BCL7B antibody

Catalog No. ABIN7227474

The Rabbit Polyclonal anti-BCL7B antibody is suitable to detect BCL7B in samples from Human and Mouse. It has been validated for WB and ELISA.

Quick Overview for BCL7B antibody (ABIN7227474)

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

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This BCL7B antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-BCL7B Antibody

Purpose: Rabbit Anti-BCL7B Polyclonal Antibody

Specificity: The antibody detects endogenous levels of BCL7B protein

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogen: Synthesized peptide derived from part region of human BCL7B protein

Isotype: IgG

Application Details

Application Notes: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-2000,ELISA 1:5000-20000

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, 50 % glycerol, 0.05 % Proclin 300, 0.05 %BSA

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: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Expiry Date: 12 months

Target Details for BCL7B

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

Alternative Name: BCL7B

Background: B-cell CLL/lymphoma 7 protein family member BBCL7B 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.

Molecular Weight: 22kD

Gene ID: 9275

UniProt: Q9BQE9