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Invitrogen™ DMGDH Polyclonal Antibody

Rabbit Polyclonal Antibody

Supplier:  Invitrogen™ PA5113450

Catalog No. PIPA5113450


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Description

Description

DMGDH Polyclonal Antibody for Western Blot, ICC/IF, IHC (P), ELISA

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.
TRUSTED_SUSTAINABILITY
Specifications

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
Protein G
RUO
29958, 74129
-20°C or -80°C if preferred
Liquid
ELISA, Immunohistochemistry (Paraffin), Western Blot, Immunocytochemistry
3.34 mg/mL
PBS with 50% glycerol and 0.03% ProClin 300; pH 7.4
Q9DBT9, Q9UI17
DMGDH
Recombinant Human Dimethylglycine dehydrogenase, mitochondrial protein (429-524AA).
100 μg
Primary
Human, Mouse
Antibody
IgG
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