Bio-Rad Launches New Website for Researchers Transfecting Mammalian Cells

25 Jun 2008

Product news

Bio-Rad Laboratories, Inc., a multinational manufacturer and distributor of life science research and clinical diagnostic products, today announced the launch of a new addition, entitled “Gene Transfer Protocols”, to the Bio-Rad Gene Expression Gateway Web-site, dedicated to researchers working with mammalian cells, including primaries, that are difficult to transfect.

The Gene Transfer Protocols offers a library where scientists can search a database of gene transfer protocols to identify conditions for transfecting mammalian cells either by cell type or cell line. The database currently contains more than 300 different protocols, many of them collected from peer reviewed journals.

Since transfection plays a critical role in gene expression, determining the right method and parameters are paramount to a successful experiment. Methods such as electroporation, particle bombardment, and lipid-mediated protocols are found on the site, providing researchers with the ability to select the protocol specific for their needs.

“We are pleased to offer our customers this service, which not only provides them a way to browse an extensive set of protocols, but also offers them the opportunity to submit a protocol, which has proved successful for them,” said Jamie Wibbenmeyer, marketing manager, Microarrays, Bio-Rad’s Gene Expression Division. “We plan to continuously update and expand this website.”

Bio-Rad instruments cited extensively throughout the posted protocol literature include the Gene Pulser series of electroporators, the MicroPulser™ electroporator, the Helios® gene gun and PDS-1000/He biolistic systems. Chemically mediated methods discussed include transfection reagents such as TransFectin lipid reagent for delivery of plasmid DNA, siLentFect lipid reagent for siRNA delivery, and HEKFectin and COSFectin lipid for cell line-specific transfection.

Links

Tags

Genome AnalysisGenomics, the study of genomes, includes functional genomics, evolutionary genomics and comparative genomics. There are many genomic technologies such as DNA sequencing of whole genomes, computational biology and bioinformatics. DNA and nucleic acids must be isolated and concentrated from cells for analysis with kits, automated analyzers and software. Other useful technologies for studying genomics include PCR, microarrays and electrophoresis.Cell Lines Stem Cells and Primary CellsPrimary cell cultures, established cell lines and stem cells are vital for <i>in vitro</i> and <i>ex vivo</i> experimentation. High-quality cells, optimized for your applications, alongside optimized cell substrates, growth medium and supplements, are critical for experimental success. Explore a range of cells suitable for your applications, including isogenic cell lines, competent cells, induced pluripotent stem cell (iPSC)-derived cell lines, fungal/bacterial/mammalian cell lines, stem cells and cancer cell lines. Find the best cells for your research in our peer-reviewed product directory: compare products, check customer reviews and receive pricing direct from manufacturers.Gene Expression and Molecular CloningMolecular cloning is a set of techniques that utilizes vectors to transfer recombinant DNA into host cells and is an essential tool for investigating the expression of genes and proteins in bacterial or mammalian cells. A variety of vectors optimized for gene cloning and expression in a range of host organisms are available, alongside competent cells for genetic replication. Here, you can explore a range of molecular tools, high-quality genomic and cDNA libraries, premade clones, transformation and transfection reagents and mutagenesis or gene expression detection assays and expression arrays. Find the best gene expression and molecular cloning products in our peer-reviewed product directory: compare products, check customer reviews and receive pricing direct from manufacturers.RNA InterferenceRNA interference (RNAi) uses siRNA or miRNA for transcriptional silencing, gene knockdown and regulation of gene expression. RNAi requires chemical synthesis, introduction of DNA vectors into cells, an assay of RNAi effects and RNAi quantification or analysis. Consider target sequence selection, reagent preparation, controls, high specificity and effectiveness and low non-specific gene knockdown.