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USH1C Produkte

(Usher Syndrome 1C (Autosomal Recessive, Severe) (USH1C))

Kategorien

This gene encodes a scaffold protein that functions in the assembly of Usher protein complexes. The protein contains PDZ domains, a coiled-coil region with a bipartite nuclear localization signal and a PEST degradation sequence. Defects in this gene are the cause of Usher syndrome type 1C and non-syndromic sensorineural deafness autosomal recessive type 18. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009].

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Ausgewählte USH1C Kategorien

USH1C Antikörper

High quality antibodies with extensive validation data.

USH1C Proteine

Proteins for various applications incl. WB, ELISA, IF etc.

Empfohlene USH1C Antikörper

Produkt
Reaktivität
Applikation
Validierungen
Kat. Nr.
Menge
Datenblatt
Reaktivität Zebrafish (Danio rerio)
Applikation WB
Validierungen
  • (4)
Kat. Nr. ABIN1683223
Menge 100 μg
Datenblatt Datenblatt
Reaktivität Human, Mouse
Applikation WB
Validierungen
  • (4)
  • (2)
Kat. Nr. ABIN1881984
Menge 400 μL
Datenblatt Datenblatt
Reaktivität Human, Mouse, Rat
Applikation IHC
Validierungen
  • (3)
Kat. Nr. ABIN7261032
Menge 200 μL
Datenblatt Datenblatt

Empfohlene USH1C ELISA Kits

Produkt
Reaktivität
Analytical Method
Validierungen
Kat. Nr.
Menge
Datenblatt
Reaktivität Human
Analytical Method Quantitative Sandwich ELISA
Validierungen
Kat. Nr. ABIN6229188
Menge 96 tests
Datenblatt Datenblatt

Empfohlene USH1C Proteine

Produkt
Reaktivität
Source
Validierungen
Kat. Nr.
Menge
Datenblatt
Reaktivität Human
Source Escherichia coli (E. coli)
Validierungen
  • (1)
Kat. Nr. ABIN667114
Menge 100 μg
Datenblatt Datenblatt
Reaktivität Human
Source Wheat germ
Validierungen
  • (1)
Kat. Nr. ABIN1324734
Menge 10 μg
Datenblatt Datenblatt
Reaktivität Human
Source Wheat germ
Validierungen
  • (1)
Kat. Nr. ABIN1324733
Menge 25 μg
Datenblatt Datenblatt

Neueste Publikationen zu unseren USH1C Produkten

Pan, Askew, Galvin, Heman-Ackah, Asai, Indzhykulian, Jodelka, Hastings, Lentz, Vandenberghe, Holt, Géléoc: "Gene therapy restores auditory and vestibular function in a mouse model of Usher syndrome type 1c." in: Nature biotechnology, Vol. 35, Issue 3, pp. 264-272, (2017) (PubMed).

McConnell, Benesh, Mao, Tabb, Tyska: "Proteomic analysis of the enterocyte brush border." in: American journal of physiology. Gastrointestinal and liver physiology, Vol. 300, Issue 5, pp. G914-26, (2011) (PubMed).

Yan, Pan, Chen, Wu, Zhang: "The structure of the harmonin/sans complex reveals an unexpected interaction mode of the two Usher syndrome proteins." in: Proceedings of the National Academy of Sciences of the United States of America, Vol. 107, Issue 9, pp. 4040-5, (2010) (PubMed).

Jaijo, Aller, García-García, Aparisi, Bernal, Avila-Fernández, Barragán, Baiget, Ayuso, Antiñolo, Díaz-Llopis, Külm, Beneyto, Nájera, Millán: "Microarray-based mutation analysis of 183 Spanish families with Usher syndrome." in: Investigative ophthalmology & visual science, Vol. 51, Issue 3, pp. 1311-7, (2010) (PubMed).

Zallocchi, Sisson, Cosgrove: "Biochemical characterization of native Usher protein complexes from a vesicular subfraction of tracheal epithelial cells." in: Biochemistry, Vol. 49, Issue 6, pp. 1236-47, (2010) (PubMed).

Pan, Yan, Wu, Zhang: "Assembling stable hair cell tip link complex via multidentate interactions between harmonin and cadherin 23." in: Proceedings of the National Academy of Sciences of the United States of America, Vol. 106, Issue 14, pp. 5575-80, (2009) (PubMed).

Verpy, Leibovici, Zwaenepoel, Liu, Gal, Salem, Mansour, Blanchard, Kobayashi, Keats, Slim, Petit: "A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C." in: Nature genetics, Vol. 26, Issue 1, pp. 51-5, (2000) (PubMed).

Hanna, Kruskal, Ezekowitz, Bloom, Collier: "Role of macrophage oxidative burst in the action of anthrax lethal toxin." in: Molecular medicine (Cambridge, Mass.), Vol. 1, Issue 1, pp. 7-18, (1996) (PubMed).

Synonyme und alternative Namen zu USH1C

USH1 protein network component harmonin (USH1C), harmonin (CpipJ_CPIJ012732), USH1 protein network component harmonin (Ush1c), Usher syndrome 1C (ush1c), USH1 protein network component harmonin L homeolog (ush1c.L), 2010016F01Rik, AIE-75, DFNB18, DFNB18A, harmonin, NY-CO-37, NY-CO-38, PDZ-45, PDZ-73, PDZ-73/NY-CO-38, PDZ73, PDZD7C, ush1c, ush1cpst, zgc:136806

Bezeichner auf Proteinebene für USH1C

  • antigen NY-CO-38/NY-CO-37
  • autoimmune enteropathy-related antigen AIE-75
  • harmonin
  • renal carcinoma antigen NY-REN-3
  • usher syndrome type-1C protein
  • PDZ domain-containing protein
  • Usher syndrome 1C homolog
  • usher syndrome type-1C protein homolog
  • harmonin a1
  • Usher syndrome 1C (autosomal recessive, severe)
  • harmonin pseudogene
  • USH1 protein network component harmonin L homeolog
  • Usher syndrome 1C L homeolog
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