Recombinant Human MMAA Protein, MYC/DDK-tagged

• Cat.No.: MMAA-573H
• Product Overview: Recombinant Human MMAA fused with MYC/DDK tag at C-terminal was expressed in HEK293.

Specification

• 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 Information

• 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