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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.
Case Report: Whole-Exome Sequencing-Based Copy Number Variation Analysis Identified a Novel DRC1 Homozygous Exon Deletion in a Patient With Primary Ciliary Dyskinesia
Islet primary cilia motility controls insulin secretion.
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 ES, Ince-Dunn G, Suomalainen A
The Journal of cell biology 2023 Jan 2;222(1)
The Journal of cell biology 2023 Jan 2;222(1)
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
Islet primary cilia motility controls insulin secretion.
Cho JH, Li ZA, Zhu L, Muegge BD, Roseman HF, Lee EY, Utterback T, Woodhams LG, Bayly PV, Hughes JW
Science advances 2022 Sep 23;8(38):eabq8486
Science advances 2022 Sep 23;8(38):eabq8486
Mutations in TP73 cause impaired mucociliary clearance and lissencephaly.
Wallmeier J, Bracht D, Alsaif HS, Dougherty GW, 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 FS, Koerner-Rettberg C, Omran H
American journal of human genetics 2021 Jul 1;108(7):1318-1329
American journal of human genetics 2021 Jul 1;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 GW, Edelbusch C, Hjeij R, Loges NT, 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 JB, Hamada H, Omran H
American journal of human genetics 2016 Aug 4;99(2):460-9
American journal of human genetics 2016 Aug 4;99(2):460-9
Loss-of-Function GAS8 Mutations Cause Primary Ciliary Dyskinesia and Disrupt the Nexin-Dynein Regulatory Complex.
Olbrich H, Cremers C, Loges NT, Werner C, Nielsen KG, Marthin JK, Philipsen M, Wallmeier J, Pennekamp P, Menchen T, Edelbusch C, Dougherty GW, Schwartz O, Thiele H, Altmüller J, Rommelmann F, Omran H
American journal of human genetics 2015 Oct 1;97(4):546-54
American journal of human genetics 2015 Oct 1;97(4):546-54
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