CSPP1 (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.
Applications:Suitable for use in Western Blot and ELISA.
Other applications not tested.
Recommended Dilution:Western Blot: 1:500-1:2000ELISA: 1:5000-1:20,000Optimal dilutions to be determined by the researcher.
Storage and Stability:May be stored at 4°C for short-term only.
Aliquot to avoid repeated freezing and thawing.
Store at -20°C.
Aliquots are stable for 12 months after receipt.
For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.
仕様
Size：100ul
Host：rabbit
Source Antibody：human
Grade：Affinity Purified
Purity：Purified by immunoaffinity chromatography.
Form：Supplied as a liquid in PBS, pH 7.4, 0.02% sodium azide, 50% glycerol.
Specificity：Recognizes endogenous levels of human CSPP1.
Isotype：IgG
Calc Applications Abbrev：E WB
Calc Crossreactivity：Hu
Immunogen：Synthetic peptide corresponding to human CSPP1 protein.
