Human Glutathione S‑Transferase mu 1/
GS Antibody Summary
Accession # P09488
Please Note: Optimal dilutions should be determined by each laboratory for each application. General Protocols are available in the Technical Information section on our website.
Detection of Human Glutathione S‑Transferase mu 1/ GS by Western Blot. Western blot shows lysates of human kidney tissue, human adrenal gland tissue, human stomach tissue, and Jurkat human acute T cell leukemia cell line. PVDF membrane was probed with 0.2 µg/mL of Sheep Anti-Human Glutathione S-Transferase mu 1/GS Antigen Affinity-purified Polyclonal Antibody (Catalog # AF6894) followed by HRP-conjugated Anti-Sheep IgG Secondary Antibody (Catalog # HAF016). A specific band was detected for Glutathione S-Transferase mu 1/GS at approximately 25 kDa (as indicated). This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 1.
Preparation and Storage
- 12 months from date of receipt, -20 to -70 °C as supplied.
- 1 month, 2 to 8 °C under sterile conditions after reconstitution.
- 6 months, -20 to -70 °C under sterile conditions after reconstitution.
Background: Glutathione S-Transferase mu 1/GSTM1
Glutathione S-Transferases (GSTs) are members of the phase II detoxification enzyme family that conjugate glutathione to various electrophilic compounds, including metabolites generated by oxidative processes in the body, environmental toxins or carcinogens, and anti-cancer drugs. GSTM1 is a cytosolic protein that belongs to the mu class of the GST superfamily. The gene encoding GSTM1 is mapped onto human chromosome 1p13.3 and is known to be highly polymorphic (1). Mostly notably, the widely occurring GSTM1-null genotype has been linked to a variety of cancers including lung (2), gastric (3), bladder (4) and prostate (5). In addition to its role in releasing oxidative stress, GSTM1 has also been suggested to act as a hormone binding protein and play a role in maintaining hormone homeostasis in the body (6, 7).
- Pearson, W. R. et al. (1993) Am. J. Hum. Genet. 53:220.
- Mohr, L.C. et al. (2003) Anticancer. Res. 23:2111.
- Wang, H. et al. (2010) Dig. Dis. Sci. 55:1824.
- Engel, L. S. et al. (2002) Am. J. Epidermiol. 156:95.
- Mo, Z. et al. (2009) Prostate. 69:662.
- Mukherjee, S. B. et al. (1999) Biochem. J. 340:309.
- Ishigaki, S. et al. (1989) Arch. Biochem. Biophys. 273:265.
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