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Anti-Glutathione Synthetase antibody

SKU Product Brand Unit Availability Price Quantity  
AB-06-1952
Anti-Glutathione Synthetase antibody
Erpan Tech In stock

Specifications        

Product Cat#: AB-06-1952
Product type: Primary antibody
Antigen: Glutathione Synthetase
Immunogen: Recombinant protein
Species immunized: Rabbit
Isotype: IgG
Applications: Western Blot (1:500-1:1000); Immunohistochemistry (1:50-1:200); Immunocytochemistry (1:50-1:200); Flow Cytometry (1:50-1:100); Immunofluorescence
Reactivity: Human, Mouse, Rat
Clonality (clone number): Monoclonal (JB95-33)
Form: Liquid
Buffer: 1*TBS (pH7.4), 1%BSA, 40%Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 1 mg/ml
Purity: Protein A affinity purified
Storage: Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
Alternative names: epididymis secretory sperm binding protein Li 64p antibody
epididymis secretory sperm binding protein Li 88n antibody
Glutathione synthase antibody
Glutathione synthetase antibody
GSH S antibody
GSH synthetase antibody
GSH-S antibody
GSHB_HUMAN antibody
GSHS antibody
GSS antibody
HEL-S-64p antibody
HEL-S-88n antibody
MGC14098 antibody
OTTHUMP00000030711 antibody
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Target information

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 β-sheet, a parallel β-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 γ-GCS and ending with GSS. In an ATP-dependent reaction, GSS produces Glutathione from γ-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.

Provider

Erpantech Laboratory

download

MSDS-AB-06-1952.pdf (132 downloads )