Human Glutathione Synthetase/GSS antibody
Glutathione synthetase, also known GSS, is the second enzyme in the glutathione biosynthesis pathway. It catalyses the condensation of gamma-glutamylcysteine and glycine, to form glutathione. Defects in GSS are the cause of glutathione synthetase deficiency (GSS deficiency) ; also known as 5-oxoprolinuria or pyroglutamic aciduria. It is a severe form characterized by an increased rate of hemolysis and defective function of the central nervous system.
Product Specifications
Product Name Alternative
Glutathione synthetase, GSHS, GSH synthetase
Host
Mouse
Antigen Species
Human
Reactivity
Human
Immunogen
Recombinant human GSS (1-474aa) purified from E. coli
Clonality
Monoclonal
Isotype
IgG1 κ
Clone
AT12F2
Conjugation
Unconjugated
Applications
ELISA, WB, ICC/IF
Purification Method
By protein-A affinity chromatography
Concentration
1 mg/mL (determined by BCA assay)
Additionnal Information
References & Citations
Polekhina G., et al. (1999) EMBO J. 18: 3204-3213. ; ; Huanq Z A., et al. (2000) Biochim Biophys Acta. 1493: 48-55.;
Storage Conditions
Can be stored at 2°C to 8°C for 1 week. For long term storage, aliquot and store at -20C to -80C. Avoid repeated freezing and thawing cycles.
Formulation
Liquid in. Phosphate-Buffered Saline (pH 7.4) with 0.02% Sodium Azide, 10% glycerol
Applications Notes
Scientific Category
Signal Transduction
NCBI Accession Number
NP_000169
Uniprot Accession Number
P48637
WB Description
IF Description
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