Site Directed Mutagenesis (SDM) Rat Deletion H9C2

- Found 5748 results

Get tips on using iScript™ Reverse Transcription Supermix for RT-qPCR to perform

Products Bio-Rad Laboratories iScript™ Reverse Transcription Supermix for RT-qPCR

Get tips on using BH ladder :: GD OneMARK B RTU Ladder to perform DNA Ladder 1 kb

Products MyBioSource.com BH ladder :: GD OneMARK B RTU Ladder

Get tips on using GD 1Kb Plus DNA Ladder RTU Ladder to perform DNA Ladder 1 kb

Products MyBioSource.com GD 1Kb Plus DNA Ladder RTU Ladder

Get tips on using QuantiNova Probe RT-PCR Kit (2500) to perform PCR Quantitative real-time PCR - Viral

Products Qiagen QuantiNova Probe RT-PCR Kit (2500)

Get tips on using QuantiTect Multiplex RT-PCR NR Kit (1000) to perform PCR Multiplex PCR - Viral

Products Qiagen QuantiTect Multiplex RT-PCR NR Kit (1000)

Get tips on using QuantiTect Probe RT-PCR Kit (1000) to perform PCR Quantitative real-time PCR - Viral

Products Qiagen QuantiTect Probe RT-PCR Kit (1000)

Get tips on using iScript™ Reverse Transcription Supermix for RT-qPCR to perform cDNA synthesis Bacteria

Products Bio-Rad Laboratories iScript™ Reverse Transcription Supermix for RT-qPCR

Plasmid isolation is an important technique in molecular biology or any kind of genetic editing. It involves amplifying plasmids overnight by transforming them into competent bacterial cells. The desired colonies of these bacteria can then be grown in shaker cultures, at appropriate shaking speed, oxygen availability and temperature. These liquid cultures can then be ultracentrifuged to pellet the bacteria, which are then used for plasmid isolation. The bacteria are first resuspended in a buffer, then lysed, neutralized, purified in a column, eluted, precipitated with ethanol and then resuspended. During plasmid isolation, it is important to lyse cells quickly because lysing bacteria for too long may lead to irreversible denaturing of the plasmid. Usually, alkaline lysis is used for isolation because it is a mild treatment. It isolates plasmid DNA and other cell components such as proteins by breaking cells apart with an alkaline solution. Precipitation removes the proteins, and the plasmid DNA recovers with alcohol precipitation. Resuspension and lysis buffers should be mixed thoroughly in order to prevent the DNA from breaking into smaller fragments. This is because broken gDNA can reanneal and remain in the solution, without binding to the column.

DNA Plasmid Isolation Bacillus smithii

Get tips on using BH50bp ladder :: GD 50bp DNA Ladder RTU Ladder to perform DNA Ladder 50 bp

Products MyBioSource.com BH50bp ladder :: GD 50bp DNA Ladder RTU Ladder

Get tips on using QuantiNova SYBR Green RT-PCR Kit (2500) to perform PCR Quantitative real-time PCR - Viral

Products Qiagen QuantiNova SYBR Green RT-PCR Kit (2500)

Outsource your experiment

Fill out your contact details and receive price quotes in your Inbox

  Outsource experiment
Become shareholder Discussions About us Contact Privacy Terms