CSPP1 antibody

Catalog No. ABIN7228078

The Rabbit Polyclonal anti-CSPP1 antibody (ABIN7228078) specifically detects CSPP1 in WB and ELISA. The antibody is reactive with Human and Mouse samples.

Quick Overview for CSPP1 antibody (ABIN7228078)

Target: CSPP1 (Cspp1) (Centrosome and Spindle Pole Associated Protein 1 (Cspp1))

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CSPP1 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-CSPP1 Antibody

Purpose: Rabbit Anti-CSPP1 Polyclonal Antibody

Specificity: The antibody detects endogenous levels of CSPP1 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 CSPP1 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 CSPP1

Target: CSPP1 (Cspp1) (Centrosome and Spindle Pole Associated Protein 1 (Cspp1))

Alternative Name: CSPP1

Background: Centrosome and spindle pole-associated protein 1CSPP1 (Centrosome And Spindle Pole Associated Protein 1) is a Protein Coding gene. Diseases associated with CSPP1 include Joubert Syndrome 21 and Joubert Syndrome With Jeune Asphyxiating Thoracic Dystrophy. CSPP1 encodes a centrosome and spindle pole associated protein. The encoded protein plays a role in cell-cycle progression and spindle organization, regulates cytokinesis, interacts with Nephrocystin 8 and is required for cilia formation. Mutations in CSPP1 result in primary cilia abnormalities and classical Joubert syndrome. Alternatively spliced transcript variants encoding distinct isoforms have been found for CSPP1.

Molecular Weight: 138kD

Gene ID: 79848

UniProt: Q1MSJ5