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[Preparation and identification of the polyclonal antibody against ATRX-C2193-2492].
Tang, Shuangyang; Liu, Zhimin; Li, Ranhui; Chen, Yan; Zhao, Lanhua; Shen, Haiyan; Wan, Yanping.
Afiliación
  • Tang S; Hunan Provincial Key Laboratory for Special Pathogens Prevention and Control, Institute of Pathogenic Biology, University of South China, Hengyang 421001, China.
  • Liu Z; Hunan Provincial Key Laboratory for Special Pathogens Prevention and Control, Institute of Pathogenic Biology, University of South China, Hengyang 421001, China.
  • Li R; Hunan Provincial Key Laboratory for Special Pathogens Prevention and Control, Institute of Pathogenic Biology, University of South China, Hengyang 421001, China.
  • Chen Y; Second Affiliated Hopsital, University of South China, Hengyang 421001, China.
  • Zhao L; Hunan Provincial Key Laboratory for Special Pathogens Prevention and Control, Institute of Pathogenic Biology, University of South China, Hengyang 421001, China.
  • Shen H; Hunan Provincial Key Laboratory for Special Pathogens Prevention and Control, Institute of Pathogenic Biology, University of South China, Hengyang 421001, China.
  • Wan Y; Hunan Provincial Key Laboratory for Special Pathogens Prevention and Control, Institute of Pathogenic Biology, University of South China, Hengyang 421001, China. *Corresponding author, E-mail: wanyy1991@aliyun.com.
Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi ; 33(4): 536-539, 2017 Apr.
Article en Zh | MEDLINE | ID: mdl-28395727
ABSTRACT
Objective To prepare the polyclonal antibody against human alpha thalassemia/mental retardation syndrome X-linked (ATRX) C-terminal and study the distribution and expression of ATRX protein in human cervical cancer tissues. Methods The antiserum was obtained from the BALB/c mice immunized with 6His-ATRX-C2193-2492 protein and then purified by the saturated ammonium sulfate precipitation and affinity chromatography. The titer of anti-ATRX polyclonal antibody was determined by ELISA. Its specificity was identified by SDS-PAGE analysis and Western blotting. The expression and location of ATRX in human cervical tissues were analyzed by immunohistochemistry. Results The titer of the polyclonal antibody against 6His-ATRX-C2193-2492 protein was about 112 800. The antibody could recognize 6His-ATRX-C2193-2492 protein specifically. With the polyclonal antibody, the target protein was found mainly in the nucleus of para-carcinoma tissues, and it was also expressed in the nucleus of cervical cancer tissue cells, but the expression in the latter was obviously lower. Conclusion The polyclonal antibody against 6His-ATRX-C2193-2492 protein has been produced successfully and used to detect ATRX protein in human cervical cancer tissues.
Asunto(s)
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Bases de datos: MEDLINE Asunto principal: Proteínas Nucleares / Talasemia alfa / ADN Helicasas / Discapacidad Intelectual Ligada al Cromosoma X / Anticuerpos Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Animals / Female / Humans Idioma: Zh Revista: Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi Asunto de la revista: ALERGIA E IMUNOLOGIA Año: 2017 Tipo del documento: Article País de afiliación: China
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Bases de datos: MEDLINE Asunto principal: Proteínas Nucleares / Talasemia alfa / ADN Helicasas / Discapacidad Intelectual Ligada al Cromosoma X / Anticuerpos Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Animals / Female / Humans Idioma: Zh Revista: Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi Asunto de la revista: ALERGIA E IMUNOLOGIA Año: 2017 Tipo del documento: Article País de afiliación: China