SOD2 Rabbit Monoclonal Antibody [Clone ID: EPR2560Y]

CAT#: TA301157

Rabbit Monoclonal Antibody against SOD2 (Clone EPR2560Y)


USD 523.00

In Stock*

Size
    • 100 ul

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Specifications

Product Data
Clone Name EPR2560Y
Applications IHC, WB
Recommended Dilution IHC-Fr: Use at an assay dependent concentration; WB: 1:1000 - 1:2000; IHC-P: 1:100 - 1:250
Reactivities Human, Mouse, Rat
Host Rabbit
Isotype IgG
Clonality Monoclonal
Immunogen A synthetic peptide corresponding to residues near the N-terminus of human SOD2 was used as an immunogen.
Formulation pH: 7.40
Preservative: 0.01% Sodium azide
Constituents: 50% Glycerol, 0.05% BSA
Purification Tissue culture supernatant
Conjugation Unconjugated
Storage Store at -20°C as received.
Stability Stable for 12 months from date of receipt.
Predicted Protein Size 25 kDa
Gene Name superoxide dismutase 2, mitochondrial
Background Superoxide dismutase comprises a family of metalloenzymes that catalyze the oxido-reduction of superoxide anion to H2O2. Manganese superoxide dismutase (SOD2) is encoded by nuclear chromatin, synthesized in the cytosol, and imported posttranslationally into the mitochondrial matrix (1). It has been shown that SOD2 activity in tumor cells is lower than that in their normal counterparts. results suggest that the reduced level of SOD2 activity observed in human tumor cells is not due to a defect in the primary structure of the SOD2 protein, a change in the dosage of the SOD2 gene, or a decrease in the stability of SOD2 mRNA in tumor cells but rather is due to a defect or defects in the expression of the gene (2). SOD2 is one of the major cellular defense enzymes that protects against toxic effects of superoxide radicals. Overexpression of human SOD2 has been shown to inhibit radiation-induced neoplastic transformation, suppress malignancy of cancer cells, and increase tolerance to various toxic agents (3).
Synonyms IPOB; MNSOD; MVCD6
Note Is unsuitable for Flow Cyt,ICC or IP.
Reference Data
Protein Families Druggable Genome, Transcription Factors
Protein Pathways Huntington's disease

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