MMAA Antibody (N-term) Blocking Peptide
€363.00
In stock
SKU
AC-BP9795a
Background:
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.
Other Names:
Methylmalonic aciduria type A protein, mitochondrial, 36--, MMAA
Gene Name: MMAA (HGNC:18871)
Gene ID: 166785
Primary Accession: Q8IVH4
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
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.
Other Names:
Methylmalonic aciduria type A protein, mitochondrial, 36--, MMAA
Gene Name: MMAA (HGNC:18871)
Gene ID: 166785
Primary Accession: Q8IVH4
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
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