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>   home   >   Products   >   Primary Antibodies   >   Signal Transduction   >   DMGDH Antibody (C-term)   

DMGDH Antibody (C-term)

Peptide Affinity Purified Rabbit Polyclonal Antibody (Pab)

  • WB - DMGDH Antibody (C-term) AP18005B
    DMGDH Antibody (C-term) (Cat. #AP18005b) western blot analysis in MDA-MB453 cell line lysates (35ug/lane).This demonstrates the DMGDH antibody detected the DMGDH protein (arrow).
Product Information
  • Applications Legend:
  • WB=Western Blot
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin-embedded Sections)
  • IHC-F=Immunohistochemistry (Frozen Sections)
  • IF=Immunofluorescence
  • FC=Flow Cytopmetry
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • IP=Immunoprecipitation
  • DB=Dot Blot
  • CHIP=Chromatin Immunoprecipitation
  • FA=Fluorescence Assay
  • IEM=Immunoelectronmicroscopy
  • EIA=Enzyme Immunoassay
Primary Accession Q9UI17
Other Accession NP_037523.2
Reactivity Human
Host Rabbit
Clonality Polyclonal
Isotype Rabbit Ig
Calculated MW 96811 Da
Antigen Region 836-864 aa
Additional Information
Gene ID 29958
Other Names Dimethylglycine dehydrogenase, mitochondrial, ME2GLYDH, DMGDH
Target/Specificity This DMGDH antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 836-864 amino acids from the C-terminal region of human DMGDH.
Dilution WB~~1:1000
Format Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.
StorageMaintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
PrecautionsDMGDH Antibody (C-term) is for research use only and not for use in diagnostic or therapeutic procedures.
Protein Information
Cellular Location Mitochondrion.
Research Areas
Citations (0)

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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.


Mostowska, A., et al. Eur. J. Oral Sci. 118(4):325-332(2010)
Bailey, S.D., et al. Diabetes Care (2010) In press :
Jugessur, A., et al. PLoS ONE 5 (7), E11493 (2010) :
Talmud, P.J., et al. Am. J. Hum. Genet. 85(5):628-642(2009)
Boyles, A.L., et al. Genet. Epidemiol. 33(3):247-255(2009)

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$ 295.00
$ 99.00
Cat# AP18005B
(40 western blots)
Availability: In Stock
Bulk Size
Seasonal Special on Bulk Order
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