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Human CHCHD10 Peptide (VGSAVGHVM) (PEP-146813CQ)

This product is synthetic peptide that is derived from Human CHCHD10 (AA 57-65). This peptide sequence corresponds to amino acid residues: VGSAVGHVM.
Specificity
Human
Format
Lyophilized powder
Storage
Store at -20°C
Introduction
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.
Alternative Name
Coiled-Coil-Helix-Coiled-Coil-Helix Domain Containing 10; C22orf16; Coiled-Coil-Helix-Coiled-Coil-Helix Domain-Containing Protein 10, Mitochondrial; Chromosome 22 Open Reading Frame 16; Protein N27C7-4; FTDALS2; N27C7-4; IMMD; SMAJ;
Entrez Gene ID
UniProt ID
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For research use only. Not intended for any clinical use.
Cat PEP-146813CQ
Conjugates
Size
Price $
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Second antibody and isotype control