Gene Editing on Zageno
Gene Editing Kits and Methods
CRISPR (Clustered regularly-interspaced short palindromic repeats) was originally discovered in E. coli during the 1980s.
Gene Silencing refers to a series of molecular biology techniques that reduces the transcription or translation of a gene.
Good gene editing controls are a critical tool for troubleshooting and ensuring that the transfer worked according to plan.
Gene Transfer is the process of inserting a specific coding sequence into a cell, either as a plasmid or as a genomic insert.
Gene Modification refers to numerous molecular biological techniques that can introduce mutations into double stranded DNA.
In vitro transcription is a method which enables you to synthesize RNA in the lab, which can be used for methods such as blot hybridizations.
Clustered regularly interspaced short palindromic repeats (CRISPR) was discovered in a prokaryotic immune defense system against foreign DNA. This technique targets specific genes and interrupts or manipulates these regions of DNA for either gene knockout or gene knock-in.
If you have any problems with your experiments, visit our CRISPR Troubleshoot.
Silencing refers to the suppression of genetic material, preventing the synthesis of proteins. RNA interference for silencing introduces foreign RNA, which binds to messenger RNA to either increase or decrease activity.
If you have any problems with your experiments, visit our Gene Silencing Troubleshoot.
Gene Editing Controls
Given the sensitivity and implications of a faulty gene editing procedure, controls enable researchers to monitor and troubleshoot to see whether the gene transfer worked according to plan.
These controls can be either:
- or Standards
Plasmid transfection is used to assess the function of a specific gene in its cellular context. With transfection and overexpression of a specific gene, researchers can evaluate the workings of that particular gene.
Transduction refers to the use of viral vectors of for genetic transfer, while transformation introduces recombinant plasmids into bacterial cells, which then express the newly acquired genetic material.
If you have any problems with your experiments, visit our Gene Transfer Troubleshoots on our troubleshooting page.
Another application to manually edit DNA is site-directed mutagenesis by PCR-driven overlap extension. This method is used to generate DNA fragments in a way that specific mutations are introduced by the use of overlapping PCR. These fragments can then serve as a primary template for further editing applications.
If you have any problems with your experiments, visit our Gene Modification Troubleshoot.
In Vitro Transcription
Many biological applications require molecular probes, including labeling and real-time PCR. In vitro transcription can make use of both radioactively labeled and non-isotopically labeled probes. The capability to manufacture these probes in the laboratory helps facilitate a wide variety of procedures like RNA amplification, expression studies, and structural analysis.
If you have any problems with your experiments, visit our In Vitro Transcription Troubleshoot.