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MMADHC Protéines

(Methylmalonic Aciduria (Cobalamin Deficiency) CblD Type, with Homocystinuria (MMADHC))

This gene encodes a mitochondrial protein that is involved in 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 and homocystinuria type cblD (MMADHC), a disorder of cobalamin metabolism that is characterized by decreased levels of the coenzymes adenosylcobalamin and methylcobalamin. Pseudogenes have been identified on chromosomes 11 and X.[provided by RefSeq, Nov 2008].

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MMADHC Protein (AA 1-296) (GST tag)

MMADHC Origine: Humain Hôte: Wheat germ Recombinant ELISA, AP, AA, WB

Image no. 1 for Methylmalonic Aciduria (Cobalamin Deficiency) CblD Type, with Homocystinuria (MMADHC) (AA 1-296) protein (GST tag) (ABIN1311045)

1 image

N° du produit ABIN1311045

MMADHC Protein (AA 39-296) (His tag)

MMADHC Origine: Humain Hôte: Escherichia coli (E. coli) Recombinant > 90 % by SDS - PAGE SDS

SDS-PAGE (SDS) image for Methylmalonic Aciduria (Cobalamin Deficiency) CblD Type, with Homocystinuria (MMADHC) (AA 39-296) protein (His tag) (ABIN5853506)

1 image

N° du produit ABIN5853506

MMADHC Protéine

MMADHC Origine: Humain Hôte: Escherichia coli (E. coli) Recombinant > 90 % pure SDS

N° du produit ABIN2130616

MMADHC Protein (Myc-DYKDDDDK Tag)

MMADHC Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD

Validation with Western Blot

1 image

N° du produit ABIN2726133

MMADHC Protein (AA 39-296) (His tag)

MMADHC Origine: Rat Hôte: Levure Recombinant > 90 % ELISA

N° du produit ABIN7590383

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