ZMYM3 anticorps (full length)

N° du produit ABIN7879345

Cet anticorps anti-ZMYM3 Monoclonal Souris (Clone PCRP-ZMYM3-2F10) (ABIN7879345) détecte spécifiquement ZMYM3 dans WB, IF, IHC (p) et FACS. L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour ZMYM3 anticorps (full length) (ABIN7879345)

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

Reactivité: Humain

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp ZMYM3 est non-conjugé

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

Classe de qualité: Carrier-free

Clone: PCRP-ZMYM3-2F10

Détail du produit anti-ZMYM3 anticorps

Épitope: full length

Fonction: ZMYM3 Antibody (azide and preservative free)

Purification: Protein A/G affinity

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

Isotype: IgG2a

Information d'application

Indications d'application: Optimal dilution of the ZMYM3 antibody should be determined by the researcher.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: 1 mg/mL in 1X PBS, BSA free, sodium azide free

Agent conservateur: Azide free

Stock: -20 °C

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

Détails sur ZMYM3

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

Autre désignation: ZMYM3

Sujet: 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