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| Product | Description | |
|---|---|---|
| Sodium citrate | Our wide distribution network, with locations coast-to-coast, helps guarantee fast, reliable service to Univar's customers. |  |
| Sodium citrate | Pharmacopeia & Metrological Institutes Standards. Uses: For analytical and research use. Group: Reagents. CAS No. 6132-4-3. Pack Sizes: 1G. |  |
| Sodium Citrate | SODIUM CITRATE, DIHYDRATE, ACS Reagent, granular, (Synonym: Trisodium Citrate, Dihydrate), Formula: Na3C6H5O7.2H2O. CAS No. 1932-4-3. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today! |  Texas TX |
| Sodium Citrate | Sodium citrate dihydrate consists of odorless, colorless, monoclinic crystals, or a white crystalline powder with a cooling, saline taste. It is slightly deliquescent in moist air, and in warm dry air it is efflorescent. Although most pharmacopeias specify that sodium citrate is the dihydrate, the USP states that sodium citrate may be either the dihydrate or anhydrous material. Synonyms: Citric acid trisodium salt; E331; natrii citras; sodium citrate tertiary; trisodium citrate. CAS No. 6132-4-3. Product ID: PE-0124. Molecular formula: C6H5Na3O7·2H2O. Mole weight: 294.1. Category: Alkalizing Agents; Buffering Agents; Emulsifying Agents; Sequestering Agents. Product Keywords: Flavoring Agents; Stabilizers; pH Modifier Excipients; ; PE-0124; Sodium Citrate; Alkalizing Agents; Buffering Agents; Emulsifying Agents; Sequestering Agents; C6H5Na3O7·2H2O; 6132-04-03. UNII: 1Q73Q2JULR. Chemical Name: Trisodium 2-hydroxypropane-1, 2, 3-tricarboxylate dihydrate. Grade: Pharmceutical Excipients. Administration route: Inhalations; injections; ophthalmic; oral; nasal, otic, rectal, topical, transdermal, and vaginal. Dosage Form: Inhalations; injections; ophthalmic products; oral solutions, suspensions, syrups and tablets; nasal, otic, rectal, topical, transdermal, and vaginal preparations. Stability and Storage Conditions: Sodium citrate dihydrate is a stable material. Aqueous solutions may be sterilized by autoclaving. On storag |  |
| Sodium Citrate | Sodium Citrate elevates the caliber and durability of edibles and drinks across diverse product arrays. With a wide-ranging buffering capacity, Sodium Citrate exhibits versatility suitable for a multitude of uses. Uses: Acidulant, antioxidant, cheese, chelating agent, food additive, buffer. Alternative names: Citric Acid Trisodium Salt, Sodium Citrate Dihydrate, Trisodium Citrate, Trisodium Citrate Dihydrate. Grades: FCC, USP. CAS No. 6132-04-3. Pack Sizes: 55lb. |  USA |
| Sodium Citrate | Sodium Citrate. Grade: FCC USP. CAS: 1545801. Packing: Bag |  New Jersey NJ |
| Sodium Citrate | Sodium Citrate. Grade: FCC USP. CAS: 6132-04-3. Packing: Bag. | New Jersey NJ |
| Sodium Citrate | Sodium Citrate. Grades: ACS. CAS No. 6132-04-3 4. Pack Sizes: Gram Quantities: 6 x 500 gm, 4 x 2.5 kg, 12 kg. Order Number: 14523. |  www.prochemonline.com |
| Sodium Citrate Anhydrous | White crystalline powder. Uses: food emulsifier, anticoagulant. Group: organic salt. Alternative Names: Trisodium Citrate. CAS No. 68-04-2. |  |
| Sodium Citrate Bp80 | Sodium Citrate Bp80 - Agriculture Chemicals. SUPPLIERS TO BUSINESS CUSTOMERS ONLY. |  North America & APAC |
| Sodium citrate dihydrate | Sodium citrate dehydrate (Trisodium citrate dihydrate) is a natural product with oral activity that can be found in citrus fruits. Sodium citrate dehydrate can inhibit the proliferation of tumor cells and induce apoptosis. Sodium citrate dehydrate has antibacterial , anti-tumor and antioxidant activities. Sodium citrate dehydrate can be prepared as a cosolvent or buffer [1] [2] [3]. Uses: Scientific research. Group: Natural products. Alternative Names: Trisodium citrate dihydrate; Citric acid trisodium salt dihydrate. CAS No. 6132-4-3. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g. Product ID: HY-B1610. |  |
| Sodium citrate dihydrate | Sodium citrate dihydrate is used as a flavouring agent and an anticoagulant. Synonyms: Sodium citrate dihydrate; Sodium citrate tribasic dihydrate; 1,2,3-Propanetricarboxylic acid, 2-hydroxy-, trisodium salt, dihydrate. CAS No. 6132-4-3. Molecular formula: C6H9Na3O9. Mole weight: 294.10. |  |
| Sodium Citrate Dihydrate | Sodium citrate dihydrate consists of odorless, colorless, monoclinic crystals, or a white crystalline powder with a cooling, saline taste. It is slightly deliquescent in moist air, and in warm dry air it is efflorescent. Although most pharmacopeias specify that sodium citrate is the dihydrate, the USP states that sodium citrate may be either the dihydrate or anhydrous material. Synonyms: Citric acid trisodium salt; E331; natrii citras; sodium citrate tertiary; trisodium citrate. CAS No. 6132-4-3. Product ID: PE-0542. Molecular formula: C6H5Na3O7·2H2O. Mole weight: 294.1. Category: Alkalizing Agents; Buffering Agents; Emulsifying Agents; Sequestering Agents. Product Keywords: Excipients for Liquid Dosage Form; Emulsifier Excipients; PE-0542; Sodium Citrate Dihydrate; Alkalizing Agents; Buffering Agents; Emulsifying Agents; Sequestering Agents; C6H5Na3O7·2H2O; 6132-04-3. UNII: 1Q73Q2JULR. Chemical Name: Trisodium 2-hydroxypropane-1, 2, 3-tricarboxylate dihydrate. Grade: Pharmceutical Excipients. Administration route: Inhalations; injections; ophthalmic; oral; nasal, otic, rectal, topical, transdermal, and vaginal. Dosage Form: Inhalations; injections; ophthalmic products; oral solutions, suspensions, syrups and tablets; nasal, otic, rectal, topical, transdermal, and vaginal preparations. Stability and Storage Conditions: Sodium citrate dihydrate is a stable material. Aqueous solutions may be sterilized by au | |
| Sodium Citrate Dihydrate | Sodium Citrate Dihydrate. Molecular Formula Na3C6H5O7 * 2H2O. Chemical Reagents |  Cater Chemicals Corp. Illinois IL |
| Sodium Citrate Dihydrate | White crystalline solid. Uses: food additive, buffer solution. Group: organic salt. CAS No. 6132-4-3. | |
| Sodium citrate dihydrate, 99.0-100.5% USP | Sodium citrate dihydrate, 99.0-100.5% USP. Group: Biochemicals. Grades: USP. Pack Sizes: 250g, 1Kg, 2.5Kg, 10Kg, 25Kg. US Biological Life Sciences. |  Worldwide |
| Sodium Citrate, Dihydrate, ACS | Sodium Citrate, Dihydrate, ACS. Group: Biochemicals. Alternative Names: Trisodium citrate, dihydrate; Citric acid, Trisodium Salt, Dihydrate. Grades: ACS Grade. CAS No. 6132-4-3. Pack Sizes: 500g, 1Kg, 2.5Kg, 10Kg. Molecular Formula: C6H5Na3O7 2H2O, Molecular Weight: 294.1. US Biological Life Sciences. | Worldwide |
| Sodium Citrate, Dihydrate, Granular, Laboratory Grade, 500 g | Formula: Na3C6H5O7 2H2O. Formula Wt: 294. 1. Characteristic: White. Storage Code: Green; general chemical storage. Alternative Names: Sodium citrate; disodium salt. Grades: chem-grade laboratory. CAS No. 6132-04-3. Product ID: 889060. -- SOLD FOR EDUCATIONAL USE ONLY -- |  |
| Sodium Citrate IP/BP/USP (Dihydrate) | Sodium Citrate IP/BP/USP (Dihydrate). CAS No. 6132-4-3. Molecular formula: C6H5Na3O7.2H2O. |  |
| Sodium citrate tribasic dihydrate | Sodium citrate tribasic dihydrate. Synonyms: Citric acid trisodium salt dihydrate, Trisodium citrate dihydrate. CAS No. 6132-4-3. Product ID: CDC10-0122. Molecular formula: C6H9Na3O9. Category: Cosmetic Chelating Chemicals. Product Keywords: Cosmetic Ingredients; Cosmetic Chelating Chemicals; Sodium citrate tribasic dihydrate; CDC10-0122; 6132-04-3; C6H9Na3O9; Citric acid trisodium salt dihydrate, Trisodium citrate dihydrate; 200-675-3; MFCD00150031; 6132-04-3. Purity: ≥99.0%. Color: White. EC Number: 200-675-3. Physical State: Powder. Solubility: water: soluble 29.4 g/L at 20 °C (completely). Quality Level: 200. Storage: Store at 5°C to 30°C. Melting Point: >300 °C (lit.). Density: 1.76 g/mL. | |
| Sodium Citrate USP (Anhydrous) | Sodium Citrate USP (Anhydrous). CAS No. 68-04-2. Molecular formula: C6H5Na3O7. | |
| monosodium citrate | DryPowder; Liquid; OtherSolid, Liquid;Crystalline white powder or colourless crystals. Group: Pvc stabilizers. Product ID: sodium; 3-carboxy-3,5-dihydroxy-5-oxopentanoate. Molecular formula: 214.1g/mol. Mole weight: (a)C6H7O7Na (anhydrous);NaC6H7O7;C6H7NaO7. C(C(=O)O)C(CC(=O)[O-])(C(=O)O)O. [Na+]. InChI=1S/C6H8O7.Na/c7-3(8)1-6(13, 5(11)12)2-4(9)10;/h13H, 1-2H2, (H, 7, 8)(H, 9, 10)(H, 11, 12);/q;+1/p-1. HWPKGOGLCKPRLZ-UHFFFAOYSA-M. |  |
| Plasma, Pigeon (non-sterile) in Sodium Citrate | Plasma, Pigeon (non-sterile) in Sodium Citrate. Group: Biologicals. Grades: Plasma. Pack Sizes: 10ml. US Biological Life Sciences. | Worldwide |
| Plasma, Pigeon (sterile) in Sodium Citrate | Plasma, Pigeon (sterile) in Sodium Citrate. Group: Biologicals. Grades: Plasma. Pack Sizes: 10ml. US Biological Life Sciences. | Worldwide |
| Sodium Acid Citrate BP | Sodium Acid Citrate BP. CAS No. 144-33-2. Molecular formula: C6H6Na2O7-1.5H2O. | |
| Sodium dihydRogen citRate | Sodium dihydRogen citRate. Group: Biochemicals. Grades: Highly Purified. CAS No. 18996-35-5. Pack Sizes: 1kg, 2kg. US Biological Life Sciences. | Worldwide |
| Sodium dihydrogen citrate anhydrous | 100g Pack Size. Group: Biochemicals, Buffers. Formula: C6H7NaO7. CAS No. 18996-35-5. Prepack ID 11207603-100g. Molecular Weight 214.11. See USA prepack pricing. |  |
| Tri-sodium citrate | Tri-sodium citrate. Group: Biochemicals. Grades: Highly Purified. CAS No. 68-04-2. Pack Sizes: 1kg, 2kg, 5kg, 10Kg, 25Kg. Molecular Formula: C6H5Na3O7. US Biological Life Sciences. | Worldwide |
| Tri Sodium citrate dihydrate | 1kg Pack Size. Group: Aroma Chemicals, Biochemicals, Flavours and Fragrance Materials. Formula: C6H5Na3O7 · 2H2O. CAS No. 6132-4-3. Prepack ID 32357040-1kg. Molecular Weight 294.1. See USA prepack pricing. | |
| KJ Ingredients Inc. | Delivering premium natural ingredients with unmatched reliability, KJ Ingredients Inc. connects businesses with high-quality food and nutrition solutions. Our extensive range includes citric acid, sodium citrate, vitamins, sweeteners, and more—sourced with strict quality standards. With strategic distribution across the U.S., we ensure timely delivery and expert support. Let’s build a lasting partnership—contact us today! featured listing |  |
| AMYLOGLUCOSIDASE | AMYLOGLUCOSIDASE. Synonyms: Amyloglucosidase from Aspergillus niger;Glucoamylase, Rhizopus sp;Saccharifying enzyMe(high conversion rate);Amyloglucosidase solution from Aspergillus niger;AMG 300L;Amyloglucosidase 2D Electrophoresis marker from Aspergillus niger;Glucoamylase from Rhizopus;1,4-α-D-Glucan glucohydrolase, Exo-1,4-α-glucosidase, Glucoamylase. CAS No. 9032-08-0. Pack Sizes: 250 g. Product ID: CDF4-0038. Molecular formula: Cd+2. Category: Enzyme Preparations. Product Keywords: Food Ingredients; Enzyme Preparations; AMYLOGLUCOSIDASE; CDF4-0038; 9032-08-0; Cd+2; 232-877-2; 9032-08-0. Purity: 0.99. Color: White. EC Number: 232-877-2. Physical State: Solution. Solubility: 0.03 M sodium citrate-phosphate buffer, pH 4.5: soluble5.0mg/mL. Storage: 2-8°C. Density: ~1.2 g/mL at 25 °C. Product Description: Amyloglucosidase, a 1,4-α-D-glucan glucohydrolase, is a disaccharidase-type α-glucosidase. It is synthesized by several Aspergillus genus species. This exo-enzyme is one of the major industrial enzymes. The stability of amyloglucosidase can be increased by immobilization. | |
| Citric acid trisodium | Citric acid trisodium is a natural preservative and food tartness enhancer. Citric acid trisodium induces apoptosis and cell cycle arrest at G2/M phase and S phase. Citric acid trisodium cause oxidative damage of the liver by means of the decrease of antioxidative enzyme activities. Citric acid trisodium causes renal toxicity in mice [1] [2] [3]. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: Sodium citrate; Trisodium citrate anhydrous. CAS No. 68-04-2. Pack Sizes: 100 mg; 500 mg; 1 g. Product ID: HY-B2201. | |
| Citric Acid, Trisodium Salt, Dihydrate 99+% USP/BP/EP | Citric Acid, Trisodium Salt, Dihydrate 99+% USP/BP/EP. Group: Biochemicals. Alternative Names: Trisodium citrate, dihydrate; Sodium Citrate, Dihydrate. Grades: USP. CAS No. 6132-4-3. Pack Sizes: 500g, 1Kg, 5Kg, 10Kg. Molecular Formula: C6H5Na3O7 2H2O, Molecular Weight: 294.1. US Biological Life Sciences. | Worldwide |
| (-)-Eburnamonine | (-)-Eburnamonine is a natural product that is obtained from the roots of Eucalyptus globulus. It is an inhibitor of sodium citrate, which is used in the treatment of infectious diseases. (-)-Eburnamonine has been shown to be effective against intestinal inflammation and bowel disease by reducing the production of inflammatory cytokines. The molecule also inhibits hydroxyl group formation and has been shown to have minimal toxicity in animal studies. It also affects brain functions, such as energy metabolism, and may have significant cytotoxicity against cancer cells. Group: Other alkaloids. CAS No. 4880-88-0. Molecular formula: C19H22N2O. Mole weight: 294.39 g/mol. Canonical SMILES: CC[C@@]12CCCN3[C@@H]1C4=C (CC3)C5=CC=CC=C5N4C (=O)C2. Catalog: ACM4880880. |  |
| N-Acetyl-L-Glutamine | N-acetyl-L-glutamine is an N(2)-acetylglutamine that has L-configuration. It has a role as a human metabolite. It is a N-acetyl-L-amino acid, a N(2)-acyl-L-glutamine and a N(2)-acetylglutamine. It is a conjugate acid of a N-acetyl-L-glutaminate. It is an enantiomer of a N(2)-acetyl-D-glutamine. CAS No. 2490-97-3. Product ID: PAP-0011. Molecular formula: C7H12N2O4. Category: Amino acid. Product Keywords: Amino Acid Series; N-Acetyl-L-Glutamine; PAP-0011; Amino acid; C7H12N2O4; 2490-97-3. Color: White to Off-White. EC Number: 219-647-7. Physical State: Solid. Solubility: DMSO (Slightly, Heated, Sonicated), Water (Sparingly, Heated, Sonicated). Storage: Sealed in dry,Room Temperature. Applications: N-Acety-L-Glutamine is an amino acid that is not synthesized by the human body and must be obtained through diet. It is a precursor to glutamate, which is an important neurotransmitter in the brain. N-Acetyl-L-glutamine has been shown to have neuroprotective effects against various metabolic disorders including diabetes, bowel disease, and microdialysis probes. The effect of N-acetyl-L-glutamine on neuronal death can be observed using a reaction solution containing sodium citrate and glucose injection. N-acetylglutamine has been shown to increase the activity of enzymes such as citrate synthase in this reaction solution. Boiling Point: 430.5±40.0 °C(Predicted). Melting Point: 206-208 °C. Density: 1.290±0.06 g/cm3(Predi | |
| Native Baker's yeast (S. cerevisiae) Nucleoside 5'-Diphosphate Kinase | Nucleoside 5'-diphosphate kinase is a cytosolic enzyme. Nucleoside 5'-diphosphate kinase from Saccharomyces cerevisiae is found highly expressed in the cytoplasm. It affects DNA synthesis, in part, by binding to Cdc8p. Nucleoside 5?-diphosphate kinase is a cytosolic enzyme. Applications: Nucleoside 5?-diphosphate kinase has been used in a study to examine a possible intracellular activity of the drug disodium cromoglycate in mast cells. it has also been used in a study to investigate protein synthesis in rabbit reticul ocytes. Group: Enzymes. Synonyms: nucleoside 5'-diphosphate kinase; nucleoside diphosphate (UDP) kinase; nucleoside diphosphokinase; nucleotide phosphate kinase; UDP kinase; uridine diphosphate kinase; nucleoside-diphosphate kinase; EC 2.7.4.6; 9026-51-1; NDPK. Enzyme Commission Number: EC 2.7.4.6. CAS No. 9026-51-1. NDPK. Storage: -20°C. Form: lyophilized powder; essentially sulfate-free powder. Contains sodium Citrate with a trace of magnesium and EDTA salts. Source: Baker's yeast (S. cerevisiae). nucleoside 5'-diphosphate kinase; nucleoside diphosphate (UDP) kinase; nucleoside diphosphokinase; nucleotide phosphate kinase; UDP kinase; uridine diphosphate kinase; nucleoside-diphosphate kinase; EC 2.7.4.6; 9026-51-1; NDPK. Cat No: NATE-0476. |  |
| Native baker's yeast (S. cerevisiae) Proteinase A | Saccharopepsin is an enzyme. This enzyme catalyses the following chemical reaction:Hydrolysis of proteins with broad specificity for peptide bonds. Cleaves-Leu-Leu-Val-Tyr bond in a synthetic substrate. This enzyme is present in baker's yeast (Saccharomyces cerevisiae). Applications: Possibly useful for producing overlap peptides in sequence studies. Group: Enzymes. Synonyms: Endopeptidase; Proteinase A; EC 3.4.23.25; yeast endopeptidase A; Saccharomyces aspartic proteinase; aspartic proteinase yscA; proteinase yscA; yeast proteinase A; Saccharomyces cerevisiae aspartic proteinase A. Enzyme Commission Number: EC 3.4.23.25. Proteinase A. Activity: 15-50 units/mg protein. Storage: -20°C. Form: Lyophilized solids containing sodium Citrate, pH 5.0. Source: S. cerevisiae. Species: baker's yeast. Endopeptidase; Proteinase A; EC 3.4.23.25; yeast endopeptidase A; Saccharomyces aspartic proteinase; aspartic proteinase yscA; proteinase yscA; yeast proteinase A; Saccharomyces cerevisiae aspartic proteinase A. Pack: Package size based on protein content. Cat No: NATE-0636. | |
| Native Bovine β(1-3,4)-Galactosidase | Hydrolyzes non-reducing terminal galactose β(1-3) and β(1-4) linkages. Can be used in conjunction with other β-galactosidases for exoglycosidase sequencing. Applications: The enzyme has applications in the analysis of a wide variety of glycoconjugates. it is particularly useful for ensuring the complete removal of β(1-3) and β(1-4)-linked non-reducing terminal galactose residues of oligosaccharides. gal β(1-6) glcnac is hydrolyzed more slowly, however this linkage is not normally encountered in native complex glycans. this activity towards β(1-3) and β(1-4)-linked galactose contrasts with that of our other β-galactosidases whi...tose residues. Group: Enzymes. Synonyms: β-galactosidase; beta-gal; β-gal; lactase; β-lactosidase; maxilact; hydrolact; β-D-lactosidase; lactozym; trilactase; β-D-galactanase; oryzatym; sumiklat; β-D-galactoside galactohydrolase. β-gal. Mole weight: ~68 kD. Form: 20 mM sodium Citrate phosphate, 150 mM NaCl (pH 4.0). Source: Bovine testis. Species: Bovine. β(1-3,4)-Galactosidase; β-galactosidase; beta-gal; β-gal; EC 3.2.1.23; lactase; β-lactosidase; maxilact; hydrolact; β-D-lactosidase; S 2107; lactozym; trilactase; β-D-galactanase; oryzatym; sumiklat; β-D-galactoside galactohydrolase. Cat No: NATE-0973. | |
| Native Bovine Thrombin | Thrombin is a serine protease that in humans is encoded by the F2 gene. Prothrombin (coagulation factor II) is proteolytically cleaved to form thrombin in the coagulation cascade, which ultimately results in the reduction of blood loss. Thrombin in turn acts as a serine protease that converts soluble fibrinogen into insoluble strands of fibrin, as well as catalyzing many other coagulation-related reactions. Thrombin is the final coagulation protease in regard to hemostasis, promoting both procoagulant and anticoagulant effects. Applications: Thrombin is used for site specific cleavage of recombinant fusion proteins containing an accessible thrombin recognition site for removal of ...Ia; E thrombin; β-thrombin; γ-thrombin. Enzyme Commission Number: EC 3.4.21.5. CAS No. 9002-4-4. Thrombin. Activity: 600-2,000 NIH units/mg protein (biuret) or > 2,000 NIH units/mg protein (E1%/280 = 19.5); > 125 NIH units/mg protein (biuret). Form: Type I, Lyophilized from saline sodium Citrate buffer, pH 6.5; Type II, buffered aqueous solution, In 0.05 M phosphate buffer, pH 7.0. Source: Bovine plasma. Species: Bovine. thrombin; 9002-04-4; EC 3.4.21.5; fibrinogenase; thrombase; thrombofort; topical; thrombin-C; tropostasin; activated blood-coagulation factor II; blood-coagulation factor IIa; factor IIa; E thrombin; β-thrombin; γ-thrombin. Cat No: NATE-0698. | |
| Native Enterobacter cloacae β-Lactamase | β--lactamase inactivates β-lactam antibiotics by breaking open the β-lactam ring. Protein determined by biuret. Applications: Β-lactamase is used to inactivate β-lactam antibiotics by breaking open the β-lactam ring. β-lactamase is used to study antibiotic resistance and resistance suppression1. this product is produced from enterobacter cloacae. Group: Enzymes. Synonyms: β-lactamase; penicillinase; cephalosporinase; neutrapen; penicillin β-lactamase; exopenicillinase; ampicillinase; penicillin amido-β-lactamhydrolase; penicillinase I, II; β-lactamase I-III; β-lactamase A, B, C; β-lactamase AME I; cephalosporin-β-lactamase; EC . Enzyme Commission Number: EC 3.5.2.6. CAS No. 9073-60-3. β-Lactamase. Activity: 6-18 units/mg protein (using benzylpenicillin); 0.2-0.6 units/mg protein (using benzylpenicillin). Storage: 2-8°C. Form: Lyophilized powder containing sodium phosphate and sodium Citrate buffer salts. Source: Enterobacter cloacae. β-lactamase; penicillinase; cephalosporinase; neutrapen; penicillin β-lactamase; exopenicillinase; ampicillinase; penicillin amido-β-lactamhydrolase; penicillinase I, II; β-lactamase I-III; β-lactamase A, B, C; β-lactamase AME I; cephalosporin-β-lactamase; EC 3.5.2.6; 9073-60-3. Cat No: NATE-0774. | |
| Native Escherichia coli L-Glutamine Synthetase | Glutamine synthetase (GS) (EC 6.3.1.2) is an enzyme that plays an essential role in the metabolism of nitrogen by catalyzing the condensation of glutamate and ammonia to form glutamine:Glutamate + ATP + NH3 ? Glutamine + ADP + phosphate. Glutamine Synthetase uses ammonia produced by Nitrate reduction, amino acid degradation, and photorespiration. The amide group of glutamate is a nitrogen source for the synthesis of glutamine pathway metabolites. Applications: L-glutamine synthetase may be used for the purification of proteases from escherichia coli. Group: Enzymes. Synonyms: glutamine synthetase; glutamylhydroxamic synthetase; L-glutamine synthetase; glutamate-ammonia ligase; L-Glutamate:ammonia ligase (ADP-forming); EC 6.3.1.2; GS; 9023-70-5. Enzyme Commission Number: EC 6.3.1.2. CAS No. 9023-70-5. Purity: affinity chromatography. GS. Activity: 400-2,000 units/mg protein. Storage: -20°C. Form: lyophilized powder; Contains potassium phosphate, sodium Citrate and magnesium acetate buffer salts. Source: Escherichia coli. glutamine synthetase; glutamylhydroxamic synthetase; L-glutamine synthetase; glutamate-ammonia ligase; L-Glutamate:ammonia ligase (ADP-forming); EC 6.3.1.2; GS; 9023-70-5. Cat No: NATE-0321. | |
| Native Human α-Amylase | α-Amylase is a protein enzyme EC 3.2.1.1 that hydrolyses alpha bonds of large, alpha-linked polysaccharides, such as starch and glycogen, yielding glucose and maltose. It is the major form of amylase found in Humans and other mammals. It is also present in seeds containing starch as a food reserve, and is secreted by many fungi. Applications: Α-amylase is used to hydrolyze α bonds of α-linked polysaccharides, such as starch and glycogen. α-amylase has been used in various plant studies, such as metabolism studies in arabidopsis. α-amylase from human saliva has been used to study the development of nutraceuticals, which may aid the treatment of diabetes and obesity. Group: Enzymes. Synonyms: glycogenase; αamylase, α-amylase; 1,4-α-D-glucan glucanohydrolase; EC 3.2.1.1; 9001-19-8; endoamylase; Taka-amylase A. Enzyme Commission Number: EC 3.2.1.1. CAS No. 9001-19-8. α-Amylase. Activity: 1,000-3,000 units/mg protein; 300-1,500 units/mg protein. Storage: -20°C. Form: Lyophilized powder containing (NH4)2SO4 and sodium Citrate. Source: Human saliva. Species: Human. glycogenase; αamylase, α-amylase; 1,4-α-D-glucan glucanohydrolase; EC 3.2.1.1; 9001-19-8; endoamylase; Taka-amylase A. Cat No: NATE-0743. | |
| Native Human Glyceraldehyde-3-phosphate Dehydrogenase | Glyceraldehyde-3-phosphate dehydrogenase catalyzes the conversion of glyceraldehyde-3-phosphate to 1,3-bisphosphoglycerate as part of glycolysis. It has also been shown to have roles in initiation of apoptosis, transcription activation and the shuttling of ER to Golgi vesicles. Group: Enzymes. Synonyms: EC 1.2.1.12; GAPDH; glyceraldehyde-3-phosphate dehydrogenase (phosphorylating); triosephosphate dehydrogenase; dehydrogenase, glyceraldehyde phosphate; phosphoglyceraldehyde dehydrogenase; 3-phosphoglyceraldehyde dehydrogenase; NAD+-dependent glyceraldehyde phosphate dehydrogenase; glyceralde. Enzyme Commission Number: EC 1.2.1.12. CAS No. 9001-50-7. Glyceraldehyde-3-phosphate Dehydrogenase. Activity: 50-150 units/mg protein. Storage: -20°C. Form: Lyophilized powder containing sodium Citrate buffer salts. Source: Human erythrocytes. Species: Human. EC 1.2.1.12; GAPDH; glyceraldehyde-3-phosphate dehydrogenase (phosphorylating); triosephosphate dehydrogenase; dehydrogenase, glyceraldehyde phosphate; phosphoglyceraldehyde dehydrogenase; 3-phosphoglyceraldehyde dehydrogenase; NAD+-dependent glyceraldehyde phosphate dehydrogenase; glyceraldehyde phosphate dehydrogenase (NAD+); glyceraldehyde-3-phosphate dehydrogenase (NAD+); NADH-glyceraldehyde phosphate dehydrogenase; glyceraldehyde-3-P-dehydrogenase; 9001-50-7. Cat No: NATE-0280. | |
| Native Penicillium janthinellum Carboxypeptidase P | Membrane Pro-Xaa carboxypeptidase (EC 3.4.17.16, carboxypeptidase P, microsomal carboxypeptidase) is an enzyme. This enzyme catalyses the following chemical reaction:Release of a C-terminal residue other than proline, by preferential cleavage of a prolyl bond. This is one of the renal brush border exopeptidases. Applications: Membrane pro-xaa carboxypeptidase (ec 3.4.17.16, carboxypeptidase p, microsomal carboxypeptidase) is an enzyme.[1][2][3] this enzyme catalyses the following chemical reaction release of a c-terminal residue other than proline, by preferential cleavage of a prolyl bond this is one of the renal brush border exopeptidases. Group: Enzymes. Synonyms: Aminoacylproline Carboxypeptidase; CPP; Penicillocarboxypeptidase S-1; Proline Carboxypeptidase; EC 3.4.17.16; Membrane Pro-Xaa carboxypeptidase; carboxypeptidase P; microsomal carboxypeptidase. Enzyme Commission Number: EC 3.4.17.16. CAS No. 9075-64-3. CPP. Storage: -20°C. Form: Lyophilized powder containing sodium Citrate. Source: Penicillium janthinellum. Aminoacylproline Carboxypeptidase; CPP; Penicillocarboxypeptidase S-1; Proline Carboxypeptidase; EC 3.4.17.16; Membrane Pro-Xaa carboxypeptidase; carboxypeptidase P; microsomal carboxypeptidase. Pack: vial of > 100 units. Cat No: NATE-0157. | |
| Native Porcine Thrombin | Thrombin is a serine protease that in humans is encoded by the F2 gene. Prothrombin (coagulation factor II) is proteolytically cleaved to form thrombin in the coagulation cascade, which ultimately results in the reduction of blood loss. Thrombin in turn acts as a serine protease that converts soluble fibrinogen into insoluble strands of fibrin, as well as catalyzing many other coagulation-related reactions. Applications: Diagnostic controls, calibrators & standards; immunoassays; testing/assay validation; life science; manufacturing; coagulation/anemia. Group: Enzymes. Synonyms: thrombin; alpha Subunit Thrombin. Thrombin. Mole weight: 362 kDa. Activity: > 1,000 NIH U/mg. Stability: 2 years. Storage: Store at -20°C. Form: Liquid in 0.05 M sodium Citrate, 0.2 M NaCl, 0.1% PEG-8,000, pH 6.5. Source: Porcine Plasma. Species: Porcine. thrombin; EC 3.4.21.5; fibrinogenase; thrombase; thrombofort; topical; thrombin-C; tropostasin; activated blood-coagulation factor II; blood-coagulation factor IIa; factor IIa; E thrombin; β-thrombin; γ-thrombin; alpha Subunit Thrombin. Cat No: NATE-0970. | |
| Native Saccharomyces cerevisiae Hexokinase | A hexokinase is an enzyme that phosphorylates hexoses (six-carbon sugars), forming hexose phosphate. In most organisms, glucose is the most important substrate of hexokinases, and glucose-6-phosphate the most important product. Hexokinase can transfer an inorganic phosphate group from ATP to a substrate. Hexokinases should not be confused with glucokinase, which is a specific isoform of hexokinase. While other hexokinases are capable of phosphorylating several hexoses, glucokinase acts with a 50-fold lower substrate affinity and its only hexose substrate is glucose. Group: Enzymes. Synonyms: hexokinase type IV glucokinase; hexokinase D; hexokinase type IV. Enzyme Commission Number: EC 2.7.1.1. CAS No. 9001-51-8. Hexokinase. Mole weight: ~ 54 kDa (monomer); ~110 kDa (dimer). Activity: Type I, > 350 units/mg protein; Type II, > 25 units/mg protein (biuret); Type III, > 130 units/mg protein (biuret). Storage: -20°C. Form: Type I, Lyophilized powder containing phosphate/Citrate pH approx. 7.0; Type II, Type III, Lyophilized powder containing approx. 15% sodium Citrate. Source: Saccharomyces cerevisiae. hexokinase type IV glucokinase; hexokinase D; hexokinase type IV; hexokinase (phosphorylating); ATP-dependent hexokinase; glucose ATP phosphotransferase; hexokinase; ATP:D-hexose 6-phosphotransferase; EC 2.7.1.1; 9001-51-8. Cat No: NATE-0342. | |
| Protoveratrine | Protoveratrine is an alkaloid that is found in the seeds of the red kidney bean. It has been shown to have a wide range of biological properties and can be used as an experimental model for congestive heart failure. Protoveratrine has also been shown to inhibit sodium citrate-induced hypernatremia and lc-ms/ms method, which is an analytical method for the quantification of human serum proteins. This compound also inhibits the expression of protein genes involved in energy metabolism, such as ATP synthase and pyruvate dehydrogenase kinase 4. Protoveratrine has been shown to be effective against autoimmune diseases, such as lupus erythematosus, which are caused by autoantibodies that attack the body's own cells. Group: Other alkaloids. Alternative Names: Protoveratrine A. CAS No. 143-57-7. Molecular formula: C41H63NO14. Mole weight: 793.94 g/mol. Canonical SMILES: CC[C@@H] (C)C (=O)O[C@H]1[C@@H] ([C@H]2[C@@H] (CN3C[C@H] (CC[C@H]3[C@@]2 (C)O)C)[C@H]4[C@@]1 ([C@@H]5[C@@H] ([C@@H] ([C@H]6[C@]7 ([C@]5 (C4)O[C@@]6 ([C@H] (CC7)OC (=O)[C@] (C) (CC)O)O)C)OC (=O)C)OC (=O)C)O)O. Catalog: ACM143577. | |
| Tetrodotoxin Citrate | Tetrodotoxin Citrate is a highly selective, reversible sodium channel blocker. Group: Biochemicals. Grades: Highly Purified. CAS No. 18660-81-6. Pack Sizes: 1mg, 10mg. Molecular Formula: C17H25N3O15. US Biological Life Sciences. | Worldwide |
| Tetrodotoxin, citrate (1:1) (salt) | Tetrodotoxin, citrate (1:1) (salt), also called as TTX citrate, is the citrate salt of tetrodotoxin. Tetrodotoxin is a neurotoxin that reversibly and selectively blocks sodium channel. Synonyms: TETRODOTOXIN;TETRODOTOXIN CITRATE;OCTAHYDRO-12-(HYDROXYMETHYL)-2-IMINO-5,9:7,10A-DIMETHANO-10AH-[1,3]DIOXOCINO[6,5-D]PYRIMIDINE-4,7,10,11,12-PENTOL CITRATE; citratodetetrodotoxina; tetrodotoxin, citrate(1:1)(salt); Octahydro-12-(hydroxymethyl)-2-imino-5, 9:7. Grades: 95%. CAS No. 18660-81-6. Molecular formula: C17H25N3O15. Mole weight: 511.39. | |
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