GSS polyclonal, anti-human, mouse, rat

Background:
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. Defects in GSS are the cause of glutathione synthetase deficiency of erythrocytes (GLUSYNDE).

Alternative Name:
Glutathione synthase, Glutathione synthetase, GSH S, GSH synthetase, GSH-S, GSHB, GSHS, GSS, MGC14098, OTTHUMP00000030711,

Application Dilution: WB: 1:500 - 1:2000

Specificity: GSS polyclonal antibody detects endogenous levels of GSS protein.

Immunogen:
Recombinant full length Human GSS.

MW: ~ 52 kDa

Swis Prot.: P48637

Purification & Purity:
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).

Format:
1mg/ml in PBS with 0.1% Sodium Azide, 50% Glycerol.

Storage:
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.

For research use only, not for use in diagnostic procedure.