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| Product | Description | |
|---|---|---|
| 2,5-didehydrogluconate reductase (2-dehydro-L-gulonate-forming) | The enzyme is involved in ketogluconate metabolism, and catalyses the reaction in vivo in the reverse direction to that shown. It is used in the commercial microbial production of ascorbate. cf. EC 1.1.1.274, 2,5-didehydrogluconate reductase (2-dehydro-D-gluconate-forming). Group: Enzymes. Synonyms: 2,5-diketo-D-gluconate-reductase (ambiguous); YqhE reductase; dkgA (gene name); dkgB (gene name). Enzyme Commission Number: EC 1.1.1.346. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0261; 2,5-didehydrogluconate reductase (2-dehydro-L-gulonate-forming); EC 1.1.1.346; 2,5-diketo-D-gluconate-reductase (ambiguous); YqhE reductase; dkgA (gene name); dkgB (gene name). Cat No: EXWM-0261. |  |
| 2-Nitrophenyl caprylate | 2-Nitrophenyl caprylate, a biomedical compound renowned for its therapeutic efficacy, stands as a cornerstone in the fight against bacterial infections due to its remarkable antimicrobial attributes. Its multifaceted utility extends further as an invaluable tool in deciphering enzyme kinetics and microbial metabolism, thereby propelling the advancement of tailored pharmaceutical interventions against infectious ailments. Synonyms: 2-Nitrophenyl octanoate ONP-caprylate. CAS No. 104809-25-8. Molecular formula: C14H19NO4. Mole weight: 265.31. |  |
| 3-Amino-3-deoxy-b-D-fructofuranose | 3-Amino-3-deoxy-b-D-fructofuranose is a highly coveted compound forging novel alliances with specific enzymes and proteins culminating in bespoke pharmaceuticals for research of metabolic dysregulation, malignancies, and microbial invasions. CAS No. 402856-08-0. Molecular formula: C6H13NO5. Mole weight: 179.17. | |
| 4,5-Dihydro-4,5-dioxo-1H-pyrrolo[2,3-f]quinoline-2,7,9-tricarboxylic Acid (Methoxatin, Pyrroloquinoline, PQQ) | A cofactor of microbial quinoprotein enzyme, and imidazopyrroline. A redox/cofactor found in a a class of enzymes called quinoproteins. Group: Biochemicals. Alternative Names: Methoxatin, Pyrroloquinoline, PQQ. Grades: Highly Purified. Pack Sizes: 2.5mg. US Biological Life Sciences. |  Worldwide |
| 4-Amino-1-(6-(hydroxymethyl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)-1,3,5-triazin-2(1H)-one | 4-Amino-1-(6-(hydroxymethyl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)-1,3,5-triazin-2(1H)-one is an intriguing organic compound that has been extensively researched in the biomedical industry. The compound displays remarkable potential as a DNA topoisomerase inhibitor, a crucial enzyme involved in DNA replication and cell growth. Its distinctive chemical structure is expected to revolutionize drug discovery and development for the treatment of various cancers and microbial infections. Synonyms: 4-amino-1-[2,3-O-(1-methylethylene)pentofuranosyl]-1,3,5-triazine-2(1H)-one. Grades: 98%. CAS No. 686300-58-3. Molecular formula: C11H16N4O5. Mole weight: 284.27. | |
| 4-Bromophenyl 2-acetamido-2-deoxy-b-D-glucopyranoside | 4-Bromophenyl 2-acetamido-2-deoxy-b-D-glucopyranoside, a biomedical compound, exhibits potential in the investigation and advancement of pharmacological interventions for diverse pathological conditions. Its exceptional attributes and intricate configuration render it a promising candidate for selectively targeting receptors and enzymes implicated in neoplastic ailments, microbial infestations, and immune-mediated dysfunctions. CAS No. 38229-80-0. Molecular formula: C14H18BrNO6. Mole weight: 376.2. | |
| 4-Methoxyphenyl 2-acetamido-4-O-(2,3,4,6-tri-O-acetyl-b-D-glucopyranosyl)-3,6-di-O-benzyl-2-deoxy-b-D-glucopyranoside | 4-Methoxyphenyl 2-acetamido-4-O-(2,3,4,6-tri-O-acetyl-b-D-glucopyranosyl)-3,6-di-O-benzyl-2-deoxy-b-D-glucopyranoside is a compound of immense academic and scientific significance, employed for the efficacious research of an array of ailments. Its multifarious potential encompasses research of inflammation, malignancies is and microbial invasions. This extraordinary compound, owing to its exceptional chemical architecture, effectively converges on precise pharmacological receptors and enzymes. Molecular formula: C43H51NO16. Mole weight: 837.86. | |
| 4-Methoxyphenyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-b-D-glucopyranoside | 4-Methoxyphenyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-b-D-glucopyranoside is an innovative biomedical compound, holding promise in the realm of disease research. Its remarkable attributes encompass potent anti-inflammatory is anti-cancer is and anti-microbial capabilities. This exceptional compound demonstrates its efficacy by precisely targeting disease pathways' distinctive receptors and enzymes is amplifying its relevance in the realm of pharmaceutical research and drug development. Synonyms: 4-Methoxyphenyl 3,4,6-Tri-O-acetyl-2-deoxy-2-phthalimido-beta-D-glucopyranoside; 4-Methoxyphenyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-b-D-glucopyranoside; (2R,3S,4R,5R,6S)-2-(Acetoxymethyl)-5-(1,3-dioxoisoindolin-2-yl)-6-(4-methoxyphenoxy)tetrahydro-2H-pyran-3,4-diyl diacetate; [(2R,3S,4R,5R,6S)-3,4-diacetyloxy-5-(1,3-dioxoisoindol-2-yl)-6-(4-methoxyphenoxy)oxan-2-yl]methyl acetate; [(2R,3S,4R,5R,6S)-3,4-bis(acetyloxy)-5-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)-6-(4-methoxyphenoxy)oxan-2-yl]methyl acetate; beta-D-Glucopyranoside, 4-methoxyphenyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-, 3,4,6-triacetate; SCHEMBL2058839; DTXSID60458947; AKOS027320196; AS-74882; M1480; D91510; (2R,3S,4R,5R,6S)-2-(Acetoxymethyl)-5-(1,3-dioxoisoindolin-2-yl)-6-(4-methoxyphenoxy)tetrahydro-2H-pyran-3,4-diyldiacetate; 4-Methoxyphenyl 3,4,6-tri-O-acetyl-2-deoxy-2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-beta-D-glucopyranoside. CAS No. 138906-41-9. Molecular formula: C27H27NO11. Mole weight: 541.52. | |
| 4-Methylumbelliferyl 2-acetamido-2-deoxy-b-D-glucopyranoside | 4-Methylumbelliferyl 2-acetamido-2-deoxy-b-D-glucopyranoside is an intricate fluorogenic substrate commonly utilized for comprehensive detection of microbial enzymes. Specifically, the substrate facilitates the identification of Escherichia coli and Salmonella Typhimurium through monitoring the hydrolization of N-acetylglucosamine, a vital facet of bacterial cell walls. The advantageous emission of fluorophores when this substrate is cleaved by the aforementioned enzymes reinforces its effectiveness in resistance determination and ailment diagnosis. Synonyms: 4-Methylumbelliferyl N-acetyl-b-D-glucosaminide; 4-MU-GlcNAc; GlcNAc-b-4MU; 2H-1-Benzopyran-2-one, 7-[[2-(acetylamino)-2-deoxy-b-D-glucopyranosyl]oxy]-4-methyl-. Grades: ≥98%. CAS No. 37067-30-4. Molecular formula: C18H21NO8. Mole weight: 379.36. | |
| 4-Methylumbelliferyl phosphocholine | 4-Methylumbelliferyl phosphocholine, a highly sought-after fluorescent substrate within the biomedical industry, boasts immense significance in elucidating the intricacies surrounding phosphocholine-hydrolyzing enzymes. Touted for its efficacy in ascertaining the activity of microbial phospholipases, pivotal actors in the realm of bacterial and fungal pathogenesis, this substrate undeniably opens Pandora's box of insights into the multifaceted mechanics governing diverse infectious diseases. CAS No. 97055-84-0. Molecular formula: C15H20NO6P. Mole weight: 341.30. | |
| 4-Nitrophenyl 6-O-DMT-2,3,4-tri-O-levulinoyl-a-D-mannopyranoside | 4-Nitrophenyl 6-O-DMT-2,3,4-tri-O-levulinoyl-α-D-mannopyranoside is a biomedical compound, finding extensive application in the pharmaceutical domain for research of infections caused by particular microbial pathogens. It demonstrates exceptional proficiency as an inhibitor of select enzymes implicated in aberrant physiological pathways linked to distinct pathological conditions. Molecular formula: C48H51NO16. Mole weight: 897.92. | |
| 4-Nitrophenyl b-D-cellotetraoside | 4-Nitrophenyl b-D-cellotetraoside, an immensely valuable chemical compound in the realm of biomedical research, stands prominently at the forefront of scientific exploration. Acknowledged for its pivotal role as a substrate, it serves as an indispensable tool for quantifying enzyme activity and delving into the enigmatic realm of carbohydrate metabolism. By virtue of its striking semblance to cellulose, this compound unveils a compelling narrative elucidating the intricate mechanisms of cellulases in microbial degradation. Synonyms: P-NITROPHENYL BETA-D-CELLOTETRAOSIDE; 4-Nitrophenyl b-D-cellotetraoside; P-NITROPHENYL B-D-CELLOTETRAOSIDE; (2S,3R,4S,5S,6R)-2-[(2R,3S,4R,5R,6S)-6-[(2R,3S,4R,5R,6S)-6-[(2R,3S,4R,5R,6S)-4,5-dihydroxy-2-(hydroxymethyl)-6-(4-nitrophenoxy)oxan-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol; p-Nitrophenyl |A-D-Cellotetraoside; p-nitrophenyl-beta-D-cellotetraoside; DTXSID40680648; 4-Nitrophenyl ??-D-Cellotetraoside; 4-nitrophenyl-beta-D-cellotetraoside; p-Nitrophenyl beta -D-Cellotetraoside; AKOS040755910; PD057547; W-201015; 4-Nitrophenyl beta-D-glucopyranosyl-(1->4)-beta-D-glucopyranosyl-(1->4)-beta-D-glucopyranosyl-(1->4)-beta-D-glucopyranoside. CAS No. 129411-62-7. Molecular formula: C30H45NO23. Mole weight: 787.67. | |
| 5-Bromo-5-nitro-1,3-dioxane | 5-Bromo-5-nitro-1,3-dioxane, an antimicrobial compound, is effective against Gram-positive and Gram-negative bacteria and fungi, including yeast. 5-Bromo-5-nitro-1,3-dioxane inhibits enzyme activity and subsequent inhibition of microbial growth by the oxidation of essential protein thiol [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 30007-47-7. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-W014316. |  |
| 5-Bromo-5-nitro-1,3-dioxane | 5-bromo-5-nitro-1,3-Dioxane is an antimicrobial compound that is effective against Gram-positive and Gram-negative bacteria and fungi, including yeast.1 Its mode of action occurs via the oxidation of essential protein thiols causing inhibition of enzyme activity and subsequent inhibition of microbial growth.1 This compound has been used as a preservative for biological molecules and solutions such as antibodies and antisera. Group: Biochemicals. Grades: Highly Purified. CAS No. 30007-47-7. Pack Sizes: 50g, 100g, 250g, 500g, 1Kg. Molecular Formula: C?H?BrNO?, Molecular Weight: 212. US Biological Life Sciences. | Worldwide |
| 6-Chloro-3-indolyl 2-acetamido-2-deoxy-b-D-galactopyranoside | 6-Chloro-3-indolyl 2-acetamido-2-deoxy-b-D-galactopyranoside, a potent biomedicine compound, serves as a crucial tool in scientific research. Its utility lies in precisely detecting and localizing targeted enzymes, making it indispensable in biomedicine exploration. Researchers harness its potential to unravel the intricacies of drug resistance, microbial infections, and various diseases, which expedites the progress of drug discovery and development. Synonyms: 6-Chloro-3-indolyl-N-acetyl-b-D-galactosaminide Salmon-b-D-GalNAc 6-Chloro-3-(2-acetamido-2-deoxy-b-D-galactopyranosyloxy)indole. CAS No. 501432-61-7. Molecular formula: C16H19ClN2O6. Mole weight: 370.78. | |
| 6-Chloro-6-deoxy-D-mannose | 6-Chloro-6-deoxy-D-mannose acts as an antimicrobial agent, inhibiting the growth of certain bacteria and fungi. It displays potent activity against specific drug-resistant strains, making it an essential tool in combating these infections. Its mechanism of action involves targeting key enzymes required for microbial growth, offering a promising solution for drug resistance challenges. CAS No. 4990-81-2. Molecular formula: C6H11ClO5. Mole weight: 198.60. | |
| 8-Hydroxyquinoline b-D-galactopyranoside | 8-Hydroxyquinoline b-D-galactopyranoside is a compound with diverse biomedical applications, showcasing exceptional capabilities in research of microbial infections. Its multifaceted functionality extends towards inhibiting specific cancer-associated enzymes. Synonyms: 8-Hydroxy-1-azanaphthalene b-D-galactoside HQGal. CAS No. 113079-84-8. Molecular formula: C15H17NO6. Mole weight: 307.3. | |
| Alanine dehydrogenase, expressed in E. coli | Alanine dehydrogenase, expressed in E. coli is a microbial enzyme that catalyzes a reversible conversion of L-alanine to pyruvate [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 9029-6-5. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P2854. | |
| alpha-Man-TEG-SH | Alpha-Man-TEG-SH is an exceedingly influential compound, encompassing a distinctive alpha-mannosidase inhibitor, which selectively directs its action towards distinct enzymes participating in carbohydrate metabolism. Notably, this remarkable compound showcases inhibitory efficacy in the control of metabolic anomalies and research of compound-resistant microbial affections. Molecular formula: C12H24O8S. Mole weight: 328.38. | |
| Benzyl 2-acetamido-3-O-(2,3,4,6-tetra-O-acetyl-b-D-galactopyranosyl)-4,6-O-benzylidene-2-deoxy-a-D-galactopyranose | Benzyl 2-acetamido-3-O-(2,3,4,6-tetra-O-acetyl-b-D-galactopyranosyl)-4,6-O-benzylidene-2-deoxy-a-D-galactopyranose, a biomedicine of significant scientific interest, demonstrates remarkable potential in the field of disease treatment. With its impressive inhibitory abilities against specific enzymes, this compound poses as an invaluable asset for the pursuit of drug discovery and development. Notably, it exhibits exceptional therapeutic effects against viral infections, microbial diseases, and select cancers by specifically targeting fundamental cellular processes. Molecular formula: C36H43NO15. Mole weight: 729.72. | |
| β-cyclopiazonate dehydrogenase | A flavoprotein (FAD). Cytochrome c and various dyes can act as acceptor. Cyclopiazonate is a microbial toxin. Group: Enzymes. Synonyms: β-cyclopiazonate oxidocyclase; β-cyclopiazonic oxidocyclase; β-cyclopiazonate:(acceptor) oxidoreductase (cyclizing). Enzyme Commission Number: EC 1.21.99.1. CAS No. 9059-00-1. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1262; β-cyclopiazonate dehydrogenase; EC 1.21.99.1; 9059-00-1; β-cyclopiazonate oxidocyclase; β-cyclopiazonic oxidocyclase; β-cyclopiazonate:(acceptor) oxidoreductase (cyclizing). Cat No: EXWM-1262. | |
| Chitosanase from Bacillus sp. (food grade) | Chitosanase is a powdered chitosanase preparation made by submerged fermentation of a selected strain of the bacterium Bacillus sp. The enzyme catalyzes the breakdown of chitosan, a partially or completely de-acetylated derivative of chitin (β-1,4 homopolymer of N-acetyl glucosamine). Applications: Chitosanase can be used for hydrolyzing chitosan (degree of de-acetylatin: 40~100%). especially, it can be used for the production of chitosan oligosaccharides from chitosan, which have a variety of biological activities such as immuno-stimulating activity, anti-tumor activity, anti-microbial activity, etc. Group: Enzymes. Synonyms: Chitosanase; EC 3.2.1.132; 51570-20-8; Chitosan N-acetylglucosaminohydrolase. Chitosanase. Mole weight: 45,000Da estimated by SDS-PAGE. Activity: 35,000U/g. Storage: The product should be stored in a cool, dry environment with temperatures below 4°C. Form: White or light yellow colored, freeze-dried powder. Chitosanase; EC 3.2.1.132; 51570-20-8; Chitosan N-acetylglucosaminohydrolase. Cat No: CHIC-001. | |
| Cholesterol oxidase | Cholesterol oxidase. Synonyms: EC 1.1.3.6;EC: 1.1.3.6;CHOLESTEROL OXIDASE;CHOLESTEROL OXIDASE MICROBIAL;CHOLESTEROL OXIDASE, NOCARDIA SPECIES;CHOLESTEROL: OXYGEN OXIDOREDUCTASE;CHOLESTEROL: OXYGEN OXIDOREDUCTASE MICROBIAL;cholesterol oxidase F. pseudomonas sp. CAS No. 9028-76-6. Product ID: CDF4-0046. Category: Enzyme Preparations. Product Keywords: Food Ingredients; Enzyme Preparations; Cholesterol oxidase; CDF4-0046; 9028-76-6; 232-842-1; 9028-76-6. Purity: 0.99. Color: Pale yellow. EC Number: 232-842-1. Physical State: Solution (Slightly hazy). Solubility: 50 mM potassium phosphate buffer, pH 7.0: soluble (Cold). Storage: -70°C. Product Description: Cholesterol Oxidase produced from Streptomyces sp corresponds to a molecular weight of 62 kDa. It has a pH and temperature optimum of 7 and 37 °C, respectively. Cholesterol Oxidase comprises a FAD-binding and a steroid-binding domain. |  |
| deuterolysin | Proteolytic activity found in Penicillium roqueforti, P. caseicolum, Aspergillus sojae and A. oryzae. Optimum pH of 5 for digesting various proteins. Strong action on protamine and histones. Insensitive to phosphoramidon. About 20 kDa. A distinct Aspergillus sojae endopeptidase is larger and has a neutral pH optimum. Type example of peptidase family M35. Formerly included in EC 3.4.24.4. Group: Enzymes. Synonyms: Penicillium roqueforti protease II; microbial neutral proteinase II; acid metalloproteinase; neutral proteinase II; Penicillium roqueforti metalloproteinase. Enzyme Commission Number: EC 3.4.24.39. CAS No. 247028-11-1. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4321; deuterolysin; EC 3.4.24.39; 247028-11-1; Penicillium roqueforti protease II; microbial neutral proteinase II; acid metalloproteinase; neutral proteinase II; Penicillium roqueforti metalloproteinase. Cat No: EXWM-4321. | |
| Dextranase 66A from Bacteroides thetaiotaomicron, Recombinant | An endodextranase that hydrolyzes-(1,6)-glucosidic linkages in dextran. Dextrans are undesirable compounds synthesized from sucrose by microbial contaminants during sugar production that increase viscosity of the flow and decrease industrial recovery. Dextranase has been used for hydrolyzing dextran at sugar mills in order to improve efficiency of sugar production. Group: Enzymes. Synonyms: EC 3.2.1.11, dextran hydrolase; endodextranase; dextranase DL 2; DL 2; endo-dextranase; α-D-1,6-glucan-6-glucanohydrolase; 1,6-α-D-glucan 6-glucanohydrolase; 9025-70-1; Dextranase. Enzyme Commission Number: EC 3.2.1.11. CAS No. 9025-70-1. Purity: >90% by SDS-PAGE. Dextranase. Mole weight: 43.8 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacteroides thetaiotaomicron. EC 3.2.1.11, dextran hydrolase; endodextranase; dextranase DL 2; DL 2; endo-dextranase; α-D-1,6-glucan-6-glucanohydrolase; 1,6-α-D-glucan 6-glucanohydrolase; 9025-70-1; Dextranase; Dextranase 66A. Cat No: NATE-1307. | |
| (-)-D-Noviose | (-)-D-Noviose, a carbohydrate derivative, possesses promising therapeutic implications in the management of metabolic ailments and microbial infections. It has been established that (-)-D-Noviose manifests inhibitory tendencies towards bacterial enzymes implicated in peptidoglycan biogenesis, vital for bacterial cell wall maintenance. Furthermore, researchers have explored the applicability of (-)-D-Noviose as a putative glycosylation inhibitor in recombinant protein production, opening new avenues for biopharmaceutical research. Synonyms: 6-Deoxy-5-C-methyl-4-O-methyl-D-lyxo-hexose. CAS No. 206185-18-4. Molecular formula: C8H16O5. Mole weight: 192.21. | |
| Ethyl 3,4-di-O-acetyl-2-O-benzyl-1-thio-b-L-fucopyranoside | Ethyl 3,4-di-O-acetyl-2-O-benzyl-1-thio-b-L-fucopyranoside is an indispensable compound in biomedicine, showcasing its significance in the realm of medication development for a wide range of diseases, with a particular focus on glycosylation processes. Serving as a pivotal intermediary, it facilitates the synthesis of prospective pharmaceuticals, specifically designed to target precise enzymes or receptors. Underpinning biomedical investigations, this pivotal tool enables profound scrutiny of glycosylation-associated proteins and their intricate involvement in afflictions such as cancer and microbial infections. Synonyms: (2S,3R,4R,5S,6R)-5-(Benzyloxy)-6-(ethylthio)-2-methyltetrahydro-2H-pyran-3,4-diyl diacetate. CAS No. 254444-59-2. Molecular formula: C19H26O6S. Mole weight: 382.5. | |
| Ethyl a-D-thioglucopyranoside | Ethyl α-D-thioglucopyranoside is a vital compound in biomedicine utilized for various purposes. It acts as a precursor in the synthesis of various drugs used in treating diabetes, cancer, and microbial infections. Moreover, it plays a crucial role in carbohydrate chemistry research, supporting the investigation of enzyme inhibitors and glycosylation reactions. Ethyl α-D-thioglucopyranoside's availability and versatility contribute to advancements in biomedicine, fostering drug development and pivotal studies on carbohydrate-based therapies. Synonyms: Ethyl a-thioglucopyranoside. CAS No. 13533-58-9. Molecular formula: C8H16O5S. Mole weight: 224.28. | |
| feruloyl esterase | Catalyses the hydrolysis of the 4-hydroxy-3-methoxycinnamoyl (feruloyl) group from an esterified sugar, which is usually arabinose in "natural" substrates. p-Nitrophenol acetate and methyl ferulate are poorer substrates. All microbial ferulate esterases are secreted into the culture medium. They are sometimes called hemicellulase accessory enzymes, since they help xylanases and pectinases to break down plant cell wall hemicellulose. Group: Enzymes. Synonyms: ferulic acid esterase, hydroxycinnamoyl esterase, hemicellulase accessory enzymes; FAE-III, cinnamoyl ester hydrolase, FAEA, cinnAE, FAE-I, FAE-II. Enzyme Commission Number: EC 3.1.1.73. CAS No. 134712-49-5. Feruloyl esterase. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3501; feruloyl esterase; EC 3.1.1.73; 134712-49-5; ferulic acid esterase, hydroxycinnamoyl esterase, hemicellulase accessory enzymes; FAE-III, cinnamoyl ester hydrolase, FAEA, cinnAE, FAE-I, FAE-II. Cat No: EXWM-3501. | |
| fructose-bisphosphate aldolase | Also acts on (3S,4R)-ketose 1-phosphates. The yeast and bacterial enzymes are zinc proteins. The enzymes increase electron-attraction by the carbonyl group, some (Class I) forming a protonated imine with it, others (Class II), mainly of microbial origin, polarizing it with a metal ion, e.g. zinc. Group: Enzymes. Synonyms: aldolase; fructose-1,6-bisphosphate triosephosphate-lyase; fructose diphosphate aldolase; diphosphofructose aldolase; fructose 1,6-diphosphate aldolase; ketose 1-phosphate aldolase; phosphofructoaldolase; zymohexase; fructoaldolase; fructose 1-phosphate aldolase; fructose 1-monophosphate aldolase; 1,6-diphosphofructose aldolase; SMALDO; D-fructose-1,6-bisph. Enzyme Commission Number: EC 4.1.2.13. CAS No. 9024-52-6. Aldolase. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4853; fructose-bisphosphate aldolase; EC 4.1.2.13; 9024-52-6; aldolase; fructose-1,6-bisphosphate triosephosphate-lyase; fructose diphosphate aldolase; diphosphofructose aldolase; fructose 1,6-diphosphate aldolase; ketose 1-phosphate aldolase; phosphofructoaldolase; zymohexase; fructoaldolase; fructose 1-phosphate aldolase; fructose 1-monophosphate aldolase; 1,6-diphosphofructose aldolase; SMALDO; D-fructose-1,6-bisphosphate D-glyceraldehyde-3-phosphate-lyase. Cat No: EXWM-4853. | |
| hypodermin C | From the larva of a warble fly, Hypoderma lineatum. Little action on small molecule substrates of trypsin, chymotrypsin, elastase or microbial collagenases. In peptidase family S1 (trypsin family). Group: Enzymes. Synonyms: Hypoderma collagenase. Enzyme Commission Number: EC 3.4.21.49. CAS No. 122191-36-0. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4142; hypodermin C; EC 3.4.21.49; 122191-36-0; Hypoderma collagenase. Cat No: EXWM-4142. | |
| Hypromellose(15000cps) | Hypromellose(15000cps). Synonyms: Cellulosehydroxypropyl methyl ether; HPMC; methyl hydroxypropylcellulose; hydroxypropyl ; methylcellulose propylene glycol ether. CAS No. 9004-65-3. Product ID: PE-0640. Molecular formula: C8H15O8-(C10H18O6 ) n- C8H15O8. Category: Thickening Agents; Suspending Agents; Gel Agents. Product Keywords: Excipients for Liquid Dosage Form; Suspending Agents; PE-0640; Hypromellose(15000cps); Thickening Agents; Suspending Agents; Gel Agents; C8H15O8-(C10H18O6 ) n- C8H15O8; 9004-65-3. UNII: 3NXW29V3WO. Chemical Name: Cellulose, 2-hydroxypropyl methyl ether. Grade: Pharmceutical Excipients. Administration route: Eye drops and oral. Dosage Form: Ophthalmic preparations, oral capsules, suspensions, syrups and tablets; Topical and vaginal preparations. Stability and Storage Conditions: Hydroxypropyl methylene cellulose after drying moisture absorption, but the property is stable. The solution is stable at pH 3 ~ 11. The viscosity of solution decreases as temperature increases. Heating - cooling can make the reversible transformation of hydroxypropyl methylene cellulose from solution to gel state. Depending on different grades and concentrations, the gelation temperature is 50 ~ 90°C. The aqueous solution of hydroxypropyl methylcellulose has anti-enzyme effect and maintains good viscosity stability during long-term storage. However, its aqueous solution is susceptible to microbial attack, so | |
| Hypromellose K100M | Hypromellose K100M. Synonyms: Cellulosehydroxypropyl methyl ether; HPMC; methyl hydroxypropylcellulose; hydroxypropyl ; methylcellulose propylene glycol ether. CAS No. 9004-65-3. Product ID: PE-0538. Molecular formula: C8H15O8-(C10H18O6)n-C8H15O8. Mole weight: 10 000~1 500 000. Category: Thickener; Stabilizer; Emulsifier; Gelling Agents; Suspension Agents. Product Keywords: Stabilizers; Emulsifier Excipients; PE-0538; Hypromellose K100M; Thickener; Stabilizer; Emulsifier; Gelling Agents; Suspension Agents; C8H15O8-(C10H18O6)n-C8H15O8; 9004-65-3. UNII: 3NXW29V3WO. Grade: Pharmceutical Excipients. Administration route: Ophthalmic, oral; Topical and vaginal. Dosage Form: Ophthalmic preparations, oral capsules, suspensions, syrups and tablets; Topical and vaginal preparations. Stability and Storage Conditions: Hydroxypropyl methylene cellulose after drying moisture absorption, but the property is stable. The solution is stable at pH 3 ~ 11. The viscosity of solution decreases as temperature increases. Heating - cooling can make the reversible transformation of hydroxypropyl methylene cellulose from solution to gel state. Depending on different grades and concentrations, the gelation temperature is 50 ~ 90°C. The aqueous solution of hydroxypropyl methylcellulose has anti-enzyme effect and maintains good viscosity stability during long-term storage. However, its aqueous solution is susceptible to microbial attack, so p | |
| Immobilized Acetyl esterase from Microbial | Catalyzed reaction: Hydrolysis of acetyl esters. Known substrates: Acetylated xylan, ethyl acetate, cephalosporin C and derivatives. Applications: Desacetylation of β-lactam antibiotics; broad range esterase; desacethylation of other substartes. Group: Enzymes. Synonyms: Acetyl esterase (Immobilized); Acetyl esterase; EC 3.1.1.72. Enzyme Commission Number: EC 3.1.1.72. Acetylxylan esterase. Activity: > 50 U/g of wet carrier. Storage: 4°C. Form: Immobilized. Source: Microbial. Acetyl esterase (Immobilized); Acetyl esterase; EC 3.1.1.72. Cat No: NATE-1168. | |
| indole-3-glycerol-phosphate lyase | Forms part of the defence mechanism against insects and microbial pathogens in the grass family, Gramineae, where it catalyses the first committed step in the formation of the cyclic hydroxamic acids 2,4-dihydroxy-2H-1,4-benzoxazin-3(4H)-one (DIBOA) and 2,4-dihydroxy-7-methoxy-2H-1,4-benzoxazin-3(4H)-one (DIMBOA). This enzyme resembles the α-subunit of EC 4.2.1.20, tryptophan synthase, for which, (1S,2R)-1-C-(indol-3-yl)glycerol 3-phosphate is also a substrate, but, unlike tryptophan synthase, its activity is independent of the β-subunit and free indole is released. Group: Enzymes. Synonyms: tryptophan synthase α; TSA; indoleglycerolphosphate aldolase; indole glycerol phosphate hydrolase; indole synthase; indole-3-glycerolphosphate D-glyceraldehyde-3-pho. Enzyme Commission Number: EC 4.1.2.8. CAS No. 9014-52-2. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4896; indole-3-glycerol-phosphate lyase; EC 4.1.2.8; 9014-52-2; tryptophan synthase α; TSA; indoleglycerolphosphate aldolase; indole glycerol phosphate hydrolase; indole synthase; indole-3-glycerolphosphate D-glyceraldehyde-3-phosphate-lyase; indole-3-glycerol phosphate lyase; IGL; BX1; (1S,2R)-1-C-(indol-3-yl)glycerol 3-phosphate D-glyceraldehyde-3-phosphate-lyase. Cat No: EXWM-4896. | |
| L-Arabinose | L(+)-Arabinose is a pentose monosaccharide whose transcription is regulated by Ara-C proteins and is a substrate for L-arabinose dehydrogenase, galactose dehydrogenase. It is not fermented by yeast. Used as a one-way or reversible switch for protein expression. It is also used to make arabinosyl nucleosides. L-Arabinose is used as a substrate to identify, differentiate and characterize pentose sugar isomerase(s). L-Arabinose is used in the bioproduction of L-ribose. L-Arabinose is the naturally occurring isomer and is a constituent of plant polysaccharides. Most bacteria contain an inducible arabinose operon that codes for a series of enzymes and transporters that allows L-arabinose to be used as the sole carbon source in microbial culture. Group: Biochemicals. Alternative Names: Beta-L-Arabinopyranose; Beta-L-(+)-ARABINOSE; L-(+)-Arabinose; Pectinose; Arabitol, L-(-)-(RG); L-Arabinopyranose; (2R,3R,4S,5S)-oxane-2,3,4,5-tetrol. Grades: Reagent Grade. CAS No. 87-72-9. Pack Sizes: 100g, 500g, 1Kg, 2.5Kg. Molecular Formula:?C5H10O5 , Molecular Weight:?150.13. US Biological Life Sciences. | Worldwide |
| mannan-binding lectin-associated serine protease-2 | Mannan-binding lectin (MBL) recognizes patterns of neutral carbohydrates, such as mannose and N-acetylglucosamine, on a wide range of microbial surfaces and is able to initiate activation of the lectin pathway of complement. This enzyme displays C1s-like esterolytic activity (cf. EC 3.4.21.42, complement subcomponent C1s). It also cleaves C4 and C2 with efficiencies that are relatively higher than those of EC 3.4.21.42. Belongs in peptidase family S1A. Group: Enzymes. Synonyms: MASP-2; MASP2; MBP-associated serine protease-2; mannose-binding lectin-associated serine protease-2; p100; mannan-binding lectin-associated serine peptidase 2. Enzyme Commission Number: EC 3.4.21.104. CAS No. 214915-16-9. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4099; mannan-binding lectin-associated serine protease-2; EC 3.4.21.104; 214915-16-9; MASP-2; MASP2; MBP-associated serine protease-2; mannose-binding lectin-associated serine protease-2; p100; mannan-binding lectin-associated serine peptidase 2. Cat No: EXWM-4099. | |
| Meropenem Sodium Carbonate | Meropenem with sodium carbonate is a salt form of Meropenem, a β-lactam antibiotic of the carbapenem subclass that has been shown to inhibit penicillinase-negative, -positive and methicillin-susceptible staphylococci. This compound demonstrates the ability to also affect strains of 11 species of streptococci. Mechanistic studies suggest that Meropenem's antimicrobial activity is based on its high affinity for the majority of penicillin-binding proteins, which are cell wall-synthesizing enzymes. Meropenem is very effective because it resists inactivation by the majority of microbial LACTB (β-lactamases) as well as kidney dehydropeptidase I. Experiments have shown Meropenem to have a low toxicity profile and, in contrast to similar compounds, no central nervous system toxicity. Synonyms: (4R, 5S, 6S)-3-[[(3S, 5S)5-[(Dimethylamino)carbonyl]-3-pyrrolidinyl]thio]-6-((1R)-1-hydroxyethyl)-4-methyl-7-oxo-1-azabicyclo[3, 2, 0]hept-2-ene-2-carboxyloc acid. CAS No. 96036-03-2 free acid. Product ID: PAP-0097. Molecular formula: C17H25N3O5S xNa2CO3. Mole weight: 383.46 (free acid). Product Keywords: Antibacterial, Anti-inflammatory and Antiviral Series; PAP-0097; Meropenem Sodium Carbonate; 96036-03-2 free acid; (4R, 5S, 6S)-3-[[(3S, 5S)5-[(Dimethylamino)carbonyl]-3-pyrrolidinyl]thio]-6-((1R)-1-hydroxyethyl)-4-methyl-7-oxo-1-azabicyclo[3, 2, 0]hept-2-ene-2-carboxyloc acid. Chemical Name: Meropenem with sodium carbona | |
| microbial collagenase | Six species of metalloendopeptidase acting on native collagen can be isolated from the medium of Clostridium histolyticum. Class I has forms α (68 kDa), β (115 kDa) and γ (79 kDa); class II has Δ (100 kDa), ε (110 kDa) and ζ (125 kDa). The two classes are immunologically crossreactive, but have significantly different sequences, and different specificities such that their actions on collagen are complementary. The enzymes also act as peptidyl-tripeptidases. Variants of the enzyme have been purified from Bacillus cereus, Empedobacter collagenolyticum, Pseudomonas marinoglutinosa, and species of Vibrio, Vibrio B-30 (ATCC 21250) and V. alginolyticu...ase-8; matirx metalloproteinase-18; interstitial collagenase. Enzyme Commission Number: EC 3.4.24.3. CAS No. 9001-12-1. Collagenase. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4311; microbial collagenase; EC 3.4.24.3; 9001-12-1; Clostridium histolyticum collagenase; clostridiopeptidase A; collagenase A; collagenase I; Achromobacter iophagus collagenase; collagenase; aspergillopeptidase C; nucleolysin; azocollase; metallocollagenase; soycollagestin; Clostridium histolyticum proteinase A; clostridiopeptidase II; MMP-8; clostridiopeptidase I; collagen peptidase; collagen protease; collagenase MM | |
| Microorganisms and enzymes blend for Petroleum sewage | This product is a microbial product, mixed by a number of high concentrations of non-pathogenic aerobic and autotrophic microorganisms and a variety of enzymes, these microorganisms can grow under aerobic and anaerobic conditions and is capable of degrading various cellulose and other organic substances in oil wastewater. This product also contains high active enzymes, can help degrade suspended solids and complex matters in the sludge. Group: Enzymes. Synonyms: microbial products; non-pathogenic aerobic microorganisms; autotrophic microorganisms; enzymes; oil wastewater; cellulose; organic substances; suspended solids; sludge; Natural microflora; Waste Management. Waste Management. Activity: 3×108 CFU/g. Appearance: Pale yellow to light brown powder. Storage: Below 25°C. microbial products; non-pathogenic aerobic microorganisms; autotrophic microorganisms; enzymes; oil wastewater; cellulose; organic substances; suspended solids; sludge; Natural microflora; Waste Management. Cat No: WME-2700. | |
| N-Acetyltaurine | N-Acetyltaurine is a sulfonate that can serve as a carbon source or a nitrogen source, and an energy source for microbial growth (such as the NAT strain). Additionally, N-Acetyltaurine is also a substrate for the amidase enzyme, porcine kidney N-acetyl-β-alanine deacetylase [EC 3.5.1.21] [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 19213-70-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-W587486. | |
| Native Acetyl esterase from Microbial | Catalyzed reaction: Hydrolysis of acetyl esters. Known substrates: Acetylated xylan, ethyl acetate, cephalosporin C and derivatives. Applications: Desacetylation of β-lactam antibiotics; broad range esterase; desacethylation of other substartes. Group: Enzymes. Synonyms: Acetyl esterase (Lyophilized); Acetyl esterase; EC 3.1.1.72. Enzyme Commission Number: EC 3.1.1.72. Acetylxylan esterase. Activity: > 50 U/mg of powder. Storage: Store at -20°C. Form: Lyophilized. Source: Microbial. Acetyl esterase (Lyophilized); Acetyl esterase; EC 3.1.1.72. Cat No: NATE-1169. | |
| Native Acid Phosphatase from Microbial | Acid phosphatases (APase) are a family of enzymes that non-specifically catalyze the hydrolysis of monoesters and anhydrides of phosphoric acid to produce inorganic phosphate at an optimum pH of 4 to 7. Acid phosphatase from potatoes is a 111 kDa diner consisting of two subunits at 41 and 35 kDa. This phosphatase has also been shown to cleave DNA. Applications: Hydrolysis of phosphate monoesters. Group: Enzymes. Synonyms: acid phosphatase; 9001-77-8; acid phosphomonoesterase; phosphomonoesterase; glycerophosphatase; acid monophosphatase; acid phosphohydrolase; acid phosphomonoester hydrolase; uteroferrin; acid nucleoside diphosphate phosphatase; orthophosphoric-monoester phosphohydrolase (acid optimum); EC 3.1.3.2; APase. Enzyme Commission Number: EC 3.1.3.2. CAS No. 9001-77-8. Apase. Activity: > 40 U/mg; > 100 U/ml. Storage: 4°C. Form: Suspension in Ammonium Sulphate. Source: Microbial. acid phosphatase; 9001-77-8; acid phosphomonoesterase; phosphomonoesterase; glycerophosphatase; acid monophosphatase; acid phosphohydrolase; acid phosphomonoester hydrolase; uteroferrin; acid nucleoside diphosphate phosphatase; orthophosphoric-monoester phosphohydrolase (acid optimum); EC 3.1.3.2; APase. Cat No: NATE-1170. | |
| Native Bacillus sp Chitosanase | Chitosanase is a powdered chitosanase preparation made by submerged fermentation of a selected strain of the bacterium Bacillus sp. The enzyme catalyzes the breakdown of chitosan, a partially or completely de-acetylated derivative of chitin (β-1,4 homopolymer of N-acetyl glucosamine). Applications: Chitosanase can be used for hydrolyzing chitosan(degree of de-acetylatin: 40?100%). especially, it can be used for the production of chitosan oligosaccharides from chitosan, which have a variety of biological activities such as immuno-stimulating activity, anti-tumor activity, anti-microbial activity, etc. Group: Enzymes. Synonyms: Chitosanase; EC 3.2.1.132; 51570-20-8; Chitosan N-acetylglucosaminohydrolase. Enzyme Commission Number: EC 3.2.1.132. CAS No. 51570-20-8. Chitosanase. Mole weight: 45,000Da estimated by SDS-PAGE. Activity: 35,000U/g. Appearance: White or light yellow colored, freeze-dried powder. Storage: The product should be stored in a cool, dry environment with temperatures below 4°C. Source: Bacillus sp. Chitosanase; EC 3.2.1.132; 51570-20-8; Chitosan N-acetylglucosaminohydrolase. Cat No: NATE-1746. | |
| Native Chaetomium erraticum Dextranase | An endodextranase that hydrolyzes-(1,6)-glucosidic linkages in dextran. Dextrans are undesirable compounds synthesized from sucrose by microbial contaminants during sugar production that increase viscosity of the flow and decrease industrial recovery. Dextranase has been used for hydrolyzing dextran at sugar mills in order to improve efficiency of sugar production. A fungal dextranase produced by submerged fermentation of chaetomium erraticum. stable in the ph range of 3-7 and at temperatures up to approx. 70 oc. for most applications, the preferred conditions are ph 5-6 and a temperature of 50-60°c. Applications: Dextranase from chaetomium erraticum has been used in a study to investigate the optimization of process conditions for enzymatic modification of alternan. dextranase from chaetomium erraticum has also been used in a study to investigate the immobilization of dextranase from chaetomium erraticum. Group: Enzymes. Synonyms: EC 3.2.1.11, dextran hydrolase; endodextranase; dextranase DL 2; DL 2; . Enzyme Commission Number: EC 3.2.1.11. CAS No. 9025-70-1. Dextranase. Storage: 2-8°C. Form: solution. Source: Chaetomium erraticum. EC 3.2.1.11, dextran hydrolase; endodextranase; dextranase DL 2; DL 2; endo-dextranase; α-D-1,6-glucan-6-glucanohydrolase; 1,6-α-D-glucan 6-glucanohydrolase; 9025-70-1; Dextranase. Cat No: NATE-0182. | |
| Native Chaetomium gracile Dextranase | An endodextranase that hydrolyzes-(1,6)-glucosidic linkages in dextran. Dextrans are undesirable compounds synthesized from sucrose by microbial contaminants during sugar production that increase viscosity of the flow and decrease industrial recovery. Dextranase has been used for hydrolyzing dextran at sugar mills in order to improve efficiency of sugar production. Group: Enzymes. Synonyms: EC 3.2.1.11, dextran hydrolase; endodextranase; dextranase DL 2; DL 2; endo-dextranase; α-D-1,6-glucan-6-glucanohydrolase; 1,6-α-D-glucan 6-glucanohydrolase; Dextranase. Enzyme Commission Number: EC 3.2.1.11. CAS No. 9025-70-1. Dextranase. Form: Liquid. Source: Chaetomium gracile. EC 3.2.1.11, dextran hydrolase; endodextranase; dextranase DL 2; DL 2; endo-dextranase; α-D-1,6-glucan-6-glucanohydrolase; 1,6-α-D-glucan 6-glucanohydrolase; Dextranase. Cat No: NATE-0873. | |
| Native Microbial α-phosphoglucomutase | Phosphoglucomutase (EC 5.4.2.2) is an enzyme that transfers a phosphate group on an α-D-glucose monomer from the 1' to the 6' position in the forward direction or the 6' to the 1' position in the reverse direction. More precisely, it facilitates the interconversion of glucose 1-phosphate and glucose 6-phosphate. High purity recombinant α-phosphoglucomutase (microbial) for use in research, biochemical enzyme assays and in vitro diagnostic analysis. Group: Enzymes. Synonyms: α-phosphoglucomutase; Phosphoglucomutase; EC 5.4.2.2; Phosphoglucomutase (alpha-D-glucose-1,6-bisphosphate-dependent); Glucose phosphomutase; Phosphoglucose mutase. Enzyme Commission Number: EC 5.4.2.2. CAS No. 9001-81-4. Phosphoglucomutase. Mole weight: MW ~ 59.2 kDa. Source: Microbial. α-phosphoglucomutase; Phosphoglucomutase; EC 5.4.2.2; Phosphoglucomutase (alpha-D-glucose-1,6-bisphosphate-dependent); Glucose phosphomutase; Phosphoglucose mutase. Cat No: DIA-265. | |
| Native Microbial Creatinine Deiminase | In enzymology, a creatinine deaminase (EC 3.5.4.21) is an enzyme that catalyzes the chemical reaction: creatinine + H2O <-> N-methylhydantoin + NH3. Thus, the two substrates of this enzyme are creatinine and H2O, whereas its two products are N-methylhydantoin and NH3. This enzyme belongs to the family of hydrolases, those acting on carbon-nitrogen bonds other than peptide bonds, specifically in cyclic amidines. The systematic name of this enzyme class is creatinine iminohydrolase. Applications: Creatinine deiminase has been used in a study to assess the application of a creatinine-sensitive biosensor for hemodialysis control. creatinine deiminase has also been used in a study to investigate the bioelectronic tongue for the simultaneous determination of urea, creatinine and alkaline ions in clinical samples. Group: Enzymes. Synonyms: EC 3.5.4.21, creatinine hydrolase; creatinine desiminase; creatinine deaminase; 37289-15-9. Enzyme Commission Number: EC 3.5.4.21. CAS No. 37289-15-9. Creatinine Deiminase. Mole weight: mol wt ~260 kDa. Activity: > 25 units/mg protein. Storage: -20°C. Form: Lyophilized powder containing mannitol as stabilizer. Source: Microbial. EC 3.5.4.21, creatinine hydrolase; creatinine desiminase; creatinine deaminase; 37289-15-9. Cat No: NATE-0164. | |
| Native Microbial Xanthine Oxidase | Xanthine oxidase is a molybdenum-containing enzyme that is found in the cytosol, and may be strongly inhibited by flavonoids. It plays a vital role in the metabolism of some drugs, as well as purines and pyrimidines. It is also known to be a biological source of reactive oxygen species. Xanthine oxidase was shown to be involved in the reduction of cytochrome c by the generation of superoxide anions following the oxidation of xanthine. These free radicals are responsible for reducing cytochrome c. Allopurinol is a synthetic drug show to inhibit xanthine oxidase. Applications: This enzyme is useful for enzymatic determination of inorganic phosphorus, 5?-nucleotidase and adenosine deaminase when coupled with purine-nucleoside phosphorylase and uricase. Group: Enzymes. Synonyms: Xanthine oxidase; XO; xanthine oxidoreductase; EC 1.17. Enzyme Commission Number: EC 1.17.3.2. CAS No. 9002-17-9. XAO. Mole weight: mol wt ~160 kDa. Activity: > 7 units/mg solid. Storage: -20°C. Form: Lyophilized powder containing BSA and sodium glutamate as stabilizers. Source: Microbial. Xanthine oxidase; XO; xanthine oxidoreductase; EC 1.17.3.2; 9002-17-9; XOD; Xanthine:oxygen oxidoreductase; hypoxanthine oxidase; hypoxanthine:oxygen oxidoreductase; Schardinger enzyme; hypoxanthine-xanthine oxidase; xanthine:O2 oxidoreductase; xanthine:xanthine oxidase. Cat No: NATE-0733. | |
| Native Penicillium sp. Dextranase | An endodextranase that hydrolyzes-(1,6)-glucosidic linkages in dextran. Dextrans are undesirable compounds synthesized from sucrose by microbial contaminants during sugar production that increase viscosity of the flow and decrease industrial recovery. Dextranase has been used for hydrolyzing dextran at sugar mills in order to improve efficiency of sugar production. Applications: Dextranase from penicillium has been used in a study to assess the purification properties of an extracellular dextranase from penicillium janthinellum. dextranase from penicillium has also been used in a study to investigate the carbohydrate component of penicillium funiculosum dextranase. it has been used for the hydrolysis of carbohydate polymers, during the study of polysaccharide synthesis by phanerochaete chrysosporium. it has also been used in the synthesis of new enzymatically degradable thermo-responsive nanogels. Group: Enzymes. Synonyms: EC 3.2.1.11, dextran hydrolase; endodextranase; dextran. Enzyme Commission Number: EC 3.2.1.11. CAS No. 9025-70-1. Dextranase. Activity: 3,000 units/mg. Storage: 2-8°C. Form: lyophilized powder. Source: Penicillium sp. EC 3.2.1.11, dextran hydrolase; endodextranase; dextranase DL 2; DL 2; endo-dextranase; α-D-1,6-glucan-6-glucanohydrolase; 1,6-α-D-glucan 6-glucanohydrolase; 9025-70-1; Dextranase. Cat No: NATE-0194. | |
| Native Porcine Lipoamide Dehydrogenase | Lipoamide dehydrogenase (or diaphorase) catalyzes the following reaction: Lipoamide + NADH + H+ ? Dihydrolipoamide + NAD+. The enzyme occurs in mammalian and microbial cells and it catalyzes a number of reactions which involve NAD+ or NADH. Lipoamide dehydrogenase from porcine heart contains two polypeptide chains which are similar. It has two molecules of tightly bound flavin adenine dinucleotide (FAD). The molecular weight of the porcine heart enzyme is between 100,000 and 114,000. Group: Enzymes. Synonyms: NADH: lipoamide oxidoreductase; EC 1.6.4.3; Lipoamide Dehydrogenase; LD. Enzyme Commission Number: EC 1.6.4.3. LD. Mole weight: 100-114 kDa. Activity: 25 U/mg protein. Stability: Store at -20°C (-4°F). Form: Freeze-dried powder. Source: Porcine Heart. Species: Porcine. NADH: lipoamide oxidoreductase; EC 1.6.4.3; Lipoamide Dehydrogenase; LD. Cat No: NATE-0894. | |
| Neutral Protease AF GMP Grade | Neutral Protease AF GMP Grade is manufactured according to cGMP guidelines using a production process completely free of animal-based components. In this way the introduction of any potential animal-derived pathogen is excluded. Neutral Protease AF GMP Grade is chromatographically purified and largely free from collagenolytic activity (PZ U) as well as endotoxins. The absence of any animal-derived ingredients and thorough microbial analysis provide the highest possible safety. Applications: Neutral protease af gmp grade is suitable for cell isolation from several tissue types for clinical applications. it is often used in combination with collagenase af-1 gmp grade. Group: Enzymes. Synonyms: Neutral Protease AF GMP Grade; Neutral Protease AF; Neutral Protease; Protease. Enzyme Commission Number: EC 3.4.21.62. CAS No. 9001-92-7. Protease. Mole weight: 34 000. Activity: ≥ 0.50 U/mg. Storage: 2 to 8 °C. Form: Lyophilized powder. Source: Clostridium histolyticum. Neutral Protease AF GMP Grade; Neutral Protease AF; Neutral Protease; Protease. Cat No: NATE-1920. | |
| Neutral proteinase from Bacillus sp. | Neutral proteinase from Bacillus sp. Applications: This enzyme is useful for synthesis of oligopeptides, for proteolysis of insoluble protein and for structural investigation of the protein. Group: Enzymes. Synonyms: Neutral proteinase; Cathepsin G; Microbial metalloproteinase; EC 3.4.24.4. Enzyme Commission Number: EC 3.4.24.4. CAS No. 70851-98-8. Neutral Protease. Mole weight: approx. 25,000 (SDS-PAGE). Activity: 1000U/mg-solid or more. Stability: Stable at 5°C for at least one year. Appearance: White amorphous powder or granule. Source: Bacillus sp. Neutral proteinase; Cathepsin G; Microbial metalloproteinase; EC 3.4.24.4. Cat No: DIA-273. | |
| O-(2-Acetamido-3,4,6-tri-O-acetyl-D-glucopyranosylidene)amino N-phenyl carbamate | O-(2-Acetamido-3,4,6-tri-O-acetyl-D-glucopyranosylidene)amino N-phenyl carbamate is a pivotal element, finding its application in research of cancer, neurodegenerative disorders and microbial infections by exerting inhibitory effects on associated enzymes. Synonyms: 2-Acetamido-3,4,6-tri-O-acetyl-2-deoxy-N-[(phenylaminocarbonyl)oxy]-D-gluconimidic acid-1,5-lactone. CAS No. 132063-04-8. Molecular formula: C21H25N3O10. Mole weight: 479.44. | |
| Phosphoenolpyruvate carboxylase | Phosphoenolpyruvate carboxylase. Synonyms: Phosphoenolpyruvic carboxylase;Phosphopyruvate carboxylase;Phosphoenol pyruvate carboxylase from maize;Phosphoenolpyruvate Carboxylase from maize leaves;Phospho(enol)pyruvate Carboxylase from Escherichia coli;Phosphoenolpyruvate carboxylase microbial;Phosphoenolpyruvate (PEP);Phosphoebolpyruvate Carboxylase. CAS No. 9067-77-0. Pack Sizes: 1 kg. Product ID: CDF4-0050. Molecular formula: NULL. Category: Enzyme Preparations. Product Keywords: Food Ingredients; Enzyme Preparations; Phosphoenolpyruvate carboxylase; CDF4-0050; 9067-77-0; 232-958-2; 9067-77-0. Purity: 0.98. EC Number: 232-958-2. Physical State: Suspension. Storage: -20°C. Application: Phosphoenolpyruvate carboxylase (PEPC) is an enzyme useful for enzymatic determination of carbon dioxide when coupled with malate dehydrogenase in clinical analysis. PEPC is also used to study carbon assimilation, post-translational regulation and allosteric regulation in various plants. | |
| Phosphoramidon disodium | Phosphoramidon disodium, a microbial metabolite , is a specific metalloprotease thermolysin inhibitor with an IC 50 of 0.4 μg/mL. Phosphoramidon disodium also inhibits endothelin-converting enzyme ( ECE ), neutral endopeptidase ( NEP ), and angiotensin-converting enzyme ( ACE ) with IC 50 values of 3.5, 0.034, and 78 μM, respectively [1] [2] [3]. Uses: Scientific research. Group: Natural products. CAS No. 164204-38-0. Pack Sizes: 5 mg; 10 mg. Product ID: HY-N2021A. | |
| prolyl aminopeptidase | A Mn2+-requiring enzyme present in the cytosol of mammalian and microbial cells. In contrast to the mammalian form, the bacterial form of the enzyme (type example of peptidase family S33) hydrolyses both polyproline and prolyl-2-naphthylamide. The mammalian enzyme, which is not specific for prolyl bonds, is possibly identical with EC 3.4.11.1, leucyl aminopeptidase. Group: Enzymes. Synonyms: proline aminopeptidase; Pro-X aminopeptidase; cytosol aminopeptidase V; proline iminopeptidase. Enzyme Commission Number: EC 3.4.11.5. CAS No. 9025-40-5. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4026; prolyl aminopeptidase; EC 3.4.11.5; 9025-40-5; proline aminopeptidase; Pro-X aminopeptidase; cytosol aminopeptidase V; proline iminopeptidase. Cat No: EXWM-4026. | |
| Pyrroloquinoline quinone | Pyrroloquinoline quinone is a cofactor of microbial quinoprotein enzyme, and imidazopyrroline. A redox/cofactor found in a a class of enzymes called quinoproteins. Applications: A redox/cofactor found in a a class of enzymes called quinoproteins. Group: Coenzymes. Synonyms: PQQ. CAS No. 72909-34-3. Mole weight: 330.2. Form: Solid. PQQ; Pyrroloquinoline quinone; 72909-34-3. Cat No: COEC-076. | |
| Ribonuclease T2 from Aspergillus oryzae, Recombinant | Aspergillus oryzae Ribonuclease T2 is a member of the RNase T2 family of endonucleases that are present in a wide variety of microbial, plant and animal species. In contrast to Aspergillus oryzae Ribonuclease T1, which is an exclusively guanylic-acid specific endonuclease, all RNase T2-like enzymes are essentially base non-specific. However, RNase T2 endonucleases from different species can show slight base preferences. The fungal enzymes, including Aspargillus oryzae RNaseT2, show slight base preference in the following order: A>G>C, U. RNase T2 cleaves between the 3-phosphate residue of one base and the 5-OH residue of the adjacent nucleotide forming a 2, 3-cyclic phosphate intermediate followed by the generation of oligonucleotides with 3-phosphate residues. This enzyme is also used as a non-mammalian source of RNase in various applications. Group: Enzymes. Synonyms: Ribonuclease T2; RNase T2; Ribonuclease. Enzyme Commission Number: EC 3.1.27.1. Rnase. Mole weight: 36 kDa. Activity: ≥10,000 units per mg protein. Stability: Stable at 12-18 months at 2-8°C. Storage: Store at 2-8°C. Form: Lyophilized powder. Source: Pichia pastoris. Species: Aspergillus oryzae. Ribonuclease T2; RNase T2; Ribonuclease. Cat No: NATE-1930. | |
| (S)-hydroxynitrile lyase | Hydroxynitrile lyases catalyses the the cleavage of hydroxynitriles into cyanide and the corresponding aldehyde or ketone. In nature the liberation of cyanide serves as a defense mechanism against herbivores and microbial attack in plants. In vitro the enzymes from Manihot esculenta and Hevea brasiliensis accept a broad range of aliphatic and aromatic carbonyl compounds as substrates and catalyse the formation of (S)-hydroxynitriles. Group: Enzymes. Synonyms: (S)-cyanohydrin producing hydroxynitrile lyase; (S)-oxynitrilase; (S)-HbHNL; (S)-MeHNL; hydroxynitrile lyase; oxynitrilase; HbHNL; MeHNL; (S)-selective hydroxynitrile lyase; (S)-cyanohydrin carbonyl-lyase (cyanide forming). Enzyme Commission Number: EC 4.1.2.47. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4883; (S)-hydroxynitrile lyase; EC 4.1.2.47; (S)-cyanohydrin producing hydroxynitrile lyase; (S)-oxynitrilase; (S)-HbHNL; (S)-MeHNL; hydroxynitrile lyase; oxynitrilase; HbHNL; MeHNL; (S)-selective hydroxynitrile lyase; (S)-cyanohydrin carbonyl-lyase (cyanide forming). Cat No: EXWM-4883. | |
| taurine-2-oxoglutarate transaminase | A pyridoxal-phosphate protein. Also acts on D,L-3-amino-isobutanoate, β-alanine and 3-aminopropanesulfonate. Involved in the microbial utilization of β-alanine. Group: Enzymes. Synonyms: taurine aminotransferase; taurine transaminase; taurine-α-ketoglutarate aminotransferase; taurine-glutamate transaminase. Enzyme Commission Number: EC 2.6.1.55. CAS No. 9076-52-2. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2896; taurine-2-oxoglutarate transaminase; EC 2.6.1.55; 9076-52-2; taurine aminotransferase; taurine transaminase; taurine-α-ketoglutarate aminotransferase; taurine-glutamate transaminase. Cat No: EXWM-2896. | |
| ureidoglycolate lyase | This microbial enzyme is involved in the degradation of ureidoglycolate, an intermediate of purine degradation. Not to be confused with EC 3.5.1.116, ureidoglycolate amidohydrolase, which releases ammonia rather than urea. Group: Enzymes. Synonyms: ureidoglycolatase (ambiguous); ureidoglycolase (ambiguous); ureidoglycolate hydrolase (misleading); (S)-ureidoglycolate urea-lyase. Enzyme Commission Number: EC 4.3.2.3. CAS No. 9014-57-7. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-5298; ureidoglycolate lyase; EC 4.3.2.3; 9014-57-7; ureidoglycolatase (ambiguous); ureidoglycolase (ambiguous); ureidoglycolate hydrolase (misleading); (S)-ureidoglycolate urea-lyase. Cat No: EXWM-5298. | |
| 2-Acetamido-1,3-di-O-benzyl-4,6-O-benzylidene-2-deoxy-b-D-glucopyranoside | 2-Acetamido-1,3-di-O-benzyl-4,6-O-benzylidene-2-deoxy-b-D-glucopyranoside is a multifaceted biomedical compound with remarkable aptitude in enzymatic modulation, bacterial growth inhibition and precise receptor targeting. It can be used to study microbial infestations, cancer, inflammation and diabetes. Synonyms: Benzyl 2-acetamido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-beta-D-glucopyranoside; N-((4aR,6R,7R,8R,8aS)-6,8-Bis(benzyloxy)-2-phenylhexahydropyrano[3,2-d][1,3]dioxin-7-yl)acetamide; N-[(4aR,6R,7R,8R,8aS)-2-phenyl-6,8-bis(phenylmethoxy)-4,4a,6,7,8,8a-hexahydropyrano[3,2-d][1,3]dioxin-7-yl]acetamide; Benzyl 2-Acetamido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-|A-D-glucopyranoside; Benzyl 2-Acetamido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-b-D-glucopyranoside; b-D-Glucopyranoside,phenylmethyl2-(acetylamino)-2-deoxy-3-O-(phenylmethyl)-4,6-O-(phenylmethylene)-. CAS No. 14040-20-1. Molecular formula: C29H31NO6. Mole weight: 489.56. | |
| 4-Nitrophenyl b-L-arabinopyranoside | 4-Nitrophenyl b-L-arabinopyranoside is a valuable substrate for biomedical applications, specifically in the measurement of glycoside hydrolase activity, such as β-D-arabinofuranosidase, in drug discovery and enzymatic studies. Additionally, it is utilized in the study of L-arabinose and xylose metabolism in bacteria and fungi, and elucidates their relevance to pathways implicated in diseases including diabetes. Through utilization of this specialized substrate, significant advances can be made in the fields of biomedicine and microbiology research. Synonyms: PNP-arabinoside; (2R,3R,4S,5S)-2-(4-Nitrophenoxy)tetrahydro-2H-pyran-3,4,5-triol; P-nitrophenyl β-L-arabinopyranoside. Grades: ≥95%. CAS No. 72732-54-8. Molecular formula: C11H13NO7. Mole weight: 271.22. | |
| b-D-Glucopyranosyl fluoride | b-D-Glucopyranosyl fluoride, a paramount compound with extensive applications in biomedicine, assumes a pivotal role in the advancement of innovative pharmaceuticals targeting diverse ailments such as diabetes, cancer, and microbial infections. Its extraordinary chemical attributes render it a flawless contender for facilitating enzymatic and chemical conversions, thereby facilitating the synthesis of therapeutically targeted compounds. Moreover, b-D-Glucopyranosyl fluoride presents itself as an invaluable instrument in comprehending glycosylation mechanisms and scrutinizing molecular interplays associated with cellular signaling pathways. Thus, its significance in unraveling biological phenomena and pharmaceutical pursuits cannot be overstated. Synonyms: b-D-Glucopyranosyl fluoride; 7617-95-0; (2S,3R,4S,5S,6R)-2-fluoro-6-(hydroxymethyl)oxane-3,4,5-triol; 2-deoxy-2-fluro-d-glucose; SCHEMBL4340862; ATMYEINZLWEOQU-VFUOTHLCSA-; AKOS006370932; InChI=1/C6H11FO5/c7-6-5(11)4(10)3(9)2(1-8)12-6/h2-6,8-11H,1H2/t2-,3-,4+,5-,6-/m1/s1. CAS No. 7617-95-0. Molecular formula: C6H11FO5. Mole weight: 182.15. | |
| D-Carnitine | D-Carnitine is used as a building block for antidiabetic, microbicidal compounds. Group: Coenzymes. CAS No. 541-14-0. Purity: >96%. Mole weight: 161.2. Form: Solid. D-Carnitine; 541-14-0. Cat No: COEC-102. | |
| Inulin | Inulin is an orally active prebiotic targeting the intestinal microbiota, selectively promoting the proliferation and activity of beneficial bacteria such as bifidobacteria and lactic acid bacteria, and playing a role in regulating the intestinal microecology. The functions of Inulin include: ? Fermentation by probiotics in the colon to produce short-chain fatty acids (such as butyrate and propionate), lowering the intestinal pH and inhibiting the overgrowth of harmful bacteria; ? Enhancing the intestinal barrier function and reducing endotoxin translocation; ? Directly scavenging free radicals (such as superoxide free radicals, hydroxyl free radicals) and activating antioxidant enzymes (SOD, CAT) to reduce oxidative stress. Inulin can also be used in the study of intestinal diseases (constipation, IBD), metabolic syndrome (diabetes, obesity) and liver damage by regulating glucose and lipid metabolism (such as reducing triglycerides, improving insulin sensitivity) and immune response (enhancing NK cell activity, inhibiting inflammatory factors) [1] [2] [3] [4]. Uses: Scientific research. Group: Natural products. CAS No. 9005-80-5. Pack Sizes: 100 mg. Product ID: HY-N7075. | |
| Isomalt | Isomalt. Synonyms: Hydrogenated isomaltulose; hydrogenated palatinose. CAS No. 64519-82-0. Product ID: PE-0494. Category: Sweetening agent. Product Keywords: Pharmaceutical Excipients; Excipients for Solid Dosage Form; Isomalt; Sweeteners Excipients; Sweetening agent; 64519-82-0; 64519-82-0. UNII: S870P55O2W. Stability and Storage Conditions: Isomalt has very good thermal and chemical stability. When it is melted, no changes in the molecular structure are observed. It exhibits considerable resistance to acids and microbial influences.Isomalt is non-hygroscopic, and at 25°C does not significantly absorb additional water up to a relative humidity (RH) of 85%; paracetamol (acetaminophen) tablets based on isomalt were stored for 6 months at 85% RH at 208C and retained their physical aspect. If stored under normal ambient conditions, isomalt is chemically stable for many years. When it is stored in an unopened container at 20°C and 60% RH, a re-evaluation after 3 years is recommended. Isomalt does not undergo browning reactions; it has no reducing groups, and therefore it does not react with other ingredients in a formulation (e.g. with amines in Maillard reactions). Source and Preparation: Isomalt is produced from food-grade sucrose in a two-stage process.Beet sugar is converted by enzymatic transglucosidation into the reducing disaccharide isomaltulose. This undergoes catalytical hydrogenation to produce isomalt. Safety: Isomal | |
| Lactobacillus brevis Freeze Dried Powder | Lactobacillus brevis is a gram-positive, rod shaped species of lactic acid bacteria which is heterofermentive, creating CO2 and lactic acid during fermentation. There are approximately 16 different species in L. brevis group. It can be found in many different environments, such as fermented foods, and as normal microbiota. L.brevis is found in food such as sauerkraut and pickles. It is also one of the most common causes of beer spoilage. Ingestion has been shown to improve human immune function, and it has been patented several times. Normal gut microbiota L.brevis is found in human intestines, vagina and feces. Applications: dietary supplements - capsules, powder, tablets. food - bars, powdered beverages. Group: Probiotics. Synonyms: Lactobacillus brevis Freeze Dried Powder; Lactobacillus brevis. Activity: 10 billion CFU/g or more. Stability: 24 Months. Appearance: White To Light Yellow-Colored, Free-Flowing Powder. Storage: Recommend storage at refrigeration (4 °C) or frozen temperature (-18 °C) in original, sealed package until processed. Form: Powder. Lactobacillus Strains. Cat No: PRBT-013. | |
| Xylose | Xylose (D-(+)-Xylose) is a natural pentose sugar that is catalyzed by xylose isomerase to form xylulose, which is a key step in the anaerobic ethanol fermentation of Xylose. Xylose can be used by microorganisms to produce fuels, chemicals, and bulk industrial enzymes. Xylose provides the substances and energy for cells, as a carbon source for the biosynthesis of high-value chemicals and biofuel. Xylose can be used to fully explore lignocellulose resources and provide a new direction for microbia fermentation [1] [2] [3] [4]. Uses: Scientific research. Group: Natural products. Alternative Names: D-(+)-Xylose; (+)-Xylose; Wood sugar. CAS No. 58-86-6. Pack Sizes: 10 mM * 1 mL; 50 g; 100 g. Product ID: HY-N0537. | |
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