Dimethylglycine Dehydrogenase (DMGDH) Antibody

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Catalogue No: abx029935
Price: US$290.00
(Size: 80 µl)

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Datasheet SDS
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.

Target Dimethylglycine Dehydrogenase (DMGDH)
Clonality Polyclonal
Reactivity Human
Tested Applications ELISA, WB
Host Rabbit
Recommended dilutions WB: 1/1000. Optimal dilutions/concentrations should be determined by the end user.
Conjugation Unconjugated
Immunogen KLH-conjugated synthetic peptide between 836-864 amino acids from the C-terminal region of human DMGDH.
Isotype IgG
Form Liquid
Purification Purified through a protein A column, followed by peptide affinity purification.
Storage Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
UniProt Primary AC Q9UI17 (UniProt, ExPASy)
UniProt Secondary AC B2RBN0, B4E1J9
UniProt Entry Name M2GD_HUMAN
Gene Symbol DMGDH
String 9606.ENSP00000255189
Molecular Weight Calculated MW: 96.8 kDa
Buffer PBS containing 0.09% sodium azide.
Availability Shipped within 5-10 working days.
Note This product is for research use only.
Research Articles on Dimethylglycine Dehydrogenase (DMGDH)


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