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DMGDH Polyclonal Antibody, Invitrogen™
Rabbit Polyclonal Antibody
Brand: Invitrogen PA557659
This item is not returnable.
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Description
Immunogen sequence: IINVVNGPIT YSPDILPMVG PHQGVRNYWV AIGFGYGIIH AGGVGKYLSD WILHGEPPFD LIELDPNRYG KWTTTQYTE Highest antigen sequence identity to the following orthologs: Mouse - 97%, Rat - 97%.
This gene encodes an enzyme involved in the catabolism of choline, catalyzing the oxidative demethylation of dimethylglycine to form sarcosine. The enzyme is found as a monomer in the mitochondrial matrix, and uses flavin adenine dinucleotide and folate as cofactors. Mutation in this gene causes dimethylglycine dehydrogenase deficiency, characterized by a fishlike body odor, chronic muscle fatigue, and elevated levels of the muscle form of creatine kinase in serum. Alternative splicing results in multiple transcript variants.Specifications
DMGDH | |
Polyclonal | |
Unconjugated | |
DMGDH | |
1200014D15Rik; AI787269; dimethylglycine dehydrogenase; dimethylglycine dehydrogenase precursor; dimethylglycine dehydrogenase, mitochondrial; Dmgdh; DMGDHD; EC 1.5.99.2; M2GD; ME2GLYDH | |
Rabbit | |
Antigen affinity chromatography | |
RUO | |
29958 | |
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles. | |
Liquid |
Immunohistochemistry | |
0.05 mg/mL | |
PBS with 40% glycerol and 0.02% sodium azide; pH 7.2 | |
Q9UI17 | |
DMGDH | |
Recombinant protein corresponding to Human DMGDH | |
100 μL | |
Primary | |
Human | |
Antibody | |
IgG |
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