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RPGRIP1L 产品

(RPGRIP1-Like (RPGRIP1L))

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The protein encoded by this gene can localize to the basal body-centrosome complex or to primary cilia and centrosomes in ciliated cells. The encoded protein has been found to interact with nephrocystin-4. Defects in this gene are a cause of Joubert syndrome type 7 (JBTS7) and Meckel syndrome type 5 (MKS5). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008].

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Featured RPGRIP1L Categories

RPGRIP1L 抗体

High quality antibodies with extensive validation data.

Recommended RPGRIP1L 抗体

Product
Reactivity
Application
Validations
Cat. No.
Quantity
Datasheet
Reactivity Human, Mouse, Rat
Application WB, IHC, ICC, IF
Validations
  • (3)
Cat. No. ABIN6264825
Quantity 100 μL
Datasheet Datasheet
Reactivity Human
Application WB, ELISA
Validations
  • (1)
Cat. No. ABIN334483
Quantity 100 μg
Datasheet Datasheet
Reactivity Human
Application WB, ELISA, IF (cc), IF (p), IHC (p), ICC, IHC (fro)
Validations
Cat. No. ABIN1385221
Quantity 100 μL
Datasheet Datasheet

Recommended RPGRIP1L ELISA试剂盒

Product
Reactivity
Analytical Method
Validations
Cat. No.
Quantity
Datasheet
Reactivity Human
Analytical Method
Validations
Cat. No. ABIN1151581
Quantity 96 tests
Datasheet Datasheet
Reactivity Mouse
Analytical Method
Validations
Cat. No. ABIN1151582
Quantity 96 tests
Datasheet Datasheet

Recommended RPGRIP1L 蛋白

Product
Reactivity
Source
Validations
Cat. No.
Quantity
Datasheet
Reactivity Human
Source Insect Cells
Validations
  • (1)
Cat. No. ABIN3092708
Quantity 1 mg
Datasheet Datasheet
Reactivity Mouse
Source Insect Cells
Validations
  • (1)
Cat. No. ABIN3136445
Quantity 1 mg
Datasheet Datasheet

Latest Publications for our RPGRIP1L Products

Yang, Su, Wang, Craige, Witman, Tsou, Liao: "Superresolution Pattern Recognition Reveals the Architectural Map of the Ciliary Transition Zone." in: Scientific reports, Vol. 5, pp. 14096, (2015) (PubMed).

Wang, Tay, Soni, Perumal, Goll, Macaluso, Asara, Amack, Tsou: "CEP162 is an axoneme-recognition protein promoting ciliary transition zone assembly at the cilia base." in: Nature cell biology, Vol. 15, Issue 6, pp. 591-601, (2013) (PubMed).

Arts, Doherty, van Beersum, Parisi, Letteboer, Gorden, Peters, Märker, Voesenek, Kartono, Ozyurek, Farin, Kroes, Wolfrum, Brunner, Cremers, Glass, Knoers, Roepman: "Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome." in: Nature genetics, Vol. 39, Issue 7, pp. 882-8, (2007) (PubMed).

Synonyms and alternative names related to RPGRIP1L

RPGRIP1 like (RPGRIP1L), RPGRIP1-like (rpgrip1l), RPGRIP1 like (rpgrip1l), Protein fantom (mks-5), Rpgrip1-like (Rpgrip1l), RPGRIP1 like (Rpgrip1l), 1700047E16Rik, 4931437C01, cors3, CORS3, FTM, Ftm, jbts7, JBTS7, mks5, MKS5, nphp8, NPHP8, Nphp8, RGD1311099, si:ch1073-301i20.1

Protein level used designations for RPGRIP1L

  • RPGRIP1-like
  • proteasome activator complex subunit 4
  • protein fantom-like
  • RPGR-interacting protein 1-like protein
  • fantom homolog
  • nephrocystin-8
  • protein fantom
  • RPGRIP1-like protein
  • fantom
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