CAMSAP1 antibody (AA 1401-1500) (Cy3)

Catalog No. ABIN1702440

This anti-CAMSAP1 antibody is a Rabbit Polyclonal antibody detecting CAMSAP1 in WB, IF (cc) and IF (p). Suitable for Human.

Quick Overview for CAMSAP1 antibody (AA 1401-1500) (Cy3) (ABIN1702440)

Target: CAMSAP1 (Calmodulin Regulated Spectrin Associated Protein 1 (CAMSAP1))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CAMSAP1 antibody is conjugated to Cy3

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

Product Details anti-CAMSAP1 Antibody (Cy3)

Binding Specificity: AA 1401-1500

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

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human CAMSAP1

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 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 CAMSAP1

Target: CAMSAP1 (Calmodulin Regulated Spectrin Associated Protein 1 (CAMSAP1))

Alternative Name: CAMSAP1

Background:

Synonyms: calmodulin regulated spectrin-associated protein 1, Calmodulin-regulated spectrin-associated protein 1, CAMP1_HUMAN, camsap1, PRO2405.

Background: CAMSAP1L1 is a 1,489 amino acid protein that contains one calponin-homology domain and one CKK domain, which serves to bind microtubules. There are three isoforms of CAMSAP1L1 that are produced as a result of alternative splicing events. The gene encoding CAMSAP1L1 maps to human chromosome 1, the largest human chromosome spanning about 260 million base pairs and making up 8 % of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1.

Gene ID: 157922