Peasy t1
WebpEASY ® - T1 Simple Cloning Vector eliminates the multi-cloning sites of pEASY ®-T1 Cloning Vector. It is designed for cloning and sequencing Taq-amplified PCR products. •5 … WebM-Wave Drag-T1 M-Wave Drag-T2 M-Wave Peasy; Zum Angebot * x Wir verlinken auf ausgewählte Online-Shops und Partner, von denen wir ggf. eine Vergütung erhalten. Zwischenzeitliche Änderung der Preise, Lieferzeit und -kosten möglich. Preise inkl. MwSt, ggf. zzgl. Versand. Wenn Sie eine ältere Version des Vergleichs aufrufen oder ansehen ...
Peasy t1
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WebMar 15, 2024 · Purified PCR products were cloned and constructed pEASY-T1-CGMMV, pEASY-T1- A. citrulli, and pEASY-T1- EF-1α (540-bp) plasmid by using a pEASY-T1 Simple Cloning Kit (TransGen Biotech, Beijing, China), respectively. WebpEASY® -T1 Cloning Kit Catalog Number:CT101-01 Price:$89.02 Specification: 20 rxns 60 rxns Quantity: Manual Vector Information MSDS COA Inquire Now Buy Now Add to …
WebApr 6, 2024 · All PCR products were separated on a 1.2% agarose gel, and the target bands were purified and then ligated into the pEASY-T1 vector (TransGen, Beijing, China). The PCR products were sequenced by Sangon Biotech (Shanghai, China) [ 25 ]. WebpEASY-T1 Simple (linearized) TA cloning vector suitable for blue-white selection, with kanamycin and ampicillin resistance markers and a T7 promoter but no multiple cloning …
WebJun 15, 2014 · The PCR product was purified and cloned into pEASY-T1 vector and transformed into E. coli DH5α. Positive clones were identified and verified by sequencing pEASY-T1-GFA1 with M13 primers (Transgen Biotech, Beijing, China) and comparison with the GFA1 sequence database. pEASY-T1 (linearized) TA cloning vector suitable for blue-white selection, with kanamycin and ampicillin resistance markers and a T7 promoter. Sequence Author: TransBionovo (TransGen Biotech) Open in SnapGene Try SnapGene for Free Download Plasmid Download SnapGene Viewer Explore Over 2.7kPlasmids:Basic Cloning Vectors More Plasmid Sets No matches
WebpEASY® -Blunt E1 Expression Vector is constructed from pET vector, it utilizes a highly efficient, five-minute blunt cloning strategy to clone PCR product into high-efficient expression vector. The size of control insert is 750 bp, and expressed target protein is about 27 kDa. • 5 minutes fast ligation of Pfu-amplified PCR products.
WebPeasy T1 Simple Cloning Vector, supplied by TransGen biotech co, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, … hr block rochester hills miWebJan 31, 2014 · The EcoR I/Not I digested fragments of pEASY-T1-ADH1B were ligated with pPICZB, resulting in pPICZB-ADH1B. The recombined plasmid was transfected by electroporation of Pichia pastoris. Enzyme purification and assays. Cells were harvested by centrifugation and washed with 50 mM Tris–HCl, pH8.0 (buffer A). The cell paste was … hr block rockaway nj phoneWebConstruction of Clone Vectors pEASY-T1-2f PF4 and pEASY-T1-3f PF4. Source publication Polycistronic Expression of Human Platelet Factor 4 with Heparin-Neutralizing Activity in … hr block rohnert park caWebpEASY® -T1 Simple Cloning Kit Catalog Number:CT111-01 Price:$97.24 Specification: 20 rxns 60 rxns Quantity: Manual Vector Information MSDS COA Inquire Now Buy Now … hr block rollover access errorWebApr 12, 2024 · The first PCR product and the intermediate vector pEASY-T1-intron were digested by Sac I and Spe I, and then ligated after gel purification. The recombinant plasmid was transformed into DH5α, verified by double digestion with Hin d III and Eco R V, and then confirmed by sequencing. hrblock roth ira backdoorWebMar 2, 2024 · The amplified GhGT23 fragment was subcloned into pEASY-T1 (TransGen Biotech, Beijing, China), thereby creating pEASY-T1::GhGT23. Flanking BamHI and SalI restriction sites were then used to cut GhGT23 from pEASY-T1::GhGT23, followed by ligation into the pBI21, pBin438, pGAL4 DBD, and pGEX6p-1 expression vectors. hr block rockford ilWebJan 30, 2015 · The amplified DNA was purified using an AxyPrep DNA gel extraction kit (Axygen), inserted into the pEASY -T1 Cloning Vector (TransGen, Beijing, China) and transformed into E. coli Trans 1-T1 competent cells (TransGen, Beijing, China). Positive clones were analyzed by PCR using vector-specific primers. hr block rogers city mi