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  1. Chemiluminescent Dideoxy DNA Sequencing Assay Standard double deoxy DNA sequencing can be easily and efficiently detected using non-isobaric labeled chemiluminescence. In the sequencing reaction, biotin-lab
  2. Junction partitioning mutagenesis of DNA Linker scanner mutations: In vitro additions of sites to restriction fragments that result in recombination of two DNA molecules, resulting in the addition of a
  3. Transfection of eukaryotic cells using DEAE-glucan Mouse L-type fibroblasts were used to perform the conditions eubiquitously, but can be applied to almost any cell with only minor modifications. It is critical
  4. Freeze-thaw method for recovery of DNA fragments The freeze-thaw method of recovering DNA fragments can be used to (1) obtain purified DNA fragments and (2) recover PCR products.
  5. Steps for SSR labeling experiments SSR simple sequence repeat markers can be used to: design pairs of primers with a specific sequence of microsatellite regions, and polymorphism of SSR loci amon
  6. Analysis of radioisotope-labeled DNA sequence determination Radioisotope-labeled DNA sequencing analysis can be applied to analyze gene structure-function relationships.
  7. DNA blot hybridization analysis experiment Hybridization analysis is based on the principle that a single-stranded DNA molecule of a specific sequence (i.e., a commonly labeled "probe") can form a base p
  8. T4 DNA polymerase assay T4 DNA polymerase has a human template-dependent polymerase activity, as well as exonuclease activity for the 3' to 5' ends of single- and double-stranded DNA,
  9. Construction of recombinant DNA by polymerase chain reaction The polymerase chain reaction constructs recombinant DNA for a wide range of uses (1) for sequencing primers (2) targeted mutagenesis (3) nucleic acid hybridiza
  10. DNA binding protein assay This experiment was used to detect sequence-specific DNA-binding proteins in crude extracts.
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