Antibody data
- Antibody Data
- Antigen structure
- References [12]
- Comments [0]
- Validations [0]
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- Product number
- 23253-1-AP - Provider product page

- Provider
- Proteintech Group
- Product name
- RSPH9 antibody
- Antibody type
- Polyclonal
- Description
- RSPH9 antibody (Cat. #23253-1-AP) is a rabbit polyclonal antibody that shows reactivity with human, mouse, rat and has been validated for the following applications: WB,ELISA.
- Reactivity
- Human, Mouse, Rat
- Host
- Rabbit
- Conjugate
- Unconjugated
- Isotype
- IgG
- Vial size
- 20ul, 150ul
Submitted references Ccdc57 regulates cilia and left-right patterning in Xenopus.
Loss-of-function variants in ciliary genes confer high risk for tetralogy of Fallot.
CFAP65 is essential for C2a projection integrity in axonemes: implications for organ-specific ciliary dysfunction and infertility.
Novel mutations in LRRC23 cause asthenozoospermia in a nonconsanguineous family.
CALR3 defects disrupt sperm-zona pellucida binding in humans: new insights into male factor fertilization failure and relevant clinical therapeutic approaches.
Adenylate kinase phosphate energy shuttle underlies energetic communication in flagellar axonemes.
Structures of sperm flagellar doublet microtubules expand the genetic spectrum of male infertility.
CFAP70 is a solid and valuable target for the genetic diagnosis of oligo-astheno-teratozoospermia in infertile men.
LRRC23 truncation impairs radial spoke 3 head assembly and sperm motility underlying male infertility.
Differential requirements of IQUB for the assembly of radial spoke 1 and the motility of mouse cilia and flagella.
Bi-allelic variants in human TCTE1/DRC5 cause asthenospermia and male infertility.
Loss of DRC1 function leads to multiple morphological abnormalities of the sperm flagella and male infertility in human and mouse.
Yang B, Mis EK, Zhou X, Aslam F, He J, Lu X, Fan H, Guo T, Deniz E, Luo H, Khokha MK
Biology open 2026 Feb 15;15(2)
Biology open 2026 Feb 15;15(2)
Loss-of-function variants in ciliary genes confer high risk for tetralogy of Fallot.
Zhou Y, Jiang T, Gao J, Zang J, Mo X, Yue S, Cui Y, Wang Q, Da M, Xu J, Li Q, Shen B, Dai J, Ma H, Jin G, Shen H, Wang C, Gu Y, Lin Y, Hu Z
Science advances 2025 Oct 10;11(41):eadt0836
Science advances 2025 Oct 10;11(41):eadt0836
CFAP65 is essential for C2a projection integrity in axonemes: implications for organ-specific ciliary dysfunction and infertility.
Chen J, Ren C, Zhao S, Wu H, Wang J, Dong Y, Liu S, Pan Y, Xiao Z, Yang S, Zhang J, Liu M
Cellular and molecular life sciences : CMLS 2025 Jan 24;82(1):61
Cellular and molecular life sciences : CMLS 2025 Jan 24;82(1):61
Novel mutations in LRRC23 cause asthenozoospermia in a nonconsanguineous family.
Tang SX, Liu SY, Xiao H, Zhang X, Xiao Z, Zhou S, Ding YL, Yang P, Chen Q, Huang HL, Chen X, Lin X, Zhou HL, Liu MX
Asian journal of andrology 2024 Sep 1;26(5):484-489
Asian journal of andrology 2024 Sep 1;26(5):484-489
CALR3 defects disrupt sperm-zona pellucida binding in humans: new insights into male factor fertilization failure and relevant clinical therapeutic approaches.
Gao Y, Xue R, Guo R, Yang F, Sha X, Li Y, Hua R, Li G, Shen Q, Li K, Liu W, Xu Y, Zhou P, Wei Z, Zhang Z, Cao Y, He X, Wu H
Human reproduction (Oxford, England) 2024 Nov 1;39(11):2608-2617
Human reproduction (Oxford, England) 2024 Nov 1;39(11):2608-2617
Adenylate kinase phosphate energy shuttle underlies energetic communication in flagellar axonemes.
Wu H, Zhang Y, Li Y, Sun S, Zhang J, Xie Q, Dong Y, Zhou S, Sha X, Li K, Chen J, Zhang X, Gao Y, Shen Q, Wang G, Zha X, Duan Z, Tang D, Xu C, Geng H, Lv M, Xu Y, Zhou P, Wei Z, Hua R, Cao Y, Liu M, He X
Science China. Life sciences 2024 Aug;67(8):1697-1714
Science China. Life sciences 2024 Aug;67(8):1697-1714
Structures of sperm flagellar doublet microtubules expand the genetic spectrum of male infertility.
Zhou L, Liu H, Liu S, Yang X, Dong Y, Pan Y, Xiao Z, Zheng B, Sun Y, Huang P, Zhang X, Hu J, Sun R, Feng S, Zhu Y, Liu M, Gui M, Wu J
Cell 2023 Jun 22;186(13):2897-2910.e19
Cell 2023 Jun 22;186(13):2897-2910.e19
CFAP70 is a solid and valuable target for the genetic diagnosis of oligo-astheno-teratozoospermia in infertile men.
Jin HJ, Wang JL, Geng XY, Wang CY, Wang BB, Chen SR
EBioMedicine 2023 Jul;93:104675
EBioMedicine 2023 Jul;93:104675
LRRC23 truncation impairs radial spoke 3 head assembly and sperm motility underlying male infertility.
Hwang JY, Chai P, Nawaz S, Choi J, Lopez-Giraldez F, Hussain S, Bilguvar K, Mane S, Lifton RP, Ahmad W, Zhang K, Chung JJ
eLife 2023 Dec 13;12
eLife 2023 Dec 13;12
Differential requirements of IQUB for the assembly of radial spoke 1 and the motility of mouse cilia and flagella.
Zhang X, Xiao Z, Zhang J, Xu C, Liu S, Cheng L, Zhou S, Zhao S, Zhang Y, Wu J, Wang Y, Liu M
Cell reports 2022 Nov 22;41(8):111683
Cell reports 2022 Nov 22;41(8):111683
Bi-allelic variants in human TCTE1/DRC5 cause asthenospermia and male infertility.
Zhou S, Wu H, Zhang J, He X, Liu S, Zhou P, Hua R, Cao Y, Liu M
European journal of human genetics : EJHG 2022 Jun;30(6):721-729
European journal of human genetics : EJHG 2022 Jun;30(6):721-729
Loss of DRC1 function leads to multiple morphological abnormalities of the sperm flagella and male infertility in human and mouse.
Zhang J, He X, Wu H, Zhang X, Yang S, Liu C, Liu S, Hua R, Zhou S, Zhao S, Hu F, Zhang J, Liu W, Cheng H, Gao Y, Zhang F, Cao Y, Liu M
Human molecular genetics 2021 Oct 13;30(21):1996-2011
Human molecular genetics 2021 Oct 13;30(21):1996-2011
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