相关文章
- 自定义路由改进 · Issue #47 ·...
- Watson Pharma Pvt Ltd进口数据及联系方式
- raykim0421的个人空间 ( ゜ ゜)つロ 乾杯~...
- 甲状腺球蛋白(tg)的在甲状腺癌复查中的重要作用_健康号微医
- 新产品jetCRISPR™——用于基因编辑的RNP转染试剂
- 人分泌性白细胞蛋白酶抑制因子(SLPI) ELISA试剂盒
- VF6SS立式加工中心,立式加工中心配置哈斯自动数控机械(上...
- 纤维样细胞特效转染试剂 GenoFect GF010303报...
- Suppliers Matching perstorp (P...
- 公司介绍_江苏普诺生生物科技有限公司_
- 哪儿可以买到质量较好的聚苯乙烯(PS)微球或者SiO2微球?...
- 转染试剂选择指南 | Thermo Fisher Scien...
促销商品
最新问答
- [08-06]【求助】哪种方法转染293T细胞的效率较高 细胞技术讨论版 ...
- [10-02][求助]转染后细胞都死了是怎么回事啊? 经验共享 分析测试百科
- [07-30]基因转染实验(脂质体介导DNA转染法) 实验方法
- [07-24]细胞转染几天后就死亡,是什么原因?_问答详情_细胞转染_细胞研究_...
- [02-13][求助]细胞转染 经验共享
- [07-28]电转染实验时,DNA有什么要求?
- [10-02]转染6孔板后,怎么收集我的细胞,然后提蛋白
- [08-16]细胞转染为什么不能加血清
- [07-19]怎样解决RAW264.7转染效率低的问题?
热卖商品
High Efficency Yeast Plasmid Rescue
- Growyeastovernight.
- Spindown1.5mlofcultureinmicrofugetubes.
- Decant.
- Add250µlofQiagenbufferP1andabout250µlofglassbeadstoeachtube.
- Beatorvortexonhighfor3-5minutes.
- Add250µlofbufferP2andgentlymixwell(Donotletlysisreactioncontinueformorethanfiveminutes).
- Add350µlofbufferN3andmiximmediately,butgently.
- Centrifugefor10minutesonfullblast.
- ApplysupernatantstoQIAprepspincolumn.
- Centrifugecolumnfor45secondsonfullblast.Discardflow-though.
- Washcolumnwith750µlofBufferPEandcentrifuge45seconds.
- Discardflowthroughandspinforanadditional45seconds.
- Placecolumninacleantubeandadd50µlofbufferEB.
- Letsitfor1min.thenspinfor1min.
- Forefficenttransformationintocoliuse1-2µlofthisprepperaliquotofE.coliusingthe90secheatshockprotocol.(NOTE:usingupto20µlwillincreaseyieldoftransformants)
ColonyPlasmidRescue
ProtocoladaptedbyJuliaSidorovaandLindaBreedenfromHoffmanandWinston,Gene,1987,Vol.57:267-272.
- Startwithafreshplateofyeast,withlargecoloniesgrownfor3-4days.
- PrepareEppendorfswith20µlaqueousbuffer(2%TritonX-100,1%SDS,100mMNaCl,10mMTris-HClpH8.0,1mMEDTApH8.0).
- PickcoloniesfromplatewithaPipettetipandresUSPendintheaqueousbuffer.Note:LablorerecommendsNOTusingatoothpicktopickyourcolony.Thereissomethingevilintoothpicksthatinhibitsbacterialtransformations.
- Add10µlphenoland10µlchloroform(or20µlphenol:chloroform)toeacheppendorftube.
- Add1/3eppendorfcap(0.65mltube)ofglassbeads.
- Vortex5min.atspeedof4-5inmultiheadvortexeratroomtemperature.
- Spinfor5min.atmaximumspeedinamicrocentrifuge.
- ThawtransformationcompetentE.colicellsonice.
- Intesttubes(formicrofugetubesseebelow;otherwiseuse14-mlsnap-captube)oniceadd:a)1µlaqueousphase(ifyouexperiencelowyield,tryusingmore)b)120µlcompetentcells
- Mixandincubateonicefor30min.
- Heatshockfor90secat42degC,thenimmediatelyadd2mlofNZYbrothtoeachtesttube.(LBwillalsowork,thoughrichermediaisusuallybetter)
- Shakegentlyat37degCfor1hr.(Ifusingmicrofugetubes,rotateat37°Cinrollerdrum)
- Pelletcellsfor5min.at3krpmintabletopcentrifuge.
- Pouroffthesupernatant,resuspendthepelletintheresidualliquid,andplatetheentiresuspensiononselectivemedium.
================ 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。