DNMT3B Antikörper (AA 1-150)

Produktnummer ABIN5542518

Produktdetails anti-DNMT3B Antikörper

Target: DNMT3B (DNA (Cytosine-5-)-Methyltransferase 3 beta (DNMT3B))

Bindungsspezifität: AA 1-150

Reaktivität: Human

Wirt: Maus

Klonalität: Monoklonal

Konjugat: Dieser DNMT3B Antikörper ist unkonjugiert

Applikation: Immunohistochemistry (IHC), ELISA, Flow Cytometry (FACS)

Verwendungszweck: DNMT3B Antibody

Aufreinigung: Purified antibody

Immunogen: Purified recombinant fragment of human DNMT3B (AA: 1-150) expressed in E. Coli.

Klon: 7E5E9C1

Isotyp: IgG1

Anwendungsinformationen

Applikationshinweise:

ELISA: 1/10000

FCM: 1/200 - 1/400

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: Purified antibody in PBS with 0.05 % 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: Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.

Details zu DNMT3B

Target: DNMT3B (DNA (Cytosine-5-)-Methyltransferase 3 beta (DNMT3B))

Andere Bezeichnung: DNMT3B (DNMT3B Produkte)

Synonyme: DNMT3B antikoerper, LOC100218113 antikoerper, ICF antikoerper, ICF1 antikoerper, M.HsaIIIB antikoerper, MmuIIIB antikoerper, cb91 antikoerper, dnmt3bl antikoerper, dnmt7 antikoerper, sb:cb91 antikoerper, wu:fb16h07 antikoerper, DNA methyltransferase 3 beta antikoerper, DNA methyltransferase 3B antikoerper, DNA (cytosine-5-)-methyltransferase 3 beta, duplicate a antikoerper, DNMT3B antikoerper, Dnmt3b antikoerper, dnmt3b antikoerper, dnmt3ba antikoerper

Hintergrund:

Description: CpG methylation is an epigenetic modification that is important for embryonic development, imprinting, and X-chromosome inactivation. Studies in mice have demonstrated that DNA methylation is required for mammalian development. This gene encodes a DNA methyltransferase which is thought to function in de novo methylation, rather than maintenance methylation. The protein localizes primarily to the nucleus and its expression is developmentally regulated. Mutations in this gene cause the immunodeficiency-centromeric instability-facial anomalies (ICF) syndrome. Eight alternatively spliced transcript variants have been described. The full length sequences of variants 4 and 5 have not been determined.

Aliases: ICF, ICF1, M.HsaIIIB

Molekulargewicht: 95.8kDa

Gen-ID: 1789

HGNC: 1789

UniProt: Q9UBC3