EHMT1 Antikörper
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- Target Alle EHMT1 Antikörper anzeigen
- EHMT1 (Euchromatic Histone-Lysine N-Methyltransferase 1 (EHMT1))
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Reaktivität
- Human, Maus, Ratte
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser EHMT1 Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB)
- Aufreinigung
- Affinity purification
- Immunogen
- Recombinant protein of human EHMT1
- Isotyp
- IgG
- Top Product
- Discover our top product EHMT1 Primärantikörper
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- Applikationshinweise
- WB 1:500 - 1:2000
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Konzentration
- 1 mg/mL
- Buffer
- Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3.
- 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
- Informationen zur Lagerung
- Store at -20°C. Avoid freeze / thaw cycles.
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- Target
- EHMT1 (Euchromatic Histone-Lysine N-Methyltransferase 1 (EHMT1))
- Andere Bezeichnung
- EHMT1 (EHMT1 Produkte)
- Hintergrund
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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.
- Molekulargewicht
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Observed_MW: 141kDa
Calculated_MW: 7kDa/86kDa/128kDa/141kDa
- Gen-ID
- 79813
- UniProt
- Q9H9B1
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