Anti SPEF2 pAb (ATL-HPA040343 w/enhanced validation)

Atlas Antibodies

Catalog No.: ATL-HPA040343-25

Protein Description: sperm flagellar 2
Gene Name: SPEF2
Alternative Gene Name: CT122, FLJ23577, KPL2
Isotype: IgG
Interspecies mouse/rat: ENSMUSG00000072663: 88%, ENSRNOG00000058275: 91%
Entrez Gene ID: 79925
Uniprot ID: Q9C093
Buffer: 40% glycerol and PBS (pH 7.2). 0.02% sodium azide is added as preservative.
Storage Temperature: Store at +4°C for short term storage. Long time storage is recommended at -20°C.

Product Specifications

• Application: IHC
• Reactivity: Human
• Clonality: Polyclonal
• Host: Rabbit
• Immunogen: LGTITFEQYMQAGLWFTGDEDIKIPENPLEPLPFNRQEHLIEFFFRLFADYEKDPPQLDYTQMLLYFACHPDTVEGVYRALSVAVGTHVFQQVKA
• Gene Sequence: LGTITFEQYMQAGLWFTGDEDIKIPENPLEPLPFNRQEHLIEFFFRLFADYEKDPPQLDYTQMLLYFACHPDTVEGVYRALSVAVGTHVFQQVKA
• Gene ID - Mouse: ENSMUSG00000072663
• Gene ID - Rat: ENSRNOG00000058275
• Buffer: 40% glycerol and PBS (pH 7.2). 0.02% sodium azide is added as preservative.

Citations for Anti SPEF2 pAb (ATL-HPA040343 w/enhanced validation) – 7 Found

Coutton, Charles; Martinez, Guillaume; Kherraf, Zine-Eddine; Amiri-Yekta, Amir; Boguenet, Magalie; Saut, Antoine; He, Xiaojin; Zhang, Feng; Cristou-Kent, Marie; Escoffier, Jessica; Bidart, Marie; Satre, Véronique; Conne, Béatrice; Fourati Ben Mustapha, Selima; Halouani, Lazhar; Marrakchi, Ouafi; Makni, Mounir; Latrous, Habib; Kharouf, Mahmoud; Pernet-Gallay, Karin; Bonhivers, Mélanie; Hennebicq, Sylviane; Rives, Nathalie; Dulioust, Emmanuel; Touré, Aminata; Gourabi, Hamid; Cao, Yunxia; Zouari, Raoudha; Hosseini, Seyedeh Hanieh; Nef, Serge; Thierry-Mieg, Nicolas; Arnoult, Christophe; Ray, Pierre F. Bi-allelic Mutations in ARMC2 Lead to Severe Astheno-Teratozoospermia Due to Sperm Flagellum Malformations in Humans and Mice. American Journal Of Human Genetics. 2019;104(2):331-340. 

Dong, Frederick N; Amiri-Yekta, Amir; Martinez, Guillaume; Saut, Antoine; Tek, Julie; Stouvenel, Laurence; Lorès, Patrick; Karaouzène, Thomas; Thierry-Mieg, Nicolas; Satre, Véronique; Brouillet, Sophie; Daneshipour, Abbas; Hosseini, Seyedeh Hanieh; Bonhivers, Mélanie; Gourabi, Hamid; Dulioust, Emmanuel; Arnoult, Christophe; Touré, Aminata; Ray, Pierre F; Zhao, Haiqing; Coutton, Charles. Absence of CFAP69 Causes Male Infertility due to Multiple Morphological Abnormalities of the Flagella in Human and Mouse. American Journal Of Human Genetics. 2018;102(4):636-648. 

Moye, Abigail R; Bedoni, Nicola; Cunningham, Jessica G; Sanzhaeva, Urikhan; Tucker, Eric S; Mathers, Peter; Peter, Virginie G; Quinodoz, Mathieu; Paris, Liliana P; Coutinho-Santos, Luísa; Camacho, Pedro; Purcell, Madeleine G; Winkelmann, Abbie C; Foster, James A; Pugacheva, Elena N; Rivolta, Carlo; Ramamurthy, Visvanathan. Mutations in ARL2BP, a protein required for ciliary microtubule structure, cause syndromic male infertility in humans and mice. Plos Genetics. 2019;15(8):e1008315. 

He, Xiaojin; Liu, Chunyu; Yang, Xiaoyu; Lv, Mingrong; Ni, Xiaoqing; Li, Qiang; Cheng, Huiru; Liu, Wangjie; Tian, Shixiong; Wu, Huan; Gao, Yang; Yang, Chenyu; Tan, Qing; Cong, Jiangshan; Tang, Dongdong; Zhang, Jingjing; Song, Bing; Zhong, Yading; Li, Hang; Zhi, Weiwei; Mao, Xiaohong; Fu, Feifei; Ge, Lei; Shen, Qunshan; Zhang, Manyu; Saiyin, Hexige; Jin, Li; Xu, Yuping; Zhou, Ping; Wei, Zhaolian; Zhang, Feng; Cao, Yunxia. Bi-allelic Loss-of-function Variants in CFAP58 Cause Flagellar Axoneme and Mitochondrial Sheath Defects and Asthenoteratozoospermia in Humans and Mice. American Journal Of Human Genetics. 2020;107(3):514-526. 

Tan, Chen; Meng, Lanlan; Lv, Mingrong; He, Xiaojin; Sha, Yanwei; Tang, Dongdong; Tan, Yaqi; Hu, Tongyao; He, Wenbin; Tu, Chaofeng; Nie, Hongchuan; Zhang, Huan; Du, Juan; Lu, Guangxiu; Fan, Li-Qing; Cao, Yunxia; Lin, Ge; Tan, Yue-Qiu. Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and mice. American Journal Of Human Genetics. 2022;109(1):157-171. 

Cho, Jung Hoon; Li, Zipeng A; Zhu, Lifei; Muegge, Brian D; Roseman, Henry F; Lee, Eun Young; Utterback, Toby; Woodhams, Louis G; Bayly, Philip V; Hughes, Jing W. Islet primary cilia motility controls insulin secretion. Science Advances. 2022;8(38):eabq8486. 

Yu, Hui; Shi, Xiao; Shao, Zhongmei; Geng, Hao; Guo, Senzhao; Li, Kuokuo; Gu, Meng; Xu, Chuan; Gao, Yang; Tan, Qing; Duan, Zongliu; Wu, Huan; Hua, Rong; Guo, Rui; Wei, Zhaolian; Zhou, Ping; Cao, Yunxia; He, Xiaojin; Li, Liang; Zhang, Xiaoping; Lv, Mingrong. Novel HYDIN variants associated with male infertility in two Chinese families. Frontiers In Endocrinology. 14( 36742411):1118841.