MMAA/cblA Polyklonale Antilichaam, PE Vervoeging

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. [provided by RefSeq, Jul 2008].

Mitochondrial; cblA; MMAA protein; Methylmalonic aciduria cobalamin deficiency cblA type; Methylmalonic aciduria cobalamin deficiency type A; Methylmalonic aciduria type A protein; Methylmalonic aciduria type A protein mitochondrial; MMAA; MMAA_HUMAN.

166785

Mouse

21-120/418

MMAA/cblA

PE

KLH conjugated synthetic peptide derived from human MMAA/cblA

WB, IF (IHC-P)

Purified by Protein A.

496,564nm/578nm

1µg/µl

WB (1:300-5000), IF (IHC-P) (1:50-200)

Aqueous buffered solution containing 0.01M TBS (pH 7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.

Unmodified

Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

166785

Human, Rat