Esta buscando: Pyrite+(FeS\u2082)

Numero del catalogo: (33621.260)

Proveedor: VWR Chemicals

Descripción: Tris-(hidroximetil) aminometano (TRIS, Trometamol) ≥99%, Gen-Apex para biología molecular

UOM: 1 * 500 g

FDS Certificados Promoción

Proveedor: Apollo Scientific

Descripción: 2-(Aminomethyl)-1H-indole methanesulphonate 95%

Proveedor: Thermo Fisher Scientific

Descripción: 1H-Indol-6-ylmethylamine 97%

FDS Certificados

Proveedor: TCI

Descripción: Tris-(hidroximetil) aminometano (TRIS, Trometamol) ≥99.0% (by titrimetric analysis)

Proveedor: Apollo Scientific

Descripción: (Pyridin-2-ylmethyl)(pyridin-3-ylmethyl)amine

Proveedor: PanReac AppliChem

Descripción: Tris-(hidroximetil) aminometano (TRIS, Trometamol) ≥99.9% para biología molecular

Certificados

Proveedor: Thermo Fisher Scientific

Descripción: Tris-(hidroximetil) aminometano (TRIS, Trometamol) 99.85% para biología molecular DNase-, RNase-, protease-free

FDS

Proveedor: Thermo Fisher Scientific

Descripción: Tris-(hidroximetil) aminometano (TRIS, Trometamol) 99.8-100.1% (base secada) ACS

FDS Certificados

Proveedor: Thermo Fisher Scientific

Descripción: Tris-(hidroximetil) aminometano (TRIS, Trometamol) 99.8% para bioquímica, para análisis

FDS

Proveedor: Apollo Scientific

Descripción: [[4-(Trifluoromethyl)cyclohexyl]methyl]amine(cis- and trans- mixture) 97%

Proveedor: Thermo Fisher Scientific

Descripción: Tris-(hidroximetil) aminometano (TRIS, Trometamol) 99.8% ACS

FDS

Proveedor: Merck

Descripción: Tris(hydroxymethyl)aminomethane volumetric standard, secondary reference material for acidimetry, traceable to NIST Standard Reference Material (SRM)

Proveedor: Apollo Scientific

Descripción: 4-(Aminomethyl)phenylboronic acid pinacol ester hydrochloride

Numero del catalogo: (BOSSBS-13370R-CY3)

Proveedor: Bioss

Descripción: The glycine cleavage system is comprised of AMT (known as Protein T), GCSH (known as Protein H), DLD (known as Protein L) and GLDC (known as Protein P), all of which work together to catalyze the cleavage and degradation of glycine. GLDC (glycine dehydrogenase ), also known as GCE, GCSP (glycine cleavage system P protein) or HYGN1, is a 1,020 amino acid protein that localizes to the mitochondria and belongs to the gcvP family. GLDC binds to glycine and enables the methylamine group from glycine to be transferred to the Protein T. GLDC exists as a homodimer and utilizes pyridoxal phosphate as a cofactor. Mutations in the gene encoding GLDC leads to nonketotic hyperglycinemia (NKH), also known as glycine encephalopathy (GCE), an autosomal recessive disease characterized by accumulation of a large amount of glycine in body fluid and by severe neurological symptoms.

UOM: 1 * 100 µl

Promoción

Numero del catalogo: (BOSSBS-13370R-FITC)

Proveedor: Bioss

Descripción: The glycine cleavage system is comprised of AMT (known as Protein T), GCSH (known as Protein H), DLD (known as Protein L) and GLDC (known as Protein P), all of which work together to catalyze the cleavage and degradation of glycine. GLDC (glycine dehydrogenase ), also known as GCE, GCSP (glycine cleavage system P protein) or HYGN1, is a 1,020 amino acid protein that localizes to the mitochondria and belongs to the gcvP family. GLDC binds to glycine and enables the methylamine group from glycine to be transferred to the Protein T. GLDC exists as a homodimer and utilizes pyridoxal phosphate as a cofactor. Mutations in the gene encoding GLDC leads to nonketotic hyperglycinemia (NKH), also known as glycine encephalopathy (GCE), an autosomal recessive disease characterized by accumulation of a large amount of glycine in body fluid and by severe neurological symptoms.

UOM: 1 * 100 µl

Promoción

Numero del catalogo: (BOSSBS-13370R-A647)

Proveedor: Bioss

Descripción: The glycine cleavage system is comprised of AMT (known as Protein T), GCSH (known as Protein H), DLD (known as Protein L) and GLDC (known as Protein P), all of which work together to catalyze the cleavage and degradation of glycine. GLDC (glycine dehydrogenase ), also known as GCE, GCSP (glycine cleavage system P protein) or HYGN1, is a 1,020 amino acid protein that localizes to the mitochondria and belongs to the gcvP family. GLDC binds to glycine and enables the methylamine group from glycine to be transferred to the Protein T. GLDC exists as a homodimer and utilizes pyridoxal phosphate as a cofactor. Mutations in the gene encoding GLDC leads to nonketotic hyperglycinemia (NKH), also known as glycine encephalopathy (GCE), an autosomal recessive disease characterized by accumulation of a large amount of glycine in body fluid and by severe neurological symptoms.

UOM: 1 * 100 µl

Promoción