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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
- HPA031703 - Provider product page
- Provider
- Atlas Antibodies
- Proper citation
- Atlas Antibodies Cat#HPA031703, RRID:AB_10602126
- Product name
- Anti-RSPH9
- Antibody type
- Polyclonal
- Description
- Polyclonal Antibody against Human RSPH9, Gene description: radial spoke head 9 homolog (Chlamydomonas), Alternative Gene Names: C6orf206, CILD12, FLJ30845, MRPS18AL1, Validated applications: IHC, Uniprot ID: Q9H1X1, 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
- 0.2 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 Mapping the Most Common Founder Variant in RSPH9 That Causes Primary Ciliary Dyskinesia in Multiple Consanguineous Families of Bedouin Arabs
Testis‐enriched kinesin KIF9 is important for progressive motility in mouse spermatozoa
Rsph4a is essential for the triplet radial spoke head assembly of the mouse motile cilia
A quantitative super-resolution imaging toolbox for diagnosis of motile ciliopathies
Zebrafish Rfx4 controls dorsal and ventral midline formation in the neural tube
Radial spoke head 6 homolog a is required for sperm flagellum formation and male fertility in mice
Accuracy of Immunofluorescence in the Diagnosis of Primary Ciliary Dyskinesia
Novel roles for the radial spoke head protein 9 in neural and neurosensory cilia
Immunofluorescence Analysis and Diagnosis of Primary Ciliary Dyskinesia with Radial Spoke Defects
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
Proteomic analysis of multiple primary cilia reveals a novel mode of ciliary development in mammals
Al-Mutairi D, Alsabah B, Pennekamp P, Omran H
Journal of Clinical Medicine 2023;12(20):6505
Journal of Clinical Medicine 2023;12(20):6505
Testis‐enriched kinesin KIF9 is important for progressive motility in mouse spermatozoa
Miyata H, Shimada K, Morohoshi A, Oura S, Matsumura T, Xu Z, Oyama Y, Ikawa M
The FASEB Journal 2020;34(4):5389-5400
The FASEB Journal 2020;34(4):5389-5400
Rsph4a is essential for the triplet radial spoke head assembly of the mouse motile cilia
Omran H, Yoke H, Ueno H, Narita A, Sakai T, Horiuchi K, Shingyoji C, Hamada H, Shinohara K
PLOS Genetics 2020;16(3):e1008664
PLOS Genetics 2020;16(3):e1008664
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)
Zebrafish Rfx4 controls dorsal and ventral midline formation in the neural tube
Sedykh I, Keller A, Yoon B, Roberson L, Moskvin O, Grinblat Y
Developmental Dynamics 2018;247(4):650-659
Developmental Dynamics 2018;247(4):650-659
Radial spoke head 6 homolog a is required for sperm flagellum formation and male fertility in mice
Abbasi F, Miyata H, Shimada K, Morohoshi A, Nozawa K, Matsumura T, Xu Z, Pratiwi P, Ikawa M
Journal of Cell Science 2018
Journal of Cell Science 2018
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
Novel roles for the radial spoke head protein 9 in neural and neurosensory cilia
Sedykh I, TeSlaa J, Tatarsky R, Keller A, Toops K, Lakkaraju A, Nyholm M, Wolman M, Grinblat Y
Scientific Reports 2016;6(1)
Scientific Reports 2016;6(1)
Immunofluorescence Analysis and Diagnosis of Primary Ciliary Dyskinesia with Radial Spoke Defects
Frommer A, Hjeij R, Loges N, Edelbusch C, Jahnke C, Raidt J, Werner C, Wallmeier J, Große-Onnebrink J, Olbrich H, Cindrić S, Jaspers M, Boon M, Memari Y, Durbin R, Kolb-Kokocinski A, Sauer S, Marthin J, Nielsen K, Amirav I, Elias N, Kerem E, Shoseyov D, Haeffner K, Omran H
American Journal of Respiratory Cell and Molecular Biology 2015;53(4):563-573
American Journal of Respiratory Cell and Molecular Biology 2015;53(4):563-573
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
Proteomic analysis of multiple primary cilia reveals a novel mode of ciliary development in mammals
Narita K, Kozuka-Hata H, Nonami Y, Ao-Kondo H, Suzuki T, Nakamura H, Yamakawa K, Oyama M, Inoue T, Takeda S
Biology Open 2012;1(8):815-825
Biology Open 2012;1(8):815-825
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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 pancreas tissues using HPA031703 antibody. Corresponding RSPH9 RNA-seq data are presented for the same tissues.
- Sample type
- Human
- Protocol
- Protocol
