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  2. Netprimer - Wikipedia

    en.wikipedia.org/wiki/Netprimer

    NetPrimer is a gratis web-based tool used for analysing primers used in PCR to amplify a DNA sequence. [2] The software predicts the melting temperature of the primers using the nearest neighbor thermodynamic algorithm. The accurate prediction of the melting temperature (Tm) is one of the most important factors that governs the success of a PCR ...

  3. OLIGO Primer Analysis Software - Wikipedia

    en.wikipedia.org/wiki/OLIGO_Primer_Analysis_Software

    OLIGO Primer Analysis Software is a software for DNA primer design. [ 1 ] [ 2 ] The first paper describing this software was published in 1989. [ 3 ] The program is a real time PCR primer and probe search and analysis tool.

  4. In silico PCR - Wikipedia

    en.wikipedia.org/wiki/In_silico_PCR

    The last 10-12 bases at the 3' end of a primer are sensitive to initiation of polymerase extension and general primer stability on the template binding site. The effect of a single mismatch at these last 10 bases at the 3' end of the primer depends on its position and local structure, reducing the primer binding, selectivity, and PCR efficiency.

  5. Primer Premier - Wikipedia

    en.wikipedia.org/wiki/Primer_Premier

    Primer Premier is a bioinformatics software used for various PCR applications. It supports the design of degenerate primers for amplifying a related set of nucleotide sequences for the detection of common traits amongst organisms, as well as to determine heredity. [1] The software also designs tagged and nested primers for multiplex PCR ...

  6. Alkaline lysis - Wikipedia

    en.wikipedia.org/wiki/Alkaline_lysis

    The first alkaline lysis was performed by Birnom and Doly in 1979. [1] Since then, slight modifications have been made to the procedure to get to today's most widely used approach. The steps of alkaline lysis can be summarized as the formation of a pellet, resuspension of the pellet in solution, cell lysis, neutralization , and centrifugation .

  7. Bradford protein assay - Wikipedia

    en.wikipedia.org/wiki/Bradford_protein_assay

    Turn on and adjust a spectrophotometer to a wavelength of 595 nm, and blank the spectrophotometer using 1.5 mL cuvettes or use a mobile smartphone camera (RGBradford method). [9] Wait 2 minutes and read the absorbance of each standard and sample at 595 nm. Plot the absorbance of the standards vs. their concentration.

  8. Touchdown polymerase chain reaction - Wikipedia

    en.wikipedia.org/wiki/Touchdown_polymerase_chain...

    The annealing temperature during a polymerase chain reaction determines the specificity of primer annealing. The melting point of the primer sets the upper limit on annealing temperature. At temperatures just above this point, only very specific base pairing between the primer and the template will occur.

  9. Lysis buffer - Wikipedia

    en.wikipedia.org/wiki/Lysis_buffer

    Lysis buffer usually contains one or more salts. The function of salts in lysis buffer is to establish an ionic strength in the buffer solution. Some of the most commonly used salts are NaCl, KCl, and (NH 4) 2 SO 4. They are usually used with a concentration between 50 and 150 mM. [4] Sodium dodecyl sulfate (SDS) structure