中文名称:小鼠抗CHCHD10单克隆抗体
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 |