CSPP1 anticorps

N° du produit ABIN7228078

Cet anticorps anti-CSPP1 Polyclonal Lapin (ABIN7228078) détecte spécifiquement CSPP1 dans WB et ELISA. L’anticorps est réactif avec des échantillons de Humain et Souris.

Aperçu rapide pour CSPP1 anticorps (ABIN7228078)

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

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CSPP1 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-CSPP1 anticorps

Fonction: Rabbit Anti-CSPP1 Polyclonal Antibody

Specificité: The antibody detects endogenous levels of CSPP1 protein

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

Immunogène: Synthesized peptide derived from part region of human CSPP1 protein

Isotype: IgG

Information d'application

Indications d'application: 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

Stockage

Format: Liquid

Concentration: 1 mg/mL

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

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: 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.

Date de péremption: 12 months

Détails sur CSPP1

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

Autre désignation: CSPP1

Sujet: 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.

Poids moléculaire: 138kD

ID gène: 79848

UniProt: Q1MSJ5