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Methylmalonic aciduria type A protein

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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.

Below are the list of possible Methylmalonic aciduria type A protein 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 protein

 Methylmalonic aciduria type A protein ELISA Kit
 Methylmalonic aciduria type A protein Recombinant
 Methylmalonic aciduria type A protein Antibody
Also known as Methylmalonic aciduria type A protein, 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
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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.-.-

Chromosomal Location of Human Ortholog: 4q31.21

Cellular Component: mitochondrial matrix

Biological Process: cobalamin metabolic process; short-chain fatty acid catabolic process

Disease: Methylmalonic Aciduria, Cbla Type
 MMAA ELISA Kit
 MMAA Recombinant
 MMAA Antibody
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