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ImmunohistochemistryAntibody data
- Antibody Data
- Antigen structure
- References [11]
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- Validations
- Immunohistochemistry [1]
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- Product number
- HPA017382 - Provider product page
- Provider
- Atlas Antibodies
- Proper citation
- Atlas Antibodies Cat#HPA017382, RRID:AB_1858392
- Product name
- Anti-RSPH1
- Antibody type
- Polyclonal
- Description
- Polyclonal Antibody against Human RSPH1, Gene description: radial spoke head 1 homolog (Chlamydomonas), Alternative Gene Names: CILD24, FLJ32753, RSP44, RSPH10A, TSGA2, Validated applications: IHC, Uniprot ID: Q8WYR4, 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
- 0.1 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 Novel variants in DNAH6 cause male infertility associated with multiple morphological abnormalities of the sperm flagella (MMAF) and ICSI outcomes
Novel HYDIN variants associated with male infertility in two Chinese families
Sperm flagellar 2 (SPEF2) is essential for sperm flagellar assembly in humans
Novel RSPH4A Variants Associated With Primary Ciliary Dyskinesia–Related Infertility in Three Chinese Families
Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and mice
Identification of DNAH6 mutations in infertile men with multiple morphological abnormalities of the sperm flagella
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
RSPH3 Mutations Cause Primary Ciliary Dyskinesia with Central-Complex Defects and a Near Absence of Radial Spokes
Targeted NGS gene panel identifies mutations in RSPH1 causing primary ciliary dyskinesia and a common mechanism for ciliary central pair agenesis due to radial spoke defects
Loss-of-Function Mutations in RSPH1 Cause Primary Ciliary Dyskinesia with Central-Complex and Radial-Spoke Defects
Shao Z, Zhu Y, Gu M, Guo S, Yu H, Li K, Tang D, Xu Y, Lv M
Asian Journal of Andrology 2024;26(1):91-98
Asian Journal of Andrology 2024;26(1):91-98
Novel HYDIN variants associated with male infertility in two Chinese families
Yu H, Shi X, Shao Z, Geng H, Guo S, Li K, Gu M, Xu C, Gao Y, Tan Q, Duan Z, Wu H, Hua R, Guo R, Wei Z, Zhou P, Cao Y, He X, Li L, Zhang X, Lv M
Frontiers in Endocrinology 2023;14
Frontiers in Endocrinology 2023;14
Sperm flagellar 2 (SPEF2) is essential for sperm flagellar assembly in humans
Li D, Yang X, Tu C, Wang W, Meng L, Lu G, Tan Y, Zhang Q, Du J
Asian Journal of Andrology 2022;24(4):359-366
Asian Journal of Andrology 2022;24(4):359-366
Novel RSPH4A Variants Associated With Primary Ciliary Dyskinesia–Related Infertility in Three Chinese Families
Wang L, Wang R, Yang D, Lu C, Xu Y, Liu Y, Guo T, Lei C, Luo H
Frontiers in Genetics 2022;13
Frontiers in Genetics 2022;13
Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and mice
Tan C, Meng L, Lv M, He X, Sha Y, Tang D, Tan Y, Hu T, He W, Tu C, Nie H, Zhang H, Du J, Lu G, Fan L, Cao Y, Lin G, Tan Y
The American Journal of Human Genetics 2022;109(1):157-171
The American Journal of Human Genetics 2022;109(1):157-171
Identification of DNAH6 mutations in infertile men with multiple morphological abnormalities of the sperm flagella
Tu C, Nie H, Meng L, Yuan S, He W, Luo A, Li H, Li W, Du J, Lu G, Lin G, Tan Y
Scientific Reports 2019;9(1)
Scientific Reports 2019;9(1)
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
RSPH3 Mutations Cause Primary Ciliary Dyskinesia with Central-Complex Defects and a Near Absence of Radial Spokes
Jeanson L, Copin B, Papon J, Dastot-Le Moal F, Duquesnoy P, Montantin G, Cadranel J, Corvol H, Coste A, Désir J, Souayah A, Kott E, Collot N, Tissier S, Louis B, Tamalet A, de Blic J, Clement A, Escudier E, Amselem S, Legendre M
The American Journal of Human Genetics 2015;97(1):153-162
The American Journal of Human Genetics 2015;97(1):153-162
Targeted NGS gene panel identifies mutations in RSPH1 causing primary ciliary dyskinesia and a common mechanism for ciliary central pair agenesis due to radial spoke defects
Onoufriadis A, Shoemark A, Schmidts M, Patel M, Jimenez G, Liu H, Thomas B, Dixon M, Hirst R, Rutman A, Burgoyne T, Williams C, Scully J, Bolard F, Lafitte J, Beales P, Hogg C, Yang P, Chung E, Emes R, O'Callaghan C, Bouvagnet P, Mitchison H
Human Molecular Genetics 2014;23(13):3362-3374
Human Molecular Genetics 2014;23(13):3362-3374
Loss-of-Function Mutations in RSPH1 Cause Primary Ciliary Dyskinesia with Central-Complex and Radial-Spoke Defects
Kott E, Legendre M, Copin B, Papon J, Dastot-Le Moal F, Montantin G, Duquesnoy P, Piterboth W, Amram D, Bassinet L, Beucher J, Beydon N, Deneuville E, Houdouin V, Journel H, Just J, Nathan N, Tamalet A, Collot N, Jeanson L, Le Gouez M, Vallette B, Vojtek A, Epaud R, Coste A, Clement A, Housset B, Louis B, Escudier E, Amselem S
The American Journal of Human Genetics 2013;93(3):561-570
The American Journal of Human Genetics 2013;93(3):561-570
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Supportive validation
- Submitted by
- Atlas Antibodies (provider)
- Enhanced method
- Orthogonal validation
- Main image
- Experimental details
- Immunohistochemistry analysis in human fallopian tube and cerebral cortex tissues using HPA017382 antibody. Corresponding RSPH1 RNA-seq data are presented for the same tissues.
- Sample type
- Human
- Protocol
- Protocol
