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Rabbit Anti-CSPP1 Antibody (CSB-PA635936DSR1HU)
Supplier: CUSABIO BIOTECH CO.
Centrosome and spindle pole-associated protein 1 Antibody,CSPP1 Antibody,CSPP AntibodyMore alternative names for the antibody
Centrosome and spindle pole associated protein 1 antibody|CSPP 1 antibody|CSPP antibody|FLJ22490 antibody|FLJ38886 antibody
Anti-CSPP1 antibody (ab102755)
Anti-CSPP1 antibody (ab102755)
Recommended applications: ELISA, IHC
Recommended dilution: Recommended dilution:IHC:1:20-1:200
Recommended protocols: check protocols
|Catalogue No.|| |
Recombinant human Centrosome and spindle pole-associated protein 1 protein (997-1256AA)
|Recommended dilution|| |
|Molecular weight|| |
Antigen Affinity Purified
Shipped at 4 Celcius Degree. Upon delivery aliquot and store at -20 Celcius Degree or -80 Celcius Degree. Avoid repeated freeze.
|Database links|| |
<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=gene&cmd=Retrieve&dopt=Graphics&list_uids=79848" target="_blank">Entrez Gene:79848( Human)</a>, <a href="http://www.ncbi.nlm.nih.gov/omim/611654" target="_blank">Omim:611654( Human)</a>, <a href="http://www.uniprot.org/uniprot/Q1MSJ5" target="_blank">SwissProt:Q1MSJ5( Human)</a>, <a href="http://www.ncbi.nlm.nih.gov/UniGene/clust.cgi?ORG=Hs&CID=370147" target="_blank">Unigene:370147( Human)</a>
|Protein function|| |
May play a role in cell-cycle-dependent microtubule organization. .
|Protein tissue specificity|| |
Expressed in adult and fetal brain with enrichment in the cerebellum. Detected in testis. .
|Involvement in disease|| |
Joubert syndrome 21 (JBTS21) [MIM:615636]: A disorder presenting with cerebellar ataxia, oculomotor apraxia, hypotonia, neonatal breathing abnormalities and psychomotor delay. Neuroradiologically, it is characterized by cerebellar vermian hypoplasia/aplasia, thickened and reoriented superior cerebellar peduncles, and an abnormally large interpeduncular fossa, giving the appearance of a molar tooth on transaxial slices (molar tooth sign). Additional variable features include retinal dystrophy, renal disease, liver fibrosis, and polydactyly. . Note=The disease is caused by mutations affecting the gene represented in this entry.
|Protein post-translational modifications|| |
Phosphorylated. Phosphorylation increases in colcemide-treated cells. .
|Protein cellular localization|| |
Cytoplasm, cytoskeleton, microtubule organizing center, centrosome. Cytoplasm, cytoskeleton, spindle. Cytoplasm, cytoskeleton, spindle pole . Note=Associated with mitotic spindles.
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CUSABIO BIOTECH CO.
|Product type|| |
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