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 | 
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 021-54845833/15800441009
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