C2ORF25 (MMADHC) Mouse Monoclonal Antibody [Kloon ID: LBI1G4]

This gene encodes a mitochondrial protein that is involved in an early step of vitamin B12 metabolism. Vitamin B12 (cobalamin) is essential for normal development and survival in humans. Mutations in this gene cause methylmalonic aciduria and homocystinuria type cblD (MMADHC), a disorder of cobalamin metabolism that is characterized by decreased levels of the coenzymes adenosylcobalamin and methylcobalamin. Pseudogenes have been identified on chromosomes 11 and X. [provided by RefSeq, Nov

Carrier-free (BSA/glycerol-free) MMADHC mouse monoclonal antibody, clone LBI1G4

C2orf25; cblD; CL25022

Homo sapiens metabolism of cobalamin associated D (MMADHC), mRNA.

27249

Q9H3L0

Unconjugated

WB 1:2000

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.

MMADHC

https://www.ncbi.nlm.nih.gov/gene/?term=27249

https://www.uniprot.org/uniprot/Q9H3L0