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作 者:Xiaoyan Sheng Chenglei Tian Linlin Liu Lingling Wang Xiaoying Ye Jie Li Ming Zeng Lin Liu
机构地区:[1]State Key Laboratory of Medicinal Chemical Biology,College of Life Sciences,Nankai University,Tianjin 300071,China [2]Department of Cell Biology and Genetics,College of Life Sciences,Nankai University,Tianjin 300071,China
出 处:《Protein & Cell》2020年第12期928-930,共3页蛋白质与细胞(英文版)
摘 要:Figure 2.Neo-meiosis and functional test of oocytes developed from Fragilis*cells.(A)Immunofluorescenee of SCP1(red)and SCP3(green,appear as yellowish by merge with SCP1)showing pachytene spread of E12.5 Fragilis*cells obtained from aggregates with fetal E12.5 somatic cells 6 days following transplantation,compared with those of E17.5 ovaries.Right panel,Percentage of synaptonemal complex elements based on count of spread at pachytene(n-22).Scale bar=5 pm.(B)Representative immunofluorescence of MLH1 foci at pachytene stage by co-immunostaining of SCP3(red)and MLH1(green).Right panel,Statistics of MLH1 foci represents 20 spread per each group.
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