missing translation for 'onlineSavingsMsg'
Learn More
Learn More
Description
CHCHD10 encodes a mitochondrial protein that is enriched at cristae junctions in the intermembrane space. It may play a role in cristae morphology maintece or oxidative phosphorylation. Mutations in this gene cause frontotemporal dementia and/or amyotrophic lateral sclerosis-2. Alternative splicing of this gene results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 7 and 19.
Specifications
Specifications
| Antigen | CHCHD10 |
| Applications | Western Blot, Immunofluorescence, Immunohistochemistry (Paraffin), Immunoprecipitation, Immunocytochemistry |
| Classification | Polyclonal |
| Concentration | 0.3 mg/mL |
| Conjugate | Unconjugated |
| Formulation | PBS with 50% glycerol and 0.1% sodium azide; pH 7.3 |
| Gene | CHCHD10 |
| Gene Accession No. | Q8WYQ3 |
| Gene Alias | C22orf16, CHCHD10, N27C7 4, Protein N27C7 4 |
| Gene Symbols | CHCHD10 |
| Show More |
Product Title
By clicking Submit, you acknowledge that you may be contacted by Fisher Scientific in regards to the feedback you have provided in this form. We will not share your information for any other purposes. All contact information provided shall also be maintained in accordance with our Privacy Policy.
Spot an opportunity for improvement?