ZNF276 anticorps (full length)

N° du produit ABIN7879347

L’anticorps anti-ZNF276 Monoclonal Souris est utilisé pour la détection de ZNF276 dans des échantillons de Humain. Il a été validé pour ELISA, IF et FACS.

Aperçu rapide pour ZNF276 anticorps (full length) (ABIN7879347)

Antigène: ZNF276 (Zinc Finger Protein 276 (ZNF276))

Reactivité: Humain

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp ZNF276 est non-conjugé

Application: ELISA, Immunofluorescence (IF), Flow Cytometry (FACS)

Classe de qualité: Carrier-free

Clone: PCRP-ZNF276-1A5

Détail du produit anti-ZNF276 anticorps

Épitope: full length

Fonction: ZNF276 Antibody (azide and preservative free)

Purification: Protein A/G affinity

Immunogène: Recombinant full-length human ZNF276 protein was used as the immunogen for the ZNF276 antibody.

Isotype: IgG2b

Information d'application

Indications d'application: Optimal dilution of the ZNF276 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 ZNF276 antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.

Détails sur ZNF276

Antigène: ZNF276 (Zinc Finger Protein 276 (ZNF276))

Autre désignation: ZNF276

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. ZNF276 is a 614 amino acid protein containing five C2H2- type zinc fingers and one zinc finger associated (ZAD) domain. Due to a loss of heterozygosity at the chromosomal location of the gene encoding ZNF276 in sporadic breast cancers, the ZNF276 gene has been targeted as a possible breast cancer tumor suppressor. The FANCA gene, which encodes a DNA repair protein, is situated at the same chromosomal location as the ZNF276 gene, suggesting a possible involvement of ZNF276 in the progression of Fanconi anemia, an autosomal recessive disorder which is caused by mutations in the gene encoding FANCA. There are two isoforms of ZNF276 that exist as a result of an alternative splicing event.

UniProt: Q8N554