Tag RNA Lab

Articles by tag "RNA Lab"

Items 41-50 of 107

Set Descending Direction
  1. RNA bulk transcription synthesis The typical recovery rate of the RNA standard transcription system is lugRNA/ug plasmid DNA, which can be increased to 5~l0ug RNA/ug plasmid DNA by using the fo
  2. Photo-activated nucleotide analog-mediated RNA-protein cross-linking experiments Photochemical cross-linking technology is an effective means to study the interaction between RNA and protein in nuclear enameled egg complexes. The basic princ
  3. PAT method for analyzing mRNA Poly(A) tail length assay The PAT method [ PCR poly(A) test ] can quickly and sensitively analyze specific mRNA from total RNA and quantitatively estimate the length of RNA poly(A) tails
  4. Fe(II)-EDTA protection assay experiment Fe(II)-EDTA is capable of catalyzing the breakage of RNA or DNA and is a complementary method to RNase protection analysis. It has the advantage that there is l
  5. RNA in situ hybridization assay In situ hybridization (ISH), also known as hybrid histochemistry or hybridization for cytology, is a technique that enables morphological demonstration of the p
  6. Primer extension method RNA analysis The primer extension method can be used for RNA mapping and RNA 5' halo. In this method, an excess of a 5' end-labeled single-stranded RNA primer is hybridized
  7. RNA SI Nuclease Mapping SI nuclease is an endonuclease that was isolated from Aspergillus oryzae. It can degrade single-stranded nucleic acids but not double-stranded nucleic acids. In
  8. Spot and slit hybridization Spot and slit hybridization analysis of RNA enables the qualitative or semi-quantitative determination of RNA by directly spotting RNA samples onto nitrocellulo
  9. Methylmercury hydroxide agarose gel electrophoresis Methylmercury hydroxide reacts with the imine bonds on uracil and guanine in RNA, which are involved in Watson-Crick base pairing. Therefore, methylmercury hydr
  10. Glyoxal/DMSO denaturing agarose gel electrophoresis Under slightly acidic conditions, the two acetaldehyde groups of glyoxal interact with the imino group of guanosine to form a cyclic compound, which inhibits th
per page