CHCHD10 Mouse Monoclonal Antibody [Kloon ID: LBI3B8]

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]

Carrier-free (BSA/glycerol-free) CHCHD10 mouse monoclonal antibody, clone LBI3B8

C22orf16; FTDALS2; IMMD; N27C7-4; SMAJ

Homo sapiens coiled-coil-helix-coiled-coil-helix domain containing 10 (CHCHD10), transcript variant 2, mRNA; nuclear gene for mitochondrial product.

400916

Q8WYQ3

Unconjugated

WB 1:500~2000, IHC 1:500

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

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.

CHCHD10

https://www.ncbi.nlm.nih.gov/gene/?term=400916

https://www.uniprot.org/uniprot/Q8WYQ3