EHMT1 Antikörper

Produktnummer ABIN7073867

Produktdetails anti-EHMT1 Antikörper

Target: EHMT1 (Euchromatic Histone-Lysine N-Methyltransferase 1 (EHMT1))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser EHMT1 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Kreuzreaktivität: Human, Ratte

Aufreinigung: Affinity purification

Immunogen: Recombinant protein corresponding to Mouse EHMT1/GLP

Anwendungsinformationen

Applikationshinweise: WB (H,M,R) 1:500-1:1000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: PBS, pH 7.4, 0.02 % 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: -20 °C

Details zu EHMT1

Target: EHMT1 (Euchromatic Histone-Lysine N-Methyltransferase 1 (EHMT1))

Andere Bezeichnung: EHMT1/GLP (EHMT1 Produkte)

Synonyme: EUHMTASE1 antikoerper, Eu-HMTase1 antikoerper, FP13812 antikoerper, GLP antikoerper, GLP1 antikoerper, KMT1D antikoerper, bA188C12.1 antikoerper, EHMT1 antikoerper, G9a antikoerper, 9230102N17Rik antikoerper, D330003E03 antikoerper, mKIAA1876 antikoerper, bZ1O1.6 antikoerper, si:rp71-1o1.6 antikoerper, zgc:136244 antikoerper, euchromatic histone lysine methyltransferase 1 antikoerper, histone-lysine N-methyltransferase EHMT2 antikoerper, euchromatic histone-lysine N-methyltransferase 1 antikoerper, euchromatic histone methyltransferase 1 antikoerper, euchromatic histone-lysine N-methyltransferase 1a antikoerper, EHMT1 antikoerper, Ehmt1 antikoerper, LOC100121084 antikoerper, ehmt1 antikoerper, ehmt1a antikoerper

Hintergrund: The protein encoded by this gene is a histone methyltransferase that is part of the E2F6 complex, which represses transcription. The encoded protein methylates the Lys-9 position of histone H3, which tags it for transcriptional repression. This protein may be involved in the silencing of MYC- and E2F-responsive genes and therefore could play a role in the G0/G1 cell cycle transition. Defects in this gene are a cause of chromosome 9q subtelomeric deletion syndrome (9q-syndrome).

Molekulargewicht: 180 kDa

Gen-ID: 77683

NCBI Accession: NP_001012536

UniProt: Q5DW34