CNTNAP3 antibody (AA 31-130)

Catalog No. ABIN1385153

The Rabbit Polyclonal anti-CNTNAP3 antibody is suitable to detect CNTNAP3 in samples from Human. It has been validated for WB, IF (cc), IF (p), IHC (fro) and IHC (p).

Quick Overview for CNTNAP3 antibody (AA 31-130) (ABIN1385153)

Target: CNTNAP3 (Contactin Associated Protein-Like 3 (CNTNAP3))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CNTNAP3 antibody is un-conjugated

Application: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Product Details anti-CNTNAP3 Antibody

Binding Specificity: AA 31-130

Purpose: CNTNAP3 Polyclonal Antibody

Cross-Reactivity: Rat

Predicted Reactivity: Human,Mouse,Dog,Cow,Sheep,Pig,Horse,Chicken,Rabbit

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human CNTNAP3

Isotype: IgG

Application Details

Application Notes: WB(1:300-5000),

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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: 4 °C,-20 °C

Storage Comment: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Expiry Date: 12 months

Target Details for CNTNAP3

Target: CNTNAP3 (Contactin Associated Protein-Like 3 (CNTNAP3))

Alternative Name: CNTNAP3

Background:

Synonyms: CASPR3, Cell recognition molecule Caspr3, CNTNAP3A, Contactin associated protein like 3, contactin associated protein-like 3B, FLJ14195, KIAA1714, CNTP3_HUMAN.

Background: CNTNAP3B is a 1,288 amino acid protein that is encoded by a gene which maps to human chromosome 9. Chromosome 9 contains 145 million base pairs and comprises 4 % of the human genome, encoding nearly 900 genes. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, and Familial dysautonomia, are both associated with chromosome 9. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in translocations that lead to the aberrant production of a BCR-ABL fusion protein often found in leukemias.