Plko.1 – trc cloning vector
WebbpLKO.1 价格: 1500元 联系方式: I47-825O-882O 相关技术服务: 质粒构建 基因合成 质粒大提 立刻购买 买家导航 载体基本信息 载体图谱质粒图谱和多克隆位点信息 载体简介 载体序列 LOCUS pLKO.1 8901 bp ds-DNA circular SYN 08-JAN-2014 DEFINITION Stuffer-containing lentiviral vector for expression of shRNA. This plasmid is the official TRC … WebbHere, the ‘stuffer’ sequence of the pLKO.1-TRC cloning vector was excised in exchange for a constructed shRNA insert targeting CDK12. Lentiviral particles were produced, carrying these modified pLKO.1- TRC plasmids, and transfected into the MDA-MB-231 breast cancer cell line in an effort to deplete the cells’ expression of CDK12.
Plko.1 – trc cloning vector
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Webb9 okt. 2011 · Incubate cells 5%CO overnight.Although cells should regularly 10%FBS penicillin/streptomycin,cells should 10%FBS without antibiotics streptomycin).Day lateafternoon because transfectionmix should only 12-15hours. polypropylenemicrofuge tubes (do usepolystyrene tubes), make eachtransfection: pLKO.1shRNA plasmid 750 ng … Webb11 feb. 2024 · Methods: The 1.9 kb insertion fragment of the original pLKO.1-TRC cloning vector was excised by digestion with Age I and EcoR I, and the annealing shRNA oligos of mSelK were cloned into the Age I and EcoR I sites to construct pLKO.1-mSelK-shRNA vector. Then the constructed pLKO.1-mSelK-shRNA vector, psPAX2 packaging plasmid …
WebbThe Genetic Perturbation Platform, formerly known as the RNA interference (RNAi) Platform, supports functional investigations of the mammalian genome that can reveal how genetic alterations lead to changes in phenotype. Webb12 juni 2024 · pcdna3.1-myc-hisB PLKO-TRC-cloning-vector pIRES2-EGFP pLVX-shRNA2 lenti MS2-P65-HSF1_Hygro addgene61426 lenti sgRNA(MS2)_puro backbone addgene73795 pcDNA3.1(+) CircRNA Mini Vector addgene60648 pCLucIPZ addgene53222 pGIPZ pJL-TRBO addgene80082 pLSLR addgene51500 pMA2775 addgene46884
WebbshRNA pLKO.1-Puro shRNA pLKO.1-TRC cloning vector shRNA pLVX-shRNA2 shRNA pLKO-Tet-ON 或Tet-pLKO-puro shRNA pHHsi-hU6-GFP-Puro shRNA pSUPER.neo+GFP shRNA pSUPER.neo+GFP-shLUC(对照NC) shRNA pMXs-miR-GFP Puro shRNA pAAV-zsgreen-shRNA(非空载,插入shSnail,酶切位点未破坏) shRNA pLKO.1-GFP-CAMP WebbFeatures of the pLKO.1-puro vector allow for transient or stable transfection of the shRNA as well as production of lentiviral particles. 1 Stable gene silencing is selected using the …
WebbShivam Mishra. I have made repeated attempts to clone shRNA into pLKO vectors, but have not produced any colonies. I have tried annealing the shRNA in a thermocycler, in PCR, and in a water bath ...
WebbA. pLKO.1-TRC Cloning Vector. A.1 The RNAi Consortium. The pLKO.1 cloning vector is the backbone upon which The RNAi Consortium has built a library of shRNAs directed against 15,000 human and 15,000 mouse genes. Addgene is working with the TRC to make this shRNA cloning vector available to the scientific community. i miss you in lithuanianWebbThis is the protocol accompanying the "pLKO.1 – TRC Cloning Vector". For information about the PLKO.1-TRC cloning vector and tips on designing shRNA oligos for pLKO.1... list of record of the year grammy winnersWebbFind the scrambled shRNA vector. pLKO.1 - TRC cloning vector - This vector from the David Root lab is a 3rd generation lentiviral transfer plasmid for cloning and expressing new shRNA sequences. For more information, see the Addgene’s pLKO.1 protocol. Pro-tip: this plasmid grows more slowly than standard plasmids. Find pLKO.1 - TRC cloning ... i miss you in other wordsWebbeISSN 0219-1032 2024 Impact Factor 4.250. Download. Articles. Current Issue On-line First i miss you in shonaWebbThe pLKO.1-puro Control Vector is provided as 10 μg of plasmid DNA in Tris-EDTA (TE) buffer at a concentration of 500 ng/μl. Application MISSION ® pLKO.1-puro Empty … list of recovery slogansWebbIn order to stably knock down RBM3 expression, shRNAs targeting two different positions of RBM3 mRNA were designed and cloned between the Age I and EcoR I restriction sites of the plasmid pLKO.1-TRC (Addgene) cloning vector, forming plasmid pLKO.1-RBM3-shRNA #1 and #2, respectively. i miss you in newariWebb所以今天,我们就来聊一聊shRNA的设计,以sigma家的为例子。. 下图是一个他们家的shRNA的载体,pLKO.1。. 大部分shRNA都由U6驱动。. 和驱动蛋白合成的PoII promoter不同,U6是Pol III promoter,意味着它主要驱动RNA而非蛋白。. 如果想要自己连入一段shRNA的话,需要设计两段 ... i miss you in number code