DMGDH Antikörper (C-Term)

Produktnummer ABIN7180160

Produktdetails anti-DMGDH Antikörper

Target: DMGDH (Dimethylglycine Dehydrogenase (DMGDH))

Bindungsspezifität: C-Term

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser DMGDH Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA

Kreuzreaktivität: Human

Aufreinigung: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogen: Synthesized peptide derived from C-terminal of Human DMGDH.

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB:1:500-1:3000,

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: Rabbit IgG in phosphate buffered saline (without Mg2+ and Ca2+), pH 7.4, 150 mM NaCl, 0.02 % sodium azide and 50 % glycerol.

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Lagerung: -20 °C,-80 °C

Informationen zur Lagerung: Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.

Details zu DMGDH

Target: DMGDH (Dimethylglycine Dehydrogenase (DMGDH))

Andere Bezeichnung: DMGDH (DMGDH Produkte)

Synonyme: MGC132281 antikoerper, DMGDHD antikoerper, ME2GLYDH antikoerper, Me2GlyDH antikoerper, 1200014D15Rik antikoerper, AI787269 antikoerper, dimethylglycine dehydrogenase antikoerper, dimethylglycine dehydrogenase L homeolog antikoerper, D-amino-acid oxidase antikoerper, Dimethylglycine dehydrogenase antikoerper, glycine cleavage system protein T antikoerper, dimethylglycine dehydrogenase precursor antikoerper, DMGDH antikoerper, dmgdh.L antikoerper, dmgdh antikoerper, SAR11_1253 antikoerper, EAMY_RS27375 antikoerper, EAMY_RS33570 antikoerper, VDBG_06516 antikoerper, Sinme_2570 antikoerper, HALXA_RS03495 antikoerper, Dmgdh antikoerper

Hintergrund:

Background: 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.

Binzak B.A., Mol. Genet. Metab. 69:181-187(2000).
Binzak B.A., Am. J. Hum. Genet. 68:839-847(2001).
Moolenaar S.H., Clin. Chem. 45:459-464(1999)

Aliases: Dimethylglycine dehydrogenase antibody, Dimethylglycine dehydrogenase, mitochondrial antibody, Dmgdh antibody, M2GD_HUMAN antibody, ME2GLYDH antibody, mitochondrial antibody

UniProt: Q9UI17