Anti-CSPP1 Antibody

$99.00$319.00

Reactivity: Human
Applications: ELISA,IHC
Conjugation: Various
Supplier: CUSABIO BIOTECH CO.

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Rabbit Anti-CSPP1 Antibody (CSB-PA635936DSR1HU)

Supplier: CUSABIO BIOTECH CO.

Alternative names:

Centrosome and spindle pole-associated protein 1 Antibody,CSPP1 Antibody,CSPP Antibody

More 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)
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Recommended applications: ELISA, IHC

Recommended dilution: Recommended dilution:IHC:1:20-1:200

Recommended protocols: check protocols

Name

Anti-CSPP1 Antibody

Catalogue No.

CSB-PA635936DSR1HU

Reactivity

Human

Immunogen

Recombinant human Centrosome and spindle pole-associated protein 1 protein (997-1256AA)

Host

Rabbit

Applications

ELISA, IHC

Recommended dilution

Recommended dilution:IHC:1:20-1:200

Clonality

Polyclonal

Conjugation

unconjugated

Isotype

IgG

Molecular weight

145 kDa

Purification

Antigen Affinity Purified

Storage

Shipped at 4 Celcius Degree. Upon delivery aliquot and store at -20 Celcius Degree or -80 Celcius Degree. Avoid repeated freeze.

Database links

Entrez Gene:79848( Human), Omim:611654( Human), SwissProt:Q1MSJ5( Human), Unigene:370147( Human)

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.

Note

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Supplier

CUSABIO BIOTECH CO.

Product type

Primary antibody

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