This webpage contains legacy information. The product is either no longer available from the supplier or has been delisted at Labome.
product summary
company name :
Proteintech Group
product type :
antibody
product name :
IFT88
catalog :
13967-1-AP
quantity :
150UL
price :
299 USD
clonality :
polyclonal
host :
domestic rabbit
conjugate :
nonconjugated
reactivity :
human, mouse, dogs
application :
western blot, ELISA, immunohistochemistry, immunocytochemistry, immunoprecipitation
citations: 154
Published Application/Species/Sample/DilutionReference
  • western blot; human; 1:1000; loading ...; fig 4b
Boukhalfa A, Nascimbeni A, Ramel D, Dupont N, Hirsch E, Gayral S, et al. PI3KC2α-dependent and VPS34-independent generation of PI3P controls primary cilium-mediated autophagy in response to shear stress. Nat Commun. 2020;11:294 pubmed publisher
  • immunocytochemistry; mouse; 1:50; loading ...; fig s10a
  • western blot; mouse; 1:1000; loading ...; fig s10e
Martin Hurtado A, Martin Morales R, Robledinos Antón N, Blanco R, Palacios Blanco I, Lastres Becker I, et al. NRF2-dependent gene expression promotes ciliogenesis and Hedgehog signaling. Sci Rep. 2019;9:13896 pubmed publisher
  • immunocytochemistry; mouse; 1:200; loading ...; fig 5
Hua K, Ferland R. Fixation methods can differentially affect ciliary protein immunolabeling. Cilia. 2017;6:5 pubmed publisher
  • immunocytochemistry; human; loading ...; fig s1b
Oliazadeh N, Gorman K, Eveleigh R, Bourque G, Moreau A. Identification of Elongated Primary Cilia with Impaired Mechanotransduction in Idiopathic Scoliosis Patients. Sci Rep. 2017;7:44260 pubmed publisher
  • immunocytochemistry; mouse; 1:300; loading ...; fig s5
  • western blot; mouse; 1:800; loading ...; fig 6d
Yu F, Sharma S, Skowronek A, Erdmann K. The serologically defined colon cancer antigen-3 (SDCCAG3) is involved in the regulation of ciliogenesis. Sci Rep. 2016;6:35399 pubmed publisher
  • western blot; human; loading ...; fig 5C
  • immunocytochemistry; mouse; fig 6F
Hong C, Hamilton B. Zfp423 Regulates Sonic Hedgehog Signaling via Primary Cilium Function. PLoS Genet. 2016;12:e1006357 pubmed publisher
  • immunocytochemistry; human; 1:200; loading ...; fig 3A
Kim M, Froese C, Xie H, Trimble W. Immunofluorescent staining of septins in primary cilia. Methods Cell Biol. 2016;136:269-83 pubmed publisher
  • immunocytochemistry; dogs; 1:100; loading ...; fig s1f
Bernabé Rubio M, Andrés G, Casares Arias J, Fernández Barrera J, Rangel L, Reglero Real N, et al. Novel role for the midbody in primary ciliogenesis by polarized epithelial cells. J Cell Biol. 2016;214:259-73 pubmed publisher
  • immunocytochemistry; human; fig 2
Wang L, Lee K, Malonis R, SANCHEZ I, Dynlacht B. Tethering of an E3 ligase by PCM1 regulates the abundance of centrosomal KIAA0586/Talpid3 and promotes ciliogenesis. elife. 2016;5: pubmed publisher
  • western blot; human; fig 5c
Kim J, Ki S, Joung J, Scott E, Heynen Genel S, Aza Blanc P, et al. Genome-wide screen identifies novel machineries required for both ciliogenesis and cell cycle arrest upon serum starvation. Biochim Biophys Acta. 2016;1863:1307-18 pubmed publisher
  • immunocytochemistry; mouse; 1:200; loading ...; fig 6h
  • western blot; mouse; 1:1000; loading ...; fig 6f
Katoh Y, Terada M, Nishijima Y, Takei R, Nozaki S, Hamada H, et al. Overall Architecture of the Intraflagellar Transport (IFT)-B Complex Containing Cluap1/IFT38 as an Essential Component of the IFT-B Peripheral Subcomplex. J Biol Chem. 2016;291:10962-75 pubmed publisher
  • immunocytochemistry; human; 1:500; loading ...; fig 5b
Khan N, Willemarck N, Talebi A, Marchand A, Binda M, Dehairs J, et al. Identification of drugs that restore primary cilium expression in cancer cells. Oncotarget. 2016;7:9975-92 pubmed publisher
Yoshida S, Aoki K, Fujiwara K, Nakakura T, Kawamura A, Yamada K, et al. The novel ciliogenesis regulator DYRK2 governs Hedgehog signaling during mouse embryogenesis. elife. 2020;9: pubmed publisher
Yu F, Li T, Sui Y, Chen Q, Yang S, Yang J, et al. O-GlcNAc transferase regulates centriole behavior and intraflagellar transport to promote ciliogenesis. Protein Cell. 2020;: pubmed publisher
Bangs F, Miller P, O Neill E. Ciliogenesis and Hedgehog signalling are suppressed downstream of KRAS during acinar-ductal metaplasia in mouse. Dis Model Mech. 2020;13: pubmed publisher
Toro Tapia G, Das R. Primary cilium remodeling mediates a cell signaling switch in differentiating neurons. Sci Adv. 2020;6:eabb0601 pubmed publisher
Ni X, Wang J, Lv M, Liu C, Zhong Y, Tian S, et al. A novel homozygous mutation in WDR19 induces disorganization of microtubules in sperm flagella and nonsyndromic asthenoteratospermia. J Assist Reprod Genet. 2020;37:1431-1439 pubmed publisher
Ran J, Liu M, Feng J, Li H, Ma H, Song T, et al. ASK1-Mediated Phosphorylation Blocks HDAC6 Ubiquitination and Degradation to Drive the Disassembly of Photoreceptor Connecting Cilia. Dev Cell. 2020;53:287-299.e5 pubmed publisher
Vitre B, Taulet N, Guesdon A, Douanier A, Dosdane A, Cisneros M, et al. IFT proteins interact with HSET to promote supernumerary centrosome clustering in mitosis. EMBO Rep. 2020;21:e49234 pubmed publisher
Chen S, Qin L, Wu X, Fu X, Lin S, Chen D, et al. Moderate Fluid Shear Stress Regulates Heme Oxygenase-1 Expression to Promote Autophagy and ECM Homeostasis in the Nucleus Pulposus Cells. Front Cell Dev Biol. 2020;8:127 pubmed publisher
Wang W, Allard B, Pottorf T, Wang H, Vivian J, Tran P. Genetic interaction of mammalian IFT-A paralogs regulates cilia disassembly, ciliary entry of membrane protein, Hedgehog signaling, and embryogenesis. FASEB J. 2020;34:6369-6381 pubmed publisher
Liu P, Dodson M, Fang D, Chapman E, Zhang D. NRF2 negatively regulates primary ciliogenesis and hedgehog signaling. PLoS Biol. 2020;18:e3000620 pubmed publisher
Lv M, Liu W, Chi W, Ni X, Wang J, Cheng H, et al. Homozygous mutations in DZIP1 can induce asthenoteratospermia with severe MMAF. J Med Genet. 2020;57:445-453 pubmed publisher
Komarynets O, Chassot A, Bernabeu E, Czogalla J, Roth I, Liaudet N, et al. Aldosterone controls primary cilium length and cell size in renal collecting duct principal cells. FASEB J. 2020;34:2625-2640 pubmed publisher
Shohayeb B, Ho U, Yeap Y, Parton R, Millard S, Xu Z, et al. The association of microcephaly protein WDR62 with CPAP/IFT88 is required for cilia formation and neocortical development. Hum Mol Genet. 2020;29:248-263 pubmed publisher
Flynn M, Whitton L, Donohoe G, Morrison C, Morris D. Altered gene regulation as a candidate mechanism by which ciliopathy gene SDCCAG8 contributes to schizophrenia and cognitive function. Hum Mol Genet. 2019;: pubmed publisher
Bae J, Kang G, Min S, Jo D, Jung Y, Kim K, et al. Primary cilia mediate mitochondrial stress responses to promote dopamine neuron survival in a Parkinson's disease model. Cell Death Dis. 2019;10:952 pubmed publisher
Volta F, Scerbo M, Seelig A, Wagner R, O Brien N, Gerst F, et al. Glucose homeostasis is regulated by pancreatic β-cell cilia via endosomal EphA-processing. Nat Commun. 2019;10:5686 pubmed publisher
Sahabandu N, Kong D, Magidson V, Nanjundappa R, Sullenberger C, Mahjoub M, et al. Expansion microscopy for the analysis of centrioles and cilia. J Microsc. 2019;: pubmed publisher
Choi H, Madhu V, Shapiro I, Risbud M. Nucleus pulposus primary cilia alter their length in response to changes in extracellular osmolarity but do not control TonEBP-mediated osmoregulation. Sci Rep. 2019;9:15469 pubmed publisher
Liu L, Sheng J, Wang M, Gan Y, Wu X, Liao J, et al. Primary Cilia Blockage Promotes the Malignant Behaviors of Hepatocellular Carcinoma via Induction of Autophagy. Biomed Res Int. 2019;2019:5202750 pubmed publisher
Wang C, Su M, Cheng H, Kuo P, Tsai P. Fetuin-A Inhibits Placental Cell Growth and Ciliogenesis in Gestational Diabetes Mellitus. Int J Mol Sci. 2019;20: pubmed publisher
Lospinoso Severini L, Quaglio D, Basili I, Ghirga F, Bufalieri F, Caimano M, et al. A Smo/Gli Multitarget Hedgehog Pathway Inhibitor Impairs Tumor Growth. Cancers (Basel). 2019;11: pubmed publisher
Shaheen R, Alsahli S, Ewida N, Alzahrani F, Shamseldin H, Patel N, et al. Biallelic mutations in TTC26 (IFT56) cause severe biliary ciliopathy in humans. Hepatology. 2019;: pubmed publisher
Lamri L, Twan W, Katoh T, Botilde Y, Takaoka K, Ikawa Y, et al. Ciliogenesis-coupled accumulation of IFT-B proteins in a novel cytoplasmic compartment. Genes Cells. 2019;24:731-745 pubmed publisher
Nozaki S, Castro Araya R, Katoh Y, Nakayama K. Requirement of IFT-B-BBSome complex interaction in export of GPR161 from cilia. Biol Open. 2019;8: pubmed publisher
Lo C, Lin I, Yang T, Huang Y, Tanos B, Chou P, et al. Phosphorylation of CEP83 by TTBK2 is necessary for cilia initiation. J Cell Biol. 2019;218:3489-3505 pubmed publisher
Frikstad K, Molinari E, Thoresen M, Ramsbottom S, Hughes F, Letteboer S, et al. A CEP104-CSPP1 Complex Is Required for Formation of Primary Cilia Competent in Hedgehog Signaling. Cell Rep. 2019;28:1907-1922.e6 pubmed publisher
Taulet N, Douanier A, Vitre B, Anguille C, Maurin J, Dromard Y, et al. IFT88 controls NuMA enrichment at k-fibers minus-ends to facilitate their re-anchoring into mitotic spindles. Sci Rep. 2019;9:10311 pubmed publisher
Wang B, Hu L, Sun Z, Zhang Y. Cilia function is associated with axon initial segment morphology. Biochem Biophys Res Commun. 2019;: pubmed publisher
Hossain D, Barbelanne M, Tsang W. Requirement of NPHP5 in the hierarchical assembly of basal feet associated with basal bodies of primary cilia. Cell Mol Life Sci. 2019;: pubmed publisher
Wheway G, Nazlamova L, Turner D, Cross S. 661W Photoreceptor Cell Line as a Cell Model for Studying Retinal Ciliopathies. Front Genet. 2019;10:308 pubmed publisher
Odabasi E, Gül S, Kavakli I, Firat Karalar E. Centriolar satellites are required for efficient ciliogenesis and ciliary content regulation. EMBO Rep. 2019;20: pubmed publisher
Hong H, Joo K, Park S, Seo J, Kim M, Shin E, et al. Extraciliary roles of the ciliopathy protein JBTS17 in mitosis and neurogenesis. Ann Neurol. 2019;86:99-115 pubmed publisher
Engelke M, Waas B, Kearns S, Suber A, Boss A, Allen B, et al. Acute Inhibition of Heterotrimeric Kinesin-2 Function Reveals Mechanisms of Intraflagellar Transport in Mammalian Cilia. Curr Biol. 2019;: pubmed publisher
Shaheen R, Jiang N, Alzahrani F, Ewida N, Al Sheddi T, Alobeid E, et al. Bi-allelic Mutations in FAM149B1 Cause Abnormal Primary Cilium and a Range of Ciliopathy Phenotypes in Humans. Am J Hum Genet. 2019;104:731-737 pubmed publisher
Chang C, Zanini M, Shirvani H, Cheng J, Yu H, Feng C, et al. Atoh1 Controls Primary Cilia Formation to Allow for SHH-Triggered Granule Neuron Progenitor Proliferation. Dev Cell. 2019;48:184-199.e5 pubmed publisher
Jeffries E, Di Filippo M, Galbiati F. Failure to reabsorb the primary cilium induces cellular senescence. FASEB J. 2019;33:4866-4882 pubmed publisher
Chen T, Lien W, Cheng H, Kuan T, Sheu S, Wang C. Chloroquine inhibits human retina pigmented epithelial cell growth and microtubule nucleation by downregulating p150glued. J Cell Physiol. 2019;234:10445-10457 pubmed publisher
Haley C, Waters A, Bader D. Malformations in the Murine Kidney Caused by Loss of CENP-F Function. Anat Rec (Hoboken). 2019;302:163-170 pubmed publisher
Xu Q, Liu X, Liu W, Hayashi T, Yamato M, Fujisaki H, et al. Type I collagen-induced YAP nuclear expression promotes primary cilia growth and contributes to cell migration in confluent mouse embryo fibroblast 3T3-L1 cells. Mol Cell Biochem. 2019;450:87-96 pubmed publisher
Vuong L, Iomini C, Balmer S, Esposito D, Aaronson S, Mlodzik M. Kinesin-2 and IFT-A act as a complex promoting nuclear localization of β-catenin during Wnt signalling. Nat Commun. 2018;9:5304 pubmed publisher
Tu H, Qin X, Liu Z, Song Z, Hu H, Zhang Y, et al. Microtubule asters anchored by FSD1 control axoneme assembly and ciliogenesis. Nat Commun. 2018;9:5277 pubmed publisher
Bowie E, Norris R, Anderson K, Goetz S. Spinocerebellar ataxia type 11-associated alleles of Ttbk2 dominantly interfere with ciliogenesis and cilium stability. PLoS Genet. 2018;14:e1007844 pubmed publisher
Oud M, Latour B, Bakey Z, Letteboer S, Lugtenberg D, Wu K, et al. Cellular ciliary phenotyping indicates pathogenicity of novel variants in IFT140 and confirms a Mainzer-Saldino syndrome diagnosis. Cilia. 2018;7:1 pubmed publisher
Vuolo L, Stevenson N, Heesom K, Stephens D. Dynein-2 intermediate chains play crucial but distinct roles in primary cilia formation and function. elife. 2018;7: pubmed publisher
Wang L, Failler M, Fu W, Dynlacht B. A distal centriolar protein network controls organelle maturation and asymmetry. Nat Commun. 2018;9:3938 pubmed publisher
Shamoto N, Narita K, Kubo T, Oda T, Takeda S. CFAP70 Is a Novel Axoneme-Binding Protein That Localizes at the Base of the Outer Dynein Arm and Regulates Ciliary Motility. Cells. 2018;7: pubmed publisher
Abdelhamed Z, Ryan T, Fuller M, Coulson Gilmer C, Abdelmottaleb D, Wang T, et al. Characterization of Primary Cilia in Normal Fallopian Tube Epithelium and Serous Tubal Intraepithelial Carcinoma. Int J Gynecol Cancer. 2018;28:1535-1544 pubmed publisher
Honda A, Kita T, Seshadri S, Misaki K, Ahmed Z, Ladbury J, et al. FGFR1-mediated protocadherin-15 loading mediates cargo specificity during intraflagellar transport in inner ear hair-cell kinocilia. Proc Natl Acad Sci U S A. 2018;115:8388-8393 pubmed publisher
Chekuri A, Guru A, Biswas P, Branham K, Borooah S, Soto Hermida A, et al. IFT88 mutations identified in individuals with non-syndromic recessive retinal degeneration result in abnormal ciliogenesis. Hum Genet. 2018;137:447-458 pubmed publisher
Dafinger C, Rinschen M, Borgal L, Ehrenberg C, Basten S, Franke M, et al. Targeted deletion of the AAA-ATPase Ruvbl1 in mice disrupts ciliary integrity and causes renal disease and hydrocephalus. Exp Mol Med. 2018;50:75 pubmed publisher
Viau A, Bienaime F, Lukas K, Todkar A, Knoll M, Yakulov T, et al. Cilia-localized LKB1 regulates chemokine signaling, macrophage recruitment, and tissue homeostasis in the kidney. EMBO J. 2018;37: pubmed publisher
Funabashi T, Katoh Y, Okazaki M, Sugawa M, Nakayama K. Interaction of heterotrimeric kinesin-II with IFT-B-connecting tetramer is crucial for ciliogenesis. J Cell Biol. 2018;217:2867-2876 pubmed publisher
Jenks A, Vyse S, Wong J, Kostaras E, Keller D, Burgoyne T, et al. Primary Cilia Mediate Diverse Kinase Inhibitor Resistance Mechanisms in Cancer. Cell Rep. 2018;23:3042-3055 pubmed publisher
Weng R, Yang T, Huang C, Chang C, Wang W, Liao J. Super-Resolution Imaging Reveals TCTN2 Depletion-Induced IFT88 Lumen Leakage and Ciliary Weakening. Biophys J. 2018;115:263-275 pubmed publisher
Barny I, Perrault I, Michel C, Soussan M, Goudin N, Rio M, et al. Basal exon skipping and nonsense-associated altered splicing allows bypassing complete CEP290 loss-of-function in individuals with unusually mild retinal disease. Hum Mol Genet. 2018;: pubmed publisher
Lee J, Yi S, Won M, Song Y, Yi H, Park Y, et al. Loss-of-function of IFT88 determines metabolic phenotypes in thyroid cancer. Oncogene. 2018;37:4455-4474 pubmed publisher
Forbes T, Howden S, Lawlor K, Phipson B, Maksimovic J, Hale L, et al. Patient-iPSC-Derived Kidney Organoids Show Functional Validation of a Ciliopathic Renal Phenotype and Reveal Underlying Pathogenetic Mechanisms. Am J Hum Genet. 2018;102:816-831 pubmed publisher
Takei R, Katoh Y, Nakayama K. Robust interaction of IFT70 with IFT52-IFT88 in the IFT-B complex is required for ciliogenesis. Biol Open. 2018;7: pubmed publisher
Wiegering A, Dildrop R, Kalfhues L, Spychala A, Kuschel S, Lier J, et al. Cell type-specific regulation of ciliary transition zone assembly in vertebrates. EMBO J. 2018;37: pubmed publisher
Revenkova E, Liu Q, Gusella G, Iomini C. The Joubert syndrome protein ARL13B binds tubulin to maintain uniform distribution of proteins along the ciliary membrane. J Cell Sci. 2018;131: pubmed publisher
Silva L, Jacobs D, Allard B, Fields T, Sharma M, Wallace D, et al. Inhibition of Hedgehog signaling suppresses proliferation and microcyst formation of human Autosomal Dominant Polycystic Kidney Disease cells. Sci Rep. 2018;8:4985 pubmed publisher
Vion A, Alt S, Klaus Bergmann A, Szymborska A, Zheng T, Perovic T, et al. Primary cilia sensitize endothelial cells to BMP and prevent excessive vascular regression. J Cell Biol. 2018;217:1651-1665 pubmed publisher
Ogungbenro Y, Tena T, Gaboriau D, Lalor P, Dockery P, Philipp M, et al. Centrobin controls primary ciliogenesis in vertebrates. J Cell Biol. 2018;217:1205-1215 pubmed publisher
Khan N, Garg A, Agostinis P, Swinnen J. Drug-induced ciliogenesis in pancreatic cancer cells is facilitated by the secreted ATP-purinergic receptor signaling pathway. Oncotarget. 2018;9:3507-3518 pubmed publisher
Canning P, Park K, Goncalves J, Li C, Howard C, Sharpe T, et al. CDKL Family Kinases Have Evolved Distinct Structural Features and Ciliary Function. Cell Rep. 2018;22:885-894 pubmed publisher
Rosengren T, Larsen L, Pedersen L, Christensen S, Møller L. TSC1 and TSC2 regulate cilia length and canonical Hedgehog signaling via different mechanisms. Cell Mol Life Sci. 2018;75:2663-2680 pubmed publisher
Schmid F, Schou K, Vilhelm M, Holm M, Breslin L, Farinelli P, et al. IFT20 modulates ciliary PDGFRα signaling by regulating the stability of Cbl E3 ubiquitin ligases. J Cell Biol. 2018;217:151-161 pubmed publisher
Deng Y, Cai Z, Shi S, Jiang H, Shang Y, Ma N, et al. Cilia loss sensitizes cells to transformation by activating the mevalonate pathway. J Exp Med. 2018;215:177-195 pubmed publisher
Hartill V, van de Hoek G, Patel M, Little R, Watson C, Berry I, et al. DNAAF1 links heart laterality with the AAA+ ATPase RUVBL1 and ciliary intraflagellar transport. Hum Mol Genet. 2018;27:529-545 pubmed publisher
Takahashi K, Nagai T, Chiba S, Nakayama K, Mizuno K. Glucose deprivation induces primary cilium formation through mTORC1 inactivation. J Cell Sci. 2018;131: pubmed publisher
Lee S, Joo K, Jung E, Hong H, Seo J, Kim J. Export of membrane proteins from the Golgi complex to the primary cilium requires the kinesin motor, KIFC1. FASEB J. 2018;32:957-968 pubmed publisher
Martin L, Kaci N, Estibals V, Goudin N, Garfa Traoré M, Benoist Lasselin C, et al. Constitutively-active FGFR3 disrupts primary cilium length and IFT20 trafficking in various chondrocyte models of achondroplasia. Hum Mol Genet. 2018;27:1-13 pubmed publisher
Agbu S, Liang Y, Liu A, Anderson K. The small GTPase RSG1 controls a final step in primary cilia initiation. J Cell Biol. 2018;217:413-427 pubmed publisher
Taulet N, Vitre B, Anguille C, Douanier A, Rocancourt M, Taschner M, et al. IFT proteins spatially control the geometry of cleavage furrow ingression and lumen positioning. Nat Commun. 2017;8:1928 pubmed publisher
Liu X, Wang J, Gao L, Liu H, Liu C. iTRAQ-Based Proteomic Analysis of Neonatal Kidney from Offspring of Protein Restricted Rats Reveals Abnormalities in Intraflagellar Transport Proteins. Cell Physiol Biochem. 2017;44:185-199 pubmed publisher
Wu C, Hou S, Orr B, Kuo B, Youn Y, Ong T, et al. mTORC1-Mediated Inhibition of 4EBP1 Is Essential for Hedgehog Signaling-Driven Translation and Medulloblastoma. Dev Cell. 2017;43:673-688.e5 pubmed publisher
Kasioulis I, Das R, Storey K. Inter-dependent apical microtubule and actin dynamics orchestrate centrosome retention and neuronal delamination. elife. 2017;6: pubmed publisher
Hsu Y, Garrison J, Kim G, Schmitz A, Searby C, Zhang Q, et al. BBSome function is required for both the morphogenesis and maintenance of the photoreceptor outer segment. PLoS Genet. 2017;13:e1007057 pubmed publisher
Pitaval A, Senger F, Letort G, Gidrol X, Guyon L, Sillibourne J, et al. Microtubule stabilization drives 3D centrosome migration to initiate primary ciliogenesis. J Cell Biol. 2017;216:3713-3728 pubmed publisher
Biswas P, Duncan J, Ali M, Matsui H, Naeem M, Raghavendra P, et al. A mutation in IFT43 causes non-syndromic recessive retinal degeneration. Hum Mol Genet. 2017;26:4741-4751 pubmed publisher
Srivastava S, Ramsbottom S, Molinari E, Alkanderi S, Filby A, White K, et al. A human patient-derived cellular model of Joubert syndrome reveals ciliary defects which can be rescued with targeted therapies. Hum Mol Genet. 2017;26:4657-4667 pubmed publisher
Hu L, Wang B, Zhang Y. Serotonin 5-HT6 receptors affect cognition in a mouse model of Alzheimer's disease by regulating cilia function. Alzheimers Res Ther. 2017;9:76 pubmed publisher
Kohli P, Höhne M, Jüngst C, Bertsch S, Ebert L, Schauss A, et al. The ciliary membrane-associated proteome reveals actin-binding proteins as key components of cilia. EMBO Rep. 2017;18:1521-1535 pubmed publisher
Ding J, Shao L, Yao Y, Tong X, Liu H, Yue S, et al. DGKδ triggers endoplasmic reticulum release of IFT88-containing vesicles destined for the assembly of primary cilia. Sci Rep. 2017;7:5296 pubmed publisher
Shimada H, Lu Q, Insinna Kettenhofen C, Nagashima K, English M, Semler E, et al. In Vitro Modeling Using Ciliopathy-Patient-Derived Cells Reveals Distinct Cilia Dysfunctions Caused by CEP290 Mutations. Cell Rep. 2017;20:384-396 pubmed publisher
Kanie T, Abbott K, Mooney N, Plowey E, Demeter J, JACKSON P. The CEP19-RABL2 GTPase Complex Binds IFT-B to Initiate Intraflagellar Transport at the Ciliary Base. Dev Cell. 2017;42:22-36.e12 pubmed publisher
Gupta A, Tsuchiya Y, Ohta M, Shiratsuchi G, Kitagawa D. NEK7 is required for G1 progression and procentriole formation. Mol Biol Cell. 2017;28:2123-2134 pubmed publisher
Lu H, Galeano M, Ott E, Kaeslin G, Kausalya P, Kramer C, et al. Mutations in DZIP1L, which encodes a ciliary-transition-zone protein, cause autosomal recessive polycystic kidney disease. Nat Genet. 2017;49:1025-1034 pubmed publisher
Das A, Qian J, Tsang W. USP9X counteracts differential ubiquitination of NPHP5 by MARCH7 and BBS11 to regulate ciliogenesis. PLoS Genet. 2017;13:e1006791 pubmed publisher
Trempus C, Song W, Lazrak A, Yu Z, Creighton J, Young B, et al. A novel role for primary cilia in airway remodeling. Am J Physiol Lung Cell Mol Physiol. 2017;313:L328-L338 pubmed publisher
Ernandez T, Komarynets O, Chassot A, Sougoumarin S, Soulie P, Wang Y, et al. Primary cilia control the maturation of tubular lumen in renal collecting duct epithelium. Am J Physiol Cell Physiol. 2017;313:C94-C107 pubmed publisher
Nguyen T, Hull S, Roepman R, van den Born L, Oud M, de Vrieze E, et al. Missense mutations in the WD40 domain of AHI1 cause non-syndromic retinitis pigmentosa. J Med Genet. 2017;54:624-632 pubmed publisher
Goetz S, Bangs F, Barrington C, Katsanis N, Anderson K. The Meckel syndrome- associated protein MKS1 functionally interacts with components of the BBSome and IFT complexes to mediate ciliary trafficking and hedgehog signaling. PLoS ONE. 2017;12:e0173399 pubmed publisher
Xin D, Christopher K, Zeng L, Kong Y, Weatherbee S. IFT56 regulates vertebrate developmental patterning by maintaining IFTB complex integrity and ciliary microtubule architecture. Development. 2017;144:1544-1553 pubmed publisher
Yeyati P, Schiller R, Mali G, Kasioulis I, Kawamura A, Adams I, et al. KDM3A coordinates actin dynamics with intraflagellar transport to regulate cilia stability. J Cell Biol. 2017;216:999-1013 pubmed publisher
Katoh Y, Michisaka S, Nozaki S, Funabashi T, Hirano T, Takei R, et al. Practical method for targeted disruption of cilia-related genes by using CRISPR/Cas9-mediated, homology-independent knock-in system. Mol Biol Cell. 2017;28:898-906 pubmed publisher
Schou K, Mogensen J, Morthorst S, Nielsen B, Aleliunaite A, Serra Marques A, et al. KIF13B establishes a CAV1-enriched microdomain at the ciliary transition zone to promote Sonic hedgehog signalling. Nat Commun. 2017;8:14177 pubmed publisher
Phua S, Chiba S, Suzuki M, Su E, Roberson E, Pusapati G, et al. Dynamic Remodeling of Membrane Composition Drives Cell Cycle through Primary Cilia Excision. Cell. 2017;168:264-279.e15 pubmed publisher
Funabashi T, Katoh Y, Michisaka S, Terada M, Sugawa M, Nakayama K. Ciliary entry of KIF17 is dependent on its binding to the IFT-B complex via IFT46-IFT56 as well as on its nuclear localization signal. Mol Biol Cell. 2017;28:624-633 pubmed publisher
Kobayashi T, Nakazono K, Tokuda M, Mashima Y, Dynlacht B, Itoh H. HDAC2 promotes loss of primary cilia in pancreatic ductal adenocarcinoma. EMBO Rep. 2017;18:334-343 pubmed publisher
Nozaki S, Katoh Y, Terada M, Michisaka S, Funabashi T, Takahashi S, et al. Regulation of ciliary retrograde protein trafficking by the Joubert syndrome proteins ARL13B and INPP5E. J Cell Sci. 2017;130:563-576 pubmed publisher
Lee J, Yi S, Kang Y, Chang J, Kim J, Sul H, et al. Defective ciliogenesis in thyroid hürthle cell tumors is associated with increased autophagy. Oncotarget. 2016;7:79117-79130 pubmed publisher
Fu W, Wang L, Kim S, Li J, Dynlacht B. Role for the IFT-A Complex in Selective Transport to the Primary Cilium. Cell Rep. 2016;17:1505-1517 pubmed publisher
Wang C, Tsai H, Syu J, Chen T, Su M. Primary Cilium-Regulated EG-VEGF Signaling Facilitates Trophoblast Invasion. J Cell Physiol. 2017;232:1467-1477 pubmed publisher
Durán I, Taylor S, Zhang W, Martin J, Forlenza K, Spiro R, et al. Destabilization of the IFT-B cilia core complex due to mutations in IFT81 causes a Spectrum of Short-Rib Polydactyly Syndrome. Sci Rep. 2016;6:34232 pubmed publisher
Nechipurenko I, Olivier Mason A, Kazatskaya A, Kennedy J, McLachlan I, Heiman M, et al. A Conserved Role for Girdin in Basal Body Positioning and Ciliogenesis. Dev Cell. 2016;38:493-506 pubmed publisher
Yang T, Chong W, Liao J. STED and STORM Superresolution Imaging of Primary Cilia. Methods Mol Biol. 2016;1454:169-92 pubmed publisher
Zhao G, Wang T, Huang Q, Pu M, Sun W, Zhang Z, et al. MicroRNA-548a-5p promotes proliferation and inhibits apoptosis in hepatocellular carcinoma cells by targeting Tg737. World J Gastroenterol. 2016;22:5364-73 pubmed publisher
Cortés C, McInerney Leo A, Vogel I, Rondón Galeano M, Leo P, Harris J, et al. Mutations in human C2CD3 cause skeletal dysplasia and provide new insights into phenotypic and cellular consequences of altered C2CD3 function. Sci Rep. 2016;6:24083 pubmed publisher
Zhong M, Zhao X, Li J, Yuan W, Yan G, Tong M, et al. Tumor Suppressor Folliculin Regulates mTORC1 through Primary Cilia. J Biol Chem. 2016;291:11689-97 pubmed publisher
Xu Q, Zhang Y, Wei Q, Huang Y, Hu J, Ling K. Phosphatidylinositol phosphate kinase PIPKIγ and phosphatase INPP5E coordinate initiation of ciliogenesis. Nat Commun. 2016;7:10777 pubmed publisher
Deren M, Yang X, Guan Y, Chen Q. Biological and Chemical Removal of Primary Cilia Affects Mechanical Activation of Chondrogenesis Markers in Chondroprogenitors and Hypertrophic Chondrocytes. Int J Mol Sci. 2016;17:188 pubmed publisher
Vo B, Wolf E, Kawauchi D, Gebhardt A, Rehg J, Finkelstein D, et al. The Interaction of Myc with Miz1 Defines Medulloblastoma Subgroup Identity. Cancer Cell. 2016;29:5-16 pubmed publisher
Mick D, Rodrigues R, Leib R, Adams C, Chien A, Gygi S, et al. Proteomics of Primary Cilia by Proximity Labeling. Dev Cell. 2015;35:497-512 pubmed publisher
Boehlke C, Janusch H, Hamann C, Powelske C, Mergen M, Herbst H, et al. A Cilia Independent Role of Ift88/Polaris during Cell Migration. PLoS ONE. 2015;10:e0140378 pubmed publisher
Yang T, Su J, Wang W, Craige B, Witman G, Tsou M, et al. Superresolution Pattern Recognition Reveals the Architectural Map of the Ciliary Transition Zone. Sci Rep. 2015;5:14096 pubmed publisher
Kim S, Lee K, Choi J, Ringstad N, Dynlacht B. Nek2 activation of Kif24 ensures cilium disassembly during the cell cycle. Nat Commun. 2015;6:8087 pubmed publisher
Siller S, Burke M, Li F, Takemaru K. Chibby functions to preserve normal ciliary morphology through the regulation of intraflagellar transport in airway ciliated cells. Cell Cycle. 2015;14:3163-72 pubmed publisher
Ran J, Yang Y, Li D, Liu M, Zhou J. Deacetylation of α-tubulin and cortactin is required for HDAC6 to trigger ciliary disassembly. Sci Rep. 2015;5:12917 pubmed publisher
Kessler K, Wunderlich I, Uebe S, Falk N, Gießl A, Brandstätter J, et al. DYNC2LI1 mutations broaden the clinical spectrum of dynein-2 defects. Sci Rep. 2015;5:11649 pubmed publisher
Shaheen R, Almoisheer A, Faqeih E, Babay Z, Monies D, Tassan N, et al. Identification of a novel MKS locus defined by TMEM107 mutation. Hum Mol Genet. 2015;24:5211-8 pubmed publisher
Taylor S, Dantas T, Durán I, Wu S, Lachman R, Nelson S, et al. Mutations in DYNC2LI1 disrupt cilia function and cause short rib polydactyly syndrome. Nat Commun. 2015;6:7092 pubmed publisher
Schmidts M, Hou Y, Cortés C, Mans D, Huber C, Boldt K, et al. TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport. Nat Commun. 2015;6:7074 pubmed publisher
Kang G, Han Y, Ko H, Kim J, Oh B, Kwon I, et al. Leptin Elongates Hypothalamic Neuronal Cilia via Transcriptional Regulation and Actin Destabilization. J Biol Chem. 2015;290:18146-55 pubmed publisher
Reales E, Bernabé Rubio M, Casares Arias J, Rentero C, Fernández Barrera J, Rangel L, et al. The MAL protein is crucial for proper membrane condensation at the ciliary base, which is required for primary cilium elongation. J Cell Sci. 2015;128:2261-70 pubmed publisher
Wong Y, Anzola J, Davis R, Yoon M, Motamedi A, Kroll A, et al. Cell biology. Reversible centriole depletion with an inhibitor of Polo-like kinase 4. Science. 2015;348:1155-60 pubmed publisher
Caparrós Martín J, De Luca A, Cartault F, Aglan M, Temtamy S, Otaify G, et al. Specific variants in WDR35 cause a distinctive form of Ellis-van Creveld syndrome by disrupting the recruitment of the EvC complex and SMO into the cilium. Hum Mol Genet. 2015;24:4126-37 pubmed publisher
Wang S, Livingston M, Su Y, Dong Z. Reciprocal regulation of cilia and autophagy via the MTOR and proteasome pathways. Autophagy. 2015;11:607-16 pubmed publisher
Hong H, Kim J, Kim J. Myosin heavy chain 10 (MYH10) is required for centriole migration during the biogenesis of primary cilia. Biochem Biophys Res Commun. 2015;461:180-5 pubmed publisher
Xu Y, Cao J, Huang S, Feng D, Zhang W, Zhu X, et al. Characterization of tetratricopeptide repeat-containing proteins critical for cilia formation and function. PLoS ONE. 2015;10:e0124378 pubmed publisher
Zhang B, Zhang T, Wang G, Wang G, Chi W, Jiang Q, et al. GSK3β-Dzip1-Rab8 cascade regulates ciliogenesis after mitosis. PLoS Biol. 2015;13:e1002129 pubmed publisher
Hoshi M, Wang J, Jain S, Mahjoub M. Imaging centrosomes and cilia in the mouse kidney. Methods Cell Biol. 2015;127:1-17 pubmed publisher
Gholkar A, Senese S, Lo Y, Capri J, Deardorff W, Dharmarajan H, et al. Tctex1d2 associates with short-rib polydactyly syndrome proteins and is required for ciliogenesis. Cell Cycle. 2015;14:1116-25 pubmed publisher
Williams C, Hempel J, Hao J, Frist A, Williams M, Fleming J, et al. An in vivo chemical genetic screen identifies phosphodiesterase 4 as a pharmacological target for hedgehog signaling inhibition. Cell Rep. 2015;11:43-50 pubmed publisher
Shin J, Kim P, Kim E, Park S, Jo Y, Hwang J, et al. BIX-01294-induced autophagy regulates elongation of primary cilia. Biochem Biophys Res Commun. 2015;460:428-33 pubmed publisher
Prosser S, Morrison C. Centrin2 regulates CP110 removal in primary cilium formation. J Cell Biol. 2015;208:693-701 pubmed publisher
Dalbay M, Thorpe S, Connelly J, Chapple J, Knight M. Adipogenic Differentiation of hMSCs is Mediated by Recruitment of IGF-1r Onto the Primary Cilium Associated With Cilia Elongation. Stem Cells. 2015;33:1952-61 pubmed publisher
Bangs F, Schrode N, Hadjantonakis A, Anderson K. Lineage specificity of primary cilia in the mouse embryo. Nat Cell Biol. 2015;17:113-22 pubmed publisher
Waters A, Asfahani R, Carroll P, Bicknell L, Lescai F, Bright A, et al. The kinetochore protein, CENPF, is mutated in human ciliopathy and microcephaly phenotypes. J Med Genet. 2015;52:147-56 pubmed publisher
Schueler M, Braun D, Chandrasekar G, Gee H, Klasson T, Halbritter J, et al. DCDC2 mutations cause a renal-hepatic ciliopathy by disrupting Wnt signaling. Am J Hum Genet. 2015;96:81-92 pubmed publisher
Barbelanne M, Hossain D, Chan D, Peränen J, Tsang W. Nephrocystin proteins NPHP5 and Cep290 regulate BBSome integrity, ciliary trafficking and cargo delivery. Hum Mol Genet. 2015;24:2185-200 pubmed publisher
Shaheen R, Schmidts M, Faqeih E, Hashem A, Lausch E, Holder I, et al. A founder CEP120 mutation in Jeune asphyxiating thoracic dystrophy expands the role of centriolar proteins in skeletal ciliopathies. Hum Mol Genet. 2015;24:1410-9 pubmed publisher
product information
CatalogNo :
13967-1-AP
AntigenName :
IFT88
Package :
150UL
Price :
299 USD
Exsists20ul :
20ul trial size available
FullName :
intraflagellar transport 88 homolog (Chlamydomonas)
Immunogen :
Recombinant Protein
Species :
chick, chicken, dog, human, mouse, rat, swine
Host :
Rabbit
IsConjugated :
Unconjugated
AntigenSpecies :
human
Application :
WB, IP, IHC, IF, CoIP, ELISA
Clonlity :
Polyclonal
IsoType :
IgG
Synonyms :
DAF19, hTg737, IFT88, TG737, TPR repeat protein 10, TTC10
PrimaryOrSecondary :
Primary
AntibodyBuffer :
PBS with 0.02% sodium azide and 50% glycerol pH 7.3.
GenBankNo :
BC030776
Category :
Binding Proteins;Ciliary Protein;Cytoskeleton/Scaffold Proteins;Disease Related;Metabolism;Signal transduction;
PurifyMethod :
Antigen affinity purification
NewAb :
False
IsSellable :
True
Feature :
siRNA
AppTiter :
IF 1:100 ; IHC 1:50 ; IP 1:800 ; WB 1:1500 ;
company information
Proteintech Group
2201 W. Campbell Park Dr. STE12
Chicago, IL 60612
Proteintech@ptglab.com
https://www.ptglab.com
1-312-455-8498
headquarters: USA
At Proteintech, we produce every single antibody we sell; we do not rely on or supply to any other antibody providers: our products are unique and we are 100% accountable for each one. We realize this accountability by validating in-house, providing extensive technical support and guaranteeing your success: in addition to helping you troubleshoot your experiment, we will offer you a full cash refund if you are in any way dissatisfied. We can guarantee satisfaction because we have confidence in our products, confidence cultivated by the science behind our antibodies: we make them using as much of the native protein as possible, and purifying them using affinity purification with the original antigen. We carry out antibody production over a 102-day period, which allows for better antigen fitting to MHC molecules and affinity maturation in the host. This approach results in higher affinity antibodies with greater sensitivity, which you can use in any application and in multiple species.
You can only buy Proteintech antibodies directly from Proteintech or via one of its approved distributors — when you receive your antibody and see the Proteintech logo on the vial, know that you hold something that is truly unique.