BAZ1B anticorps

N° du produit ABIN6572045

Détail du produit anti-BAZ1B anticorps

Antigène: BAZ1B (Bromodomain Adjacent To Zinc Finger Domain, 1B (BAZ1B))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp BAZ1B est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC)

Purification: Affinity purification

Immunogène: Recombinant protein of human BAZ1B

Isotype: IgG

Information d'application

Indications d'application: WB 1:500 - 1:2000 IHC 1:50 - 1:200

Restrictions: For Research Use only

Stockage

Concentration: 1 mg/mL

Buffer: Buffer: PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur BAZ1B

Antigène: BAZ1B (Bromodomain Adjacent To Zinc Finger Domain, 1B (BAZ1B))

Autre désignation: BAZ1B (BAZ1B Produits)

Synonymes: anticorps BAZ1B, anticorps wstf, anticorps wbscr9, anticorps wbscr10, anticorps LOC100220420, anticorps WBSCR10, anticorps WBSCR9, anticorps WSTF, anticorps C87820, anticorps Wbscr9, anticorps fi60d02, anticorps im:7137554, anticorps wu:fi60d02, anticorps bromodomain adjacent to zinc finger domain 1B, anticorps bromodomain adjacent to zinc finger domain, 1B, anticorps bromodomain adjacent to zinc finger domain 1B S homeolog, anticorps BAZ1B, anticorps baz1b, anticorps Baz1b, anticorps baz1b.S

Sujet:

Synonyms: Bromodomain Adjacent To Zinc Finger Domain 1B,Williams-Beuren Syndrome Chromosomal Region 10 Protein,Williams-Beuren Syndrome Chromosomal Region 9 Protein,Williams Syndrome Transcription Factor,Transcription Factor WSTF,EC 2.7.10.2,WBSCR10,WBSCR9.

Background: This gene encodes a member of the bromodomain protein family. The bromodomain is a structural motif characteristic of proteins involved in chromatin-dependent regulation of transcription. This gene is deleted in Williams-Beuren syndrome, a developmental disorder caused by deletion of multiple genes at 7q11.23.

Poids moléculaire:

Observed_MW: 190kDa

Calculated_MW: 170kDa

ID gène: 9031

UniProt: Q9UIG0

Pathways: Nuclear Hormone Receptor Binding, Chromatin Binding