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GSS Antibody (C-5): sc-365863

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Datasheets
  • GSS Antibody (C-5) is a mouse monoclonal IgG2b κ, cited in 4 publications, provided at 200 µg/ml
  • specific for an epitope mapping between amino acids 357-385 within an internal region of GSS of human origin
  • recommended for detection of GSS of mouse, rat, human, and, to a lesser extent, hamster origin by WB, IP, IF, IHC(P) and ELISA; also reactive with additional species, including and equine, canine, bovine, porcine and avian
  • m-IgG2b BP-HRP is the preferred secondary detection reagent for GSS Antibody (C-5) for WB and IHC(P) applications. This reagent is now offered in a bundle with GSS Antibody (C-5) (see ordering information below).

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GSS Antibody (C-5) is a mouse monoclonal IgG2b antibody that detects Glutathione synthetase (GSS) in mouse, rat, human, and hamster samples through various applications including western blotting (WB), immunoprecipitation (IP), immunofluorescence (IF), immunohistochemistry, and enzyme-linked immunosorbent assay (ELISA). GSS is a crucial enzyme involved in the biosynthesis of glutathione, a vital antioxidant that protects cells from oxidative stress and maintains cellular redox balance. GSS (C-5) antibody targets proteins primarily located in the cytoplasm of cells, where GSS plays a significant role in detoxifying harmful compounds and regulating cellular metabolism. Proper functioning of GSS is essential for maintaining adequate levels of glutathione, and deficiencies in this enzyme can lead to serious health issues, including 5-oxoprolinuria, which is characterized by neurological damage and metabolic disorders. GSS occurs as a homodimer and is encoded by a gene located on human chromosome 20q11.2, with its structure comprising three loops projecting from an antiparallel β-sheet, a parallel β-sheet, and a lid of anti-parallel sheets that facilitate access to the ATP-binding site. Anti-GSS antibody (C-5) is an invaluable tool for researchers studying the role of glutathione in cellular processes and the implications of GSS deficiencies in various diseases.

For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.

Alexa Fluor® is a trademark of Molecular Probes Inc., OR., USA

LI-COR® and Odyssey® are registered trademarks of LI-COR Biosciences

GSS Antibody (C-5) References:

  1. Glutathione synthetase homologs encode alpha-L-glutamate ligases for methanogenic coenzyme F420 and tetrahydrosarcinapterin biosyntheses.  |  Li, H., et al. 2003. Proc Natl Acad Sci U S A. 100: 9785-90. PMID: 12909715
  2. Function of conserved residues of human glutathione synthetase: implications for the ATP-grasp enzymes.  |  Dinescu, A., et al. 2004. J Biol Chem. 279: 22412-21. PMID: 14990577
  3. S-Acetylglutathione normalizes intracellular glutathione content in cultured fibroblasts from patients with glutathione synthetase deficiency.  |  Okun, JG., et al. 2004. J Inherit Metab Dis. 27: 783-6. PMID: 15617191
  4. Glutathione is essential for early embryogenesis--analysis of a glutathione synthetase knockout mouse.  |  Winkler, A., et al. 2011. Biochem Biophys Res Commun. 412: 121-6. PMID: 21802407
  5. Protein levels of clusterin and glutathione synthetase in platelets allow for early detection of colorectal cancer.  |  Strohkamp, S., et al. 2018. Cell Mol Life Sci. 75: 323-334. PMID: 28849249
  6. Erythrocyte glutathione synthetase deficiency leads not only to glutathione but also to glutathione-S-transferase deficiency.  |  Beutler, E., et al. 1986. J Clin Invest. 77: 38-41. PMID: 3944259
  7. Glutathione synthetase deficiency, an inborn error of metabolism involving the gamma-glutamyl cycle in patients with 5-oxoprolinuria (pyroglutamic aciduria).  |  Wellner, VP., et al. 1974. Proc Natl Acad Sci U S A. 71: 2505-9. PMID: 4152248
  8. Oxidative damage to neutrophils in glutathione synthetase deficiency.  |  Spielberg, SP., et al. 1979. Br J Haematol. 42: 215-23. PMID: 465367
  9. Sequencing and expression of a cDNA for human glutathione synthetase.  |  Gali, RR. and Board, PG. 1995. Biochem J. 310 (Pt 1): 353-8. PMID: 7646467
  10. Effect of decreased glutathione levels in hereditary glutathione synthetase deficiency on dibromoethane-induced genotoxicity in human fibroblasts.  |  DeLeve, LD. 1997. Mutat Res. 389: 291-7. PMID: 9093395

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

GSS Antibody (C-5)

sc-365863
200 µg/ml
$316.00

GSS Antibody (C-5): m-IgG2b BP-HRP Bundle

sc-548564
200 µg Ab; 10 µg BP
$354.00

GSS (C-5) Neutralizing Peptide

sc-365863 P
100 µg/0.5 ml
$68.00

What application is the blocking peptide sc-365863 P appropriate for?

Asked by: Dr Ninau Qelp
Thank you for your question. The blocking peptide is intended for use as a negative control, by pre-adsorbing the mouse monoclonal antibody against the antigen. For full protocol details, please contact our Technical Services Department or view our online protocol here: https://www.scbt.com/scbt/resources/protocols/peptide-neutralization
Answered by: Technical Support
Date published: 2017-02-25
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Rated 5 out of 5 by from Nice Western blot data of GSS expression in nonNice Western blot data of GSS expression in non-transfected 293T, human GSS transfected 293T CHO-K1 and HeLa whole cell lysates. -SCBT QC
Date published: 2013-09-22
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GSS Antibody (C-5) is rated 5.0 out of 5 by 1.
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