CHCHD10 Mouse Monoclonal Antibody [Clone ID: LBI3D7]
Product Specifications
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. [provided by RefSeq, Aug 2014]
Synonyms
C22orf16; FTDALS2; IMMD; N27C7-4; SMAJ
Gene Name
Homo sapiens coiled-coil-helix-coiled-coil-helix domain containing 10 (CHCHD10), transcript variant 2, mRNA; nuclear gene for mitochondrial product.
Gene ID
400916
UniProt
Q8WYQ3
Conjugation
Unconjugated
Dilution
WB 1:500~2000
Form
Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)
Buffer
Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)
Storage Conditions
Stable for 1 year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. Aliquot will be stable at 4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.
Symbol
CHCHD10
Overview
Carrier-free (BSA/glycerol-free) CHCHD10 mouse monoclonal antibody, clone LBI3D7
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/?term=400916
Uniprot URL
https://www.uniprot.org/uniprot/Q8WYQ3
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