BEND2 antibody (AbBy Fluor® 488)

Catalog No. ABIN1403374

Product Details anti-BEND2 Antibody (AbBy Fluor® 488)

Target: BEND2 (BEN Domain Containing 2 (BEND2))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This BEND2 antibody is conjugated to AbBy Fluor® 488

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

Cross-Reactivity: Human

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human BEND2/CXorf56

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 BEND2

Target: BEND2 (BEN Domain Containing 2 (BEND2))

Alternative Name: BEND2 (BEND2 Products)

Synonyms: CXorf20 antibody, BEN domain containing 2 antibody, BEND2 antibody

Background:

Synonyms: BEN domain-containing protein 2, BEN domain containing 2, BEND 2, BEND2, BEND-2, Chromosome X open reading frame 20, MGC33653, BEND2_HUMAN, CXorf56.

Background: BEND2 is a 799 amino acid protein that contains two BEN domains. BEND2 exists as two alternatively spliced isoforms and is considered a complete proteome. BEN domain mediates proteinDNA and proteinprotein interactions during chromatin organization and transcription. BEN domain may play a role in organization of viral DNA during replication or transcription. The BEND2 gene maps to human chromosome Xp22.13. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The X and Y chromosomes are the human sex chromosomes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.