Recombinant Human MMAA Protein, MYC/DDK-tagged


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Recombinant Human MMAA Protein, MYC/DDK-tagged

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Cat.No. : MMAA-573H
Product Overview : Recombinant Human MMAA fused with MYC/DDK tag at C-terminal was expressed in HEK293.
Description : 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.
Source : HEK293
Species : Human
Form : 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol.
Molecular Mass : 39 kDa
Purity : > 80% as determined by SDS-PAGE and Coomassie blue staining
Concentration : >50 ug/mL as determined by microplate BCA method
Gene Name : MMAA methylmalonic aciduria (cobalamin deficiency) cblA type [ Homo sapiens ]
Official Symbol : MMAA
Synonyms : MMAA; methylmalonic aciduria (cobalamin deficiency) cblA type; methylmalonic aciduria (cobalamin deficiency) type A; methylmalonic aciduria type A protein, mitochondrial; cblA; MGC120010; MGC120011; MGC120012; MGC120013;
Gene ID : 166785
mRNA Refseq : NM_172250
Protein Refseq : NP_758454
MIM : 607481
UniProt ID : Q8IVH4

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