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This peptide corresponds to 15 amino acid peptide near the center of human CISD2.
PEP-1588 can be used as a blocking peptide with polyclonal antibody PA5-34545. For use as a blocking peptide in Western blot, incubate the peptide with equal volume of antibody for 30 min at 37ºC.
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.
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Protein Aliases: CDGSH iron-sulfur domain-containing protein 2; Endoplasmic reticulum intermembrane small protein; Miner1; mitoNEET related 1; MitoNEET-related 1 protein; NAF-1; Nutrient-deprivation autophagy factor-1; zinc finger, CDGSH-type domain 2
Gene Aliases: CDGSH2; CISD2; ERIS; Miner1; NAF-1; WFS2; ZCD2
UniProt ID: (Human) Q8N5K1
Entrez Gene ID: (Human) 493856
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