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CISD2 Monoclonal Antibody (OTI4F8), TrueMAB™, OriGene
SDP

Catalog No. 501683351
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100 μL
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50-168-3351 100 μL
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Catalog No. 50-168-3351 Supplier OriGene Supplier No. TA810357
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Mouse Monoclonal Antibody

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

Antigen CISD2
Applications Immunohistochemistry (Paraffin), Western Blot
Classification Monoclonal
Clone OTI4F8
Concentration 1 mg/mL
Conjugate Unconjugated
Formulation PBS with 1% BSA, 50% glycerol and 0.02% sodium azide
Gene CISD2
Gene Accession No. Q8N5K1
Gene Alias ERIS, Miner1, NAF-1, WFS2, ZCD2
Gene Symbols CISD2
Host Species Mouse
Immunogen Full length human recombit protein of human CISD2 produced in E.coli.
Purification Method Affinity Chromatography
Quantity 100 μL
Regulatory Status RUO
Primary or Secondary Primary
Gene ID (Entrez) 493856
Target Species Human
Content And Storage -20° C, Avoid Freeze/Thaw Cycles
Product Type Antibody
Form Liquid
Isotype IgG1
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