中文名稱(chēng):小鼠抗CHCHD10單克隆抗體

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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. |
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Applications: |
WB, IHC |
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Name of antibody: |
CHCHD10 |
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Immunogen: |
Fusion protein of human CHCHD10 |
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Full name: |
coiled-coil-helix-coiled-coil-helix domain containing 10 |
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Synonyms: |
IMMD; SMAJ; FTDALS2; N27C7-4; C22orf16 |
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SwissProt: |
Q8WYQ3 |
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IHC positive control: |
Human liver cancer and Human liver tissue; Human appendix tissue |
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IHC Recommend dilution: |
200-500 |
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WB Predicted band size: |
14 KD |
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WB Positive control: |
293T cell lysate |
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WB Recommended dilution: |
500-2000 |
購(gòu)物車(chē)
幫助
021-54845833/15800441009
