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Product Name | Recombinant Rabbit Methylmalonic aciduria type A homolog, mitochondrial (MMAA) |
Description | 66-413aa, Full Length of Mature Protein. MW: 45,682 Da. Purity >85% (SDS-PAGE). This protein 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. |
Size | 0.05 mg (E-Coli), 0.2 mg (E-Coli), 0.05 mg (Baculovirus), 0.5 mg (E-Coli), 0.2 mg (Yeast) |
Concentration | n/a |
Applications | n/a |
Other Names | [methylmalonic aciduria type A homolog, mitochondrial; Methylmalonic aciduria type A homolog, mitochondrial; methylmalonic aciduria type A homolog, mitochondrial] |
Gene, Accession, CAS # | MMAA, Gene ID: 100009376, Accession: NP_001076131.1 |
Catalog # | MBS1440080 |
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Order / More Info | Recombinant Rabbit Methylmalonic aciduria type A homolog, mitochondrial (MMAA) from MYBIOSOURCE INC. |
Product Specific References | n/a |
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