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
  • Gene Information
  • Related Products
  • Download
Species : Human
Source : HEK293
Tag : DDK&Myc
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.
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

Not For Human Consumption!

Inquiry

  • Reviews
  • Q&As

Customer Reviews (0)

Write a review

Q&As (0)

Ask a question

Ask a Question for All MMAA Products

Required fields are marked with *

My Review for All MMAA Products

Required fields are marked with *

0

Inquiry Basket

cartIcon