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Invitrogen™ MMAA Monoclonal Antibody (OTI3G5)
Mouse Monoclonal Antibody
Supplier: Invitrogen™ MA525384
Description
MMAA Monoclonal Antibody for Western Blot, ICC/IF, IHC (P)
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.
Specifications
MMAA | |
Monoclonal | |
1 mg/mL | |
PBS with 1% BSA, 50% glycerol and 0.02% sodium azide; pH 7.3 | |
Q8IVH4 | |
MMAA | |
Full length human recombinant protein of MMAA produced in HEK293T cell. | |
100 μL | |
Primary | |
Human | |
Antibody | |
IgG2a |
Immunohistochemistry (Paraffin), Western Blot, Immunocytochemistry | |
OTI3G5 | |
Unconjugated | |
MMAA | |
2810018E08Rik; AI840684; cblA; methylmalonic aciduria (cobalamin deficiency) cblA type; methylmalonic aciduria (cobalamin deficiency) type A; methylmalonic aciduria type A homolog, mitochondrial; Methylmalonic aciduria type A protein, mitochondrial; MMAA; mutant adenosylcobalamin | |
Mouse | |
Affinity Chromatography | |
RUO | |
166785 | |
-20°C, Avoid Freeze/Thaw Cycles | |
Liquid |
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