- 法国vilber凝胶&化学发光成像系统 360实验室
- John Morgan:黎曼几何、曲率、Ricci流以及在三...
- QPOD Element终端精制器网
- 常德市畜牧水产事务中心仪器采购项目(第二次) 常德市政府采...
- Cancer discovery:一基因突变可增强癌细胞对药...
- 北航网络实验室首页
- 浙大再现“黑科技”!3D打印迷你器官不再是梦!_细胞形
- Waters液相色谱柱,Waters液相色谱柱现货北京科益恒...
- Yeast Nuclear Extract (Small S...
- Gen5 数据分析软件杭州生科仪器有限公司
- 双链DNA探针随机引物合成法资讯
- 果糖胺的疑问 临床检验医学讨论版论坛
- [07-21]线粒体提取试剂盒
- [10-12]第二代测序原理的详细解析!
- [07-27]建库试剂盒怎么选择?
- [10-12]nextseq500简易操作流程
- [10-12]肺癌靶向药基因测序需要多长时间
- [08-05]一种与乳腺癌辅助诊断相关的位于X染色体上的循环miRNA标志物及其...
- [10-12]靶向深度测序和单细胞基因测序的区别
- [09-15]【求助】组织切片提DNA
- [07-26]EGFR和KRAS基因检测意义
Whole Cell Extracts
WholeCellExtracts REFERENCE:Hoffman,G.,Garrison,T.R.,andDohlman,H.G.,AnalysisofRGSproteinsinSaccharomycescerevisiae,MethodsEnzymol.344:617-631,2002. -Usesteriletechniqueandsterilesolutionsinsteps1to3.- 1.Usingasaturatedstarterculture,inoculate25to30mlofappropriatemediaina125mlflask. ***Sinceitisoftendifficulttoestimatethegrowthrateofyeast,itishelpfultostartseveral25mlcultures,eachwithadifferentdilutionofthestarterculture(e.g.1:100,1:300,1:900). 2.Growat30Cshaking(250rpm)untiltheOD600nm~1.0(Thisisusuallydoneovernight). ***Whengrowingseveralstrainsatonce,itislikelythattheywillallreachOD600nm~1.0atdifferenttimes.Ifdesired,sodiumazide(1Mstockinwater,dilutedtoafinalconcentrationof10mM)canbeaddedtoacultureonceitreachesanOD600nm~1.0.Theculturecanthenbeplacedoniceuntiltheothersareready. 3.Transfertoa50mlconicaltubeandcentrifugefor10minat2000xgat4C. 4.ResUSPendeachsamplein1mlof10mMsodiumazideandplaceonice. 5.CalculatethevolumeofresuspendedcellsthatwouldtranslatetoanOD600nmreADIngof10.Forexample,thiswouldequal1mlif10mlofcultureatOD600nm=1.0hadbeencentrifugedandresuspended. ***Thisstepisnecessarytoequalizetheamountofcells(andprotein)inagivenvolumeofwholecellextract. 6.Transferthecalculatedvolumeofresuspendedcellstoamicrofugetubeandcentrifugeat16,000xgfor1min. 7.Aspiratethesupernatent. 8.Resuspendthepelletin200ulof1XSDS-PAGEsamplebuffer. 9.Immediatelyplaceina100Cheatblockfor10min. 10.Allowthetubetocoolandadd200ulofglassbeads(Sigma,#G-8772). 11.Vortexathighspeedfor2min.Invertafterthefirstmin. ***Severaltubescanbevortexedatthesametimebyusingafoamtubefloatertoholdthemtogether. 12.Usinga21gaugeneedle,pokeaholeinthebottomofeachtubeandplaceitintoanewmicrofugetube. 13.Centrifugeat2000xgfor10sectoexpeltheliquidintothebottomtube,leavingtheglassbeadsinthetoptube. 14.Discardtheglassbeadsandcentrifugethebottomtubeat16,000xgfor2min.Thissedimentsanyinsolublematerial. 15.Transferthesupernatanttoanewmicrofugetube.Storeat-20C. 16.Whenreadytouse,heatat37Cfor10min,vortex,andcentrifugeat16,000xgfor1min. ***Keepinmindthatrepeatedfreezingandthawingcandegradetheproteinsample. 17.Immunoblotscanbeperformedusingstandardmethods. Updated01/23/02
================ 蚂蚁淘在线 ================
免责声明:本文仅代表作者个人观点,与本网无关。其创作性以及文中陈述文字和内容未经本站证实,对本文以及其中全部或者部分内容、文字的真实性、完整性、及时性本站不做任何保证或承诺,请读者仅作参考,并请自行核实相关内容
版权声明:未经蚂蚁淘在线授权不得转载、摘编或利用其他方式使用上述作品。已经经本网授权使用作品的,应该授权范围内使用,并注明“来源:蚂蚁淘在线”。违反上述声明者,本网将追究其相关法律责任。

