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Methylmalonic aciduria

Probable GTPase. May function as chaperone. May be involved in the transport of cobalamin (Cbl) into mitochondria for the final steps of adenosylcobalamin (AdoCbl) synthesis (By similarity).

Below are the list of possible Methylmalonic aciduria products. If you cannot find the target and/or product is not available in our catalog, please click here to contact us and request the product or submit your request for custom elisa kit production, custom recombinant protein production or custom antibody production. Custom ELISA Kits, Recombinant Proteins and Antibodies can be designed, manufactured and produced according to the researcher's specifications.

Methylmalonic aciduria type A homolog

 Methylmalonic aciduria type A homolog ELISA Kit
 Methylmalonic aciduria type A homolog Recombinant
 Methylmalonic aciduria type A homolog Antibody
Also known as Methylmalonic aciduria type A homolog, mitochondrial.
MMAA: Probable GTPase. May function as chaperone. May be involved in the transport of cobalamin (Cbl) into mitochondria for the final steps of adenosylcobalamin (AdoCbl) synthesis. Defects in MMAA are the cause of methylmalonic aciduria type cblA (MMAA); also known as methylmalonic aciduria type A or vitamin B12-responsive meth
ylmalonicaciduria of cblA complementation type. MMAA is a disorder of methylmalonate and cobalamin metabolism due to defective synthesis of adenosylcobalamin. Inheritance is autosomal recessive. Belongs to the ArgK family.

Protein type: Chaperone; EC 3.6.-.-
 Mmaa ELISA Kit
 Mmaa Recombinant
 Mmaa Antibody
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