BCL7B antibody (AbBy Fluor® 647)

Catalog No. ABIN1401912

Product Details anti-BCL7B Antibody (AbBy Fluor® 647)

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

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This BCL7B antibody is conjugated to AbBy Fluor® 647

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

Cross-Reactivity: Human, Mouse, Rat

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human BCL7B

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 1:50-200

Restrictions: For Research Use only

Handling

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.

Preservative: ProClin

Precaution of Use: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Expiry Date: 12 months

Target Details for BCL7B

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

Alternative Name: BCL7B (BCL7B Products)

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

Background:

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.

Gene ID: 9275