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Key Documents

ABN1710

Sigma-Aldrich

Anti-CEP290

from rabbit

Synonyme(s) :

Cep290, Bardet-Biedl syndrome 14 protein homolog, Nephrocystin-6

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About This Item

Code UNSPSC :
12352203
eCl@ss :
32160702
Nomenclature NACRES :
NA.41

Source biologique

rabbit

Niveau de qualité

Forme d'anticorps

affinity isolated antibody

Type de produit anticorps

primary antibodies

Clone

polyclonal

Espèces réactives

rat, human, mouse

Technique(s)

immunocytochemistry: suitable
immunofluorescence: suitable
immunohistochemistry: suitable
immunoprecipitation (IP): suitable
western blot: suitable

Numéro d'accès NCBI

Numéro d'accès UniProt

Conditions d'expédition

ambient

Modification post-traductionnelle de la cible

unmodified

Informations sur le gène

mouse ... Cep290(216274)

Description générale

Centrosomal protein of 290 kDa (UniProt: Q6A078; also known as Cep290; Bardet-Biedl syndrome 14 protein homolog; Nephrocystin-6) is encoded by the Cep290 (also known as Kiaa0373, Nphp6) gene (Gene ID: 216274) in murine species. Cep290 is a centrosomal protein that is expressed in multiple organs during early postnatal development, with highest levels in the hindbrain region. Cep290 has 13 putative coiled-coil domains, a region with homology to SMC chromosome segregation ATPases, six KID motifs, three tropomyosin homology domains and an ATP/GTP binding site motif. Cep290 is part of the tectonic-like complex, which is required for tissue-specific ciliogenesis and may also regulate ciliary membrane composition. It is also required for the correct localization of ciliary and phototransduction proteins in retinal photoreceptor cells. Defects in Cep290 gene are known to cause Leber congenital amaurosis (LCA), an early-onset retinal degenerative disease. Mutations in Cep290 gene are also known to cause Joubert syndrome that is characterized by psychomotor delay, hypotonia, ataxia, oculomotor apraxia and neonatal breathing abnormalities.

Spécificité

This polyclonal antibody detects centrosomal protein of 290 kDa in HEK293 cells.

Immunogène

His-tagged recombinant fragment corresponding to 80 amino acids from the C-terminal half of mouse Centrosomal protein of 290 kDa.

Application

Anti-CEP290, Cat. No. ABN1710, is a highly specific rabbit polyclonal antibody that targets Centrosomal protein of 290 kDa and has been tested in and Immunocytochemistry, Immunofluorescence, Immunohistochemistry, Immunoprecipitation, and Western Blotting,
Western Blotting Analysis: A representative lot detected CEP290 in transfected HEK293 cells (Rachel, R.A., et. al. (2012). J Clin Invest. 122(4):1233-45) and COS-1 cells (Chang, B., et. al. (2006). Hum Mol Genet. 15(11):1847-57).

Immunoprecipitation Analysis: A representative lot detected CEP290 in WT and rd16 retinal extract(Chang, B., et. al. (2006). Hum Mol Genet. 15(11):1847-57).

Immunohistochemistry Analysis: A representative lot detected CEP290 in WT mouse retina (Chang, B., et. al. (2006). Hum Mol Genet. 15(11):1847-57).

Western Blotting Analysis: 1:1,000-1:2,000 dilution from a representative lot detected CEP290 in mouse retina (Courtesy of Dr. Tiansen at NIH).

Immunofluorescence Analysis: A representative lot detected CEP290 in ciliated sensory cells (Rachel, R.A., et. al. (2012). J Clin Invest. 122(4):1233-45) and WT mouse retina (Chang, B., et. al. (2006). Hum Mol Genet. 15(11):1847-57).

Immunofluorescence Analysis: 1:500-1:2,000 dilution from a representative lot detected CEP290 in frozen mouse retina (Courtesy of Dr. Tiansen at NIH).

Immunocytochemistry Analysis: A representative lot detected CEP290 in IMCD-3 cells (Chang, B., et. al. (2006). Hum Mol Genet. 15(11):1847-57).

Qualité

Evaluated by Western Blotting in HEK293 cell lysate.

Western Blotting Analysis: 1:500 dilution of this antibody detected CEP290 in 10 µg of HEK293 cell lysate.

Description de la cible

~260 kDa observed; 289.08 kDa calculated. Uncharacterized bands may be observed in some lysate(s).

Forme physique

Format: Purified

Autres remarques

Concentration: Please refer to lot specific datasheet.

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Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

WGK 2


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Consulter la Bibliothèque de documents

Poppy Datta et al.
The Journal of biological chemistry, 294(50), 19119-19136 (2019-11-07)
Mutations in the centrosomal protein 290 (CEP290) gene cause various ciliopathies involving retinal degeneration. CEP290 proteins localize to the ciliary transition zone and are thought to act as a gatekeeper that controls ciliary protein trafficking. However, precise roles of CEP290

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