MMADHC Antibody (C-term) Blocking Peptide
€363.00
In stock
SKU
AC-BP18061b
Background:
This gene encodes a mitochondrial protein that is involvedin an early step of vitamin B12 metabolism. Vitamin B12 (cobalamin)is essential for normal development and survival in humans.Mutations in this gene cause methylmalonic aciduria andhomocystinuria type cblD (MMADHC), a disorder of cobalaminmetabolism that is characterized by decreased levels of thecoenzymes adenosylcobalamin and methylcobalamin. Pseudogenes havebeen identified on chromosomes 11 and X.
Other Names:
Methylmalonic aciduria and homocystinuria type D protein, mitochondrial, MMADHC, C2orf25, CL25022
Gene Name: MMADHC (HGNC:25221)
Gene ID: 27249
Primary Accession: Q9H3L0
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
This gene encodes a mitochondrial protein that is involvedin an early step of vitamin B12 metabolism. Vitamin B12 (cobalamin)is essential for normal development and survival in humans.Mutations in this gene cause methylmalonic aciduria andhomocystinuria type cblD (MMADHC), a disorder of cobalaminmetabolism that is characterized by decreased levels of thecoenzymes adenosylcobalamin and methylcobalamin. Pseudogenes havebeen identified on chromosomes 11 and X.
Other Names:
Methylmalonic aciduria and homocystinuria type D protein, mitochondrial, MMADHC, C2orf25, CL25022
Gene Name: MMADHC (HGNC:25221)
Gene ID: 27249
Primary Accession: Q9H3L0
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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