Sie suchten nach: N-(tert-Butoxycarbonyl)-L-pyroglutamic+acid

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N-(tert-Butoxycarbonyl)-L-pyroglutamic acid 95+%

Artikel-Nr: (APOSOR309165-25G)

Lieferant: Apollo Scientific

Beschreibung: N-(tert-Butoxycarbonyl)-L-pyroglutamic acid 95+%

VE: 1 * 25 g

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Boc-L-pyroglutamic acid methyl ester

Artikel-Nr: (APOSOR18848-500G)

Lieferant: Apollo Scientific

Beschreibung: Boc-L-pyroglutamic acid methyl ester

VE: 1 * 500 g

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Anti-GSS Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Artikel-Nr: (BOSSBS-11850R-HRP)

Lieferant: Bioss

Beschreibung: GSS (Glutathione synthetase) is a 474 amino acid protein encoded by the gene located at human chromosome 20q11.2. GSS consists of three loops projecting from an antiparallel âˆ«-sheet, a parallel âˆ«-sheet and a lid of anti-parallel sheets, which provide access to the ATP-binding site. Although Southern blot and gene analysis suggest that GSS may be the only member of a unique family, the crystal structure indicates that GSS belongs to the ATP-GRASP superfamily. GSS is expressed in hemocytes and nucleated cells, including the brain. GSS occurs as a homodimer. There are two steps in the production of Glutathione, begining with GSS (Glutathione synthetase) is a 474 amino acid protein encoded by the gene located at human chromosome 20q11.2. GSS consists of three loops projecting from an antiparallel âˆ«-sheet, a parallel âˆ«-sheet and a lid of anti-parallel sheets, which provide access to the ATP-binding site. Although Southern blot and gene analysis suggest that GSS may be the only member of a unique family, the crystal structure indicates that GSS belongs to the ATP-GRASP superfamily. GSS is expressed in hemocytes and nucleated cells, including the brain. GSS occurs as a homodimer. There are two steps in the production of Glutathione, begining with ©-GCS and ending with GSS. In an ATP-dependent reaction, GSS produces Glutathione from ©-glutamylcysteine and glycine precursors. Partial hepatectomy, diethyl maleate, buthionine sulfoximine, tert-butylhaydroquinone and thioacetamide increase the ex-pression of GSS, which causes an increase in Glutathione levels. An inherited autosomal recessive disorder, 5-oxoprolinuria (pyroglutamic aciduria), is caused by GSS deficiencies, which leads to central nervous system damage, hemolytic anemia, metabolic acidosis and urinary excretion of 5-oxoproline. A missense mutation in the gene encoding GSS leads to a GSS deficiency restricted to erythrocytes, which causes only hemolytic anemia.-GCS and ending with GSS.

VE: 1 * 100 µl

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