Votre recherche pour: N-Fmoc-glycine

Numéro de catalogue: (BOSSBS-13370R-A647)

Fournisseur: Bioss

Description: 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

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Fournisseur: Thermo Fisher Scientific

Description: N-Benzyloxycarbonylglycine 98.5%

MSMD

Numéro de catalogue: (TCIAR0103-1G)

Fournisseur: TCI

Description: Racecadotril ≥99.0% (par HPLC, azote total)

UOM: 1 * 1 g

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Numéro de catalogue: (BOSSBS-13370R-CY5)

Fournisseur: Bioss

Description: 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

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Numéro de catalogue: (BOSSBS-13370R-A350)

Fournisseur: Bioss

Description: 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

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Fournisseur: TCI

Description: N-Benzyloxycarbonylglycine ≥98.0% (par HPLC, analyse par titration)

Numéro de catalogue: (APOSOR451084-5G)

Fournisseur: Apollo Scientific

Description: L-Cyclopropylglycine

UOM: 1 * 5 g

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Numéro de catalogue: (USBIC9001-21)

Fournisseur: US Biological

Description: Anti-Cysteine and Glycine-rich Protein 3 Chicken Polyclonal Antibody

UOM: 1 * 50 µG

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Numéro de catalogue: (ACRO369320010)

Fournisseur: Thermo Fisher Scientific

Description: tert-Butyl-2-((diphenylmethylene)amino)acetate 98%

UOM: 1 * 1 g

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Fournisseur: Apollo Scientific

Description: Methyl-2-((diphenylmethylene)amino)acetate

Numéro de catalogue: (APOSOR30359-100G)

Fournisseur: Apollo Scientific

Description: Pipérazine-2,5-dione 98%

UOM: 1 * 100 g

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Fournisseur: Apollo Scientific

Description: An NMDA receptor agonist acting at the glycine site.

Fournisseur: SIGMA ALDRICH MICROSCOPY

Description: Benzophenone imine plays a vital role as an ammonia surrogate. It is primarily used as ammonia equivalents for the selective formation of protected primary amines. Benzophenone imine is useful as a synthetic intermediate, especially for the synthesis of glycine Schiff base. Benzophenone imine is useful for the preparation of nitrile yield dimers.

Numéro de catalogue: (APOSOR17705-100G)

Fournisseur: Apollo Scientific

Description: tert-Butyl-2-((diphenylmethylene)amino)acetate 98%

UOM: 1 * 100 g

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Fournisseur: TCI

Description: Acide 4-aminohippurique ≥99.0% (par analyse titrimétrique)

Fournisseur: Apollo Scientific

Description: Acide 2-hydroxyhippurique