Protocols

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  1. Rapid isolation of mammalian DNA Mammalian DNA prepared according to this protocol is approximately 20-50 kb and is suitable for use as a template for PCR reactions. the DNA yield varies betwee
  2. Pulsed-field gel electrophoresis with clamped uniform electric field In clamped homogeneous electric field (CHEF) gel electrophoresis, the electric field is generated by multiple electrodes. These electrodes are arranged in a qua
  3. Pulsed-field gel electrophoresis with transverse alternating fields Gardiner et al. (1986; Gardiner and Patterson 1989) used a gel electrophoresis device with two sets of platinum wire electrodes placed on either side of a verti
  4. Molecular quality criteria for pulsed-field gel electrophoresis PFGE is used to isolate very large DNA molecules and thus requires standards of very high molecular mass. Such standards can be obtained from phages such as T7
  5. Neutral polyacrylamide gel electrophoresis The source of this experiment is "Guide to Molecular Cloning Experiments, Third Edition", translated by Huang Peitang et al.
  6. Alkaline agarose gel electrophoresis Alkaline agarose gel electrophoresis is performed at high pH, which causes the loss of a proton from thymine and guanine residues, thus preventing the formation
  7. Recovery of DNA from agarose and polyacrylamide gels (electroelution to dialysis bags) This technique (McDonell et al., 1977) allows the recovery of double-stranded DNA from agarose or polyacrylamide gel slices over a wide range of molecular masse
  8. Analysis of interacting proteins using BIAcore BIAcore surface plasmon resonance is widely used for (1) studying the interaction process between various biomolecules (e.g., peptides, proteins, oligonucleotid
  9. Immunoprecipitation assay to determine binding proteins Many of the protein-protein interactions present in intact cells are maintained when cells are lysed under nondenaturing conditions. This rhopper can be used to
  10. GFP and fluorescence resonance energy transfer techniques for protein interaction assays We have divided the protocol into three phases: the first phase describes the preparation of proteins and the labeling of proteins with fluorescent dyes; the se
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