Recombinant Human MMAA Protein, MYC/DDK-tagged MMAA-573H

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
Tag :	MYC/DDK
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