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时间:2020-05-20
《小鼠附睾特异性辅脂酶的原核表达及其抗体的制备.pdf》由会员上传分享,免费在线阅读,更多相关内容在行业资料-天天文库。
1、第31卷第2期暨南大学学报(医学版)VO1.31No.22010年4月JounlalofJinanUniversity(MedicineEdition)Apr.2010小鼠附睾特异性辅脂酶的原核表达及其抗体的制备关艺青,禹艳红,黄丹,潘善培(暨南大学生命科学技术学院生殖免疫研究所,广东广州510632)[摘要]目的:利用原核表达系统重组表达小鼠附睾特异性辅脂酶(meClps),并制备抗meClps抗体。方法:通过生物信息分析meClps蛋白结构,Oligo6设计引物,PCR法从小鼠附睾eDNA中扩增胱C全长序列并克隆到pMD19一T载体中。将含脚c序列pMD19一T载体通过PC
2、R扩增成熟肽区段序列,重组到pET-21b原核表达载体上,经菌落PCR及测序鉴定后,转化到表达菌株EcoliBL21(DE3),经IPTG诱导蛋白表达后用Trieine.SDS.PAGE和Westernblotting检测重组meClps的表达。包涵体沉淀经浓度为2mol/L尿素洗涤,Trieine.SDS.PAGE分离、染色、脱色,切下目的条带用生理盐水浸泡、磨碎与弗氏佐剂混合后免疫新西兰大白兔获取免疫血清,Westernblotting检测抗体与meClps反应。结果:在原核表达系统成功重组表达meClps,目的蛋白主要以包涵体形式存在,制备了高效价的兔抗meClps抗体。
3、结论:成功建立meClps的原核表达系统和获得兔抗meClps抗体。[关键词]附睾;辅脂酶;原核表达;抗体[中图分类号】R715.2[文献标志码】A[文章编号】1000—9965(2010)02—0105—06Prokaryoticexpressionofmouseepididymis-specificcolipaseandpreparationofitsantibodyGUANYi—qing,YUYan—hong,HUANGDan,PANShan—pei(InstituteofReproductiveImmunology,ColegeofLifeScienceandTechn
4、ology,JinanUniversity,Guangzhou510632,P.R.China)[Abstract]Ainl:Toexpressmouseepididymis—specificcolipase(meClps)inpmkaryoticsystemandpreparetheanti—meClpsantibody.Methods:ThemeClpsproteinstructurewasanalysedbyusingbioin—formation,andprimersweredesignedwithOligo6.Thefull—lengthofmeClpswasampl
5、ifiedfrommouseepididymalcDNAandclonedintopMD]9一Tvector.ThesequenceofmaturepeptidewasobtainedbyPCRfrompMD19一TvectorwithmeClps.Thentheproductwasrecombinedintothepmkaryoticexpressionvec—torpET-21b.TherecombinantplasmidwasidentifiedbyclonePCRandsequencingbefore~ansformationintocoliBL21(DE3).Afte
6、rinducedbyIPTG,therecombinantmeClpsproteinwasexpressedandsepreatedbyTrieine—SDS—PAGE,andthenidentifiedbyWesternblotting.Theinclusionbodieswerewashedwith2mol/LureaandsepreatedbyTricine—SDS—PAGE.Afterstaininganddestaining,thegelcontainingmeClpsproteinwascut,equilibratedwithphysiologicalsalines
7、olution,rubbed,andemulsi—fledwithFreundadjuvant,thenusedasantigentoimmunizerabbitandprepareantibodies.Theanti-meClpsantibodyresponsewasidentifiedbyWesternblotting.Results:ThemeClpsproteinwassuccess-fullyexpressedinprokaryoticsystem.butmainlyininclu
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