小鼠抗CHCHD10單克隆抗體

Background:

This gene encodes a mitochondrial protein that is enriched at cristae junctions in the intermembrane space. It may play a role in cristae morphology maintenance 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.

Applications:

WB, IHC

Name of antibody:

CHCHD10

Immunogen:

Fusion protein of human CHCHD10

Full name:

coiled-coil-helix-coiled-coil-helix domain containing 10

Synonyms:

IMMD; SMAJ; FTDALS2; N27C7-4; C22orf16

SwissProt:

Q8WYQ3

IHC positive control:

Human liver cancer and Human liver tissue; Human appendix tissue

IHC Recommend dilution:

200-500

WB Predicted band size:

14 KD

WB Positive control:

293T cell lysate

WB Recommended dilution:

500-2000