BCL7B anticorps (C-Term)

N° du produit ABIN1536707

L’anticorps anti-BCL7B Polyclonal Lapin est utilisé pour la détection de BCL7B dans des échantillons de Humain et Souris. Il a été validé pour WB et IHC (p).

Aperçu rapide pour BCL7B anticorps (C-Term) (ABIN1536707)

Antigène: BCL7B (B-Cell CLL/lymphoma 7B (BCL7B))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp BCL7B est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone: RB36546

Détail du produit anti-BCL7B anticorps

Épitope: AA 137-164, C-Term

Homologie: B

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogène: This BCL7B antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 137-164 amino acids from the C-terminal region of human BCL7B.

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:1000. WB: 1:1000. IHC-P: 1:10~50

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

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: 4 °C,-20 °C

Stockage commentaire: BCL7B Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

Date de péremption: 6 months

Détails sur BCL7B

Antigène: BCL7B (B-Cell CLL/lymphoma 7B (BCL7B))

Autre désignation: BCL7B

Sujet: This gene encodes a member of the BCL7 family including BCL7A, BCL7B and BCL7C proteins. This member is BCL7B, which contains a region that is highly similar to the N-terminal segment of BCL7A or BCL7C proteins. The BCL7A protein is encoded by the gene known to be directly involved in a three-way gene translocation in a Burkitt lymphoma cell line. This gene is located at a chromosomal region commonly deleted in Williams syndrome. This gene is highly conserved from C. elegans to human. Multiple alternatively spliced transcript variants have been found for this gene.

Poids moléculaire: 22195

ID gène: 9275

NCBI Accession: NP_001184173, NP_001698

UniProt: Q9BQE9