EHMT1 anticorps

N° du produit ABIN6571811

L’anticorps Lapin Polyclonal anti-EHMT1 a été validé pour WB. Il convient pour détecter EHMT1 dans des échantillons de Humain, Souris et Rat.

Aperçu rapide pour EHMT1 anticorps (ABIN6571811)

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

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp EHMT1 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-EHMT1 anticorps

Purification: Affinity purification

Immunogène: Recombinant protein of human EHMT1

Isotype: IgG

Information d'application

Indications d'application: WB 1:500 - 1:2000

Restrictions: For Research Use only

Stockage

Concentration: 1 mg/mL

Buffer: Buffer: PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.

Agent conservateur: Sodium azide

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

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur EHMT1

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

Autre désignation: EHMT1

Sujet:

Synonyms: bA188C12.1,DKFZp667M072,EHMT 1,EHMT1,EHMT1,Eu-HMTase1,Euchromatic histone lysine N methyltransferase 1,Euchromatic histone methyltransferase 1,Euchromatic histone-lysine N-methyltransferase 1,EUHMTASE1,FLJ12879,FP13812,G9a like protein 1,G9a like protein,G9a-like protein 1,GLP 1,GLP,GLP1,H3 K9 HMTase 5,H3-K9-HMTase 5,Histone H3 K9 methyltransferase 5,Histone H3-K9 methyltransferase 5,Histone lysine N methyltransferase H3 lysine 9 specific 5,Histone-lysine N-methyltransferase EHMT1,KIAA1876,Lysine N methyltransferase 1D,Lysine N-methyltransferase 1D,RP11 188C12.1

Background: 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, also known as Kleefstra syndrome). Alternative splicing results in multiple transcript variants.

Poids moléculaire:

Observed_MW: 141kDa

Calculated_MW: 7kDa/86kDa/128kDa/141kDa

ID gène: 79813

UniProt: Q9H9B1