A directory of where to buy chemicals in the USA, including: distributors, industrial manufacturers, bulk supplies and wholesalers of raw ingredients & finished goods.
The enzyme shows no activity with UDP-4-amino-4-deoxy-β-L-arabinose. Group: Enzymes. Synonyms: undecaprenyl-phosphate Ara4FN transferase; Ara4FN transferase; polymyxin resistance protein PmrF; UDP-4-amino-4-deoxy-α-L-arabinose:ditrans,polycis-undecaprenyl phosphate 4-amino-4-deoxy-α-L-arabinosyltransferase. Enzyme Commission Number: EC 2.4.2.53. 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-2683; undecaprenyl-phosphate 4-deoxy-4-formamido-L-arabinose transferase; EC 2.4.2.53; undecaprenyl-phosphate Ara4FN transferase; Ara4FN transferase; polymyxin resistance protein PmrF; UDP-4-amino-4-deoxy-α-L-arabinose:ditrans,polycis-undecaprenyl phosphate 4-amino-4-deoxy-α-L-arabinosyltransferase. Cat No: EXWM-2683.
This enzyme belongs to the family of transferases, specifically those transferring non-standard substituted phosphate groups. Group: Enzymes. Synonyms: poly(isoprenol)-phosphate galactose phosphotransferase; poly(isoprenyl)phosphate galactosephosphatetransferase; undecaprenyl phosphate galactosyl-1-phosphate transferase; UDP-galactose:undecaprenyl-phosphate galactose phosphotransferase. Enzyme Commission Number: EC 2.7.8.6. CAS No. 37278-29-8. 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-3344; undecaprenyl-phosphate galactose phosphotransferase; EC 2.7.8.6; 37278-29-8; poly(isoprenol)-phosphate galactose phosphotransferase; poly(isoprenyl)phosphate galactosephosphatetransferase; undecaprenyl phosphate galactosyl-1-phosphate transferase; UDP-galactose:undecaprenyl-phosphate galactose phosphotransferase. Cat No: EXWM-3344.
undecaprenyl-phosphate glucose phosphotransferase
The enzyme is involved in biosynthesis of xanthan. Group: Enzymes. Synonyms: GumD; undecaprenylphosphate glucosylphosphate transferase. Enzyme Commission Number: EC 2.7.8.31. 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-3330; undecaprenyl-phosphate glucose phosphotransferase; EC 2.7.8.31; GumD; undecaprenylphosphate glucosylphosphate transferase. Cat No: EXWM-3330.
undecaprenyl-phosphate mannosyltransferase
Requires phosphatidylglycerol. Group: Enzymes. Synonyms: guanosine diphosphomannose-undecaprenyl phosphate mannosyltransferase; GDP mannose-undecaprenyl phosphate mannosyltransferase; GDP-D-mannose:lipid phosphate transmannosylase. Enzyme Commission Number: EC 2.4.1.54. CAS No. 37277-62-6. 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-2600; undecaprenyl-phosphate mannosyltransferase; EC 2.4.1.54; 37277-62-6; guanosine diphosphomannose-undecaprenyl phosphate mannosyltransferase; GDP mannose-undecaprenyl phosphate mannosyltransferase; GDP-D-mannose:lipid phosphate transmannosylase. Cat No: EXWM-2600.
Isolated from Campylobacter jejuni. Part of a bacterial N-linked glycosylation pathway. Group: Enzymes. Synonyms: PglC. Enzyme Commission Number: EC 2.7.8.36. 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-3335; undecaprenyl phosphate N,N'-diacetylbacillosamine 1-phosphate transferase; EC 2.7.8.36; PglC. Cat No: EXWM-3335.
Undecyl 2-acetamido-2-deoxy-b-D-glucopyranoside is a powerful yet versatile compound found in many biomedical applications, particularly as a surfactant for protein extraction and purification. This unique substance has also demonstrated efficacy in treating bacterial infections, including notoriously resistant strains like Streptococcus pneumoniae and Staphylococcus aureus. By disrupting bacterial cell walls, Undecyl 2-acetamido-2-deoxy-b-D-glucopyranoside represents a promising frontier in the quest to combat drug-resistant pathogens. Whether used in the lab or the clinic, this potent molecule has much to offer the biomedical community. CAS No. 152914-68-6. Molecular formula: C19H37NO6. Mole weight: 375.5.
Undecyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-b-D-glucopyranose, renowned as an indispensable intermediary in the biomedicine sector, exhibits an array of applications in the manufacture of antibiotics and antiviral medications. It serves as a pivotal agent for combating an assortment of bacterial and viral afflictions, encompassing respiratory tract infections, urinary tract infections, and cutaneous infections. Synonyms: UNDECYL 2-ACETAMIDO-2-DEOXY-3,4,6-TRI-O-ACETYL-beta-D-GLUCOPYRANOSIDE; UNDECYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-B-D-GLUCOPYRANOSE; [(2R,3S,4R,5R,6R)-5-acetamido-3,4-diacetyloxy-6-undecoxyoxan-2-yl]methyl acetate; DTXSID001153086; beta-D-Glucopyranoside, undecyl 2-(acetylamino)-2-deoxy-, 3,4,6-triacetate. CAS No. 173725-24-1. Molecular formula: C25H43NO9. Mole weight: 501.61.
Undecyl a-D-maltopyranoside
Undecyl a-D-maltopyranoside is a versatile compound used in the biomedical industry. It exhibits potential as a pharmaceutical excipient due to its surfactant properties. It has been utilized in drug delivery systems to enhance the solubility and stability of various drugs. Synonyms: Undecyl 4-O-a-D-glucopyranosyl-a-D-glucopyranoside. CAS No. 168037-13-6. Molecular formula: C23H44O11. Mole weight: 496.59.
Undecyl b-D-glucopyranoside
Undecyl b-D-glucopyranoside, a sugar-based detergent, is utilized in the field of biomedicine as an aid in solubilizing and purifying membrane proteins. It has exhibited remarkable effectiveness in research probes on myosin, being a motor protein engaged in muscle contraction. In addition, it has been utilized for alleviating a variety of medical conditions, including cardiovascular and neuromuscular diseases. CAS No. 70005-86-6. Molecular formula: C17H34O6. Mole weight: 334.45.
Undecyl b-D-maltopyranoside
Undecyl b-D-maltopyranoside is a prevalent compound in the biomedical sector, exhibiting notable significance as a surfactant, enabling efficient solubilization and stabilization of hydrophobic proteins and membrane-bound molecules. Its remarkable applicability lies in drug delivery systems, wherein it substantiates drug absorption and targeting. Synonyms: Undecyl 4-O-a-D-glucopyranosyl-b-D-glucopyranoside. CAS No. 253678-67-0. Molecular formula: C23H44O11. Mole weight: 496.59.
Undecyl b-D-thiomaltopyranoside
Undecyl b-D-thiomaltopyranoside is a detergent widely used in drug research to isolate and purify membrane proteins. It is also used in the treatment of diseases such as Alzheimer's, Parkinson's, and Huntington's, as well as in the study of cell signaling pathways and protein-protein interactions. CAS No. 148565-57-5. Molecular formula: C23H44O10S. Mole weight: 512.66.
Undecyl-beta-D-glucopyranoside
250mg Pack Size. Group: Biochemicals, Building Blocks, Carbohydrates. Formula: C17H34O6. CAS No. 70005-86-6. Prepack ID 72880752-250mg. Molecular Weight 334.44826. See USA prepack pricing.
Undecyl-β-D-selenomaltoside
Seleniated Detergents. CAS No. 1423294-14-7. Molecular formula: C23H44O10Se. Mole weight: 573.6. Appearance: White solid. Purity: ≥97%.
Undecyl cyanide. Group: Biochemicals. Grades: Highly Purified. CAS No. 2437-25-4. Pack Sizes: 10g, 25g. Molecular Formula: C12H23N. US Biological Life Sciences.
Worldwide
Undecylenate sodium
Undecylenate SodiumIt is an organic compound belonging to the class of carboxylates. It is formed by the reaction of undecylenic acid and sodium hydroxide. Undecylenate SodiumIt has a variety of applications in the cosmetic and personal care industries, especially as an antifungal agent in products such as face creams, lotions and shampoos. In addition, it can be used as a preservative in various formulations. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 3398-33-2. Pack Sizes: 5 g; 10 g; 25 g. Product ID: HY-W127452.
Undecylenic Acid
Undecylenic Acid. We stock inventory in warehouses throughout the United States, allowing us to serve customers in all regions in a timely and cost effective manner.
Aldehydes. Alternative Names: 10-Undecenyl Aldehyde, 10-Undecenal. CAS No. 112-45-8. Molecular formula: C11H20O. Mole weight: 168.28. Canonical SMILES: C=CCCCCCCCCC=O. Catalog: ACM112458-2.
Undecylenic monoglyceride
Undecylenic monoglyceride
Sarchem Laboratories New Jersey NJ
Undecylenoyl phenylalanine
Animal Pharmaceuticals, Skin Care Treatments. Group: Heterocyclic organic compound. Alternative Names: N-Undecenoyl-L-phenylalanine. CAS No. 175357-18-3. Molecular formula: C20H29NO3. Mole weight: 331.45. Appearance: White powder. IUPACName: (2S)-3-phenyl-2-(undec-10-enoylamino)propanoic acid. Canonical SMILES: C=CCCCCCCCCC (=O)N[C@@H] (CC1=CC=CC=C1)C (=O)O. Density: 1.047±0.06g/ml. ECNumber: 209-553-4. Catalog: ACM175357183.
Undecylenyl b-D-maltoside
Undecylenyl b-D-maltoside is a multifunctional bioactive compound fostering targeted drug delivery systems and studying sundry diseases. By ingeniously formulating drugs designed to study cancer, bacterial infections and dermatological disorders, Undecylenyl b-D-maltoside emerges as an indispensable ingredient. Molecular formula: C23H42O11. Mole weight: 494.57.
Tripyrrolic pigment like prodigiosin. Antimalarial agent. Apoptosis inducer. Anticancer agent with multiple modes of action. Immunosuppressant in non-toxic concentrations. Bone resorption inhibitor. Antiulcer agent. Group: Biochemicals. Grades: Highly Purified. CAS No. 56247-02-0, 52340-48-4 (parent). Pack Sizes: 250ug, 1mg. US Biological Life Sciences.
Worldwide
undermodified hydroxywybutosine
Undermodified Hydroxywybutosine, a nucleoside analog, demonstrates potential as a chemotherapeutic agent in the biomedical industry. It selectively targets cancer cells, leaving healthy cells unscathed due to its ability to suppress protein synthesis, thereby obstructing growth and replication. Synonyms: 1H-Imidazo[1,2-a]purine-7-butanoic acid, a-amino-4,9-dihydro-b-hydroxy-4,6-dimethyl-9-oxo-1-b-D-ribofuranosyl-. CAS No. 84270-20-2. Molecular formula: C13H16N6O4. Mole weight: 452.42.
Undulatine (Alstonia)
Heterocyclic Organic Compound. CAS No. 123871-90-9. Catalog: ACM123871909.
Unesbulin (PTC596) is an orally active and selective B-cell-specific Moloney murine leukemia virus integration site 1 ( BMI-1 ) inhibitor. Unesbulin downregulates MCL-1 and induces p53-independent mitochondrial apoptosis in acute myeloid leukemia (AML) cells. Unesbulin has anti-leukemic activity [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: PTC596. CAS No. 1610964-64-1. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-112041.
Unguinol
Unguinol is a metabolite of the fungi Aspergillus unguis and Aspergillus nidulans. It has been found to be an active growth promotant in animals, in particular, monogastric animals such as chickens. It is an inhibitor of pyruvate phosphate dikinase (PPDK). Synonyms: 3,8-Dihydroxy-1,9-dimethyl-6-(1-methyl-1-propenyl)-11H-dibenzo[b,e][1,4]dioxepin-11-one; Yasimin. Grades: ≥95%. CAS No. 36587-59-4. Molecular formula: C19H18O5. Mole weight: 326.34.
Unguisin A
Unguisin A is a cyclic heptapeptide produced by the strain of the marine fungus E. unguis whose structure is comprised of amino acids and GABA. It binds to phosphate, pyrophosphate, and chloride but has no effect on chloride transport in a liposome-based assay. Synonyms: cyclo(D-alanyl-D-tryptophyl-4-aminobutanoyl-D-alanyl-D-valyl-L-phenylalanyl-D-valyl). Grades: >95% by HPLC. CAS No. 226956-06-5. Molecular formula: C40H54N8O7. Mole weight: 758.90.
Unguisin B
Unguisin B is a cyclic heptapeptide produced by the strain of the marine fungus E. unguis whose structure is comprised of amino acids and GABA. Synonyms: cyclo(D-alanyl-D-tryptophyl-4-aminobutanoyl-D-alanyl-D-valyl-L-leucyl-D-valyl). Grades: >95% by HPLC. CAS No. 226956-07-6. Molecular formula: C37H56N8O7. Mole weight: 724.89.
Uniblue A Sodium Salt
Uniblue A sodium salt is a reactive protein stain. It can also be used in engineering or chemical process of heterogeneous chemical modification of cotton cellulose with vinyl sulfone dyes in non-nucleophilic organic solvents. Group: Biochemicals. Grades: Highly Purified. CAS No. 14541-90-3. Pack Sizes: 1g, 2.5g. Molecular Formula: C22H16N2O7S2; Na, Molecular Weight: 484.502298999999. US Biological Life Sciences.
Worldwide
Uniconazole
Uniconazole is a plant growth hormone that inhibits cytochrome P450 707As, resulting in a suppression of gibberellin production. Uses: Fungicides, industrial. Synonyms: 1H-1,2,4-Triazole-1-ethanol, β-[(4-chlorophenyl)methylene]-α-(1,1-dimethylethyl)-, (βE)-; (βE)-β-[(4-Chlorophenyl)methylene]-α-(1,1-dimethylethyl)-1H-1,2,4-triazole-1-ethanol; 1H-1,2,4-Triazole-1-ethanol, β-[(4-chlorophenyl)methylene]-α-(1,1-dimethylethyl)-, (E)-(±)-; (E)-1-(4-Chlorophenyl)-4,4-dimethyl-2-(1,2,4-triazol-1-yl)-1-penten-3-ol; 1H-1,2,4-Triazole-1-ethanol, β-[(4-chlorophenyl)methylene]-α-(1,1-dimethylethyl)-, (E)-; M 13144; Majic; Majic S 3307D; Pentefenzol; Prunit; S 07; S 327D; S 3307; S 3307D; Sumagic; Sumiseven; XE 1019; XE 1019D. Grades: 95%. CAS No. 83657-22-1. Molecular formula: C15H18ClN3O. Mole weight: 291.77.
Uniconazole
Uniconazole, a plant growth retardant, is a potent inhibitor of abscisic acid (ABA) catabolism with an IC 50 of 68 nM against ABA 8-hydroxylase. Uniconazole is a potent competitive inhibitor of CYP707A3 activity with a K i of 8 nM. Uniconazole evidently inhibits gibberellin biosynthesis, and brassinosteroid biosynthesis is also inhibited to some extent [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 83657-22-1. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g. Product ID: HY-B0873.
UNIL088 is a water-soluble prodrug of cyclosporine A (CsA), can be rapidly hydrolysed under physiological conditions, and can retain a long shelf-life in aqueous media. Uses: Prodrug of cyclosporine. Synonyms: UNIL-088, UNIL 088, UNIL088, Cyclosporin A; (1R, 2R, E)-1-((2S, 5S, 11S, 14S, 17S, 20S, 23R, 26S, 29S, 32S)-5-ethyl-11, 17, 26, 29-tetraisobutyl-14, 32-diisopropyl-1, 7, 10, 16, 20, 23, 25, 28, 31-nonamethyl-3, 6, 9, 12, 15, 18, 21, 24, 27, 30, 33-undecaoxo-1, 4, 7, 10, 13, 16, 19, 22, 25, 28, 31-undecaazacyclotritriacontan-2-yl)-2-methylhex-4-en-1-yl N-(N-((1-acetoxyethoxy)carbonyl)-O-phosphono-L-seryl)-N-methylglycinate. Grades: ≥95%. CAS No. 473545-11-8. Molecular formula: C73H128N13O22P. Mole weight: 1570.86.
UniPR1331
UniPR1331 is a 3β-hydroxy-Δ5-choline acid derivative that inhibits Eph-ephrin interactions. UniPR1331 interacts with VEGFR2 and blocks the interaction of VEGFR2 with its natural ligand vascular endothelial growth factor and subsequent autophosphorylation, signaling, and pro-angiogenic activation of endothelial cells in vitro. UniPR1331 also inhibits tumor cell-driven angiogenesis in zebrafish [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1809170-59-9. Pack Sizes: 5 mg; 10 mg. Product ID: HY-123927.
Unique protease 1 from Porphyromonas gingivalis
Digestion of human IgG1 with Unique protease 1 generates a homogenous pool of precise Fab and Fc fragments. There is no over-digestion or further degradation of the fragments typically associated with other proteolytic enzymes. Very mild reducing reaction conditions give intact Fab and Fc fragments. Best activity is obtained at 37°C. Group: Enzymes. Synonyms: GingisKHAN; unique protease 1. Purity: > 80% homogeneity as determined by SDS-PAGE analysis using Coomassie Blue detection. Unique protease 1. Stability: After reconstitution Unique protease 1 is stable for at least 1 month +4-8°C. Reconstituted Unique protease 1 Reducing Agent cannot be stored, use freshly prepared. Appearance: White to light yellow powder. Storage: Unique protease 1 and Unique protease 1 Reducing Agent are shipped on ice and should be stored at -20°C upon arrival. Form: Lyophilized preparation together with 5 vials of lyophilized reducing agent for convenient and reliable performance. Source: Porphyromonas gingivalis. GingisKHAN Enzyme; GingisKHAN; unique protease 1; protease. Cat No: NATE-1601.
Unithiol
Unithiol is a chelating agent used as an antidote against for the treatment of heavy metals and metalloid intoxication. It can also be used for animals. Synonyms: DMPS. Grades: >98%. CAS No. 4076-2-2. Molecular formula: C3H7O3S3Na. Mole weight: 210.27.
Universal
Heterocyclic Organic Compound. CAS No. 102962-70-9. Catalog: ACM102962709.
Universal Protein Lysates: Group: Biologicals. Grades: Molecular Biology Grade. Pack Sizes: 2x500ug, 4x500ug. US Biological Life Sciences.
Worldwide
Universal Protein Lysate, Chicken Adult Normal
Universal Protein Lysates: Group: Biologicals. Grades: Molecular Biology Grade. Pack Sizes: 2x500ug, 4x500ug. US Biological Life Sciences.
Worldwide
Universal Protein Lysate, Human Adult Normal
Universal Protein Lysates: Group: Biologicals. Grades: Molecular Biology Grade. Pack Sizes: 2x500ug, 4x500ug. US Biological Life Sciences.
Worldwide
Universal Protein Lysate, Monkey Adult Normal
Universal Protein Lysates: Group: Biologicals. Grades: Molecular Biology Grade. Pack Sizes: 2x500ug, 4x500ug. US Biological Life Sciences.
Worldwide
Universal Protein Lysate, Mouse Adult Normal
Universal Protein Lysates: Group: Biologicals. Grades: Molecular Biology Grade. Pack Sizes: 2x500ug, 4x500ug. US Biological Life Sciences.
Worldwide
Universal Protein Lysate, Rat Adult Normal
Universal Protein Lysates: Group: Biologicals. Grades: Molecular Biology Grade. Pack Sizes: 2x500ug, 4x500ug. US Biological Life Sciences.
Worldwide
Unoprostone
Unoprostone, a prostaglandin F2α analogs (PGAs), activates BK channels to reduce oxidative stress- and light-induced retinal cell death, and phagocytotic dysfunction. Unoprostone reduces intraocular pressure and is used topically for glaucoma or ocular hypertension [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 120373-36-6. Pack Sizes: 1 mg (26.14 mM * 100 μL in Methyl acetate). Product ID: HY-106916.
Unoprostone
Heterocyclic Organic Compound. Alternative Names: Unoprostone. CAS No. 120373-36-6. Molecular formula: C22H38O5. Mole weight: 382.53. Appearance: A solution in methyl acetate. Purity: >98%. IUPACName: 7-[(2R)-3,5-dihydroxy-2-(3-oxodecyl)cyclopentyl]hept-5-enoic acid. Density: 1.069g/cm³. Catalog: ACM120373366.
Unoprostone-d15 Isopropyl Ester
Antiglaucoma; used in treatment of ocular hypertension. Group: Biochemicals. Alternative Names: (5Z)-7-[(1R,2R,3R,5S)-3,5-Dihydroxy-2-(3-oxodecyl)cyclopenthyl]-5-heptenoic Acid-d15 Isopropyl Ester; UF-021-d15; Rescula-d15. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences.
An intermediate in the preparation of Unoprostone and respective derivatives. Group: Biochemicals. Alternative Names: (5Z)-7-[(1R,2R,3R,5S)-2-[2-(2-Heptyl-1,3-dioxolan-2-yl)ethyl]-3,5-dihydroxycyclopentyl]-5-heptenoic Acid. Grades: Highly Purified. CAS No. 120373-42-4. Pack Sizes: 10mg. US Biological Life Sciences.
Worldwide
Unoprostone isopropyl ester
Unoprostone isopropyl ester. Group: Biochemicals. Alternative Names: (5Z)-7-[(1R,2R,3R,5S)-3,5-Dihydroxy-2-(3-oxodecyl)cyclopenthyl]-5-heptenoic acid isopropyl ester; UF-021; Rescula. Grades: Highly Purified. CAS No. 120373-24-2. Pack Sizes: 1mg, 2mg, 5mg, 10mg, 25mg. Molecular Formula: C25H44O5. US Biological Life Sciences.
The enzyme releases 4-deoxy-4,5-didehydro D-glucuronic acid or 4-deoxy-4,5-didehydro L-iduronic acid from chondroitin disaccharides, hyaluronan disaccharides and heparin disaccharides and cleaves both glycosidic (1?3) and (1?4) bonds. It prefers the sulfated disaccharides to the unsulfated disaccharides. Group: Enzymes. Synonyms: UGL (ambiguous); unsaturated glucuronyl hydrolase (ambiguous). Enzyme Commission Number: EC 3.2.1.180. 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-3864; unsaturated chondroitin disaccharide hydrolase; EC 3.2.1.180; UGL (ambiguous); unsaturated glucuronyl hydrolase (ambiguous). Cat No: EXWM-3864.
Unsaturated Polyester Resin
Unsaturated Polyester Resin. Group: Polymers.
unsaturated rhamnogalacturonyl hydrolase
The enzyme is part of the degradation system for rhamnogalacturonan I in Bacillus subtilis strain 168. Group: Enzymes. Synonyms: YteR; YesR. Enzyme Commission Number: EC 3.2.1.172. Unsaturated rhamnogalacturonyl hydrolase. 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-3855; unsaturated rhamnogalacturonyl hydrolase; EC 3.2.1.172; YteR; YesR. Cat No: EXWM-3855.
Unsaturated rhamnogalacturonyl hydrolase 105A from Bacillus subtilis, Recombinant
Unsaturated rhamnogalacturonyl hydrolase (EC 3.2.1.172, YteR, YesR) is an enzyme with systematic name 2-O-(4-deoxy-beta-L-threo-hex-4-enopyranuronosyl)-alpha-L-rhamnopyranose hydrolase. This enzyme catalyses the following chemical reaction: 2-O-(4-deoxy-beta-L-threo-hex-4-enopyranuronosyl)-alpha-L-rhamnopyranose + H2O ? 5-dehydro-4-deoxy-D-glucuronate + L-rhamnopyranose. Group: Enzymes. Synonyms: Unsaturated rhamnogalacturonyl hydrolase; EC 3.2.1.172; YteR; YesR. Enzyme Commission Number: EC 3.2.1.172. Purity: >90% as judged by SDS-PAGE. Unsaturated rhamnogalacturonyl hydrolase. Mole weight: 43.4 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: Bacillus subtilis. Unsaturated rhamnogalacturonyl hydrolase; EC 3.2.1.172; YteR; YesR. Cat No: NATE-1508.
Unsaturated rhamnogalacturonyl hydrolase 105A from Bacteroides thetaiotaomicron, Recombinant
Unsaturated rhamnogalacturonyl hydrolase (EC 3.2.1.172, YteR, YesR) is an enzyme with systematic name 2-O-(4-deoxy-beta-L-threo-hex-4-enopyranuronosyl)-alpha-L-rhamnopyranose hydrolase. This enzyme catalyses the following chemical reaction: 2-O-(4-deoxy-beta-L-threo-hex-4-enopyranuronosyl)-alpha-L-rhamnopyranose + H2O ? 5-dehydro-4-deoxy-D-glucuronate + L-rhamnopyranose. Group: Enzymes. Synonyms: Unsaturated rhamnogalacturonyl hydrolase; EC 3.2.1.172; YteR; YesR. Enzyme Commission Number: EC 3.2.1.172. Purity: >90% as judged by SDS-PAGE. Unsaturated rhamnogalacturonyl hydrolase. Mole weight: 52.6 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. Unsaturated rhamnogalacturonyl hydrolase; EC 3.2.1.172; YteR; YesR. Cat No: NATE-1509.
unspecific monooxygenase
A group of P-450 heme-thiolate proteins, acting on a wide range of substrates including many xenobiotics, steroids, fatty acids, vitamins and prostaglandins; reactions catalysed include hydroxylation, epoxidation, N-oxidation, sulfooxidation, N-, S- and O-dealkylations, desulfation, deamination, and reduction of azo, nitro and N-oxide groups. Together with EC 1.6.2.4, NADPH-hemoprotein reductase, it forms a system in which two reducing equivalents are supplied by NADPH. Some of the reactions attributed to EC 1.14.15.3, alkane 1-monooxygenase, belong here. Group: Enzymes. Synonyms: microsomal monooxygenase; xenobiotic monooxygenase; aryl-4-monooxygenase; aryl hydrocarbon hydroxylase; microsomal P-450; flavoprotein-linked monooxygenase; flavoprotein monooxygenase; substrate,reduced-flavoprotein:oxygen oxidoreductase (RH-hy. Enzyme Commission Number: EC 1.14.14.1. CAS No. 9038-14-6. 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-0906; unspecific monooxygenase; EC 1.14.14.1; 9038-14-6; microsomal monooxygenase; xenobiotic monooxygenase; aryl-4-monooxygenase; aryl hydrocarbon hydroxylase; microsomal P-450; flavoprotein-linked monooxygenase; flavoprotein monooxygenase; substrate,reduced-flavoprotein:oxygen oxidoreductase (RH-hydroxylating or -epoxidizing). Cat No: EXWM-0906.
unspecific peroxygenase
A heme-thiolate protein (P-450). Enzymes of this type include glycoproteins secreted by agaric basidiomycetes. They catalyse the insertion of an oxygen atom from H2O2 into a wide variety of substrates, including aromatic rings such as naphthalene, toluene, phenanthrene, pyrene and p-nitrophenol, recalcitrant heterocycles such as pyridine, dibenzofuran, various ethers (resulting in O-dealkylation) and alkanes such as propane, hexane and cyclohexane. Reactions catalysed include hydroxylation, epoxidation, N-oxidation, sulfooxidation, O- and N-dealkylation, bromination and one-electron oxidations. They have little or no activity toward chloride. Mechanistically, the catalytic cycle of unspecific (mono)-peroxygenases combines elements of the "shunt" pathway of cytochrome P-450s (a side activity that utilizes a peroxide in place of dioxygen and NAD[P]H) and the classic heme peroxidase cycle. Group: Enzymes. Synonyms: aromatic peroxygenase; mushroom peroxygenase; haloperoxidase-peroxygenase; Agrocybe aegerita peroxidase. Enzyme Commission Number: EC 1.11.2.1. 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-0512; unspecific peroxygenase; EC 1.11.2.1; aromatic peroxygenase; mushroom peroxygenase; haloperoxidase-peroxygenase; Agrocybe aegerita peroxidase. Cat No: EXWM-0512.