Glutathione Synthetase (GSS) Mouse Monoclonal Antibody (HRP conjugated) [Clone ID: OTI1A12]

CAT#: TA501932BM

GSS (Glutathione Synthetase) mouse monoclonal antibody, clone OTI1A12 (formerly 1A12), HRP conjugated

Product Images

HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY GSS (RC203174, Right lane) cDNA for 48 hrs and lysed. Equivalent amounts of cell lysates (5 ug per lane) were separated by SDS-PAGE and immunoblotted with anti-GSS. Positive lysates LY424876 (100ug) and LC424876 (20ug) can be purchased separately from OriGene.

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  Immunohistochemical staining of paraffin-embedded Human colon tissue within the normal limits using anti-GSS mouse monoclonal antibody at 1:150 (TA501932)

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  Immunohistochemical staining of paraffin-embedded Human liver tissue within the normal limits using anti-GSS mouse monoclonal antibody at 1:150 (TA501932)

Specifications

Product Data

• Clone Name: OTI1A12
• Applications: IHC, WB
• Recommended Dilution: WB: 1:500, IHC: 1:50-1:150
• Reactivities: Human, Mouse, Rat
• Host: Mouse
• Isotype: IgG1
• Clonality: Monoclonal
• Immunogen: Full length human recombinant protein of human GSS (NP_000169) produced in HEK293T cell.
• Formulation: PBS (pH 7.3) containing 1% BSA, 50% glycerol.
• Concentration: 0.5 mg/ml
• Purification: Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G)
• Conjugation: HRP
• Storage: Store at -20°C as received.
• Stability: Stable for 12 months from date of receipt.
• Predicted Protein Size: 52.2 kDa
• Gene Name: glutathione synthetase
• Database Link:
  NP_000169
  Entrez Gene 14854 MouseEntrez Gene 25458 RatEntrez Gene 2937 Human
  UniProt ID P48637
• Background: Glutathione is important for a variety of biological functions, including protection of cells from oxidative damage by free radicals, detoxification of xenobiotics, and membrane transport. The protein encoded by this gene functions as a homodimer to catalyze the second step of glutathione biosynthesis, which is the ATP-dependent conversion of gamma-L-glutamyl-L-cysteine to glutathione. Defects in this gene are a cause of glutathione synthetase deficiency. [provided by RefSeq]
• Synonyms: GSHS; HEL-S-64p; HEL-S-88n

Reference Data

• Protein Families: Druggable Genome
• Protein Pathways: Glutathione metabolism, Metabolic pathways