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| Product | Description | |
|---|---|---|
| EDTA Acid | EDTA Acid. CAS No. 60-00-4. Molecular Formula C10H16N2O8. Chemical Reagents |  Cater Chemicals Corp. Illinois IL |
| arachidonic acid-EDTA | arachidonic acid-EDTA. CAS No. 105028-29-3. Catalog: ACM105028293. |  |
| EDTA (Ethylenediamine-N,N,N,N-tetraacetic Acid), 99.4-100.6% ACS | Ethylenediamine-N,N,N,N-tetraacetic Acid (EDTA) is a powerful chelating agent which forms stable complexes with most metal ions. EDTA is used in treatment of lead and heavy metal poisoning of farm animals. Group: Biochemicals. Alternative Names: N, N-1, 2-Ethanediylbis[N- (carboxymethyl) glycine; Celon ATH; Cheelox; EDTA; Edathamil; Edetic acid; Endrate; Ethylene-N,N'-biscarboxymethyl-N,N'-diglycine; Ethylene dinitrilotetraacetic Acid; Sequestric Acid; Sequestrol; Titriplex; Trilon BW; Trilon BX; Versene. Grades: ACS Grade. CAS No. 60-00-4. Pack Sizes: 100g, 500g, 1Kg, 2.5Kg. Molecular Formula: C??H??N?O?, Molecular Weight: 292.24. US Biological Life Sciences. |  Worldwide |
| EDTA (Ethylenediamine tetraacetic acid) | 100g Pack Size. Group: Ligands. Formula: (HO2CCH2)2NCH2CH2N(CH2CO2H)2. CAS No. 60-00-4. Prepack ID 18670081-100g. Molecular Weight 292.24. See USA prepack pricing. |  |
| EDTA (Ethylenediamine tetraacetic acid) | 1kg Pack Size. Group: Ligands. Formula: (HO2CCH2)2NCH2CH2N(CH2CO2H)2. CAS No. 60-00-4. Prepack ID 18670081-1kg. Molecular Weight 292.24. See USA prepack pricing. | |
| EDTA Iron(III) sodium salt (Ethylene diaminetetraacetic acid iron(III), Edathamil, Komplexon® II) | Used to eliminate inhibition of enzyme catalyzed reactions due to traces of heavy metals. Group: Biochemicals. Alternative Names: (Ethylenedinitrilo) tetraacetato]ferrate (1-) Sodium; (OC-6-21) -[[N, N'-1, 2-Ethanediylbis[N- (carboxymethyl) glycinato]] (4-) -N, N', O, O', ON, ON']ferrate (1-) Sodium; (OC-6-21)-[[N, N'-1, 2-Ethanediylbis[N-[(carboxy-κ O)methyl]glycinato-κ N, κ O]](4-)]-Ferrate(1-) Sodium; Sodium [ (ethylenedinitrilo) tetraacetato]ferrate (III) ; AL 3037A; Edathamil Monosodium Ferric Salt; Ethylene diaminetetraacetic Acid Ferric Monosodium Salt; Fe-EDTA; Ferisan; Ferrazone; Ferric Sodium EDTA; Ferric Sodium edetate; Ferric Sodium Ethylene diaminetetraacetate; Ferrostrane; Ferrostrene; Ferroxx; Iron Monosodium EDTA; Iron Sodium EDTA; Iron Sodium ethylene diaminetetraacetate; Iron Sodium Ethylene diaminetetraacetate (1:1:1); Monosodium ferric EDTA; NSC 5237; Sequestrene NaFe; Sodium (N, N, N', N'-Ethylene diaminetetraacetato) ferrate (1-) . Grades: Purified. CAS No. 15708-41-5. Pack Sizes: 50g. Molecular Formula: C??H??FeN?NaO?. US Biological Life Sciences. | Worldwide |
| Ethylenediaminetetraacetic (EDTA) Acid 98% Powder | Ethylenediaminetetraacetic (EDTA) Acid 98% Powder. |  CA, FL & NJ |
| [S-Methane thiosulfonyl cysteaminyl ] ethyl ene diamine-N, N, N', N'-Tetraacetic Acid (MTS-EDTA) | A thiol reactive iron chelator. Group: Biochemicals. Alternative Names: MTS-EDTA. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| 1-(4-Isothiocyanatobenzyl)ethylenediamine-N,N,N',N'-tetraacetic acid | Heterocyclic Organic Compound. Alternative Names: 1-(4-ISOTHIOCYANATOBENZYL)ETHYLENEDIAMINE-N,N,N',N'-TETRAACETIC ACID;ISOTHIOCYANATOBENZYL-EDTA;1-(4-isothiocyanatobenzyl)ethylenedia-mine-tetraac. acid; Isothiocyanobenzyl-Edta; 1-(4-Isothiocyanatobenzyl)ethylenediamine; Tetraac.acid. CAS No. 105394-74-9. Molecular formula: C18H21N3O8S. Mole weight: 439.44. Catalog: ACM105394749. | |
| Acetyl-CoA Carboxylase 1 from Human, Recombinant | Acetyl-CoA Carboxylase (ACC) regulates the metabolism of fatty acids. This enzyme catalzes the formation of Malonyl CoA through the irreversible carboxylation of acetyl CoA. There are two main isoforms of Acetyl-CoA carboxylase expressed in mammals, Acetyl-CoA carboxylase 1 (ACACA) and Acetyl-CoA carboxylase 2 (ACACB). ACACA has broad tissue distribution but is enriched in tissues critical for fatty acid sythesis such as adipose tissue. ACACB is enriched in tissues such as skeletal muscle and heart that are critical for fatty acid oxidation. The Acetyl-CoA Carboxylase enzymes are activated by Citrate, glutamate, and dicarboxylic acids and negatively regulated by long ...he study of enzyme kinetics, screening inhibitors, and selectivity profiling. Group: Enzymes. Synonyms: ACAC; ACACA; ACC1; ACC; ACCA; acetyl-CoA carboxylase alpha; acetyl coenzyme A carboxylase; acetyl-CoA carboxylase. Enzyme Commission Number: EC 6.4.1.2. CAS No. 9023-93-2. ACC. Mole weight: 292.5 kDa. Activity: > 20 units/μg protein. Storage: Store at -70°C. Avoid multiple freeze-thaw cycles. Form: Supplied as a solution in 50 mM Tris-HCl, pH 8.0, 275 mM NaCl, 10% glycerol, 1 mM EDTA and 2 mM DTT. Source: Sf9 cells. Species: Human. ACAC; ACACA; ACC1; ACC; ACCA; acetyl-CoA carboxylase alpha; acetyl coenzyme A carboxylase; acetyl-CoA carboxylase. Cat No: NATE-0942. |  |
| Acetyl-CoA Carboxylase 2 from Human, Recombinant | Acetyl-CoA Carboxylase (ACC) regulates the metabolism of fatty acids. This enzyme catalzes the formation of Malonyl CoA through the irreversible carboxylation of acetyl CoA. There are two main isoforms of Acetyl-CoA carboxylase expressed in mammals, Acetyl-CoA carboxylase 1 (ACACA) and Acetyl-CoA carboxylase 2 (ACACB). ACACA has broad tissue distribution but is enriched in tissues critical for fatty acid sythesis such as adipose tissue. ACACB is enriched in tissues such as skeletal muscle and heart that are critical for fatty acid oxidation. The Acetyl-CoA Carboxylase enzymes are activated by Citrate, glutamate, and dicarboxylic acids and negatively regulated by long ...ercise. the enzyme also may be used for acc regulation study in anti-obesity and anti-type 2 diabetes therapeutics. Group: Enzymes. Synonyms: ACACB; ACC2; acetyl-CoA carboxylase beta; acetyl coenzyme A carboxylase; acetyl-CoA carboxylase. Enzyme Commission Number: EC 6.4.1.2. CAS No. 9023-93-2. ACC. Mole weight: 277 kDa. Activity: > 25 units/μg protein. Storage: Store at -70°C. Avoid multiple freeze-thaw cycles. Form: Supplied as a solution in 50 mM Tris-HCl, pH 8.0, 275 mM NaCl, 10% glycerol, 1 mM EDTA and 2 mM DTT. Source: Sf9 cells. Species: Human. ACACB; ACC2; acetyl-CoA carboxylase beta; acetyl coenzyme A carboxylase; acetyl-CoA carboxylase. Cat No: NATE-0943. | |
| α(1-2,3) Mannosidase from Xanthomonas manihotis, Recombinant | α-Mannosidase is an acid hydrolase which is located in plant vacuoles and is thought to be involved with the turnover of N-linked glycoproteins. α-Mannosidase has been shown to inhibit the proliferation of B-lymphocytes. Α1-2,3 mannosidase is a highly specific exoglycosidase that catalyzes the hydrolysis of α1-2 and α1-3 linked d-mannopyranosyl residues from oligosaccharides. Group: Enzymes. Synonyms: alpha-D-mannosidase; alpha-mannosidase; alpha-D-mannoside mannohydrolase; α-D-Mannosidase; EC 3.2.1.24; 9025-42-7. Mannosidase. Mole weight: 90 kDa. Activity: 80,000 units/mg. Storage: 4°C. Form: 50 mM NaCl, 20 mM Tris-HCl (pH 7.5 25°C) and 1 mM Na2 EDTA. Source: E. coli. Species: Xanthomonas manihotis. alpha-D-mannosidase; alpha-mannosidase; alpha-D-mannoside mannohydrolase; α-D-Mannosidase; EC 3.2.1.24; 9025-42-7; α(1-2,3) Mannosidase. Cat No: NATE-1269. | |
| α(2?3,6,8,9) Neuraminidase from Arthrobacter ureafaciens, Recombinant | Neuraminidase is the common name for Acetyl-neuraminyl hydrolase (Sialidase). α2-3,6,8,9 Neuraminidase catalyzes the hydrolysis of all linear and branched non-reducing terminal sialic acid residues from glycoproteins and oligosaccharides. The enzyme releases α2-3 and α2-6 linkages at a slightly higher rate than α2-8 and α2-9 linkages. Group: Enzymes. Synonyms: neuraminidase; sialidase; α-neuraminidase; acetylneuraminidase; exo-α-sialidase; EC 3.2.1.18; 9001-67-6; α2-3,6,8,9 Neuraminidase A; α2-3,6,8,9 Neuraminidase; α(2?3,6,8,9) Neuraminidase. Enzyme Commission Number: EC 3.2.1.18. CAS No. 9001-67-6. Neuraminidase. Mole weight: 100,000 daltons. Activity: ~316,000 units/mg. Storage: at -20°C. Form: Supplied in: 50 mM NaCl, 20 mM Tris-HCl (pH 7.5 @ 25°C) and 1 mM EDTA. Source: E. coli. Species: Arthrobacter ureafaciens. neuraminidase; sialidase; α-neuraminidase; acetylneuraminidase; exo-α-sialidase; EC 3.2.1.18; 9001-67-6; α2-3,6,8,9 Neuraminidase A; α2-3,6,8,9 Neuraminidase; α(2?3,6,8,9) Neuraminidase. Cat No: NATE-0758. | |
| α(2-3) Neuraminidase S from Streptococcus pneumoniae, Recombinant | Neuraminidase enzymes are glycoside hydrolase enzymes (EC 3.2.1.18) that cleave the glycosidic linkages of neuraminic acids. Neuraminidase enzymes are a large family, found in a range of organisms. The best-known neuraminidase is the viral neuraminidase, a drug target for the prevention of the spread of influenza infection. The viral neuraminidases are frequently used as antigenic determinants found on the surface of the Influenza virus. Some variants of the influenza neuraminidase confer more virulence to the virus than others. Other homologs are found in mammalian cells, which have a range of functions. Neuraminidase is the common name for acetyl-neurami...;2-3 linked n-acetyl-neuraminic acid residues from glycoproteins and oligosaccharides. Group: Enzymes. Synonyms: neuraminidase; sialidase; α-neuraminidase; acetylneuraminidase; exo-α-sialidase; EC 3.2.1.18; 9001-67-6. Purity: > 95% determined by SDS-PAGE. Neuraminidase. Mole weight: 74000 daltons. Activity: 160,000 units/mg. Storage: at -20°C. Form: 50 mM NaCl, 20 mM Tris-HCl (pH 7.5 25°C) and 1 mM EDTA. Source: E. coli. Species: Streptococcus pneumoniae. neuraminidase; sialidase; α-neuraminidase; acetylneuraminidase; exo-α-sialidase; EC 3.2.1.18; 9001-67-6; α(2-3) Neuraminidase S; α(2-3) Neuraminidase. Cat No: NATE-1275. | |
| Calcium disodium edetate hydrate | Calcium disodium edetate hydrate is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: EDTA disodium calcium salt hydrate; Ethylenediaminetetraacetic acid disodium calcium salt hydrate. CAS No. 23411-34-9. Pack Sizes: 100 mg. Product ID: HY-W250119. |  |
| Calmodulin-dependent Protein Kinase II from Rat, Recombinant | Serine-threonine protein kinase:these kinases appear to be involved in neurotransmitter release, control of stimulus-induced gene expression, and in the phosphorylation of microtubule related proteins. Calmodulin-dependent protein kinase ii (camkII) is a serine/threonine kinase. it is a ca2+/calmodulin-dependent, truncated monomer (1-325 amino acid residues) of the α subunit. autophosphorylation of threonine 286 in the presence of ca2+ and calmodulin activates camkii and produces substantial ca2+/calmodulin-independent activity. Group: Enzymes. Synonyms: Calmodulin-dependent Protein Kinase II; 9026-43-1. Purity: > 95% determined by SDS-PAGE. Calmodulin-dependent Protein Kinase II. Mole weight: Apparent: 33 kDa Theoretical: 36 kDa. Activity: 5,000,000 units/mg. Storage: at -70°C. Avoid repeated freeze/thaw cycles. Form: 100 mM NaCl, 50 mM HEPES (pH 7.5 25°C), 0.1 mM EDTA, 1 mM DTT, 0.01% Brij 35 and 50% glycerol. Source: S. frugiperda Sf9. Species: Rat. Calmodulin-dependent Protein Kinase II; 9026-43-1; CaMKII. Cat No: NATE-1273. | |
| Disodium edetate | Disodium edetate. Product ID: PE-0311. Molecular formula: C10H14N2Na2O8 · 2H2O. Category: Mucosal Drug Delivery Systems Materials. Product Keywords: Pharmaceutical Excipients; Mucosal Drug Delivery Systems Materials; Disodium edetate; PE-0311; C10H14N2Na2O8 · 2H2O. Appearance: Crystals. Synonym(s): Ethylenediaminetetraacetic acid disodium salt dihydrate, Disodium ethylenediaminetetraacetate dihydrate, EDTA disodium salt, EDTA-Na2, Edathamil, Edetate disodium salt dihydrate, Sequestrene Na2. Storage: 2-8°C. Melting Point: 248 °C (dec.) (lit.). |  |
| Dispase II | Dispase II is a neutral protease that hydrolyzes the N-terminal peptide bonds of non-polar amino acid residues. It may be used for separating many tissues and cells grown in vitro. The enzyme is very gentle and does not damage cell membranes. It can also be used to prevent clumping in suspension cultures. This protease cleaves fibronectin and type IV collagen, but not laminin, type V collagen, serum albumin, or transferrin.[3] Dispase II is specific for the cleavage of Leucine-Phenylalanine bonds. Ca2+, Mg2+, Mn2+, Fe2+, Fe3+ and Al3+ activate the enzyme. EDTA, EGTA, Hg2+ and other heavy metals inhibit the enzyme activity.[6] The enzyme contains 1g-atom of zinc per g-mol of purified enzyme. If this zinc component is removed by chelating agents such as EDTA or EGTA, an inactive apoenzyme is obtained. The enzyme is not inhibited by serum. Group: Biochemicals. Grades: Highly Purified. CAS No. 42613-33-2. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. US Biological Life Sciences. | Worldwide |
| EDTA | Food Additives, Flavours & Adulterants; Standards for Food Regulatory Methods; Metal alloys. Uses: For analytical and research use. Group: Reagents. Alternative Names: Dissolvine NA-X, EDTA, Ethylenediaminetetraacetate, Techrun DO, Versene, Cheelox, N,N'-1,2-Ethanediylbis[N-(carboxymethyl)glycine], Nullapon B acid, Sequestrene AA, Titriplex II, Perma Kleer 50 acid, Sequestric acid, Zonon AO, Dissolvine E, Celon A, Chelest 3A, Edetic acid, PrefGel, Trilon BW, Nullapon BF acid, Gluma Cleanser, Nervanaid B acid, Complexon II, WS,Glycine, N,N'-1,2-ethanediylbis[N-(carboxymethyl)-, Acetic acid, (ethylenedinitrilo)tetra- (8CI), Endrate, Clewat TAA, NSC 97404, Sequestrol, Dotite 4H, EDETA B, EDTA (chelating agent), Quastal Special, Dissolvine Z, NSC 97243, Sequestrene K 4, Ethylenedinitrilotetraacetic acid, Chemcolox 340, Ethylene-N,N'-biscarboxymethyl-N,N'-diglycine, Havidote, YD 30, Clewat TTA, Celon ATH, Ethylenediamine-N,N,N',N'-tetraacetic acid, Trilon BS, 3,6-Diazaoctanedioic acid, 3,6-bis(carboxymethyl)-, ICRF 185, WS (chelating agent), Titriplex, Acroma DH 700, Ethylenediaminetetraacetic acid, Chelest A, Edathamil, Acetic acid, 2,2',2'',2'''-(1,2-ethanediyldinitrilo)tetrakis-, Metaquest A, 2,2',2'',2'''-(ethane-1,2-diylbis(azanetriyl))tetraacetic acid. CAS No. 60-00-4. IUPAC Name: 2-[2-[bis(carboxymethyl)amino]ethyl-(carboxymethyl)amino]acetic acid. |  |
| EDTA dipotassium dihydrate | EDTA dipotassium dihydrate is a metal ion chelator that forms stable and water-soluble chelates with a variety of metal ions. EDTA dipotassium is commonly used as a blood anticoagulant, which can effectively prevent blood coagulation and maintain the morphology and function of cells in blood samples. In the industrial field, EDTA dipotassium can be used to remove the adverse effects of metal ions and prevent oxidation and deterioration caused by metal ions [1] [2]. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: Ethylenediaminetetraacetic acid dipotassium dihydrate. CAS No. 25102-12-9. Pack Sizes: 50 g; 100 g. Product ID: HY-D0836. | |
| EDTA disodium | EDTA disodium salt, also known as ethylenediaminetetraacetic acid disodium, belongs to the chelating agent category, which is formed by chelating a central metal ion with four carboxylate groups and two amine groups. This compound, with its ability to bind and chelate metal ions such as calcium, magnesium and iron, is commonly used in a variety of applications, including industrial, medical and research settings. It is used as a preservative in food and beverage, as a stabilizer in medicine, as a chelating agent in water treatment, and as a reagent in biochemical and biomedical research. In addition, EDTA disodium salt has been studied for potential research effects such as improving heavy metal poisoning and cardiovascular disease. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: Ethylenediaminetetraacetic acid disodium. CAS No. 139-33-3. Pack Sizes: 10 g; 25 g. Product ID: HY-W018746. | |
| EDTA Disodium Salt, 0.25M Solution | Ultrapure solution for electrophoresis, manufactured with 99%+ EDTA and Molecular Biology Grade water. Sterile and nuclease free. Group: Biochemicals. Alternative Names: Edetate disodium salt dihydrate; Disodium ethylene diaminetetraacetate dihydrate; Edathamil; Ethylene diaminetetraacetic acid disodium salt dihydrate; EDTA-Na2; Sequestrene Na2. Grades: Molecular Biology Grade. CAS No. 6381-92-6. Pack Sizes: 100ml, 500ml, 1L, 2.5L, 4L. Molecular Formula: C10H14N2O8Na2 2H2O, Molecular Weight: 372.24. US Biological Life Sciences. | Worldwide |
| EDTA Disodium Salt Dihydrate | Used as an ingredient in electrophoresis buffers and as a routine protectant of DNA. Hexadentate chelator. Group: Biochemicals. Alternative Names: Edetate disodium salt dihydrate; Disodium ethylene diaminetetraacetate dihydrate; Edathamil; Ethylene diaminetetraacetic acid disodium salt dihydrate; EDTA-Na2; Sequestrene Na2. Grades: Molecular Biology Grade. CAS No. 6381-92-6. Pack Sizes: 100g, 500g, 1Kg, 2.5Kg, 5Kg, 10Kg. Molecular Formula: C10H14N2O8Na2 2H2O, Molecular Weight: 372.24. US Biological Life Sciences. | Worldwide |
| EDTA iron sodium | EDTA iron sodium (NaFeEDTA; Sodium iron EDTA) is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: Ethylenediaminetetraacetic acid iron sodium. CAS No. 15708-41-5. Pack Sizes: 10 mM * 1 mL; 100 g. Product ID: HY-131926. | |
| Ethanolamine hydrochloride | Ethanolamine hydrochloride, is an organic compound used in various industrial applications. It is a white or colorless solid that is soluble in water and has a faint odor. One of the major uses of Ethanolamine hydrochloride is in the production of detergents and surfactants. Used as a raw material in the manufacture of compounds such as ethylenediaminetetraacetic acid (EDTA) and diethanolamine, which are commonly used in household and industrial cleaning products. Ethanolamine hydrochloride is also used in the synthesis of pharmaceuticals, agrochemicals and rubber processing agents. It acts as a buffer in certain chemical reactions, helping to adjust pH and maintain stability. Ethanolamine hydrochloride can be used for gas purification and metal corrosion inhibitor. Its ability to react with acid gases such as carbon dioxide and sulfur dioxide makes it useful for removing impurities from natural gas and other industrial gases. Overall, Ethanolamine hydrochloride is a multifunctional compound with many potential industrial applications. Its ability to act as a buffer, chelating agent, and corrosion inhibitor makes it an important tool in a variety of industries. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: 2-Aminoethanol hydrochloride. CAS No. 2002-24-6. Pack Sizes: 25 g; 50 g. Product ID: HY-W035903. | |
| Ethylenediamine-N,N,N,N-tetraacetic Acid-13C4 | Labeled Ethylene diaminetetraacetic Acid. EDTA is a powerful chelating agent; EDTA forms stable complexes with most metal ions. EDTA is used in treatment of lead and heavy metal poisoning of farm animals. Group: Biochemicals. Alternative Names: N,N-1,2-Ethanediylbis[N-(carboxymethyl)glycine-13C4; Celon ATH-13C4; Cheelox-13C4; EDTA-13C4; Edathamil-13C4; Edetic Acid-13C4; Endrate-13C4; Ethylene-N,N'-biscarboxymethyl-N,N-diglycine-13C4; Ethylene dinitrilotetraacetic Acid-13C4; Sequestric Acid-13C4; Sequestrol-13C4; Titriplex-13C4; Trilon BW-13C4; Trilon BX-13C4; Versene-13C4. Grades: Highly Purified. CAS No. 1215408-17-5. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Ethylenediaminetetraacetic acid | Ethylenediaminetetraacetic acid (EDTA) is a kind of metal chelating agent (binds to bivalent and trivalent metal cations, including calcium). Ethylenediaminetetraacetic acid has antibacterial, anti-inflammatory, antioxidant, anti-hypercalcemia and anticoagulant activities. Ethylenediaminetetraacetic acid decreases the metal ion-catalyzed oxidative damage to proteins, and allows maintenance of reducing environment during protein purification. Ethylenediaminetetraacetic acid can alleviate the liver fibrosis. Ethylenediaminetetraacetic acid can be used for coronary artery disease and neural system disease research [1] [2] [3] [4] [5] [6] [7]. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: EDTA. CAS No. 60-00-4. Pack Sizes: 500 mg; 1 g. Product ID: HY-Y0682. | |
| Ethylenediaminetetraacetic acid | Ethylenediaminetetraacetic acid. Synonyms: (Ethylenedinitrilo)tetraacetic acid, EDTA, Edathamil, Ethylenedinitrilotetraacetic acid. CAS No. 60-00-4. Pack Sizes: 100, 500 g in poly bottle. Product ID: CDC10-0093. Molecular formula: C10H16N2O8. Category: Cosmetic Chelating Chemicals. Product Keywords: Cosmetic Ingredients; Cosmetic Chelating Chemicals; Ethylenediaminetetraacetic acid; CDC10-0093; 60-00-4; C10H16N2O8; (Ethylenedinitrilo)tetraacetic acid, EDTA, Edathamil, Ethylenedinitrilotetraacetic acid; 200-449-4; MFCD00003541; 60-00-4. Purity: 99.4-100.6%. Color: White to almost white. EC Number: 200-449-4. Physical State: Powder. Solubility: water: soluble 0.4 g/L at 20 °C. Quality Level: 200. Storage: 2-8°C. Boiling Point: 434.18°C (rough estimate). Melting Point: 250 °C (dec.) (lit.). Density: 1.46 g/cm3 at 20 °C. Product Description: Ethylenediaminetetraacetic acid (EDTA) is a hydrophilic metal chelating agent that transforms metal ions into inactive, cyclic metal complexes. Hence, it has industrial application for resolving metal contamination. | |
| Ethylenediaminetetraacetic acid | Ethylenediaminetetraacetic acid. Synonyms: (Ethylenedinitrilo)tetraacetic acid, EDTA, Edathamil, Ethylenedinitrilotetraacetic acid. CAS No. 60-00-4. Product ID: PE-0106. Molecular formula: C10H16N2O8. Category: Antioxidants. Product Keywords: Pharmaceutical Excipients; Injections & Sterile Formulation; Antioxidants; Ethylenediaminetetraacetic acid; PE-0106; C10H16N2O8; 60-00-4; 60-00-4. Purity: 99.4-100.6%. Color: White to almost white. EC Number: 200-449-4. Physical State: Powder. Synonym(s): EDTA. Solubility: water: soluble 0.4 g/L at 20 °C. Quality Level: 200. Storage: 2-8°C. Boiling Point: 434.18°C (rough estimate). Melting Point: 250 °C (dec.) (lit.). Density: 1.46 g/cm3 at 20 °C. Product Description: Ethylenediaminetetraacetic acid (EDTA) is a hydrophilic metal chelating agent that transforms metal ions into inactive, cyclic metal complexes. Hence, it has industrial application for resolving metal contamination. | |
| Ethylenediaminetetraacetic Acid | ETHYLENEDIAMINETETRAACETIC ACID, ACS Reagent, powder (Synonym: EDTA, Free Acid; (Ethylenedinitrilo)tetraacetic Acid), Formula: C10H16N2O8. CAS No. 60-00-4. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today! |  Texas TX |
| Ethylenediaminetetraacetic Acid | ETHYLENEDIAMINETETRAACETIC ACID, DISODIUM, DIHYDRATE, ACS Reagent, crystalline powder, (Disodium EDTA; (Ethylenedinitrilo)tetraacetic Acid Disodium Salt),Formula: C10H14O8N2Na2.2H2O. CAS No. 6381-92-6. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today! | Texas TX |
| Ethylenediaminetetraacetic acid dipotassium salt dihydrate | Ethylenediaminetetraacetic acid dipotassium salt dihydrate. Synonyms: (Ethylenedinitrilo)tetraacetic acid dipotassium salt, Dipotassium ethylenediaminetetraacetate dihydrate, EDTA dipotassium salt, Edathamil, Potassium ethylenediaminetetraacetate dibasic. CAS No. 25102-12-9. Pack Sizes: 100, 500 g in poly bottle. Product ID: CDC10-0106. Category: Cosmetic Chelating Chemicals. Product Keywords: Cosmetic Ingredients; Cosmetic Chelating Chemicals; Ethylenediaminetetraacetic acid dipotassium salt dihydrate; CDC10-0106; 25102-12-9; (Ethylenedinitrilo)tetraacetic acid dipotassium salt, Dipotassium ethylenediaminetetraacetate dihydrate, EDTA dipotassium salt, Edathamil, Potassium ethylenediaminetetraacetate dibasic; 217-895-0; 25102-12-9. Purity: ≥98%. Color: White. EC Number: 217-895-0. Physical State: Powder. Solubility: 3 M KOH: 160 mg/mL, clear to very slightly hazy, colorless to faintly yellow. Quality Level: 200. Storage: room temp. Boiling Point: N/A. Melting Point: 255-280 °C (dec.) (lit.). | |
| Ethylenediaminetetraacetic acid disodium cobalt salt | Heterocyclic Organic Compound. Alternative Names: Ethylenediamine-N,N,N',N'-tetraacetic acid cobalt-disodium salt;EDTA.Na2Co;ETHYLENEDIAMINE-N,N,N'',N''-TETRAACETIC ACID COBALT(II) DISODIUM SALT TETRAHYDRATE (CO(II)-EDTA);Ethylenediamine tetraacetic Acid Cobalt(?)Disodium Salt. CAS No. 11079-03-1. Molecular formula: C10H12Co2N2Na4O8. Mole weight: 498.03636. Catalog: ACM11079031. | |
| Ethylenediaminetetraacetic acid disodium dihydrate | Ethylenediaminetetraacetic acid (EDTA) disodium dehydrate is a kind of metal chelating agent (binds to bivalent and trivalent metal cations, including calcium). Ethylenediaminetetraacetic acid disodium dehydrate has antibacterial, anti-inflammatory, antioxidant, anti-hypercalcemia and anticoagulant activities. Ethylenediaminetetraacetic acid disodium dehydrate decreases the metal ion-catalyzed oxidative damage to proteins, and allows maintenance of reducing environment during protein purification. Ethylenediaminetetraacetic acid disodium dehydrate can alleviate the liver fibrosis. Ethylenediaminetetraacetic acid disodium dehydrate can be used for coronary artery disease and neural system disease research [1] [2] [3] [4] [5] [6] [7]. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: EDTA disodium dihydrate. CAS No. 6381-92-6. Pack Sizes: 500 mg; 1 g. Product ID: HY-Y0682A. | |
| Ethylenediaminetetraacetic acid disodium salt | Ethylenediaminetetraacetic acid disodium salt. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: EDTA; sodium 2, 2'- ( (2- (bis (carboxymethyl) amino) ethyl) azanediyl) diacetate. CAS No. 139-33-3. Molecular Formula: C10H14N2Na2O8. Mole Weight: 336.21. Catalog: APB139333. | |
| Ethylenediaminetetraacetic acid disodium salt dihydrate | Ethylenediaminetetraacetic acid disodium salt dihydrate. Synonyms: Disodium ethylenediaminetetraacetate dihydrate, EDTA disodium salt, EDTA-Na2, Edathamil, Edetate disodium salt dihydrate, Sequestrene Na2. CAS No. 6381-92-6. Pack Sizes: 50, 100, 250, 500 g in poly bottle. Product ID: CDC10-0107. Molecular formula: C10H14N2Na2O8·2H2O. Category: Cosmetic Chelating Chemicals. Product Keywords: Cosmetic Ingredients; Cosmetic Chelating Chemicals; Ethylenediaminetetraacetic acid disodium salt dihydrate; CDC10-0107; 6381-92-6; C10H14N2Na2O8·2H2O; Disodium ethylenediaminetetraacetate dihydrate, EDTA disodium salt, EDTA-Na2, Edathamil, Edetate disodium salt dihydrate, Sequestrene Na2; 205-358-3; MFCD00150037; 6381-92-6. Purity: 99.0-101.0% (titration). EC Number: 205-358-3. Physical State: Powder. Solubility: Soluble in water (100 g/L) at 20 °C, and 3 M NaOH (100 mg/ml). Quality Level: 300. Storage: Store at room temperature. Boiling Point: >100° C. Melting Point: 248 °C (dec.) (lit.). Density: 1.01 g/cm3 at 25° C. Product Description: EDTA, Disodium Salt, Dihydrate is an extensively used chelator of divalent cations such as Ca2+. EDTA (Ethylenediaminetetraacetic acid) is a chelating agent, a general chemical, and a sequestrant. In molecular biology applications, it is used to minimize metal ion contaminants. Also used to facilitate enzymatic reactions that could be inhibited by heavy | |
| Ethylenediaminetetraacetic Acid Disodium Salt, Dihydrate, Reagent Grade, 100 g | Formula: C10H14N2Na2O8 2H2O. Formula Wt: 372. 24. Characteristic: White powder; metal chelating agent. Notes: More water-soluble than EDTA free acid. Storage Code: Green; general chemical storage. Alternative Names: EDTA disodium salt dihydrate. Grades: chem-grade reagent. CAS No. No. 6381-92-6. Product ID: 861778. -- SOLD FOR EDUCATIONAL USE ONLY -- |  |
| Ethylenediaminetetraacetic Acid Disodium Salt, Dihydrate, Reagent Grade, 25 g | Formula: C10H14N2Na2O8 2H2O. Formula Wt: 372. 24. Characteristic: White powder; metal chelating agent Notes: More water-soluble than EDTA free acid. Storage Code: Green; general chemical storage. Alternative Names: EDTA disodium salt dihydrate. Grades: chem-grade reagent. CAS No. No. 6381-92-6. Product ID: 861776. -- SOLD FOR EDUCATIONAL USE ONLY -- | |
| Ethylenediaminetetraacetic acid monosodium bismuth salt | Heterocyclic Organic Compound. Alternative Names: Bismuth Sodium Ethylenediaminetetraacetate, 12558-49-5, ACMC-1C27R, CTK4B4440, ANW-18344, AKOS015839770, AG-D-54004, Sodium Bismuth Ethylenediaminetetraacetate, E0086, FT-0626323, Ethylenediaminetetraacetic Acid Sodium Bismuth Salt, I14-100572, Bismuthate(1-), [(ethylenedinitrilo)tetraacetato]-, sodium (8CI); Bismuthate (1-), [[N, N-1, 2-ethanediylbis[N- (carboxymethyl)glycinato]] (4-)-N, N, O, O, ON, ON]-, sodium, (OC-6-21)-; Bismuth sodium EDTA, Bismuthate(1-),[[N,N-1,2-ethanediylbis[N-[(carboxy-kO)methyl]glycinato-kN,kO]](4-)]-, sodium, (OC-6-21)- (9CI). CAS No. 12558-49-5. Molecular formula: C10H12BiN2NaO8. Mole weight: 520.18. Purity: >98.0%(T). IUPACName: bismuth; sodium; 2-[2-[bis (carboxylatomethyl)amino]ethyl- (carboxylatomethyl)amino]acetate. Canonical SMILES: C (CN (CC (=O)[O-])CC (=O)[O-])N (CC (=O)[O-])CC (=O)[O-]. [Na+]. [Bi+3]. Catalog: ACM12558495. | |
| Ethylenediaminetetraacetic acid sodium hydrate | Ethylenediaminetetraacetic acid (EDTA) sodium hydrate is a kind of metal chelating agent (binds to bivalent and trivalent metal cations, including calcium). Ethylenediaminetetraacetic acid sodium hydrate has antibacterial, anti-inflammatory, antioxidant, anti-hypercalcemia and anticoagulant activities. Ethylenediaminetetraacetic acid sodium hydrate decreases the metal ion-catalyzed oxidative damage to proteins, and allows maintenance of reducing environment during protein purification. Ethylenediaminetetraacetic acid sodium hydrate can alleviate the liver fibrosis. Ethylenediaminetetraacetic acid sodium hydrate can be used for coronary artery disease and neural system disease research [1] [2] [3] [4] [5] [6] [7]. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: EDTA sodium hydrate. CAS No. 10378-23-1. Pack Sizes: 50 g. Product ID: HY-W105700. | |
| Ethylenediaminetetraacetic acid tetrasodium | Ethylenediaminetetraacetic acid (EDTA) tetrasodium is a kind of metal chelating agent (binds to bivalent and trivalent metal cations, including calcium). Ethylenediaminetetraacetic acid tetrasodium has antibacterial, anti-inflammatory, antioxidant, anti-hypercalcemia and anticoagulant activities. Ethylenediaminetetraacetic acid tetrasodium decreases the metal ion-catalyzed oxidative damage to proteins, and allows maintenance of reducing environment during protein purification. Ethylenediaminetetraacetic acid tetrasodium can alleviate the liver fibrosis. Ethylenediaminetetraacetic acid tetrasodium can be used for coronary artery disease and neural system disease research [1] [2] [3] [4] [5] [6] [7]. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: EDTA tetrasodium. CAS No. 64-02-8. Pack Sizes: 5 g; 10 g. Product ID: HY-Y0682B. | |
| Ethylene diaminetetraacetic acid tetrasodium salt dihydrate | Ethylene diaminetetraacetic acid tetrasodium salt dihydrate. Group: Biochemicals. Alternative Names: EDTA·4Na·2H2O; Tetrasodium ethylene diaminetetraacetate dihydrate. Grades: Highly Purified. CAS No. 10378-23-1. Pack Sizes: 1kg, 2kg, 5kg. US Biological Life Sciences. | Worldwide |
| Ethylenediaminetetraacetic acid tetrasodium salt dihydrate | Ethylenediaminetetraacetic acid tetrasodium salt dihydrate. Synonyms: EDTA tetrasodium salt, Edathamil, Tetrasodium ethylenediaminetetraacetate dihydrate. CAS No. 10378-23-1. Pack Sizes: 100, 500 g in poly bottle. Product ID: CDC10-0108. Molecular formula: (NaOOCCH2)2NCH2CH2N(CH2COONa)2 · 2H2O. Category: Cosmetic Chelating Chemicals. Product Keywords: Cosmetic Ingredients; Cosmetic Chelating Chemicals; Ethylenediaminetetraacetic acid tetrasodium salt dihydrate; CDC10-0108; 10378-23-1; (NaOOCCH2)2NCH2CH2N(CH2COONa)2 · 2H2O; EDTA tetrasodium salt, Edathamil, Tetrasodium ethylenediaminetetraacetate dihydrate; 200-573-9; MFCD00150026; 10378-23-1. Purity: 99.0-102.0% (titration). Color: Yellow-Orange. EC Number: 200-573-9. Physical State: Liquid. Solubility: H2O: soluble, clear, colorless. Quality Level: 300. Storage: room temp. Melting Point: >300°C. | |
| Ethylene diaminetetraacetic acid tetrasodium salt hydrate | Ethylene diaminetetraacetic acid tetrasodium salt hydrate. Group: Biochemicals. Alternative Names: EDTA-tetrasodium salt hydrate. Grades: Highly Purified. CAS No. 64-02-8,194491-31-1,13235-36-4. Pack Sizes: 500g, 1kg, 2kg. Molecular Formula: C10H12N2Na4O8. US Biological Life Sciences. | Worldwide |
| Ethylene diaminetetraacetic acid tripotassium salt dihydrate | Ethylene diaminetetraacetic acid tripotassium salt dihydrate. Group: Biochemicals. Alternative Names: EDTA tripotassium salt. Grades: Highly Purified. CAS No. 65501-24-8. Pack Sizes: 50g, 100g, 250g, 500kg, 1kg. Molecular Formula: C10H13K3N2O8·2H2O. US Biological Life Sciences. | Worldwide |
| Fpg Protein from Escherichia coli, Recombinant | Fpg protein, a key enzyme in the DNA base excision repair pathway (BER), catalyses the excision of a broad spectrum of modified purines such as formamidopyrimidine (Fapy) and 8-oxoguanine (8-oxo-G). Fpg possess both DNA glycosylase activity that removes the mutated base and AP-lyase activity that releases ribose, leaving both 5'-and 3'-phosphorylated ends in the DNA. Several analytical methods based on Fpg protein activity in vitro were developed for detection and quantitation of oxidative damage to DNA mainly for FapyA, FapyG and 8-oxo-G. The fpg gene was cloned by Boiteux, et al. Fpg protein possess a zinc finger motif at its C-terminus (one zinc atom per molecule). ... Protein. Mole weight: mol wt 30.2 kDa (269 amino acids, predicted from the nucleotide sequence). Activity: >20 ,000 units/mg protein. Storage: -20°C. Form: buffered aqueous glycerol solution; Solution in 50% glycerol containing 50 mM potassium HEPES, pH 7.5, 1 mM DTT, 1 mM EDTA, and 200 mM NaCl. Source: E. coli. Species: Escherichia coli. Fapy-DNA glycosylase; deoxyribonucleate glycosidase; 2,6-diamino-4-hydroxy-5N-formamidopyrimidine-DNA glycosylase; 2,6-diamino-4-hydroxy-5 (N-methyl)formamidopyrimidine-DNA glycosylase; formamidopyrimidine-DNA glycosylase; DNA-formamidopyrimidine glycosidase; Fpg protein; DNA-formamidopyrimidine glycosylase; EC 3.2.2.23; 78783-53-6; | |
| Immobilized Endoproteinase Glu-C on F7m | Endoproteinase Glu-C hydrolyzes peptide and ester linkages specifically at the carboxyl end of glutamic acid (-Glu/-X; in ammonium carbonate pH 7. 8, or ammonium acetate pH 4. 0, buffer A) or of glutamic and aspartic acid (-Glu/-X and -Asp/-X; in phosphate buffer pH 7. 8, buffer B). F7m: 1. 0 mg endoproteinase Glu-C immobilized on matrix F7m per CR-column. 900 units immobilized per CR-column. Nr. 7 Storage buffer: 50 mM Tris/HCl at pH 7. 5, 5 mM EDTA. Nr. 31 Reaction buffer A: 25 mM ammonium acetate, pH 4. 0 (see above)Nr. 32 Washing buffer A: 25 mM ammonium acetate, pH 4. 0, 1 M NaClNr. 62 Reaction buffer B: 50 mM phosphate buffer, pH 7. 8 (see above)Nr. 63 Washing buffer B: 50 mM phosphate buffer, pH 7. 8, 1 M NaCl. Group: Enzymes. Synonyms: EC 3. 4. 21. 19; Staph aureus V8 Protease; Protease, Staph aureus (Endoproteinase Glu-C); Glutamyl endopeptidase; V8 proteinase, endoproteinase Glu-C; staphylococcal serine proteinase. Enzyme Commission Number: EC 3. 4. 21. 19. Storage: 4 °C. Source: Staphylococcus aureus. EC 3. 4. 21. 19; Staph aureus V8 Protease; Protease, Staph aureus (Endoproteinase Glu-C); Glutamyl endopeptidase; V8 proteinase, endoproteinase Glu-C; staphylococcal serine proteinase; Immobilized Endoproteinase Glu-C. Cat No: NATE-1763. | |
| Immobilized Endoproteinase Glu-C on G3m | Endoproteinase Glu-C hydrolyzes peptide and ester linkages specifically at the carboxyl end of glutamic acid (-Glu/-X; in ammonium carbonate pH 7. 8, or ammonium acetate pH 4. 0, buffer A) or of glutamic and aspartic acid (-Glu/-X and -Asp/-X; in phosphate buffer pH 7. 8, buffer B). G3m: 25 ug (22 units) endoproteinase Glu-C per CR-column immobilized on dextran. This CR-column cuts at least 12 ug tubulin or 5 ug BSA per application in phosphate buffer. Nr. 7 Storage buffer: 50 mM Tris/HCl at pH 7. 5, 5 mM EDTA. Nr. 31 Reaction buffer: 25 mM NH4-acetate, pH 4. 0 (see above)Nr. 32 Washing buffer: 25 mM NH4-acetate, pH 4. 0, 1 M NaClNr. 62 Reaction buffer: 50 mM phosphate buffer, pH 7. 8 (see above)Nr. 63 Washing buffer: 50 mM phosphate buffer, pH 7. 8, 1 M NaCl. Group: Enzymes. Synonyms: EC 3. 4. 21. 19; Staph aureus V8 Protease; Protease, Staph aureus (Endoproteinase Glu-C); Glutamyl endopeptidase; V8 proteinase, endoproteinase Glu-C; staphylococcal serine proteinase. Enzyme Commission Number: EC 3. 4. 21. 19. Storage: 4 °C. Source: Staphylococcus aureus. EC 3. 4. 21. 19; Staph aureus V8 Protease; Protease, Staph aureus (Endoproteinase Glu-C); Glutamyl endopeptidase; V8 proteinase, endoproteinase Glu-C; staphylococcal serine proteinase; Immobilized Endoproteinase Glu-C. Cat No: NATE-1764. | |
| Inosine Monophosphate Dehydrogenase Type II from Human, Recombinant | Type II is the predominant IMPDH isoform and is specifically linked to a wide range of cancers and lymphocyte proliferation. Group: Enzymes. Synonyms: inosine-5'-phosphate dehydrogenase; inosinic acid dehydrogenase; inosinate dehydrogenase; inosine 5'-monophosphate dehydrogenase; inosine monophosphate dehydrogenase; IMP oxidoreductase; inosine monophosphate oxidoreductase; IMP dehydrogenase; IMP:NAD+ oxidoreductase; EC 1.1.1.205; IMPDH II; IMPDH2; IMPD 2. Enzyme Commission Number: EC 1.1.1.205. CAS No. 231-791-2. IMPDH2. Storage: -70°C. Form: Solution in 20 mM Tris-HCl, pH 8.0, containing 0.5 mM EDTA and 1 mM DTT. Source: E. coli. Species: Human. inosine-5'-phosphate dehydrogenase; inosinic acid dehydrogenase; inosinate dehydrogenase; inosine 5'-monophosphate dehydrogenase; inosine monophosphate dehydrogenase; IMP oxidoreductase; inosine monophosphate oxidoreductase; IMP dehydrogenase; IMP:NAD+ oxidoreductase; EC 1.1.1.205; IMPDH II; IMPDH2; IMPD 2. Pack: vial of > 0.002 unit. Cat No: NATE-0352. | |
| Lambda Protein Phosphatase, Recombinant | λ Protein Phosphatase (λ-PPase) is a Mn+2-dependent protein phosphatase with activity towards phosphorylated serine, threonine, tyrosine and histidine residues. It is the 221 amino-acid product of ORF221 open reading frame on bacteriophage lambda (1, 2). λ-PPase was expressed as a recombinant protein in E.coli and highly purified (2). This product is an intact enzyme of high quality without tag. Applications: Λ-ppase can be used to release phosphate groups from phosphorylated serine, threonine, tyrosine and histidine residues in proteins (2). it should be noted that different proteins are dephosphorylated at different rates. optimal reaction temperature is 30°c. inclusion of protease inhibitor cocktail and shortest incubation time is desired when assays are done with crude samples. Group: Enzymes. Synonyms: Protein phosphatase 1F; PPM1F; CAMKP; CaMKPase; FEM-2; POPX2; hFEM-2; Lambda Protein. Purity: >98% by SDS-PAGE. λ-PPase. Activity: 400,000 U/mg (400 U/ul). Storage: Store at -80°C. Avoid repeating freeze-thaw cycles. Form: 400 U/ul λ-PPase in 50mM HEPES (pH 7.5), 100mM NaCl, 2mM dithiothreitol, 0.1 mM MnCl2, 0.1mM EDTA, 50% glycerol, 0.01% Brij 35. Source: E. coli. Protein phosphatase 1F; PPM1F; CAMKP; CaMKPase; FEM-2; POPX2; hFEM-2; Lambda Protein Phosphatase; λ-PPase. Cat No: NATE-0990. | |
| L-Asparaginase from Guinea pig, Recombinant | Asparaginase (EC 3.5.1.1, USAN) or Colaspase (BAN) is an enzyme that catalyzes the hydrolysis of asparagine to aspartic acid. Asparaginases are enzymes expressed and produced by microorganisms. Group: Enzymes. Synonyms: EC 3.5.1.1; Asparaginase; Colaspase; L-asparaginase; L-asparagine amidohydrolase. Enzyme Commission Number: EC 3.5.1.1. CAS No. 9015-68-3. Purity: >99% (SDS-PAGE). Asparaginase. Mole weight: ~63 kDa. Activity: > 1,400 IU/mg. Storage: at -80°C. Form: 25 mM Tris pH7.5, 500 mM NaCl, 2 mM DTT, 1 mM EDTA. Source: E. coli. Species: Guinea pig. EC 3.5.1.1; Asparaginase; Colaspase; L-asparaginase; L-asparagine amidohydrolase. Cat No: NATE-1577. | |
| Manganese EDTA Disodium Dihydrate | Ethylene diaminetetraacetic acid manganese disodium salt hydrate is a metal chelating compound. used as an inert ingredient in non-food pesticide products. Group: Biochemicals. Alternative Names: Disodium ( (ethylenedinitrilo) tetraacetato) manganese; Disodium manganese ethylene diaminetetraacetate; EDTA disodium manganese salt; Ethylene diaminetetraacetic acid, disodium manganese salt; Glycine, N,N'-1,2-ethanediylbis(N-(carboxymethyl)-, manganese disodium salt; Manganese disodium ethylene diamine tetraacetate; Disodium ( (N, N'-ethylenebis (N- (carboxymethyl) glycinato) ) (4-) -N, N', O, O', ON, ON') manganate (2-) ; Manganate(2-), ( (N, N'-1, 2-ethanediylbis (N- ( (carboxy-kappaO) methyl) glycinato-kappaN, kappaO) ) (4-) ) -, disodium, (OC-6-21)-; Manganate(2-), ( (N, N'-1, 2-ethanediylbis (N- ( (carboxy-kappaO) methyl) glycinato-kappaN, kappaO) ) (4-) ) -, sodium (1:2), (OC-6-21)-; Manganate(2-), ( (N, N'-1, 2-ethanediylbis (N- (carboxymethyl) glycinato) ) (4-) -N, N', O, O', ON, ON') -, disodium, (OC-6-21)- (9CI); Manganate(2-), ( (ethylenedinitrilo) tetraacetato) -, disodium (8CI); [ChemIDplus] Ethylene diaminetetraacetic acid (EDTA), disodium manganese (II) salt; [EPA]. Grades: Highly Purified. CAS No. 15375-84-5. Pack Sizes: 5g, 25g, 100g. Molecular Formula: C10H12MnN2O8 2Na 2H2O, Molecular Weight: 407.1. US Biological Life Sciences. | Worldwide |
| meso-2,3-Dimercaptosuccinic acid | meso-2,3-Dimercaptosuccinic Acid is used as a chelating agent and masking agent for cadmium in EDTA titration of zinc. Detoxification of heavy metal. Uses: Api. Synonyms: (2S,3R)-2,3-bis(sulfanyl)butanedioic acid. Grades: 98 %. CAS No. 304-55-2. Molecular formula: C4H6O4S2. Mole weight: 182.22. |  |
| Native Bacillus polymyxa Dispase II | Dispase II is a neutral protease that hydrolyzes the N-terminal peptide bonds of non-polar amino acid residues. It may be used for separating many tissues and cells grown in vitro. The enzyme is very gentle and does not damage cell membranes. It can also be used to prevent clumping in suspension cultures. This protease cleaves fibronectin and type IV collagen, but not laminin, type V collagen, serum albumin, or transferrin. Dispase II is specific for the cleavage of Leucine-Phenylalanine bonds. Ca2+, Mg2+, Mn2+, Fe2+, Fe3+ and Al3+ activate the enzyme. EDTA, EGTA, Hg2+ and other heavy metals inhibit the enzyme activity. The enzyme contains 1g-atom of zinc per g-mol of purif... it has been used in the treatment of rat heart pieces during the isolation of mitochondria from rat heart. it has also been used for the isolation of dental pulp stem cells (dpscs) by enzymatic hydrolysis. these cells have been compared with dpscs isolated by explant method to analyse their stem cell and differentiation properties. Group: Enzymes. Synonyms: Dispase II; Dispase; 42613-33-2; Protease from Bacillus polymyxa. CAS No. 42613-33-2. Dispase. Activity: > 0.5 units/mg solid. Storage: 2-8°C. Form: lyophilized powder containing calcium acetate and milk sugar. Source: Bacillus polymyxa. Dispase II; Dispase; 42613-33-2; Protease from Bacillus polymyxa. Cat No: NATE-0192. | |
| Native Baker's yeast (S. cerevisiae) Pyruvate Decarboxylase | Pyruvate decarboxylase (PDC) is a homotetrameric enzyme that catalyses the decarboxylation of pyruvic acid to acetaldehyde and carbon dioxide in the cytoplasm. Pyruvate decarboxylase depends on cofactors thiamine pyrophosphate (TPP) and magnesium. PDC contains a β-α-β structure, yielding parallel β-sheets. Applications: Pyruvate decarboxylase (pdc) is used to study residues involved in thiamine pyrophosphate (tpp) binding. it is used to study the regulation of fermentation pathways in plant species. Group: Enzymes. Synonyms: Pyruvate decarboxylase; EC 4.1.1.1; α-carboxylase (ambiguous); pyruvic decarboxylase; α-ketoacid carboxylase; 2-oxo-acid carboxy-lyase; 9001-04-1; 2-Oxo-acid carboxy-lyase; PDC. Enzyme Commission Number: EC 4.1.1.1. CAS No. 9001-4-1. PDC. Activity: 5.0-20.0 units/mg protein (biuret). Storage: 2-8°C. Form: ammonium sulfate suspension; Suspension in 3.2 M (NH4)2SO4 pH 6.5, stabilized with 5% glycerol, 5 mM potassium phosphate, 1 mM magnesium acetate, 0.5 mM EDTA, and 25 μM c ocarboxylase. Source: Baker's yeast (S. cerevisiae). Pyruvate decarboxylase; EC 4.1.1.1; α-carboxylase (ambiguous); pyruvic decarboxylase; α-ketoacid carboxylase; 2-oxo-acid carboxy-lyase; 9001-04-1; 2-Oxo-acid carboxy-lyase; PDC. Cat No: NATE-0510. | |
| Native Clostridium perfringens (C. welchII) Phospholipase C | Phospholipase C is induced by thrombin and platelet-activating factor, forming 1,2-diacylglycerol and phosphatidic acid. PLC hydrolyzes the phosphate bond on phosphatidylcholine and other glycerophospholipids yielding diacylglycerol; this enzyme will also hydrolyze the phosphate bonds of sphingomyelin, cardiolipin, choline plasmalogen and ceramide phospholipids. Group: Enzymes. Synonyms: Phospholipase C; PLC; 9001-86-9; lipophosphodiesterase I; lecithinase C; Clostridium welchii α-toxin; Clostridium oede. Enzyme Commission Number: EC 3.1.4.3. CAS No. 9001-86-9. Phospholipase C. Activity: Type I, > 150 units/mg protein; Type II, 10-50 units/mg protein; Type III, Type IV, > 1,000 units/mg protein (Lowry). Storage: -20°C. Form: Type I, Lyophilized powder in buffered salts; Type II, lyophilized powder; Type III, buffered aqueous glycerol solution; Solution in 60% (v/v) glycerol containing 10 mM Tris-HCl, pH 8.0 and 10 mM EDTA; Type IV, lyophilized powder, Contains phosphate buffer salts, EDTA and stabilizer. Source: Clostridium perfringens (C. welchII). Phospholipase C; PLC; 9001-86-9; lipophosphodiesterase I; lecithinase C; Clostridium welchii α-toxin; Clostridium oedematiens β-and γ-toxins; lipophosphodiesterase C; phosphatidase C; heat-labile hemolysin; α-toxin; EC 3.1.4.3. Cat No: NATE-0593. | |
| Native Crotalus adamanteus venom Phosphodiesterase I | Venom exonuclease (Phosphodiesterase I) successively hydrolyzes 5'-mononucleotides from 3'-OH-terminated ribo- and deoxyribo-oligonucleotides. The enzyme has an optimal pH range of 9.8-10.4 and a molecular weight of 115 kDa. Phosphodiesterase is inhibited by reducing agents such as glutathione, cysteine and ascorbic acids. It is completely inhibited by 5mM EDTA while ATP, ADP and AMP are partial inhibitors. The enzyme has an absolute requirement for Mg2+. Group: Enzymes. Synonyms: Phosphodiesterase I; EC 3.1.4.1; 5'-exonuclease; 5'-phosphodiesterase; 5'-nucleotide phosphodiesterase; oligonucleate 5'-nucleotidohydrolase; 5' nucleotide phosphodiesterase/alkaline phosphodiesterase I; 5'-NPDase; 5'-PDase; 5'-PDE; 5'NPDE; alkaline phosphodies. Enzyme Commission Number: EC 3.1.4.1. CAS No. 9025-82-5. PDE. Activity: > 20 units per mg dry weight. Storage: -20°C. Form: Lyophilized in vials. Source: Crotalus adamanteus venom. Phosphodiesterase I; EC 3.1.4.1; 5'-exonuclease; 5'-phosphodiesterase; 5'-nucleotide phosphodiesterase; oligonucleate 5'-nucleotidohydrolase; 5' nucleotide phosphodiesterase/alkaline phosphodiesterase I; 5'-NPDase; 5'-PDase; 5'-PDE; 5'NPDE; alkaline phosphodiesterase; nucleotide pyrophosphatase/phosphodiesterase I; orthophosphoric diester phosphohydrolase; PDE I; phosphodiesterase; exonuclease I. Cat No: NATE-0512. | |
| Native Escherichia coli Thioredoxin Reductase | Thioredoxin reductase (TrxR) is an NADPH-dependent oxidoreductase containing one FAD per subunit that reduces the active site disulfide in oxidised thioredoxin (Trx). The molecular weight of the isozymes from mammalian sources vary between 55-67 kDa as compared with 35 kDa in prokaryotes, plants or yeast. The substrate specificity of the mammalian enzyme is much broader than the prokaryotic enzyme reducing both mammalian and E. coli thioredoxins as well as well as non-disulfide substrates such selenite, lipoic acids, lipid hydroperoxides and hydrogen peroxide. Applications: Thioredoxin reductase from escherichia coli can be used in peroxidase-coupled thioredoxin system assay for assessing the peroxidase activitiy of cys-based thiol peroxidases. the product was used for determining the enzymatic activity of his6-ahp1p. Group: Enzymes. Synonyms: NADP-thioredoxi. Enzyme Commission Number: EC 1.8.1.9. CAS No. 9074-14-0. TrxR. Activity: >25 units/mg protein (Bradford). Storage: 2-8°C. Form: ammonium sulfate suspension; Suspension in 3.6 M (NH4)2SO4 containing 30 mM potassium phosphate buffer, pH 7.5, and 2 mM EDTA. Source: Escherichia coli. NADP-thioredoxin reductase; NADPH-thioredoxin reductase; thioredoxin reductase (NADPH); NADPH2:oxidized thioredoxin oxidoreductase; thioredoxin-disulfide reductase; EC 1.8.1.9; TrxR. Cat No: NATE-0718. | |
| Native Leuconostoc mesenteroides Dextran Sucrase | Dextransucrases are glucansucrases that are able to produce dextran, a glucose polymer linked mainly through α1-6 bonds. However, α1-3, α1-6, α1-4 and α1-2 bonds are also found, in both the main chain and the branching linkages. The peptide has approximately 1600 amino acids. The aspartic acid in position 551 is essential for catalytic activity, while glutamic acid 589 and aspartic acid 662 complement the catalytic triad. The activity of dextransucrase is decreased by EDTA, and is restored by the addition of calcium ions. Zinc, cadmium, lead, mercury and copper ions are inhibitory to various degrees. Applications: Dextran sucrase from leu... immobilized sphere for the production of dextran from sucrose. Group: Enzymes. Synonyms: EC 2.4.1.5, sucrose 6-glucosyltransferase; SGE; CEP; sucrose-1,6-α-glucan glucosyltransferase; sucrose:1,6-α-D-glucan 6-α-D-glucosyltransferase; 9032-14-8. Enzyme Commission Number: EC 2.4.1.5. CAS No. 9032-14-8. SGE. Activity: > 100 units/mg protein. Storage: -20°C. Form: Lyophilized powder containing dextran, MES buffer salts and CaCl2. Source: Leuconostoc mesenteroides. EC 2.4.1.5, sucrose 6-glucosyltransferase; SGE; CEP; sucrose-1,6-α-glucan glucosyltransferase; sucrose:1,6-α-D-glucan 6-α-D-glucosyltransferase; 9032-14-8. Cat No: NATE-0669. | |
| Native Porcine α-Ketoglutarate Dehydrogenase | The oxoglutarate dehydrogenase complex (OGDC) or α-ketoglutarate dehydrogenase complex is an enzyme complex, most commonly known for its role in the citric acid cycle. Group: Enzymes. Synonyms: 2-ketoglutarate dehydrogenase; 2-oxoglutarate dehydrogenase; 2-oxoglutarate:lipoate oxidoreductase; 2-oxoglutarate:lipoamide 2-oxidoreductase (decarboxylating and acceptor-succinylating); α-k. Enzyme Commission Number: EC 1.2.4.2. CAS No. 9031-2-1. AKGDH. Activity: 0.1-1.0 units/mg protein (Lowry). Storage: -20°C. Form: buffered aqueous glycerol solution. Supplied as a 50% glycerol solution containing ~9 mg per mL bovine serum albumin, 30% sucrose, 1.5 mM EDTA, 1.5 mM EGTA, 1.5 mM 2-mercaptoethanol, 0.3% TRITON(TM) X-100, 0.003% sodium azide, and 15 mM potassium phosphate, pH 6.8. Source: Porcine heart. Species: Porcine. 2-ketoglutarate dehydrogenase; 2-oxoglutarate dehydrogenase; 2-oxoglutarate:lipoate oxidoreductase; 2-oxoglutarate:lipoamide 2-oxidoreductase (decarboxylating and acceptor-succinylating); α-ketoglutarate dehydrogenase; αketoglutaric acid dehydrogenase; α-ketoglutaric dehydrogenase; α-oxoglutarate dehydrogenase; AKGDH; OGDC; ketoglutaric dehydrogenase; oxoglutarate decarboxylase; oxoglutarate dehydrogenase; oxoglutarate dehydrogenase (lipoamide); EC 1.2.4.2; 9031-02-1. Cat No: NATE-0495. | |
| Native Porcine Aminopeptidase M | Native amino peptidase M from porcine kidney. Metalloprotease that hydrolyzes N-terminal amino acids from almost all unsubstituted oligopeptides. Does not cleave X-Pro bonds or N-blocked amino acids. Useful in peptide sequencing. Inhibited by EDTA, bestatin, and amastatin. Group: Enzymes. Synonyms: Aminopeptidase M. Enzyme Commission Number: EC 3.4.11.2. CAS No. 9054-63-1. Aminopeptidase M. Activity: > 50 units/ml. Stability: Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 4 months at -20°C. Appearance: White crystalline suspension. Storage: 2 - 8°C. Source: Porcine kidney. Species: Porcine. Aminopeptidase M. Cat No: NATE-1912. | |
| Native Porcine Isocitric Dehydrogenase (NADP) | Isocitrate dehydrogenase (IDH) is an enzyme that catalyzes the oxidative decarboxylation of Isocitrate, producing alpha-ketoglutarate (α-ketoglutarate) and CO2. This is a two-step process, which involves oxidation of Isocitrate (a secondary alcohol) to oxalosuccinate (a ketone), followed by the decarboxylation of the carboxyl group beta to the ketone, forming alpha-ketoglutarate. In humans, IDH exists in three isoforms:IDH3 catalyzes the third step of the citric acid cycle while converting NAD+ to NADH in the mitochondria. The isoforms IDH1 and IDH2 catalyze the same reaction outside the context of the citric acid cycle and use NADP+ as a cofactor instead of NAD+. They localize to the cytosol as well as the mitochondrion and peroxisome. Group: Enzymes. Synonyms: oxalosuccinate decarboxylase; Isocitrate dehyd. Enzyme Commission Number: EC 1.1.1.42. CAS No. 9028-48-2. IDH. Activity: Type I, 0.5-3.0 unit/mg solid; Type II, 3-20 units/mg protein. Storage: -20°C. Form: Type II, buffered aqueous glycerol solution, Solution in 50% glycerol in EDTA buffer salts, pH 6.0. Source: Porcine heart. Species: Porcine. oxalosuccinate decarboxylase; Isocitrate dehydrogenase (NADP); oxalsuccinic decarboxylase; Isocitrate (NADP) dehydrogenase; Isocitrate (nicotinamide adenine dinucleotide phosphate) dehydrogenase; NADP-specific Isocitrate dehydrog | |
| Native Proteus sp. Glutamate Dehydrogenase (NADP-dependent) | Glutamate dehydrogenase (GLDH) is an enzyme, present in most microbes and the mitochondria of eukaryotes, as are some of the other enzymes required for urea synthesis, that converts glutamate to α-ketoglutarate, and vice versa. In animals, the produced ammonia is usually used as a substrate in the urea cycle. Typically, the α-ketoglutarate to glutamate reaction does not occur in mammals, as glutamate dehydrogenase equilibrium favours the production of ammonia and α-ketoglutarate. Applications: This enzyme is useful for enzymatic determination of nh3, α-ketoglutaric acid and l-glutamic acid, and for assay of leucine aminopeptidase and urea...lutamate dehydrogenase (NADP); EC 1.4.1.4; GLDH. Enzyme Commission Number: EC 1.4.1.4. Mole weight: approx. 300 kDa. Activity: 300U/mg-protein or more (9,000U/ml or more). Appearance: Solution with 50mM Tris-HCl buffer containing 0.05% NaN3 and 5.0mM EDTA, pH 7.8. Form: Freeze dried powder. Source: Proteus sp. glutamate dehydrogenase (NADP+); glutamic dehydrogenase; dehydrogenase; glutamate (nicotinamide adenine dinucleotide (phosphate)); glutamic acid dehydrogenase; L-glutamate dehydrogenase; L-glutamic acid dehydrogenase; NAD(P)-glutamate dehydrogenase; NAD(P)H-dependent glutamate dehydrogenase; glutamate dehydrogenase (NADP); EC 1.4.1.4; GLDH. Cat No: DIA-196. | |
| Native Rabbit Phosphorylase a | Phosphorylase A is the active form of glycogen phosphorylase which converts glycogen and orthophosphate (Pi) to glucose 1-phoshate (G-1-P). Phosphorylase A can be inhibited by these compounds:Polychlorinated biphenyls, polychlorinated biphenylols and polybrominated biphenyls. Dimeric phosphorylase b is converted to the more active tetramer, phosphorylase a, by the action of phosphorylase kinase. Phosphorylase a is the active form of glycogen phosphorylase which converts glycogen and orthophosphate (pi) to glucose 1-phoshate (g-1-p). Applications: Phosphorylase from rabbit muscle has been used in a study to assess the molecular mechanisms of oleanolic acid. it has also been use...mission Number: EC 2.4.1.1. CAS No. 9035-74-9. Purity: 2× crystallization. GPBB. Activity: 20-30 units/mg protein. Storage: -20°C. Form: Lyophilized powder containing β-glycerophosphate and EDTA. Source: Rabbit muscle. Species: Rabbit. Phosphorylase a; EC 2.4.1.1; 9032-10-4; muscle phosphorylase a and b; amylophosphorylase; polyphosphorylase; amylopectin phosphorylase; glucan phosphorylase; α-glucan phosphorylase; 1,4-α-glucan phosphorylase; glucosan phosphorylase; granulose phosphorylase; maltodextrin phosphorylase; muscle phosphorylase; myophosphorylase; potato phosphorylase; starch phosphorylase; 1,4-α-D-glucan:phosphate α-D-glucosyltransferase; | |
| Native Rat Thioredoxin Reductase | Thioredoxin reductase (TrxR) is an NADPH-dependent oxidoreductase containing one FAD per subunit that reduces the active site disulfide in oxidised thioredoxin (Trx). The molecular weight of the isozymes from mammalian sources vary between 55-67 kDa as compared with 35 kDa in prokaryotes, plants or yeast. The substrate specificity of the mammalian enzyme is much broader than the prokaryotic enzyme reducing both mammalian and E. coli thioredoxins as well as well as non-disulfide substrates such selenite, lipoic acids, lipid hydroperoxides and hydrogen peroxide. Applications: Thioredoxin reductase from rat liver can be used for studying the uptake and reduction of a-lipoic acid... NADP-thioredoxin reductase; NADPH-thioredoxin reductase; thioredoxin reductase (NADPH); NADPH2:oxidized thioredoxin oxidoreductase; thioredoxin-disulfide reductase; EC 1.8.1.9; TrxR; 9074-14-0. Enzyme Commission Number: EC 1.8.1.9. CAS No. 9074-14-0. TrxR. Activity: > 100 units/mg protein (Bradford). Storage: -20°C. Form: buffered aqueous glycerol solution; Solution in 50 mM Tris-HCl, pH 7.5, 300 mM NaCl, 1 mM EDTA, and 10% glycerol. Source: Rat liver. Species: Rat. NADP-thioredoxin reductase; NADPH-thioredoxin reductase; thioredoxin reductase (NADPH); NADPH2:oxidized thioredoxin oxidoreductase; thioredoxin-disulfide reductase; EC 1.8.1.9; TrxR; 9074-14-0. Cat No: NATE-0713. | |
| Native Streptomyces griseus Protease | Protease from Streptomyces griseus is a mixture of at least three proteolytic activities including an extracellular serine protease. In general, serine proteases display a wide range of substrate specificities, which are believed to be mediated by an active site composed of one Asp, one His, and a Ser residue in the molecule. This enzyme prefers to hydrolyze peptide bonds on the carboxyl side of glutamic or aspartic acid. Collected from culture broth of s. griseus and purified by successive column procedures. a mixture of at least three proteolytic activities including an extracellular serine protease. in general, serine proteases display a wide range of substrate specifici...de aldehydes and serine proteases. protease is typically used in nucleic acid isolation procedures in incubations of 0.5-3.0 hours supplemented with 0.2% sodium dodecyl sulfate and 10 mm edta. the enzyme from creative enzymes has been used for the digestion and analysis of antithrombin-heparin complexes. it has also been used for the isolation of enzyme-resistant starch. this enzyme is more active at a higher ph range than the known alkaline protease, showing the proteolytic activity even in 0.2n naoh solution. this enzyme is useful for proteolysis of insoluble protein and for structure investigation of protein. Group: Enzymes. Synonyms: Protease; 9036-06-0; Actinase E, Pro | |
| Native Tritirachium album limber Proteinase K | Proteinase K (PROK) is a serine protease with broad specificity towards aliphatic, aromatic and other hydrophobic amino acids. PROK has a molecular weight of 27,000 daltons and is Ca2+ dependent. It is not inactivated by metal ion chelating agents such as EDTA, sulfhydryl reagents, PCMB, TLCK, or TPCK. It also retains activity in 0.5% SDS. It can be inhibited by PMSF or DFP. Applications: Useful for the proteolytic inactivation of nucleases during the isolation of dna and rna. removes endotoxins that bind to cationic proteins such as lysozyme and ribonuclease a. reported useful for the isolation of hepatic, yeast, and mung bean mit ochondria determination of enzyme l o...oteinase; Tritirachium album proteinase K; endopeptidase K; 39450-01-6; protease K. Enzyme Commission Number: EC 3.4.21.64. CAS No. 39450-01-6. Purity: Purified to remove DNase and RNase. Proteinase K. Mole weight: 27 kDa. Activity: Type I, > 20 units per mg dry weight; Type II, > 400 u/ml. Storage: Powder: 2-8°C; Liquid: -20°C. Form: Type I, powder; Type II, Liquid in 20mg/ml in 10mM Tris-HCl, 1mM calcium acetate, pH 7.5 containing 50% glycerol. Source: Tritirachium album limber. Proteinase K; EC 3.4.21.64; Tritirachium alkaline proteinase; Tritirachium album serine proteinase; Tritirachium album proteinase K; endopeptidase K; 39450-01-6; protease K. Cat No: NATE-0637. | |
| Nitrate Reductase from Arabidopsis thaliana, Recombinant | Nitrate reductase (NADH) is an enzyme with system name nitrite:NAD+ oxidoreductase. This enzyme catalises the following chemical reaction:nitrite + NAD+ + H2O<-> nitrate + NADH + H+. Nitrate reductase us an iron-sulfur molybdenum flavoprotein. Applications: Catalyzes the nadh-dependent reduction of nitrate to nitrite. nitrate reductase from arabidopsis thaliana has been used in a study to assess the amino acid sequence of chicken hepatic sulfite oxidase. Group: Enzymes. Synonyms: Nitrate reductases; assimilatory nitrate reductase; NADH-nitrate reductase; NADH-dependent nitrate reductase; assimilatory NADH:nitrate reductase; nitrate reductase (NADH2); NADH2:nitrate oxidoreductase; nitrate reductase (NADH); EC 1.7.1.1. Enzyme Commission Number: EC 1.7.1.1. CAS No. 9013-03-0. Nitrate reductase. Activity: vial of > 0.5 unit. Storage: -20°C. Form: Supplied as a lyophilized powder containing 50 mM MOPS, pH 7.0, 1 mM EDTA and a proprietary sugar. Source: Pichia pastoris. Species: Arabidopsis thaliana. Nitrate reductases; assimilatory nitrate reductase; NADH-nitrate reductase; NADH-dependent nitrate reductase; assimilatory NADH:nitrate reductase; nitrate reductase (NADH2); NADH2:nitrate oxidoreductase; nitrate reductase (NADH); EC 1.7.1.1. Pack: vial of > 0.5 unit. Cat No: NATE-0486. | |
| O-Glycanase from Streptococcus pneumoniae, Recombinant | O-Glycanase from Streptococcus pneumoniae, Recombinant. The enzyme is inactivated with sulfhydryl reagents such as p-chloro-mercuribenzene sulfonic acid and transition metals such as mn2+ or zn2+. the enzyme is also inhibited with 1 mm edta. in a highly purified form, o-glycanase adsorbs to glass surfaces and is inactivated or gives variable activities. assays with purified substrates should be carried out in polypropylene vessels, and transfer of the enzyme solutions with glass pipettes should be avoided. the purified enzyme, as formulated, is stable at 2-8°c but about 30% of its activity is lost with a single freeze-thaw cycle. the enzyme activity is not signific...Glycanase. Purity: O-Glycanase is free of contaminating endo-and exoglycosidase activity. No protease activity was detectable after incubation of the enzyme with 0.2 mg resorufin-labeled casein for ~18 hours at 37°C according to the method described by Twining. The production host strain has been extensively tested and does not produce any detectable glycosidases. O-Glycanase. Mole weight: ~180 kDa daltons. Activity: > 12 U/mg. Storage: Shipped on cold pack for next day delivery. Store at 2-8°C. DO NOT FREEZE. Form: A sterile-filtered solution in 20 mM Tris-HCl, 25 mM NaCl (pH 7.5). Source: E. coli. Species: Streptococcus pneumoniae. O-Glycanase. Cat No: NATE-0496. | |
| Protein Kinase A Catalytic Subunit from Bovine, Recombinant | Protein Kinase A (PKA) catalyzes the transfer of the terminal phosphate of ATP to threonine or serine residues in a variety of protein substrates. The enzyme is composed of two subunit types: a catalytic subunit and a regulatory subunit. In the absence of cAMP, the two subunits are bound to each other and no catalysis can take place. In the presence of cAMP, the regulatory subunit binds cAMP, thus releasing the catalytic subunit. In the presence of cAMP, the catalytic subunit exists as a monomer of 40,862 Da (amino acid sequence), but on SDS-PAGE the apparent molecular mass is 43,000 Da. Group: Enzymes. Synonyms: PKA; cAMP-dependent protein kinase; ATP:protein phosphotransferase (cAMP-dependent); Protein K. Enzyme Commission Number: EC 2.7.11.11. Activity: >9 units/μg protein. Storage: Store at -20°C. Form: Lyophilized from a solution containing approximately: 80% sucrose, 19% potassium phosphate buffer, pH 6.7, 0.0625% 2-mercaptoethanol(2-ME), 0.002% EDTA, 0.016% dithiothreitol (DTT), and ≤1% protein. The lyophilized product may contain traces of DTT or 2-ME. Source: Bovine Heart. Species: Bovine. PKA; cAMP-dependent protein kinase; ATP:protein phosphotransferase (cAMP-dependent); Protein Kinase A catalytic subunit; Protein kinase A; PKAC; cAMP-dependent protein kinase catalytic subunit; PRKAC. Cat No: NATE-1889. | |
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