DNA Ladder

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Get tips on using EpiTect 96 Bisulfite Kit (2) to perform Bisulfite DNA Modification Fluids

Products Qiagen EpiTect 96 Bisulfite Kit (2)

Get tips on using Qubit dsDNA HS Assay Kit to perform DNA quantification Human - MCF10A

Products Thermo Fisher Scientific Qubit dsDNA HS Assay Kit

Get tips on using Qubit dsDNA HS Assay Kit to perform DNA quantification Human - BJ

Products Thermo Fisher Scientific Qubit dsDNA HS Assay Kit

Get tips on using Qubit dsDNA HS Assay Kit to perform DNA quantification Human - BMDM

Products Thermo Fisher Scientific Qubit dsDNA HS Assay Kit

Get tips on using 7-AAD (7-Aminoactinomycin D) to perform DNA quantification Human - BMDM

Products Thermo Fisher Scientific 7-AAD (7-Aminoactinomycin D)

Get tips on using Qubit dsDNA HS Assay Kit to perform DNA quantification Human - HeLa

Products Thermo Fisher Scientific Qubit dsDNA HS Assay Kit

Get tips on using Qubit dsDNA HS Assay Kit to perform DNA quantification Brain tissue

Products Thermo Fisher Scientific Qubit dsDNA HS Assay Kit

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 Enterobacteriaceae

Get tips on using CometAssay Electrophoresis System II to perform DNA Damage Assay Human Skin Fibroblast Cell (FSK)

Products Bio-Techne CometAssay Electrophoresis System II

Get tips on using CometChip Electrophoresis Starter Kit to perform DNA Damage Assay Human bronchial epithelial cells (hBE)

Products Bio-Techne CometChip Electrophoresis Starter Kit

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