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CISD2 Mouse anti-Human, Mouse, Rat, Zebrafish, Clone: 3D7A3, Proteintech
Shop All Proteintech ProductsDescription
This monoclonal antibody is specific to CISD2 and does not cross-react with CISD1.
Defects in the CISD2 (CDGSH iron sulfur domain 2) gene are a cause of the neurodegenerative disorder Wolfram syndrome 2. CISD2 is a zinc finger protein that localizes to the endoplasmic reticulum and mitochondria and binds an iron/sulfur cluster. CISD2 interacts with Bcl-2 and can be displaced by the BH3-only protein BIK and contributes to the regulation of BIK-initiated autophagy. CISD2 deficiency in mice causes mitochondrial breakdown accompanied by autophagic cell death as well as the development of premature aging phenotype.
Specifications
Specifications
| Antigen | CISD2 |
| Applications | Western Blot, Immunohistochemistry (Paraffin), Immunocytochemistry, Immunofluorescence |
| Classification | Monoclonal |
| Clone | 3D7A3 |
| Concentration | 1.65 mg/mL |
| Conjugate | Unconjugated |
| Formulation | PBS with 50% glycerol and 0.02% sodium azide; pH 7.3 |
| Gene | CISD2 |
| Gene Accession No. | Q7T326, Q8N5K1, Q9CQB5 |
| Gene Alias | CDGSH iron sulfur domain 2, CDGSH2, CISD2, CISD2-Specific, ERIS, Miner1, MitoNEET related 1 protein, NAF 1, WFS2, ZCD2 |
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