ZMYM3 Antikörper (full length)

Produktnummer ABIN7879346

Dieser Maus Monoklonal Antikörper detektiert spezifisch ZMYM3 in WB, IF, IHC (p) und FACS. Es zeigt Reaktivität gegenüber Proben von Human.

Kurzübersicht für ZMYM3 Antikörper (full length) (ABIN7879346)

Target: ZMYM3 (Zinc Finger Protein 261 (ZMYM3))

Reaktivität: Human

Wirt: Maus

Klonalität: Monoklonal

Konjugat: Dieser ZMYM3 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS)

Klon: PCRP-ZMYM3-2F10

Produktdetails anti-ZMYM3 Antikörper

Bindungsspezifität: full length

Verwendungszweck: ZMYM3 Antibody

Aufreinigung: Protein A/G affinity

Immunogen: Recombinant full-length human ZMYM3 protein was used as the immunogen for the ZMYM3 antibody.

Isotyp: IgG2a

Anwendungsinformationen

Applikationshinweise: Optimal dilution of the ZMYM3 antibody should be determined by the researcher.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.2 mg/mL

Buffer: 0.2 mg/mL in 1X PBS with 0.1 mg/mL BSA (US sourced), 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: -20 °C

Informationen zur Lagerung: Aliquot the ZMYM3 antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.

Details zu ZMYM3

Target: ZMYM3 (Zinc Finger Protein 261 (ZMYM3))

Andere Bezeichnung: ZMYM3

Hintergrund: Zinc-finger proteins contain DNA-binding domains and have a wide variety of functions, most of which encompass some form of transcriptional activation or repression. ZMYM3 (zinc finger MYM-type protein 3), also known as ZNF261 (zinc finger protein 261), XFIM, DXS6673E or MYM, is a 1,370 amino acid nuclear protein that contains nine MYM-type zinc fingers. Expressed in a variety of tissues, including heart, muscle and brain, ZMYM3 is thought to function as part of a histone deacetylase-containing complex that contains other proteins, such as HDAC1 and HDAC2, and may play a role in gene silencing through the modification of chromatin structure. Defects in the gene encoding ZMYM3 that lead to chromosomal translocations may be a cause of X-linked mental retardation. Two isoforms of ZMYM3 exist due to alternative splicing events.

UniProt: Q14202