MMADHC Antilichaam

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.

27249

Q9H3L0

Human, Mouse, Rat

Recombinant fusion protein containing a sequence corresponding to amino acids 1-296 of human MMADHC (NP_056517.1) .

Unconjugated

Primary Antibodies

Other

Affinity purification

293T

Batch dependent

PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

None

Blue Ice

Store at -20˚ C. Avoid freeze / thaw cycles.

Observed: 33kDa

IgG

WB: 1:500 - 1:2000

MMADHC

NIH/3T3

HeLa

MCF7

Methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria

Homo sapiens

C2orf25, CL25022, cblD, C2orf25

WB

Liquid