WebThe obtained PCR product was also digested with DpnI (Thermo Fisher, Waltham, MA, USA) at 37 °C for 1 h. The indicated PTC harboring gB fragment was electro-transformed into SW102-JS-galK as described above. After 3 h at 32 °C, the transformed cells were washed and suspended in an M9 medium. WebThermo Scientific FastDigest快速内切酶试用套装包含13种最常用的FastDigest快速内切酶,涵盖FastDigest EcoR I、Bgl II、Nde I、Sal I、Xba I、Kpn I、Eco32I、Xho I、Not I、BamH I、Hind III、Sma I、Pst I,每种酶可进行20次反应。
DpnI (10 U/µL) - Thermo Fisher Scientific
Webtemplate DNA can be removed by Anza 10 DpnI digestion following PCR (DpnI is fully active in the SuperFi buffer). † Recommended for targets with >65% GC content. or Cycling protocols PCR cycles Step 2-step protocol 3-step protocol Long PCR (>10 kb) Temp. Time Temp. Time Temp. Time 1 Initial denaturation 98°C 30 sec 98°C 30 sec 95°C 2 min ... WebAfter digesting with BamHI and DpnI, the resultant DNA was self-ligated with T4 DNA ligase (Ligation-Convenience kit, Nippon Gene, Tokyo). ... Subsequently, using the Ion 540 Chef Kit on an Ion Chef system (Thermo Fisher Scientific Inc., Waltham, MA, USA), RNA-Seq templates were prepared. Sequencing of the amplicon libraries was performed using ... tsn brier 2022 scores
Fast and efficient site-directed mutagenesis - Thermo …
WebThermo Scientific DpnI restriction enzyme recognizes Gm6A^TC sites and cuts best at 37°C in Tango buffer (isoschizomers: MalI). See Reaction Conditions for Restriction … Thermo Scientific FastDigest DpnI is one of an advanced line of fast restriction … Thermo Scientific DpnI restriction enzyme recognizes Gm6A^TC sites and cuts … TaqMan Real-Time PCR Assays. Antibodies. Oligos, Primers & Probes Web1.A method of inhibiting antibiotic resistance in bacteria comprising modifying a bacterial plasmid gene for antibiotic resistance with a prokaryotic-active genetics (Pro-AG) system comprising: (a) a first plasmid encoding an inducible Cas9 protein; and (b) a second plasmid encoding: (a) a first plasmid encoding an inducible Cas9 protein; and (b) a WebMar 20, 2024 · Mutagenic primers were designed using SnapGene 6.0.2 software (GSL Biotech). PCRs were performed using the SuperFi II Master Mix (Thermo Fisher 12368010), and the products were gel purified using the Machary-Nagel NucleoSpin Gel and PCR Clean-up kit (740609). Amplicons were assembled using the NEB Builder HiFi DNA … ph inc