MMAA Antilichaam

The protein encoded by this gene is involved in the translocation of cobalamin into the mitochondrion, where it is used in the final steps of adenosylcobalamin synthesis. Adenosylcobalamin is a coenzyme required for the activity of methylmalonyl-CoA mutase. Defects in this gene are a cause of methylmalonic aciduria.

166785

Q8IVH4

Q8IVH4

Human, Mouse

This MMAA antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 56-84 amino acids from the N-terminal region of human MMAA.

Unconjugated

Primary Antibodies

Obesity, Signal Transduction

This antibody is purified through a protein A column, followed by peptide affinity purification.

Batch dependent

Supplied in PBS with 0.09% (W/V) sodium azide.

None

Blue Ice

Store at 4˚ C for three months and -20˚ C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

47 kDa

Rabbit Ig

MMAA

Methylmalonic aciduria type A protein, mitochondrial

Homo sapiens

Honjo, R.S., et al. Genet Test Mol Biomarkers 13 (2) :181-183 (2009)

Merinero, B., et al. J. Inherit. Metab. Dis. 31 (1) :55-66 (2008)

Horster, F., et al. Pediatr. Res. 62 (2) :225-230 (2007)

Padovani, D., et al. J. Biol. Chem. 281 (26) :17838-17844 (2006)

Methylmalonic aciduria type A protein, mitochondrial, 36--, MMAA

WB, IHC-P

38258173

Liquid