DMGDH Antikörper (C-Term)

Produktnummer ABIN1537626

Produktdetails anti-DMGDH Antikörper

Target: DMGDH (Dimethylglycine Dehydrogenase (DMGDH))

Bindungsspezifität: AA 836-864, C-Term

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser DMGDH Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Aufreinigung: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: 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.

Klon: RB23867

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: WB: 1:1000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

Konservierungsmittel: Sodium azide

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

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: DMGDH Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

Haltbarkeit: 6 months

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: 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.

Molekulargewicht: 96811

Gen-ID: 29958

NCBI Accession: NP_037523

UniProt: Q9UI17