missing translation for 'onlineSavingsMsg'
Learn More
Learn More
Invitrogen™ Human CISD2 Synthetic Peptide
Description
CISD2 Synthetic Peptide, PEP-1588, from Invitrogen.
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.
Spécifications
Spécifications
| Gene ID (Entrez) | 493856 |
| Species | Human |
| Purification Method | purified |
| Accession Number | Q8N5K1 |
| Common Name | Human CISD2 |
| Concentration | 200 μg/mL |
| Content And Storage | -20°C |
| Description | Synthetic Peptide |
| Format | Liquid |
| Formulation | PBS with 0.1% BSA and 0.02% sodium azide; pH 7.2 |
| Afficher plus de résultats |