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| Product | Description | |
|---|---|---|
| α(1-2) Fucosidase from Xanthomonas manihotis, Recombinant | 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-L-fucoside fucohydrolase; Alpha-Fucosidase; FUCA1; FUCA; EC 3.2.1.51. FUCA. Mole weight: 70000 daltons. Storage: 4°C. Source: E. coli. Species: Xanthomonas manihotis. α-L-fucoside fucohydrolase; Alpha-Fucosidase; FUCA1; FUCA; EC 3.2.1.51. Cat No: NATE-1258. |  |
| α(1-3,4) Fucosidase from Sweet almond, Recombinant | 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. Α1-3,4 fucosidase, (also known as amf) is a broad specificity exoglycosidase that catalyzes the hydrolysis of α1-3 and α1-4 linked fucose residues from oligosaccharides and glycoproteins. Group: Enzymes. Synonyms: α-L-fucoside fucohydrolase; Alpha-Fucosidase; FUCA1; FUCA; EC 3.2.1.51. FUCA. Mole weight: 56000 daltons. Activity: 75,000 units/mg. Storage: 4°C. Form: 20 mM Tris-HCl (pH 7.5), 50 mM NaCl and 1 mM EDTA. Source: Pichia pastoris. Species: Sweet almond tree. α-L-fucoside fucohydrolase; Alpha-Fucosidase; FUCA1; FUCA; EC 3.2.1.51; α(1-3,4) Fucosidase. Cat No: NATE-1264. | |
| 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. | |
| Native Almond α (1-3,4) Fucosidase | 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 ...buffer supplied with the enzyme, >85% of the original activity is observed after two months at 2-8°C. In the buffer solution at 37°C, the half-life is approximately 80 hours. Storage: Shipped on ice pack for next day delivery. Store at -20°C. Store lyophilized enzyme at-20°C. Enzyme reconstituted with the provided reaction buffer is stable at 2-8°C for at least two months and may be stored at-20°C for at least six months. Avoid repeated freeze/thaw cycles. Form: Lyophilized from 50 mM sodium acetate, 3 mg/ml bovine serum albumin (pH 5.0). Source: Almond meal. Species: Almond. α (1-3,4) Fucosidase; alpha-L-fucosidase; Alpha-Fucosidase; FUCA1; FUCA. Cat No: NATE-0260. | |
| Native α-1,2-Fucosidase solution | 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-1,2-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: > 0.4 units/mg protein. Storage: 2-8°C. Form: buffered aqueous solution, Solution in 20 mM Tris-HCl, pH 7.5, 25 mM NaCl. α-1,2-Fucosidase; alpha-L-fucosidase; Alpha-Fucosidase; FUCA1; FUCA; 9037-65-4. Pack: vial of 0.004 unit. Cat No: NATE-0259. | |
| Native Bovine α (1-2,3,4,6) Fucosidase | 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 (1-2,3,4,6) Fucosidase; alpha-L-fucosidase; Alpha-Fucosidase; FUCA1; FUCA. FUCA. Source: Bovine kidney. Species: Bovine. α (1-2,3,4,6) Fucosidase; alpha-L-fucosidase; Alpha-Fucosidase; FUCA1; FUCA. Cat No: NATE-0261. | |
| Native Bovine α-L-Fucosidase | In enzymology, an alpha-L-fucosidase (EC 3.2.1.51) is an enzyme that catalyzes the chemical reaction:an alpha-L-fucoside + H2O<-> L-fucose + an alcohol. Thus, the two substrates of this enzyme are alpha-L-fucoside and H2O, whereas its two products are L-fucose and alcohol. This enzyme belongs to the family of hydrolases, specifically those glycosidases that hydrolyse O-and S-glycosyl compounds. This enzyme participates in n-glycan degradation and glycan structures-degradation. Group: Enzymes. Synonyms: α-L-Fucosidase; EC 3.2.1.51; α-fucosidase. Enzyme Commission Number: EC 3.2.1.51. CAS No. 9037-65-4. FUCA. Activity: > 2.0 units/mg protein (biuret). Storage: 2-8°C. Form: ammonium sulfate suspension. Suspension in 3.2 M (NH4)2SO4, 10 mM NaH2PO4 10 mM Citrate, pH 6.0. Source: Bovine kidney. Species: Bovine. α-L-Fucosidase; EC 3.2.1.51; α-fucosidase. Cat No: NATE-0266. | |
| Native environmental DNA α-Fucosidase | In enzymology, an alpha-L-fucosidase (EC 3.2.1.51) is an enzyme that catalyzes the chemical reaction:an alpha-L-fucoside + H2O<-> L-fucose + an alcohol. Thus, the two substRates of this enzyme are alpha-L-fucoside and H2O, whereas its two products are L-fucose and alcohol. This enzyme belongs to the family of hydrolases, specifically those glycosidases that hydrolyse O-and S-glycosyl compounds. This enzyme participates in n-glycan degradation and glycan structures-degradation. Group: Enzymes. Synonyms: alpha-L-fucoside fucohydrolase; alpha-fucosidase; EC 3.2.1.51; alpha-L-fucosidase. Enzyme Commission Number: EC 3.2.1.51. CAS No. 9037-65-4. FUCA. Source: Proprietary environmental DNA. Species: environmental DNA. alpha-L-fucoside fucohydrolase; alpha-fucosidase; EC 3.2.1.51; alpha-L-fucosidase. Cat No: NATE-0749. | |
| Native Xanthomonas sp. α-1? (2,3,4) Fucosidase solution | 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? (2,3,4) Fucosidase; alpha-L-fucosidase; Alpha-Fucosidase; FUCA1; FUCA; EC 3.2.1.51; 9037-65-4. Enzyme Commission Number: EC 3.2.1.51. CAS No. 9037-65-4. FUCA. Activity: > 0.5 units/mg protein. Storage: 2-8°C. Form: buffered aqueous solution, Solution in 20 mM Tris-HCl, pH 7.5, 25 mM NaCl. Source: Xanthomonas sp. α-1? (2,3,4) Fucosidase; alpha-L-fucosidase; Alpha-Fucosidase; FUCA1; FUCA; EC 3.2.1.51; 9037-65-4. Pack: vial of 0.004 unit. Cat No: NATE-0262. | |
| Native Xanthomonas sp. α-1? (3,4) Fucosidase solution | 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? (3,4) Fucosidase; alpha-L-fucosidase; Alpha-Fucosidase; FUCA1; FUCA; EC 3.2.1.51; 9037-65-4. Enzyme Commission Number: EC 3.2.1.51. CAS No. 9037-65-4. FUCA. Activity: > 2 units/mg protein. Storage: 2-8°C. Form: buffered aqueous solution, Solution in 20 mM Tris-HCl, pH 7.5, 25 mM NaCl. Source: Xanthomonas sp. α-1? (3,4) Fucosidase; alpha-L-fucosidase; Alpha-Fucosidase; FUCA1; FUCA; EC 3.2.1.51; 9037-65-4. Pack: vial of 0.02 unit. Cat No: NATE-0263. | |
| 1-Deoxyfuconojirimycin | It is a potent and specific inhibitor of several alpha-L-fucosidases. Synonyms: DFJ; Deoxyfuconojirimycin; (2S,3R,4S,5R)-2-Methyl-3,4,5-piperidinetriol; 1,5-Dideoxy-1,5-imino-L-fucitol; 1,2,6-Trideoxy-2,6-imino-D-galactitol; L-fuco-Deoxynojirimycin. Grades: ≥95% by HPLC. CAS No. 99212-30-3. Molecular formula: C6H13NO3. Mole weight: 147.17. |  |
| 2-Chloro-4-nitrophenyl a-L-fucopyranoside | 2-Chloro-4-nitrophenyl α-L-fucopyranoside is a biomedical compound commonly used in research. It acts as a substrate for α-L-fucosidase enzymes, facilitating their study and characterization. This compound enables the investigation of glycan structure and its role in various biological processes. It has potential applications in drug development and understanding diseases associated with aberrant fucosidase activity. Synonyms: CNP-AFU; 2-Chloro-4-nitrophenyl-alpha-L-fucopyranoside; 2-Chloro-4-nitrophenyl a-L-fucopyranoside; (2S,3S,4R,5S,6S)-2-(2-chloro-4-nitrophenoxy)-6-methyloxane-3,4,5-triol; alpha-L-Galactopyranoside, 2-chloro-4-nitrophenyl 6-deoxy-; MFCD04972056; SCHEMBL4263599; DTXSID40463539; EX-A4782; AKOS015899699; AKOS040744200; AC-37021; AS-69565; HY-15911; 2-Chloro-4-nitrophenyl ?-D-Fucopyranoside; 2-Chloro-4-nitrophenyl alpha-D-fucopyranoside; 2-Chloro-4-nitrophenyl alpha -D-Fucopyranoside; 2-Chloro-4-nitrophenyl 6-deoxy-?-L-galactopyranoside; (2S,3S,4R,5S,6S)-2-(2-chloro-4-nitrophenoxy)-6-methyltetrahydro-2H-pyran-3,4,5-triol. CAS No. 157843-41-9. Molecular formula: C12H14ClNO7. Mole weight: 319.69. | |
| 2-Naphthyl a-L-fucopyranoside | 2-Naphthyl a-L-fucopyranoside is a critical compound extensively used in biomedical research. It serves as a substrate for enzymes like fucosidase and alpha-L-fucosidase, enabling the analysis of their activity. Additionally, this product plays a vital role in studying diseases associated with abnormal fucosylation, such as cancer and congenital disorders. Synonyms: b-Nap-a-L-Fuc b-Naphthyl-a-L-fucopyranoside. CAS No. 63503-05-9. Molecular formula: C16H18O5. Mole weight: 290.31. | |
| 4-Methylumbelliferyl 2-acetamido-2-deoxy-3-O-(a-L-fucopyranosyl)-b-D-glucopyranoside | 4-Methylumbelliferyl 2-acetamido-2-deoxy-3-O-(a-L-fucopyranosyl)-b-D-glucopyranoside, an essential biochemical compound within the biomedical industry, is instrumental for the detection and measurement of the alpha-L-fucosidase enzyme's activity. Its wide-ranging utility encompasses the exploration of lysosomal storage disorders and glycosylation disorders, particularly fucosidosis. Synonyms: Fuc-a-1,3-GlcNAc-b-4MU. CAS No. 383160-12-1. Molecular formula: C24H31NO12. Mole weight: 525.5. | |
| 4-Methylumbelliferyl a-L-fucopyranoside | 4-Methylumbelliferyl a-L-fucopyranoside is a biochemical reagent widely used in the biomedical industry. It is commonly employed for the detection and quantification of a-L-fucosidase activity in various biological samples. This product plays a crucial role in studying lysosomal storage diseases, cancer biomarkers, and carbohydrate metabolism disorders. Synonyms: 4-MU-a-L-Fuc; 4-Methylumbelliferyl α-L-Fucoside; 4-Methyl-7-(alpha-L-fucopyranosyloxy)-2H-1-benzopyran-2-one; 7-((6-Deoxy-alpha-L-galactopyranosyl)oxy)-4-methyl-2H-1-benzopyran-2-one; 4-Methyl-7-(((2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-2H-chromen-2-one. Grades: ≥97%. CAS No. 54322-38-2. Molecular formula: C16H18O7. Mole weight: 322.31. | |
| Deoxyfuconojirimycin Hydrochloride | It is a potent and specific inhibitor of several alpha-L-fucosidases. Synonyms: (2S,3R,4S,5R)-2-Methyl-3,4,5-piperidinetriol Hydrochloride; 1,5-Dideoxy-1,5-imino-L-fucitol Hydrochloride; 1,2,6-Trideoxy-2,6-imino-D-galactitol Hydrochloride; L-fuco-Deoxynojirimycin Hydrochloride; 1-Deoxyfuconojirimycin Hydrochloride. Grades: 98%. CAS No. 210174-73-5. Molecular formula: C6H14ClNO3. Mole weight: 183.63. | |
| Deoxyfuconojirimycin Hydrochloride (DFJ) | A powerful and specific inhibitor of several alpha-L-fucosidases. Deoxyfuconojirimycin (1,5-dideoxy-1,5-imino-L-fucitol) is a potent, specific and competitive inhibitor (Ki 1 x 10(-8) M) of human liver alpha-L-fucosidase (EC 3.2.1.51). Six structural analogues of this compound were synthesized and tested for their ability to inhibit alpha-L-fucosidase and other human liver glycosidases. It is concluded that the minimum structural requirement for inhibition of alpha-L-fucosidase is the correct configuration of the hydroxy groups at the piperidine ring carbon atoms 2, 3 and 4. Different substituents in either configuration at carbon atom 1 (i.e. 1 alpha- and beta-homofuconojirimycins) and at carbon atom 5 may alter the potency but do not destroy the inhibition of alpha-L-fucosidase. The pH-dependency of the inhibition by these amino sugars suggests very strongly that inhibition results from the formation of an ion-pair between the protonated inhibitor and a carboxylate group in the activ Group: Biochemicals. Alternative Names: (2S,3R,4S,5R)-2-Methyl-3,4,5-piperidinetriol; 1,5-Dideoxy-1,5-imino-L-fucitol. Grades: Highly Purified. CAS No. 210174-73-5. Pack Sizes: 5mg, 10mg. Molecular Formula: C6H13NO3 HCl, Molecular Weight: 183.63. US Biological Life Sciences. |  Worldwide |
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