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CEP290 Produkte

(Centrosomal Protein 290kDa (CEP290))

Kategorien

This gene encodes a protein with 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 A. The protein is localized to the centrosome and cilia and has sites for N-glycosylation, tyrosine sulfation, phosphorylation, N-myristoylation, and amidation. Mutations in this gene have been associated with Joubert syndrome and nephronophthisis and the presence of antibodies against this protein is associated with several forms of cancer. [provided by RefSeq, Jul 2008].

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Ausgewählte CEP290 Kategorien

CEP290 Antikörper

High quality antibodies with extensive validation data.

CEP290 ELISA Kits

Reliable ELISA kits for a wide range of species.

Empfohlene CEP290 Antikörper

Produkt
Reaktivität
Applikation
Validierungen
Kat. Nr.
Menge
Datenblatt
Reaktivität Human
Applikation ELISA, IHC, IF
Validierungen
  • (3)
Kat. Nr. ABIN334371
Menge 100 μg
Datenblatt Datenblatt
Reaktivität Human
Applikation ELISA, IHC, ICC
Validierungen
  • (3)
Kat. Nr. ABIN570714
Menge 100 μg
Datenblatt Datenblatt
Reaktivität Human, Mouse
Applikation ELISA, WB, IF, ICC
Validierungen
  • (2)
Kat. Nr. ABIN6257056
Menge 100 μL
Datenblatt Datenblatt

Empfohlene CEP290 ELISA Kits

Produkt
Reaktivität
Analytical Method
Validierungen
Kat. Nr.
Menge
Datenblatt
Reaktivität Human
Analytical Method
Validierungen
  • (1)
Kat. Nr. ABIN1742835
Menge 96 tests
Datenblatt Datenblatt
Reaktivität Sheep
Analytical Method
Validierungen
Kat. Nr. ABIN1773739
Menge 96 tests
Datenblatt Datenblatt
Reaktivität Mouse
Analytical Method Quantitative Competition ELISA
Validierungen
Kat. Nr. ABIN1745275
Menge 96 tests
Datenblatt Datenblatt

Empfohlene CEP290 Proteine

Produkt
Reaktivität
Source
Validierungen
Kat. Nr.
Menge
Datenblatt
Reaktivität Human
Source Wheat germ
Validierungen
  • (1)
Kat. Nr. ABIN1349148
Menge 10 μg
Datenblatt Datenblatt

Neueste Publikationen zu unseren CEP290 Produkten

Barny, Perrault, Michel, Soussan, Goudin, Rio, Thomas, Attié-Bitach, Hamel, Dollfus, Kaplan, Rozet, Gerard: "Basal exon skipping and nonsense-associated altered splicing allows bypassing complete CEP290 loss-of-function in individuals with unusually mild retinal disease." in: Human molecular genetics, (2018) (PubMed).

Dulla, Aguila, Lane, Jovanovic, Parfitt, Schulkens, Chan, Schmidt, Beumer, Vorthoren, Collin, Garanto, Duijkers, Brugulat-Panes, Semo, Vugler, Biasutto, Adamson, Cheetham: "Splice-Modulating Oligonucleotide QR-110 Restores CEP290 mRNA and Function in Human c.2991+1655A>G LCA10 Models." in: Molecular therapy. Nucleic acids, Vol. 12, pp. 730-740, (2018) (PubMed).

Bangs, Schrode, Hadjantonakis, Anderson: "Lineage specificity of primary cilia in the mouse embryo." in: Nature cell biology, Vol. 17, Issue 2, pp. 113-22, (2015) (PubMed).

Alby, Piquand, Huber, Megarbané, Ichkou, Legendre, Pelluard, Encha-Ravazi, Abi-Tayeh, Bessières, El Chehadeh-Djebbar, Laurent, Faivre, Sztriha, Zombor, Szabó, Failler, Garfa-Traore, Bole, Nitschké et al.: "Mutations in KIAA0586 Cause Lethal Ciliopathies Ranging from a Hydrolethalus Phenotype to Short-Rib Polydactyly Syndrome. ..." in: American journal of human genetics, Vol. 97, Issue 2, pp. 311-8, (2015) (PubMed).

Slaats, Saldivar, Bacal, Zeman, Kile, Hynes, Srivastava, Nazmutdinova, den Ouden, Zagers, Foletto, Verhaar, Miles, Sayer, Cimprich, Giles: "DNA replication stress underlies renal phenotypes in CEP290-associated Joubert syndrome." in: The Journal of clinical investigation, Vol. 125, Issue 9, pp. 3657-66, (2015) (PubMed).

Garanto, van Beersum, Peters, Roepman, Cremers, Collin: "Unexpected CEP290 mRNA splicing in a humanized knock-in mouse model for Leber congenital amaurosis." in: PLoS ONE, Vol. 8, Issue 11, pp. e79369, (2013) (PubMed).

Hopp, Heyer, Hommerding, Henke, Sundsbak, Patel, Patel, Consugar, Czarnecki, Gliem, Torres, Rossetti, Harris: "B9D1 is revealed as a novel Meckel syndrome (MKS) gene by targeted exon-enriched next-generation sequencing and deletion analysis." in: Human molecular genetics, Vol. 20, Issue 13, pp. 2524-34, (2011) (PubMed).

Allocca, Doria, Petrillo, Colella, Garcia-Hoyos, Gibbs, Kim, Maguire, Rex, Di Vicino, Cutillo, Sparrow, Williams, Bennett, Auricchio: "Serotype-dependent packaging of large genes in adeno-associated viral vectors results in effective gene delivery in mice." in: The Journal of clinical investigation, Vol. 118, Issue 5, pp. 1955-64, (2008) (PubMed).

McEwen, Koenekoop, Khanna, Jenkins, Lopez, Swaroop, Martens: "Hypomorphic CEP290/NPHP6 mutations result in anosmia caused by the selective loss of G proteins in cilia of olfactory sensory neurons." in: Proceedings of the National Academy of Sciences of the United States of America, Vol. 104, Issue 40, pp. 15917-22, (2007) (PubMed).

Kurtenbach, Gießl, Strömberg, Kremers, Atorf, Rasche, Neuhaus, Hervé, Brandstätter, Asan, Hatt, Kilimann: "The BEACH Protein LRBA Promotes the Localization of the Heterotrimeric G-protein Golfto Olfactory Cilia." in: Scientific reports, Vol. 7, Issue 1, pp. 8409 (PubMed).

Synonyme und alternative Namen zu CEP290

centrosomal protein 290 (CEP290), centrosomal protein 290 L homeolog (cep290.L), centrosomal protein 290kDa (CEP290), centrosomal protein 290 (cep290), centrosomal protein 290 (Cep290), 3h11ag, 3H11Ag, b2b1454Clo, b2b1752Clo, bbs14, BBS14, BC004690, ct87, CT87, im:7145703, im:7147820, jbts5, JBTS5, jbts6, lca10, LCA10, MGC81471, mks4, MKS4, nphp6, Nphp6, NPHP6, POC3, rd16, RGD1311640, sh11ag, slsn6, SLSN6

Bezeichner auf Proteinebene für CEP290

  • centrosomal protein 290kDa
  • nephrocystin-6
  • centrosomal protein of 290 kDa
  • centrosomal protein of 290 kDa-like
  • Bardet-Biedl syndrome 14 protein homolog
  • Bardet-Biedl syndrome 14 protein
  • CTCL tumor antigen se2-2
  • Meckel syndrome, type 4
  • POC3 centriolar protein homolog
  • cancer/testis antigen 87
  • monoclonal antibody 3H11 antigen
  • nephrocytsin-6
  • prostate cancer antigen T21
  • tumor antigen se2-2
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