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- Antibody Data
- Antigen structure
- References [10]
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- Product number
- HPA041311 - Provider product page
- Provider
- Atlas Antibodies
- Proper citation
- Atlas Antibodies Cat#HPA041311, RRID:AB_2677402
- Product name
- Anti-GAS8
- Antibody type
- Polyclonal
- Description
- Polyclonal Antibody against Human GAS8, Gene description: growth arrest-specific 8, Alternative Gene Names: GAS11, Validated applications: IHC, WB, Uniprot ID: O95995, Storage: Store at +4°C for short term storage. Long time storage is recommended at -20°C.
- Reactivity
- Human
- Host
- Rabbit
- Conjugate
- Unconjugated
- Isotype
- IgG
- Vial size
- 100 µl
- Concentration
- 0.4 mg/ml
- Storage
- Store at +4°C for short term storage. Long time storage is recommended at -20°C.
- Handling
- The antibody solution should be gently mixed before use.
Submitted references Structure, interaction and nervous connectivity of beta cell primary cilia
Mitochondrial dysfunction compromises ciliary homeostasis in astrocytes
Islet primary cilia motility controls insulin secretion
Case Report: Whole-Exome Sequencing-Based Copy Number Variation Analysis Identified a Novel DRC1 Homozygous Exon Deletion in a Patient With Primary Ciliary Dyskinesia
Mutations in TP73 cause impaired mucociliary clearance and lissencephaly
A quantitative super-resolution imaging toolbox for diagnosis of motile ciliopathies
Bi-allelic Mutations in ARMC2 Lead to Severe Astheno-Teratozoospermia Due to Sperm Flagellum Malformations in Humans and Mice
Accuracy of Immunofluorescence in the Diagnosis of Primary Ciliary Dyskinesia
TTC25 Deficiency Results in Defects of the Outer Dynein Arm Docking Machinery and Primary Ciliary Dyskinesia with Left-Right Body Asymmetry Randomization
Loss-of-Function GAS8 Mutations Cause Primary Ciliary Dyskinesia and Disrupt the Nexin-Dynein Regulatory Complex
Müller A, Klena N, Pang S, Garcia L, Topcheva O, Aurrecoechea Duran S, Sulaymankhil D, Seliskar M, Mziaut H, Schöniger E, Friedland D, Kipke N, Kretschmar S, Münster C, Weitz J, Distler M, Kurth T, Schmidt D, Hess H, Xu C, Pigino G, Solimena M
Nature Communications 2024;15(1)
Nature Communications 2024;15(1)
Mitochondrial dysfunction compromises ciliary homeostasis in astrocytes
Ignatenko O, Malinen S, Rybas S, Vihinen H, Nikkanen J, Kononov A, Jokitalo E, Ince-Dunn G, Suomalainen A
Journal of Cell Biology 2023;222(1)
Journal of Cell Biology 2023;222(1)
Islet primary cilia motility controls insulin secretion
Cho J, Li Z, Zhu L, Muegge B, Roseman H, Lee E, Utterback T, Woodhams L, Bayly P, Hughes J
Science Advances 2022;8(38)
Science Advances 2022;8(38)
Case Report: Whole-Exome Sequencing-Based Copy Number Variation Analysis Identified a Novel DRC1 Homozygous Exon Deletion in a Patient With Primary Ciliary Dyskinesia
Liu Y, Lei C, Wang R, Yang D, Yang B, Xu Y, Lu C, Wang L, Ding S, Guo T, Liu S, Luo H
Frontiers in Genetics 2022;13
Frontiers in Genetics 2022;13
Mutations in TP73 cause impaired mucociliary clearance and lissencephaly
Wallmeier J, Bracht D, Alsaif H, Dougherty G, Olbrich H, Cindric S, Dzietko M, Heyer C, Teig N, Thiels C, Faqeih E, Al-Hashim A, Khan S, Mogarri I, Almannai M, Al Otaibi W, Alkuraya F, Koerner-Rettberg C, Omran H
The American Journal of Human Genetics 2021;108(7):1318-1329
The American Journal of Human Genetics 2021;108(7):1318-1329
A quantitative super-resolution imaging toolbox for diagnosis of motile ciliopathies
Liu Z, Nguyen Q, Guan Q, Albulescu A, Erdman L, Mahdaviyeh Y, Kang J, Ouyang H, Hegele R, Moraes T, Goldenberg A, Dell S, Mennella V
Science Translational Medicine 2020;12(535)
Science Translational Medicine 2020;12(535)
Bi-allelic Mutations in ARMC2 Lead to Severe Astheno-Teratozoospermia Due to Sperm Flagellum Malformations in Humans and Mice
Coutton C, Martinez G, Kherraf Z, Amiri-Yekta A, Boguenet M, Saut A, He X, Zhang F, Cristou-Kent M, Escoffier J, Bidart M, Satre V, Conne B, Fourati Ben Mustapha S, Halouani L, Marrakchi O, Makni M, Latrous H, Kharouf M, Pernet-Gallay K, Bonhivers M, Hennebicq S, Rives N, Dulioust E, Touré A, Gourabi H, Cao Y, Zouari R, Hosseini S, Nef S, Thierry-Mieg N, Arnoult C, Ray P
The American Journal of Human Genetics 2019;104(2):331-340
The American Journal of Human Genetics 2019;104(2):331-340
Accuracy of Immunofluorescence in the Diagnosis of Primary Ciliary Dyskinesia
Shoemark A, Frost E, Dixon M, Ollosson S, Kilpin K, Patel M, Scully J, Rogers A, Mitchison H, Bush A, Hogg C
American Journal of Respiratory and Critical Care Medicine 2017;196(1):94-101
American Journal of Respiratory and Critical Care Medicine 2017;196(1):94-101
TTC25 Deficiency Results in Defects of the Outer Dynein Arm Docking Machinery and Primary Ciliary Dyskinesia with Left-Right Body Asymmetry Randomization
Wallmeier J, Shiratori H, Dougherty G, Edelbusch C, Hjeij R, Loges N, Menchen T, Olbrich H, Pennekamp P, Raidt J, Werner C, Minegishi K, Shinohara K, Asai Y, Takaoka K, Lee C, Griese M, Memari Y, Durbin R, Kolb-Kokocinski A, Sauer S, Wallingford J, Hamada H, Omran H
The American Journal of Human Genetics 2016;99(2):460-469
The American Journal of Human Genetics 2016;99(2):460-469
Loss-of-Function GAS8 Mutations Cause Primary Ciliary Dyskinesia and Disrupt the Nexin-Dynein Regulatory Complex
Olbrich H, Cremers C, Loges N, Werner C, Nielsen K, Marthin J, Philipsen M, Wallmeier J, Pennekamp P, Menchen T, Edelbusch C, Dougherty G, Schwartz O, Thiele H, Altmüller J, Rommelmann F, Omran H
The American Journal of Human Genetics 2015;97(4):546-554
The American Journal of Human Genetics 2015;97(4):546-554
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