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anti-Human RPGRIP1L Antikörper:
anti-Mouse (Murine) RPGRIP1L Antikörper:
anti-Rat (Rattus) RPGRIP1L Antikörper:
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Human Polyclonal RPGRIP1L Primary Antibody für IHC, IHC (p) - ABIN4351046
Yang, Su, Wang, Craige, Witman, Tsou, Liao: Superresolution Pattern Recognition Reveals the Architectural Map of the Ciliary Transition Zone. in Scientific reports 2015
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Human Polyclonal RPGRIP1L Primary Antibody für ELISA, WB - ABIN314338
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 2007
findings expand the repertoire of MKS (zeige MKKS Antikörper) module-associated proteins and suggest an MKS-5 and CEP-290 (zeige CEP290 Antikörper)-dependent assembly pathway for building a functional ciliary transition zone
MKS-5 acts to exclude membrane-associated signalling proteins from the transition zone and limits PIP2 ciliary abundance, creating an optimal, discrete ciliary signalling compartment.
these data suggest that NPHP-8/RPGRIP1L plays an important role in cilia formation and cilia-mediated chemosensation in a cell type-specific manner.
Importantly, one Japanese and one Omani families carried compound biallelic mutations in two distinct genes (TMEM67 (zeige TMEM67 Antikörper)/RPGRIP1L and TMEM138 (zeige TMEM138 Antikörper)/BBS1 (zeige BBS1 Antikörper), respectively).
All Spanish families with Alstrom syndrome were homozygous for 229A allele of RPGRIP1L, with the exception of a p.A229T heterozygous patient.
First evidence of the association between RPGRIP1L gene and susceptibility of Vascular Dementia.
Data show that the minor allele (N) of I393N in IQCB1 (zeige IQCB1 Antikörper) and the common allele (R) of R744Q in RPGRIP1L were associated with severe disease in XlRP with RPGR (zeige RPGR Antikörper) mutations.
Nek4 interaction with both RPGRIP1 (zeige RPGRIP1 Antikörper) and the RPGRIP1L is involved in cilium assembly.
Insulin (zeige INS Antikörper) was identified as a key factor regulating FTM expression during human preadipocyte differentiation.
CSPP (zeige Cspp1 Antikörper) isoforms require their common C-terminal domain to interact with Nephrocystin 8 (NPHP8/RPGRIP1L) and to form a ternary complex with NPHP8 and NPHP4 (zeige NPHP4 Antikörper).
RPGRIP1L interacts with retinitis pigmentosa GTPase (zeige RACGAP1 Antikörper), loss of which causes retinal degeneration.
Mutations in MKS3 (zeige TMEM67 Antikörper) are responsible for the majority of COACH syndrome, with minor contributions from CC2D2A (zeige CC2D2A Antikörper) and RPGRIP1L.
Mutations can cause the multiorgan phenotypic abnormalities found in cerebello-oculo-renal syndrome or Meckel syndrome.
Rpgrip1l controls ciliary signaling by regulating the activity of the ciliary proteasome via Psmd2 (zeige PSMD2 Antikörper).
RPGRIP1L, a ciliopathy gene, is essential for hair follicle morphogenesis likely through regulating primary cilia formation and the hedgehog (zeige SHH Antikörper) signaling pathway.
Rpgrip1l/ mice are hyperphagic.
loss of Ftm leads to shortened cilia and a reduced proliferation in distinct atrial and ventricular ciliary regions at E11.5. Consequently, wall thickness is diminished in these areas
Cut-like homeobox 1 (CUX1 (zeige CUX1 Antikörper)) regulates expression of the fat mass and obesity-associated (zeige FTO Antikörper) and retinitis pigmentosa GTPase regulator-interacting protein-1 (zeige RPGRIP1 Antikörper)-like (RPGRIP1L) genes and coordinates leptin receptor (zeige LEPR Antikörper) signaling.
As Ftm is not essential for cilia assembly but for full Shh (zeige SHH Antikörper) response, Ftm can be considered as a novel component for cilium-related Hh signalling.
Inactivation of mouse ortholog Rpgrip1l (Ftm) recapitulates the cerebral, renal and hepatic defects of cerebello-oculo-renal syndrome and Meckel syndrome.
Examined Fto (zeige FTO Antikörper)/Ftm expression in obese mice exposed to overfeeding,underfeeding and cold.
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.
, proteasome activator complex subunit 4
, protein fantom-like
, RPGR-interacting protein 1-like protein
, fantom homolog
, protein fantom
, RPGRIP1-like protein