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Adenosine 5'-O-(3-thiotriphosphate) serves as a nucleotide analogue that efficiently gauges intracellular signal pathways and G protein-coupled receptors. It identifies diverse G protein subtypes and expedites their functional analysis. Meanwhile, BODIPY FL thioester sodium salt-5mM buffered aqueous solution is a fluorescent dye that acts as a preferred biomolecule detector and protein label. It harmoniously couples with Adenosine 5'-O-(3-thiotriphosphate) to produce optimal results for GPCR activity tracing and signal transduction analysis. Synonyms: BODIPY FL ATP-gamma-S thioester. Grade: 98%. Molecular formula: C24H27BF2N8Na3O13P3S. Mole weight: 878.28.
TBE buffer solution (10X)
1lt Pack Size. Group: Biochemicals, Buffers. Formula: N/A. Prepack ID 10590369-1lt. See USA prepack pricing.
TBE buffer solution (10X)
5lt Pack Size. Group: Biochemicals, Buffers. Formula: N/A. Prepack ID 10590369-5lt. See USA prepack pricing.
14-3-3 Beta histidine-tagged human
recombinant, expressed in E. coli, ?90% (SDS-PAGE), buffered aqueous glycerol solution. Group: Fluorescence/luminescence spectroscopy.
14-3-3 Epsilon histidine-tagged human
recombinant, expressed in E. coli, C-terminal, ?90% (SDS-PAGE), buffered aqueous solution. Group: Fluorescence/luminescence spectroscopy.
14-3-3 Eta histidine-tagged human
recombinant, expressed in E. coli, C-terminal, ?90% (SDS-PAGE), buffered aqueous glycerol solution. Group: Fluorescence/luminescence spectroscopy.
14-3-3 ? , GST tagged human
recombinant, expressed in E. coli, ?70% (SDS-PAGE), buffered aqueous glycerol solution. Group: Fluorescence/luminescence spectroscopy.
recombinant, expressed in E. coli, ?70% (SDS-PAGE), buffered aqueous glycerol solution. Group: Fluorescence/luminescence spectroscopy.
14-3-3 Tau/Theta histidine-tagged human
recombinant, expressed in E. coli, C-terminal, ?90% (SDS-PAGE), buffered aqueous glycerol solution. Group: Fluorescence/luminescence spectroscopy.
14-3-3 ?, untagged human
recombinant, expressed in E. coli, ?70% (SDS-PAGE), buffered aqueous glycerol solution. Group: Fluorescence/luminescence spectroscopy.
14-3-3 ?/?, untagged human
recombinant, expressed in E. coli, ?70% (SDS-PAGE), buffered aqueous glycerol solution. Group: Fluorescence/luminescence spectroscopy.
14-3-3 Zeta, histidine-tagged human
recombinant, expressed in E. coli, ?90% (SDS-PAGE), buffered aqueous glycerol solution. Group: Fluorescence/luminescence spectroscopy.
2-Amino-2-methyl-1-propanol
Used for the preparation of buffer solutions, suitable for the determination of alkaline phosphatase. Group: Biochemicals. Alternative Names: 2-Amino-2-methyl-1-propanol; AMP; 1,1-Dimethyl-2-hydroxyethylamine; β-Aminoisobutyl alcohol. Grades: Highly Purified. CAS No. 124-68-5. Pack Sizes: 250g, 500g, 1Kg, 2Kg, 5Kg. Molecular Formula: C?H??NO, Molecular Weight: 89.14. US Biological Life Sciences.
Worldwide
3,3-Dimethyl-1,5-dioxacycloundecane-6,11-dione
3,3-Dimethyl-1,5-dioxacycloundecane-6,11-dione is a contamination formed in the buffer solution from a polyolefin plastic container. Group: Biochemicals. Grades: Highly Purified. CAS No. 94113-47-0. Pack Sizes: 1mg. US Biological Life Sciences.
Worldwide
3,3-Dimethyl-1,5-dioxacycloundecane-6,11-dione
3,3-Dimethyl-1,5-dioxacycloundecane-6,11-dione is a contamination formed in the buffer solution from a polyolefin plastic container. Synonyms: Hexanedioic acid 2,2-dimethyl-1,3-propanediyl ester. Grade: > 95%. CAS No. 94113-47-0. Molecular formula: C11H18O4. Mole weight: 214.26.
4EBP1, GST tagged human
recombinant, expressed in E. coli, ?70% (SDS-PAGE), buffered aqueous glycerol solution. Group: Fluorescence/luminescence spectroscopy.
Absolute Mag PEI Magnetic Particles, 200 nm (# WHM-X072) are water soluble iron oxide particles with organic layers consist of a monolayer of oleic acid, a monolayer of amphiphilic polymer and a monolayer of polyethylenimine (PEI). There is no linkable reactive groups on the surface of nanoparticles. PEI is very stable in most buffer solutions of pH 5-10 and can capture negatively charged molecules, such as DNA and RNA, through charge-charge interaction. Uses: The pei magnetic particles can capture negatively charged molecules, such as dna and rna, through charge-charge interaction. Pack Sizes: 5 mL. Product ID: WHM-X072.
Absolute Mag Streptavidin Iron Oxide Nanoparticles, 10 nm
Absolute Mag Streptavidin Iron Oxide Nanoparticles, which are coated with amphiphilic polymer, are water soluble materials and covalently linked with streptavidin. These particles are very stable in most buffer solutions. Their zeta potential ranges from -20mV to -40mV. Their organic layers contain both monolayer of oleic acid and monolayer of amphiphilic polymer, whose thickness is about 4nm. The target molecules are always biotinylated molecules such as DNA, peptide and protein. Also for the reaction between biotinylated molecules and AMS, it's necessary to use monobiotinylated molecules, which have only one biotin linked to each biomolecule, to avoid aggregation of nanoparticles. Pack Sizes: 1 mL, 5 mL. Product ID: WNM-X002.
Absolute Mag Streptavidin Iron Oxide Nanoparticles, 20 nm
Absolute Mag Streptavidin Iron Oxide Nanoparticles, which are coated with amphiphilic polymer, are water soluble materials and covalently linked with streptavidin. These particles are very stable in most buffer solutions. Their zeta potential ranges from -20mV to -40mV. Their organic layers contain both monolayer of oleic acid and monolayer of amphiphilic polymer, whose thickness is about 4nm. The target molecules are always biotinylated molecules such as DNA, peptide and protein. Also for the reaction between biotinylated molecules and AMS, it's necessary to use monobiotinylated molecules, which have only one biotin linked to each biomolecule, to avoid aggregation of nanoparticles. Pack Sizes: 1 mL, 5 mL. Product ID: WNM-X004.
Alcohol Dehydrogenase (NADP+ dependent) from Entamoeba species, Recombinant
NADP-dependent isopropanol dehydrogenase belongs to the superfamily of alcohol dehydrogenases with a preference for medium chain secondary alcohols, such as 2- butanol and isopropanol, while it has low activity with primary alcohols, such as ethanol. Under physiological conditions, the enzyme reduces aldehydes and 2-ketones to produce secondary alcohols. It is also active with acetaldehyde and propionaldehyde. Group: Enzymes. Synonyms: EC 1.1.1.2; Aromatic Alcohol Dehy. Purity: > 95% by SDS-PAGE. ALR. Mole weight: ~40.9 kDa (SDS-PAGE). Activity: > 60U/mg. Storage: Aliquot and store at -20°C. Avoid repeated freeze thaw cycles. Form: Liquid, 1 mg/mL solution in 50 mM Tris-HCl buffer (pH 8.0) containing 100 mM NaCl and 50% glycerol. Source: E. coli. Species: Entamoeba species. EC 1.1.1.2; Aromatic Alcohol Dehydrogenase; Alcohol:NADP+ oxidoreductase; AKR1A1; ALDR1; ALR; ARM; DD3; HEL-S-6; aldehyde reductase; aldo-keto reductase family 1 member A1; alcohol dehydrogenase (NADP+); aldehyde reductase (NADPH2); NADP-alcohol dehydrogenase; NADP+-aldehyde reductase; NADP+-dependent aldehyde reductase; NADPH-aldehyde reductase; NADPH-dependent aldehyde reductase; nonspecific succinic semialdehyde reductase; ALR 1; low-Km aldehyde reductase; high-Km aldehyde reductase; alcohol dehydrogenase (NADP). Cat No: NATE-1590.
Allene Oxide Synthase from Parthenium argentatum, Recombinant
Potent anti-oxidant enzyme to remove lipid hydroperoxides in biological samples. Allene oxide synthase converts lipoxygenase derived fatty acid hydroperoxides to unstable allene epoxides. In plants, allene oxide is a precursor of jasmonic acid, which is important for growth regulation. Applications: Allene oxide synthase is a potent anti-oxidant enzyme used to remove lipid hydroperoxides in various biological samples. it may also be used to study stress induced gene expression in plants. Group: Enzymes. Synonyms: hydroperoxide isomerase; linoleate hydroperoxide isomerase; linoleic acid hydroperoxide isomerase; HPI; (9Z,11E,14Z)-(13S)-hydroperoxyoctadeca-9,11,14-trienoate 12,13-hydr. Enzyme Commission Number: EC 4.2.1.92. AOS. Activity: 25,000-40,000 units/mg protein. Storage: Store at -20°C. Form: Supplied as a solution in phosphate buffered sale pH 7.2. Source: E. coli. Species: Parthenium argentatum. hydroperoxide isomerase; linoleate hydroperoxide isomerase; linoleic acid hydroperoxide isomerase; HPI; (9Z,11E,14Z)-(13S)-hydroperoxyoctadeca-9,11,14-trienoate 12,13-hydro-lyase; (9Z,11E,14Z)-(13S)-hydroperoxyoctadeca-9,11,14-trienoate 12,13-hydro-lyase [(9Z)-(13S)-12,13-epoxyoctadeca-9,11-dienoate-forming]; allene oxide synthase; AOS; EC 4.2.1.92; hydroperoxide dehydratase. Pack: vial of ~300 μg. Cat No: NATE-0808.
α-1,6-Fucosidase solution from Elizabethkingia miricola, Recombinant
Tissue alpha-L-fucosidase is an enzyme that in humans is encoded by the FUCA1 gene. Alpha-Fucosidase is an enzyme that breaks down fucose. Fucosidosis is an autosomal recessive lysosomal storage disease caused by defective alpha-L-fucosidase with accumulation of fucose in the tissues. Different phenotypes include clinical features such as neurologic deterioration, growth retardation, visceromegaly, and seizures in a severe early form; coarse facial features, angiokeratoma corporis diffusum, spasticity and delayed psychomotor development in a longer surviving form; and an unusual spondylometaphyseoepiphyseal dysplasia in yet another form. Group: Enzymes. Synonyms: α-1,6-Fucosidase; alpha-L-fucosidase; Alpha-Fucosidase; FUCA1; FUCA; 9037-65-4. Enzyme Commission Number: EC 3.2.1.51. CAS No. 9037-65-4. FUCA. Activity: > 1.8 units/mg protein. Storage: 2-8°C. Form: buffered aqueous solution, Solution in 20 mM Tris-HCl, pH 7.5, 25 mM NaCl. Source: E. coli. Species: Elizabethkingia miricola. α-1,6-Fucosidase; alpha-L-fucosidase; Alpha-Fucosidase; FUCA1; FUCA; 9037-65-4. Pack: 0.04 unit in glass bottle. Cat No: NATE-0264.
Amidase from Pseudomonas aeruginosa, Recombinant
The amidase from Pseudomonas aeruginosa catalyzes the hydrolysis of a small range of short aliphatic amides. Each amidase monomer is formed by a globular four-layer αββα sandwich domain with an additional 81-residue long C-terminal segment. This enzyme belongs to the family of hydrolases, those acting on carbon-nitrogen bonds other than peptide bonds, specifically in linear amides. Applications: The importance of these hydrolases in biotechnology is growing rapidly, because their potential applications span through chemical and pharmaceutical industries as well as in bioremediation. immobilized amidase can be used efficiently for production of ac.onyms: acylamidase; acylase (misleading); amidohydrolase (ambiguous); deaminase (ambiguous); fatty acylamidase; N-acetylaminohydrolase (ambiguous); amidase; EC 3.5.1.4; acylamide amidohydrolase. Enzyme Commission Number: EC 3.5.1.4. CAS No. 9012-56-0. Amidase. Activity: >200 units/mg protein (biuret). Storage: Store at -20°C. Form: Solution in 50% glycerol containing 7 mM 2-mercaptoethanol and phosphate buffer salt. Source: E. coli. Species: Pseudomonas aeruginosa. acylamidase; acylase (misleading); amidohydrolase (ambiguous); deaminase (ambiguous); fatty acylamidase; N-acetylaminohydrolase (ambiguous); amidase; EC 3.5.1.4; acylamide amidohydrolase. Cat No: NATE-0809.
Amphotericin B Solution, 100X
Amphotericin B is a polyene antifungal agent for yeast, mold and mycoplasma. It was first isolated by Gold, et a., from Streptomyces nodosus in 1955. It is an amphoteric compound composed of a hydrophilic polyhydroxyl chain along one side and a lipophilic polyene hydrocarbon chain on the other. Amphotericin B is poorly soluble in water. Amphotericin B binds to sterols, preferentially to the primary fungal cell membrane sterol, ergosterol. This binding disrupts osmotic integrity of the fungal membrane, resulting in leakage of intracellular potassium, magnesium, sugars, and metabolites and then cellular death.Used in the preparation of baculoviral stocks.Amphotericin B Solution, 100X is composed of USP grade Amphotericin B in a High pH buffer (NaOH/Na+,H2O). The concentration of Amphotericin B in the final product is 0.25 g/L. Group: Biochemicals. Alternative Names: Abelcet; Abelecet; AmBisome; Ampho-Moronal; Amphocin; Amphozone; Apothecon; Fungilin; Fungizona; Fungizone; Halizon; LNS-AmB; NS 718; NSC 527017. Grades: Cell Culture Grade. CAS No. 1397-89-3. Pack Sizes: 50ml, 100ml. Molecular Formula: C47H73NO17, Molecular Weight: 924.09. US Biological Life Sciences.
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.
Amyloid Precursor Protein ? (304-612), Secreted human
>90% (SDS-PAGE), recombinant, expressed in E. coli (N-terminal histidine tagged), buffered aqueous solution. Group: Fluorescence/luminescence spectroscopy.
Amyloid Precursor Protein ?, Secreted human
>90% (SDS-PAGE), recombinant, expressed in E. coli (N-terminal histidine tagged), buffered aqueous solution. Group: Fluorescence/luminescence spectroscopy.
Anhydrous Citric Acid
Anhydrous Citric Acid. Synonyms: Citric acid, anhydrous. CAS No. 77-92-9. Product ID: PE-0426. Molecular formula: C6H8O7·H2O. Mole weight: 192.13. Category: Buffer; pH regulator; Flavoring Agents; Stabilizer; Excipient; Disintegrant. Product Keywords: Flavoring Agents; Stabilizers; PE-0426; Anhydrous Citric Acid; Buffer; pH regulator; Flavoring Agents; Stabilizer; Excipient; Disintegrant; C6H8O7·H2O; 77-92-9. UNII: XF417D3PSL. Chemical Name: 2-Hydroxypropane-1, 2, 3-tricarboxylic acid. Grade: Pharmceutical Excipients. Administration route: Oral, intravenous, eye, ear and nose, inhalation general external use. Dosage Form: Oral, intravenous, eye, ear and nose, inhalation general external use. Stability and Storage Conditions: Dilute citric acid solution can be fermented while standing. Store in air-tight container in a cool and dry place. Source and Preparation: Citric acid occurs naturally in large quantities in plants and is extracted from lemon juice, which contains 5 to 8% citric acid, or from pear residue. Citric acid can be purified by double junction and monohydrate can be prepared from cooled concentrated aqueous solution. Applications: Often used as buffer, pH regulator, flavor correction agent, stabilizer, excipatory agent, disintegrating agent, etc. Safety: Citric acid is found in the human body, mostly in the bones. Usually consumed as part of a normal diet. Citric acid can be absorbed orally and i