Protocols

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  1. Transfer and immobilization of denatured RNA on membranes In most cases, to detect a specific target mRNA, the RNA is separated by agarose electrophoresis and then transferred from the gel to a two-dimensional support,
  2. Detection of DNA staining in polyacrylamide gels Unlike agarose gels, ethidium bromide cannot be added to polyacrylamide gels as this dye interferes with the polymerization of acrylamide. However, ethidium bro
  3. Simultaneous Preparation of DNA, RNA and Proteins from Cells and Tissues in a One-Step Process Like the rapid RNA extraction method reported by Chomczynski and Sacchi in 1987, this method consists of lysing cells with a single-phase solution containing gu
  4. Recovery of Concentrated DNA Fragments from Pulsed Field Gels DNA from low melting point agarose sections is first concentrated by electrophoresis into high percentage agarose gels and then separated by treatment with agar
  5. Isolation of high molecular mass DNA from mammalian cells using proteinase K and phenol This procedure is adapted from a method first described by Daryl Stafford and colleagues (Blin and Stanfford 1976). This method should be used when large quanti
  6. Isolation of high molecular mass DNA from mammalian cells using formamide This protocol is a modified version of the method described by Kupiec et al. (1987), which consists of digestion of cells and tissues with proteinase K, separat
  7. Isolation of DNA from mammalian cells by the winding method This method is a modification of the Bowtell method (1987), which allows for the simultaneous preparation of DNA from many different cell or tissue samples.The
  8. Rapid isolation of yeast DNA Yeast DNA prepared according to this protocol can be used as a template for PCR reactions. The shuttle plasmid, which replicates in both E. coli and Saccharomyc
  9. Southern blotting (capillary transfer of DNA to a membrane) Genomic DNA samples are prepared by digestion with one or more restriction endonucleases, and the digested fragments are separated by electrophoresis on a stand
  10. Isolation of DNA from mammalian cells grown in 96-well microculture plates This protocol, modified from the method of Ramirez-solis et al. 1992, 1993, is a simple and efficient method for extracting genomic DNA from eukaryotic cells gr
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