BCL7B anticorps (Alexa Fluor 647)

N° du produit ABIN1401912

Détail du produit anti-BCL7B anticorps (Alexa Fluor 647)

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

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp BCL7B est conjugé à/à la Alexa Fluor 647

Application: Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Réactivité croisée: Humain, Souris, Rat

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human BCL7B

Isotype: IgG

Information d'application

Indications d'application: IF(IHC-P) 1:50-200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur BCL7B

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

Autre désignation: BCL7B (BCL7B Produits)

Synonymes: anticorps bcl7b, anticorps zgc:103501, anticorps wu:fb94h01, anticorps zgc:85678, anticorps B-cell CLL/lymphoma 7B, b, anticorps B-cell CLL/lymphoma 7B, a, anticorps B-cell CLL/lymphoma 7B, anticorps B-cell CLL/lymphoma 7b, anticorps B cell CLL/lymphoma 7B, anticorps BCL tumor suppressor 7B, anticorps bcl7bb, anticorps bcl7ba, anticorps bcl7b, anticorps Bcl7b, anticorps BCL7B

Sujet:

Synonyms: B cell CLL/lymphoma 7 protein family member B, B cell CLL/lymphoma 7B, BCL 7B, BCL7B_HUMAN.

Background: BCL7B shows high homology to the BCL7A protein, which is known to be directly involved in a complex chromosomal translocation in Burkitt lymphoma cell lines. The specific function of BCL7B has not yet been determined. However, it may play a role in lung tumor development or progression. The BCL7B gene is located at a chromosomal region commonly deleted in the congenital disorder, Williams syndrome.

ID gène: 9275