DNA methylation profiling Whole genome profiling

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Get tips on using One-step TUNEL Assay Kit to perform DNA Damage Assay HEK 293T

Products Elabscience One-step TUNEL Assay Kit

Get tips on using CometAssay Single Cell Gel Electrophoresis Assay to perform DNA Damage Assay MCF7

Products Bio-Techne CometAssay Single Cell Gel Electrophoresis Assay

Get tips on using CometAssay Single Cell Gel Electrophoresis Assay to perform DNA Damage Assay HT1080

Products Bio-Techne CometAssay Single Cell Gel Electrophoresis Assay

Get tips on using CometAssay Single Cell Gel Electrophoresis Assay to perform DNA Damage Assay HeLa

Products Bio-Techne CometAssay Single Cell Gel Electrophoresis Assay

Get tips on using CometAssay Single Cell Gel Electrophoresis Assay to perform DNA Damage Assay A549

Products Bio-Techne CometAssay Single Cell Gel Electrophoresis Assay

Get tips on using CometAssay Single Cell Gel Electrophoresis Assay to perform DNA Damage Assay U266

Products Bio-Techne CometAssay Single Cell Gel Electrophoresis Assay

Get tips on using CometAssay Single Cell Gel Electrophoresis Assay to perform DNA Damage Assay U266 -

Products Bio-Techne CometAssay Single Cell Gel Electrophoresis Assay

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 DNeasy Blood & Tissue Kit to perform DNA isolation / purification Bacteria - Gram positive piezophilic bacteria [AT7 and AT12 Strains]

Products Qiagen DNeasy Blood & Tissue Kit
JetPrime Product

Get tips on using JetPrime to perform DNA transfection Mammalian cells - Immortalized cell lines HeLa

Products Polyplus transfections JetPrime

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