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anti-Mouse (Murine) IFT88 Antibodies:
anti-Human IFT88 Antibodies:
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Human Polyclonal IFT88 Primary Antibody for ICC, IF - ABIN250922
Macaluso, Perumal, Kolstrup, Satir: CLEM Methods for Studying Primary Cilia. in Methods in molecular biology (Clifton, N.J.) 2016
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Human Polyclonal IFT88 Primary Antibody for IHC, ELISA - ABIN185555
Vogel: News focus: Betting on cilia. in Science (New York, N.Y.) 2005
Show all 3 Pubmed References
Human Polyclonal IFT88 Primary Antibody for ELISA, WB - ABIN521769
Boldt, Mans, Won, van Reeuwijk, Vogt, Kinkl, Letteboer, Hicks, Hurd, Naggert, Texier, den Hollander, Koenekoop, Bennett, Cremers, Gloeckner, Nishina, Roepman, Ueffing: Disruption of intraflagellar protein transport in photoreceptor cilia causes Leber congenital amaurosis in humans and mice. in The Journal of clinical investigation 2011
Human Polyclonal IFT88 Primary Antibody for IF, IHC (p) - ABIN655090
Lehner, Semple, Brown, Counsell, Campbell, Sanderson: Analysis of a high-throughput yeast two-hybrid system and its use to predict the function of intracellular proteins encoded within the human MHC class III region. in Genomics 2003
Show all 2 Pubmed References
NOMPB is required for the assembly of sensory cilia but not for the extension or function of the sperm flagellum.
Tg737 regulates a Wnt (show WNT2 Antibodies)/beta-catenin (show CTNNB1 Antibodies)/Snail (show SNAI1 Antibodies)-HNF4alpha (show HNF4A Antibodies) negative feedback circuit, thereby blocking EMT (show ITK Antibodies) and the malignant transformation of liver stem cells to liver cancer stem cells.
genetically ablated Kif3a (show KIF3A Antibodies), Ift88, and Ttc21b (show TTC21B Antibodies) in a series of specific spatiotemporal domains. The resulting phenotypes allow us to draw several conclusions. First, we conclude that the Ttc21b (show TTC21B Antibodies) cortical phenotype is not due to the activity of Ttc21b (show TTC21B Antibodies) within the brain itself
In order to evaluate the function of IFT88 in regulating craniofacial development, we generated Wnt1 (show WNT1 Antibodies)-Cre;Ift88fl/fl mice to eliminate Ift88 specifically in cranial neural crest (CNC) cells. Wnt1 (show WNT1 Antibodies)-Cre;Ift88fl/flpups died at birth due to severe craniofacial defects including bilateral cleft lip and palate and tongue agenesis, following the loss of the primary cilia in the CNC-derived palatal mesenchyme
IFT88 influences chondrocyte actin organization and biomechanics.
These data indicate that TGF-beta (show TGFB1 Antibodies) regulates Ift88 gene expression at least in part via posttrascriptional manner.
Results suggest that EGF (show EGF Antibodies) exerts mitogenic effects in the orpk cilia (-) cells via activation of growth-associated amiloride-sensitive NHEs and ERK (show EPHB2 Antibodies).
We propose that Ift88 and primary cilia regulate expression of Sfrp5 (show SFRP5 Antibodies) and Wnt (show WNT2 Antibodies) signaling pathways in growth plate via regulation of Ihh (show IHH Antibodies) signaling.
Knockout of Bbs7 (show BBS7 Antibodies) combined with a hypomorphic Ift88 allele (orpk as a model for Shh (show SHH Antibodies) dysfuction) results in embryonic lethality with e12.5 embryos having exencephaly, pericardial edema, cleft palate and abnormal limb development.
Data show that IFT88 is present in the Golgi of spermatids, that the microtubule-associated golgin GMAP210 (show TRIP11 Antibodies) and IFT88 participate in acrosome, HTCA, and tail biogenesis.
Epidermal cilia function was analyzed using conditional alleles of the ciliogenic genes Ift88 and Kif3a (show KIF3A Antibodies).
Data suggest that the function of the fusion transcript crystallin, lambda 1 protein - intraflagellar transport 88 (CRYL1 (show CRYL1 Antibodies)-IFT88) is closed to CRYL1 (show CRYL1 Antibodies) because it contained most of domain of CRYL1 (show CRYL1 Antibodies).
multivariate Cox (show COX8A Antibodies) regression analyses demonstrated that Tg737 expression was an independent factor for predicting the overall survival of hepatocellular carcinoma patients
MiR (show MLXIP Antibodies)-548a-5p negatively regulates the tumor inhibitor gene Tg737 and promotes tumorigenesis in vitro and in vivo, indicating its potential as a novel therapeutic target for hepatocellular carcinoma.
subtle regulation of IFT and associated cilia structure, tunes the wnt (show WNT2 Antibodies) response controlling stem cell differentiation.
this work suggests that Tg737 is involved in the invasion and migration of hepatoma cells under hypoxia, with the involvement of the polycystin-1 (show PKD1 Antibodies), IL-8 (show IL8 Antibodies), and TGF-beta1 (show TGFB1 Antibodies) signaling pathway
A mutation in IFT88 causes a hitherto unknown human ciliopathy.
Data show that IFT88 depletion induces mitotic defects in human cultured cells, in kidney cells from the IFT88 mouse mutant Tg737(orpk) and in zebrafish embryos.
The results indicate that loss of heterozygosity of the tumor suppressor gene Tg737 may play an important role in the carcinogenetic mechanism of liver cancer stem cells.
IFT88 is a centrosomal protein regulating G1-S transition in non-ciliated cells.
This gene encodes a member of the tetratrico peptide repeat (TPR) family. Mutations of a similar gene in mouse can cause polycystic kidney disease. Two transcript variants encoding distinct isoforms have been identified for this gene.
intraflagellar transport protein 88 homolog
, intraflagellar transport 88 homolog (Chlamydomonas)
, TPR repeat protein 10
, intraflagellar transport 88 homolog
, recessive polycystic kidney disease protein Tg737
, tetratricopeptide repeat domain 10
, tetratricopeptide repeat protein 10
, transgene insert site 737, insertional mutation, polycystic kidney disease
, polaris homolog
, probe hTg737 (polycystic kidney disease, autosomal recessive)
, recessive polycystic kidney disease protein Tg737 homolog