BAZ1B anticorps

N° du produit ABIN6989742

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), Immunofluorescence (Cultured Cells) (IF (cc)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (IF)

Réactivité croisée: Humain, Souris, Rat

Purification: Purified by Protein A.

Immunogène: Recombinant fusion protein containing a sequence corresponding to amino acids 1-260 of human BAZ1B (NP_115784.1).

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
IHC-P 1:200-400
IF(ICC) 1:50-200
IHC()
IF()

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

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

Stock: -20 °C

Stockage commentaire: Store at -20°C for 12 months.

Date de péremption: 12 months

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: BAZ1B,WBSCR10,WBSCR9,WSTF

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.

ID gène: 9031

UniProt: Q9UIG0

Pathways: Nuclear Hormone Receptor Binding, Chromatin Binding