Antibody data
- Antibody Data
- Antigen structure
- References [48]
- Comments [0]
- Validations
- Western blot [1]
- Immunoprecipitation [1]
- Immunohistochemistry [1]
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Validation data
Reference
Comment
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- Product number
- 11744-1-AP - Provider product page
- Provider
- Proteintech Group
- Proper citation
- Proteintech Cat#11744-1-AP, RRID:AB_2121966
- Product name
- IFT81 antibody
- Antibody type
- Polyclonal
- Description
- KD/KO validated IFT81 antibody (Cat. #11744-1-AP) is a rabbit polyclonal antibody that shows reactivity with human, mouse, Canine and has been validated for the following applications: IF, IHC, IP, WB,ELISA.
- Reactivity
- Human, Mouse, Canine
- Host
- Rabbit
- Conjugate
- Unconjugated
- Isotype
- IgG
- Vial size
- 20ul, 150ul
Submitted references Fine-tuning FAM161A gene augmentation therapy to restore retinal function.
PIH1D3-knockout rats exhibit full ciliopathy features and dysfunctional pre-assembly and loading of dynein arms in motile cilia.
The IFT81-IFT74 complex acts as an unconventional RabL2 GTPase-activating protein during intraflagellar transport.
Dynein-2-driven intraciliary retrograde trafficking indirectly requires multiple interactions of IFT54 in the IFT-B complex with the dynein-2 complex.
Primary cilia are WNT-transducing organelles whose biogenesis is controlled by a WNT-PP1 axis.
Centriolar satellites expedite mother centriole remodeling to promote ciliogenesis.
ANKS1A-Deficiency Aberrantly Increases the Entry of the Protein Transport Machinery into the Ependymal Cilia.
Ttc21b deficiency attenuates autosomal dominant polycystic kidney disease in a kidney tubular- and maturation-dependent manner.
Endothelial β-arrestins regulate mechanotransduction by the type II bone morphogenetic protein receptor in primary cilia.
The ciliary gene INPP5E confers dorsal telencephalic identity to human cortical organoids by negatively regulating Sonic hedgehog signaling.
IQCN disruption causes fertilization failure and male infertility due to manchette assembly defect.
Phylogenetic profiling and cellular analyses of ARL16 reveal roles in traffic of IFT140 and INPP5E.
A WDR35-dependent coat protein complex transports ciliary membrane cargo vesicles to cilia.
Cilia locally synthesize proteins to sustain their ultrastructure and functions.
Disrupted intraflagellar transport due to IFT74 variants causes Joubert syndrome.
Separable roles for RanGTP in nuclear and ciliary trafficking of a kinesin-2 subunit.
Rabl2 GTP hydrolysis licenses BBSome-mediated export to fine-tune ciliary signaling.
Quantitative Determination of Primary Cilia Protein Distribution Using Immunofluorescence Staining and MATLAB Analysis.
Mutations in GRK2 cause Jeune syndrome by impairing Hedgehog and canonical Wnt signaling.
Genetic interaction of mammalian IFT-A paralogs regulates cilia disassembly, ciliary entry of membrane protein, Hedgehog signaling, and embryogenesis.
IFT proteins interact with HSET to promote supernumerary centrosome clustering in mitosis.
The essential role of intraflagellar transport protein IFT81 in male mice spermiogenesis and fertility.
Intraflagellar-transport A dysfunction causes hyperphagia-induced systemic insulin resistance in a pre-obese state.
The novel ciliogenesis regulator DYRK2 governs Hedgehog signaling during mouse embryogenesis.
Murine germ cell-specific disruption of Ift172 causes defects in spermiogenesis and male fertility.
Intraflagellar transport protein 74 is essential for spermatogenesis and male fertility in mice†.
Inhibition of Hedgehog signaling suppresses proliferation and microcyst formation of human Autosomal Dominant Polycystic Kidney Disease cells.
Primary Cilia Mediate Diverse Kinase Inhibitor Resistance Mechanisms in Cancer.
The small GTPase RSG1 controls a final step in primary cilia initiation.
Intraflagellar transporter protein 140 (IFT140), a component of IFT-A complex, is essential for male fertility and spermiogenesis in mice.
Spinocerebellar ataxia type 11-associated alleles of Ttbk2 dominantly interfere with ciliogenesis and cilium stability.
The Meckel syndrome- associated protein MKS1 functionally interacts with components of the BBSome and IFT complexes to mediate ciliary trafficking and hedgehog signaling.
Palmitoylation of the ciliary GTPase ARL13b is necessary for its stability and its role in cilia formation.
IFT25, an intraflagellar transporter protein dispensable for ciliogenesis in somatic cells, is essential for sperm flagella formation.
The CEP19-RABL2 GTPase Complex Binds IFT-B to Initiate Intraflagellar Transport at the Ciliary Base.
Dynamic Remodeling of Membrane Composition Drives Cell Cycle through Primary Cilia Excision.
IFT proteins spatially control the geometry of cleavage furrow ingression and lumen positioning.
Intraflagellar transporter protein (IFT27), an IFT25 binding partner, is essential for male fertility and spermiogenesis in mice.
KDM3A coordinates actin dynamics with intraflagellar transport to regulate cilia stability.
IFT56 regulates vertebrate developmental patterning by maintaining IFTB complex integrity and ciliary microtubule architecture.
Immunofluorescent staining of septins in primary cilia.
Destabilization of the IFT-B cilia core complex due to mutations in IFT81 causes a Spectrum of Short-Rib Polydactyly Syndrome.
IFT52 mutations destabilize anterograde complex assembly, disrupt ciliogenesis and result in short rib polydactyly syndrome.
Novel role for the midbody in primary ciliogenesis by polarized epithelial cells.
IFT81, encoding an IFT-B core protein, as a very rare cause of a ciliopathy phenotype.
Systematic proteomics of the VCP-UBXD adaptor network identifies a role for UBXN10 in regulating ciliogenesis.
The kinesin-4 protein Kif7 regulates mammalian Hedgehog signalling by organizing the cilium tip compartment.
BBS proteins interact genetically with the IFT pathway to influence SHH-related phenotypes.
Arsenijevic Y, Chang N, Mercey O, El Fersioui Y, Koskiniemi-Kuendig H, Joubert C, Bemelmans AP, Rivolta C, Banin E, Sharon D, Guichard P, Hamel V, Kostic C
EMBO molecular medicine 2024 Apr;16(4):805-822
EMBO molecular medicine 2024 Apr;16(4):805-822
PIH1D3-knockout rats exhibit full ciliopathy features and dysfunctional pre-assembly and loading of dynein arms in motile cilia.
Zhang T, Cui S, Xiong X, Liu Y, Cao Q, Xia XG, Zhou H
Frontiers in cell and developmental biology 2023;11:1282787
Frontiers in cell and developmental biology 2023;11:1282787
The IFT81-IFT74 complex acts as an unconventional RabL2 GTPase-activating protein during intraflagellar transport.
Boegholm N, Petriman NA, Loureiro-López M, Wang J, Vela MIS, Liu B, Kanie T, Ng R, Jackson PK, Andersen JS, Lorentzen E
The EMBO journal 2023 Sep 18;42(18):e111807
The EMBO journal 2023 Sep 18;42(18):e111807
Dynein-2-driven intraciliary retrograde trafficking indirectly requires multiple interactions of IFT54 in the IFT-B complex with the dynein-2 complex.
Hiyamizu S, Qiu H, Tsurumi Y, Hamada Y, Katoh Y, Nakayama K
Biology open 2023 Jul 15;12(7)
Biology open 2023 Jul 15;12(7)
Primary cilia are WNT-transducing organelles whose biogenesis is controlled by a WNT-PP1 axis.
Zhang K, Da Silva F, Seidl C, Wilsch-Bräuninger M, Herbst J, Huttner WB, Niehrs C
Developmental cell 2023 Jan 23;58(2):139-154.e8
Developmental cell 2023 Jan 23;58(2):139-154.e8
Centriolar satellites expedite mother centriole remodeling to promote ciliogenesis.
Hall EA, Kumar D, Prosser SL, Yeyati PL, Herranz-Pérez V, García-Verdugo JM, Rose L, McKie L, Dodd DO, Tennant PA, Megaw R, Murphy LC, Ferreira MF, Grimes G, Williams L, Quidwai T, Pelletier L, Reiter JF, Mill P
eLife 2023 Feb 15;12
eLife 2023 Feb 15;12
ANKS1A-Deficiency Aberrantly Increases the Entry of the Protein Transport Machinery into the Ependymal Cilia.
Lee H, Lee J, Shin M, Park S
Molecules and cells 2023 Dec 31;46(12):757-763
Molecules and cells 2023 Dec 31;46(12):757-763
Ttc21b deficiency attenuates autosomal dominant polycystic kidney disease in a kidney tubular- and maturation-dependent manner.
Wang W, Silva LM, Wang HH, Kavanaugh MA, Pottorf TS, Allard BA, Jacobs DT, Dong R, Cornelius JT, Chaturvedi A, Swenson-Fields KI, Fields TA, Pritchard MT, Sharma M, Slawson C, Wallace DP, Calvet JP, Tran PV
Kidney international 2022 Sep;102(3):577-591
Kidney international 2022 Sep;102(3):577-591
Endothelial β-arrestins regulate mechanotransduction by the type II bone morphogenetic protein receptor in primary cilia.
Park S, Ma Z, Zarkada G, Papangeli I, Paluri S, Nazo N, Rivera-Molina F, Toomre D, Rajagopal S, Chun HJ
Pulmonary circulation 2022 Oct;12(4):e12167
Pulmonary circulation 2022 Oct;12(4):e12167
The ciliary gene INPP5E confers dorsal telencephalic identity to human cortical organoids by negatively regulating Sonic hedgehog signaling.
Schembs L, Willems A, Hasenpusch-Theil K, Cooper JD, Whiting K, Burr K, Bøstrand SMK, Selvaraj BT, Chandran S, Theil T
Cell reports 2022 May 17;39(7):110811
Cell reports 2022 May 17;39(7):110811
IQCN disruption causes fertilization failure and male infertility due to manchette assembly defect.
Dai J, Li Q, Zhou Q, Zhang S, Chen J, Wang Y, Guo J, Gu Y, Gong F, Tan Y, Lu G, Zheng W, Lin G
EMBO molecular medicine 2022 Dec 7;14(12):e16501
EMBO molecular medicine 2022 Dec 7;14(12):e16501
Phylogenetic profiling and cellular analyses of ARL16 reveal roles in traffic of IFT140 and INPP5E.
Dewees SI, Vargová R, Hardin KR, Turn RE, Devi S, Linnert J, Wolfrum U, Caspary T, Eliáš M, Kahn RA
Molecular biology of the cell 2022 Apr 1;33(4):ar33
Molecular biology of the cell 2022 Apr 1;33(4):ar33
A WDR35-dependent coat protein complex transports ciliary membrane cargo vesicles to cilia.
Quidwai T, Wang J, Hall EA, Petriman NA, Leng W, Kiesel P, Wells JN, Murphy LC, Keighren MA, Marsh JA, Lorentzen E, Pigino G, Mill P
eLife 2021 Nov 4;10
eLife 2021 Nov 4;10
Cilia locally synthesize proteins to sustain their ultrastructure and functions.
Hao K, Chen Y, Yan X, Zhu X
Nature communications 2021 Nov 30;12(1):6971
Nature communications 2021 Nov 30;12(1):6971
Disrupted intraflagellar transport due to IFT74 variants causes Joubert syndrome.
Luo M, Lin Z, Zhu T, Jin M, Meng D, He R, Cao Z, Shen Y, Lu C, Cai R, Zhao Y, Wang X, Li H, Wu S, Zou X, Luo G, Cao L, Huang M, Jiao H, Gao H, Sui R, Zhao C, Ma X, Cao M
Genetics in medicine : official journal of the American College of Medical Genetics 2021 Jun;23(6):1041-1049
Genetics in medicine : official journal of the American College of Medical Genetics 2021 Jun;23(6):1041-1049
Separable roles for RanGTP in nuclear and ciliary trafficking of a kinesin-2 subunit.
Huang S, Dougherty LL, Avasthi P
The Journal of biological chemistry 2021 Jan-Jun;296:100117
The Journal of biological chemistry 2021 Jan-Jun;296:100117
Rabl2 GTP hydrolysis licenses BBSome-mediated export to fine-tune ciliary signaling.
Duan S, Li H, Zhang Y, Yang S, Chen Y, Qiu B, Huang C, Wang J, Li J, Zhu X, Yan X
The EMBO journal 2021 Jan 15;40(2):e105499
The EMBO journal 2021 Jan 15;40(2):e105499
Quantitative Determination of Primary Cilia Protein Distribution Using Immunofluorescence Staining and MATLAB Analysis.
Jenks AD, Fivaz M, Tanos BE
Bio-protocol 2021 Dec 5;11(23):e4248
Bio-protocol 2021 Dec 5;11(23):e4248
Mutations in GRK2 cause Jeune syndrome by impairing Hedgehog and canonical Wnt signaling.
Bosakova M, Abraham SP, Nita A, Hruba E, Buchtova M, Taylor SP, Duran I, Martin J, Svozilova K, Barta T, Varecha M, Balek L, Kohoutek J, Radaszkiewicz T, Pusapati GV, Bryja V, Rush ET, Thiffault I, Nickerson DA, Bamshad MJ, University of Washington Center for Mendelian Genomics, Rohatgi R, Cohn DH, Krakow D, Krejci P
EMBO molecular medicine 2020 Nov 6;12(11):e11739
EMBO molecular medicine 2020 Nov 6;12(11):e11739
Genetic interaction of mammalian IFT-A paralogs regulates cilia disassembly, ciliary entry of membrane protein, Hedgehog signaling, and embryogenesis.
Wang W, Allard BA, Pottorf TS, Wang HH, Vivian JL, Tran PV
FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2020 May;34(5):6369-6381
FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2020 May;34(5):6369-6381
IFT proteins interact with HSET to promote supernumerary centrosome clustering in mitosis.
Vitre B, Taulet N, Guesdon A, Douanier A, Dosdane A, Cisneros M, Maurin J, Hettinger S, Anguille C, Taschner M, Lorentzen E, Delaval B
EMBO reports 2020 Jun 4;21(6):e49234
EMBO reports 2020 Jun 4;21(6):e49234
The essential role of intraflagellar transport protein IFT81 in male mice spermiogenesis and fertility.
Qu W, Yuan S, Quan C, Huang Q, Zhou Q, Yap Y, Shi L, Zhang D, Guest T, Li W, Yee SP, Zhang L, Cazin C, Hess RA, Ray PF, Kherraf ZE, Zhang Z
American journal of physiology. Cell physiology 2020 Jun 1;318(6):C1092-C1106
American journal of physiology. Cell physiology 2020 Jun 1;318(6):C1092-C1106
Intraflagellar-transport A dysfunction causes hyperphagia-induced systemic insulin resistance in a pre-obese state.
Jacobs DT, Allard BA, Pottorf TS, Silva LM, Wang W, Al-Naamani A, Agborbesong E, Wang T, Carr DA, Tran PV
FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2020 Jan;34(1):148-160
FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2020 Jan;34(1):148-160
The novel ciliogenesis regulator DYRK2 governs Hedgehog signaling during mouse embryogenesis.
Yoshida S, Aoki K, Fujiwara K, Nakakura T, Kawamura A, Yamada K, Ono M, Yogosawa S, Yoshida K
eLife 2020 Aug 6;9
eLife 2020 Aug 6;9
Murine germ cell-specific disruption of Ift172 causes defects in spermiogenesis and male fertility.
Zhang S, Liu Y, Huang Q, Yuan S, Liu H, Shi L, Yap YT, Li W, Zhen J, Zhang L, Hess RA, Zhang Z
Reproduction (Cambridge, England) 2020 Apr;159(4):409-421
Reproduction (Cambridge, England) 2020 Apr;159(4):409-421
Intraflagellar transport protein 74 is essential for spermatogenesis and male fertility in mice†.
Shi L, Zhou T, Huang Q, Zhang S, Li W, Zhang L, Hess RA, Pazour GJ, Zhang Z
Biology of reproduction 2019 Jul 1;101(1):188-199
Biology of reproduction 2019 Jul 1;101(1):188-199
Inhibition of Hedgehog signaling suppresses proliferation and microcyst formation of human Autosomal Dominant Polycystic Kidney Disease cells.
Silva LM, Jacobs DT, Allard BA, Fields TA, Sharma M, Wallace DP, Tran PV
Scientific reports 2018 Mar 21;8(1):4985
Scientific reports 2018 Mar 21;8(1):4985
Primary Cilia Mediate Diverse Kinase Inhibitor Resistance Mechanisms in Cancer.
Jenks AD, Vyse S, Wong JP, Kostaras E, Keller D, Burgoyne T, Shoemark A, Tsalikis A, de la Roche M, Michaelis M, Cinatl J Jr, Huang PH, Tanos BE
Cell reports 2018 Jun 5;23(10):3042-3055
Cell reports 2018 Jun 5;23(10):3042-3055
The small GTPase RSG1 controls a final step in primary cilia initiation.
Agbu SO, Liang Y, Liu A, Anderson KV
The Journal of cell biology 2018 Jan 2;217(1):413-427
The Journal of cell biology 2018 Jan 2;217(1):413-427
Intraflagellar transporter protein 140 (IFT140), a component of IFT-A complex, is essential for male fertility and spermiogenesis in mice.
Zhang Y, Liu H, Li W, Zhang Z, Zhang S, Teves ME, Stevens C, Foster JA, Campbell GE, Windle JJ, Hess RA, Pazour GJ, Zhang Z
Cytoskeleton (Hoboken, N.J.) 2018 Feb;75(2):70-84
Cytoskeleton (Hoboken, N.J.) 2018 Feb;75(2):70-84
Spinocerebellar ataxia type 11-associated alleles of Ttbk2 dominantly interfere with ciliogenesis and cilium stability.
Bowie E, Norris R, Anderson KV, Goetz SC
PLoS genetics 2018 Dec;14(12):e1007844
PLoS genetics 2018 Dec;14(12):e1007844
The Meckel syndrome- associated protein MKS1 functionally interacts with components of the BBSome and IFT complexes to mediate ciliary trafficking and hedgehog signaling.
Goetz SC, Bangs F, Barrington CL, Katsanis N, Anderson KV
PloS one 2017;12(3):e0173399
PloS one 2017;12(3):e0173399
Palmitoylation of the ciliary GTPase ARL13b is necessary for its stability and its role in cilia formation.
Roy K, Jerman S, Jozsef L, McNamara T, Onyekaba G, Sun Z, Marin EP
The Journal of biological chemistry 2017 Oct 27;292(43):17703-17717
The Journal of biological chemistry 2017 Oct 27;292(43):17703-17717
IFT25, an intraflagellar transporter protein dispensable for ciliogenesis in somatic cells, is essential for sperm flagella formation.
Liu H, Li W, Zhang Y, Zhang Z, Shang X, Zhang L, Zhang S, Li Y, Somoza AV, Delpi B, Gerton GL, Foster JA, Hess RA, Pazour GJ, Zhang Z
Biology of reproduction 2017 May 1;96(5):993-1006
Biology of reproduction 2017 May 1;96(5):993-1006
The CEP19-RABL2 GTPase Complex Binds IFT-B to Initiate Intraflagellar Transport at the Ciliary Base.
Kanie T, Abbott KL, Mooney NA, Plowey ED, Demeter J, Jackson PK
Developmental cell 2017 Jul 10;42(1):22-36.e12
Developmental cell 2017 Jul 10;42(1):22-36.e12
Dynamic Remodeling of Membrane Composition Drives Cell Cycle through Primary Cilia Excision.
Phua SC, Chiba S, Suzuki M, Su E, Roberson EC, Pusapati GV, Schurmans S, Setou M, Rohatgi R, Reiter JF, Ikegami K, Inoue T
Cell 2017 Jan 12;168(1-2):264-279.e15
Cell 2017 Jan 12;168(1-2):264-279.e15
IFT proteins spatially control the geometry of cleavage furrow ingression and lumen positioning.
Taulet N, Vitre B, Anguille C, Douanier A, Rocancourt M, Taschner M, Lorentzen E, Echard A, Delaval B
Nature communications 2017 Dec 4;8(1):1928
Nature communications 2017 Dec 4;8(1):1928
Intraflagellar transporter protein (IFT27), an IFT25 binding partner, is essential for male fertility and spermiogenesis in mice.
Zhang Y, Liu H, Li W, Zhang Z, Shang X, Zhang D, Li Y, Zhang S, Liu J, Hess RA, Pazour GJ, Zhang Z
Developmental biology 2017 Dec 1;432(1):125-139
Developmental biology 2017 Dec 1;432(1):125-139
KDM3A coordinates actin dynamics with intraflagellar transport to regulate cilia stability.
Yeyati PL, Schiller R, Mali G, Kasioulis I, Kawamura A, Adams IR, Playfoot C, Gilbert N, van Heyningen V, Wills J, von Kriegsheim A, Finch A, Sakai J, Schofield CJ, Jackson IJ, Mill P
The Journal of cell biology 2017 Apr 3;216(4):999-1013
The Journal of cell biology 2017 Apr 3;216(4):999-1013
IFT56 regulates vertebrate developmental patterning by maintaining IFTB complex integrity and ciliary microtubule architecture.
Xin D, Christopher KJ, Zeng L, Kong Y, Weatherbee SD
Development (Cambridge, England) 2017 Apr 15;144(8):1544-1553
Development (Cambridge, England) 2017 Apr 15;144(8):1544-1553
Immunofluorescent staining of septins in primary cilia.
Kim MS, Froese CD, Xie H, Trimble WS
Methods in cell biology 2016;136:269-83
Methods in cell biology 2016;136:269-83
Destabilization of the IFT-B cilia core complex due to mutations in IFT81 causes a Spectrum of Short-Rib Polydactyly Syndrome.
Duran I, Taylor SP, Zhang W, Martin J, Forlenza KN, Spiro RP, Nickerson DA, Bamshad M, Cohn DH, Krakow D
Scientific reports 2016 Sep 26;6:34232
Scientific reports 2016 Sep 26;6:34232
IFT52 mutations destabilize anterograde complex assembly, disrupt ciliogenesis and result in short rib polydactyly syndrome.
Zhang W, Taylor SP, Nevarez L, Lachman RS, Nickerson DA, Bamshad M, University of Washington Center for Mendelian Genomics Consortium, Krakow D, Cohn DH
Human molecular genetics 2016 Sep 15;25(18):4012-4020
Human molecular genetics 2016 Sep 15;25(18):4012-4020
Novel role for the midbody in primary ciliogenesis by polarized epithelial cells.
Bernabé-Rubio M, Andrés G, Casares-Arias J, Fernández-Barrera J, Rangel L, Reglero-Real N, Gershlick DC, Fernández JJ, Millán J, Correas I, Miguez DG, Alonso MA
The Journal of cell biology 2016 Aug 1;214(3):259-73
The Journal of cell biology 2016 Aug 1;214(3):259-73
IFT81, encoding an IFT-B core protein, as a very rare cause of a ciliopathy phenotype.
Perrault I, Halbritter J, Porath JD, Gérard X, Braun DA, Gee HY, Fathy HM, Saunier S, Cormier-Daire V, Thomas S, Attié-Bitach T, Boddaert N, Taschner M, Schueler M, Lorentzen E, Lifton RP, Lawson JA, Garfa-Traore M, Otto EA, Bastin P, Caillaud C, Kaplan J, Rozet JM, Hildebrandt F
Journal of medical genetics 2015 Oct;52(10):657-65
Journal of medical genetics 2015 Oct;52(10):657-65
Systematic proteomics of the VCP-UBXD adaptor network identifies a role for UBXN10 in regulating ciliogenesis.
Raman M, Sergeev M, Garnaas M, Lydeard JR, Huttlin EL, Goessling W, Shah JV, Harper JW
Nature cell biology 2015 Oct;17(10):1356-69
Nature cell biology 2015 Oct;17(10):1356-69
The kinesin-4 protein Kif7 regulates mammalian Hedgehog signalling by organizing the cilium tip compartment.
He M, Subramanian R, Bangs F, Omelchenko T, Liem KF Jr, Kapoor TM, Anderson KV
Nature cell biology 2014 Jul;16(7):663-72
Nature cell biology 2014 Jul;16(7):663-72
BBS proteins interact genetically with the IFT pathway to influence SHH-related phenotypes.
Zhang Q, Seo S, Bugge K, Stone EM, Sheffield VC
Human molecular genetics 2012 May 1;21(9):1945-53
Human molecular genetics 2012 May 1;21(9):1945-53
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Supportive validation
- Submitted by
- Proteintech Group (provider)
- Main image
- Experimental details
- human brain tissue were subjected to SDS PAGE followed by western blot with 11744-1-AP(IFT81 antibody) at dilution of 1:600
- Sample type
- tissue
Supportive validation
- Submitted by
- Proteintech Group (provider)
- Main image
- Experimental details
- IP Result of anti-IFT81 (IP:11744-1-AP, 3ug; Detection:11744-1-AP 1:500) with mouse brain tissue lysate 7500ug.
- Sample type
- tissue
Supportive validation
- Submitted by
- Proteintech Group (provider)
- Main image
- Experimental details
- Immunohistochemical of paraffin-embedded human prostate cancer using 11744-1-AP(IFT81 antibody) at dilution of 1:50 (under 10x lens)
- Sample type
- tissue