You are viewing an incomplete version of our website. Please click to reload the website as full version.

Methylmalonic Aciduria (Cobalamin Deficiency) CblA Type (MMAA) ELISA Kits

The protein encoded by MMAA is involved in the translocation of cobalamin into the mitochondrion, where it is used in the final steps of adenosylcobalamin synthesis. Additionally we are shipping MMAA Antibodies (13) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
Anti-Human MMAA MMAA 166785 Q8IVH4
How to order from antibodies-online
  • +1 877 302 8632
  • +1 888 205 9894 (toll-free)
  • Order online
  • orders@antibodies-online.com

More ELISA Kits for MMAA Interaction Partners

Human Methylmalonic Aciduria (Cobalamin Deficiency) CblA Type (MMAA) interaction partners

  1. Ten novel mutational MMAA variants have been identified in patients with methylmalonic aciduria.

  2. MMAA acts as a chaperone of human MCM protein.

  3. Structures of the human GTPase (show RACGAP1 ELISA Kits) MMAA and vitamin B12 (show NDUFB3 ELISA Kits)-dependent methylmalonyl-CoA mutase (show MUT ELISA Kits) and insight into their complex formation.

  4. A candidate gene for mutations (deletion, insertion, stop-codon, missense)in cblA patient cells was identified as MMAA on chromosome 4q31.1-2. It encodes a predicted protein of 418 AA.

  5. DNA from 37 cblA patients was analyzed for deleterious mutations in the MMAA gene by DNA sequencing of exons and flanking sequences

  6. Long-term outcome in methylmalonic acidurias is influenced by the underlying genetic defects in MCM/MMAA/MMAB (show MMAB ELISA Kits).

  7. Methylmalonic acidaemia: examination of genotype and biochemical data in 32 patients belonging to mut, cblA or cblB complementation group.

  8. Spondylocostal dysostosis associated with MMAA is presented in a young boy.

MMAA Antigen Profile

Antigen Summary

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.

Gene names and symbols associated with MMAA

  • methylmalonic aciduria (cobalamin deficiency) cblA type (MMAA) antibody
  • cblA antibody

Protein level used designations for MMAA

methylmalonic aciduria type A protein, mitochondrial , methylmalonic aciduria type A homolog, mitochondrial

GENE ID SPECIES
166785 Homo sapiens
100009376 Oryctolagus cuniculus
Did you look for something else?