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  2. Buffer P2 - Wikipedia

    en.wikipedia.org/wiki/Buffer_P2

    Buffer P2 is a lysis buffer solution produced by Qiagen.It contains 1% sodium dodecyl sulfate (SDS) (w/v) to puncture holes in cellular membranes, and 200mM NaOH.It is used in conjunction with other resuspension buffers and lysis buffers to release DNA from cells, often as part of the alkaline lysis method of purifying plasmid DNA from bacterial cell culture.

  3. Alkaline lysis - Wikipedia

    en.wikipedia.org/wiki/Alkaline_lysis

    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. [ 2 ] Alkaline lysis takes advantage of the small and supercoiled physical composition of plasmid DNA compared to chromosomal DNA, along with its ability to reanneal double stranded ...

  4. Plasmid preparation - Wikipedia

    en.wikipedia.org/wiki/Plasmid_preparation

    Plasmid miniprep. 0.8% agarose gel ethidium bromide-stained.. A plasmid preparation is a method of DNA extraction and purification for plasmid DNA.It is an important step in many molecular biology experiments and is essential for the successful use of plasmids in research and biotechnology.

  5. Lysis buffer - Wikipedia

    en.wikipedia.org/wiki/Lysis_buffer

    RIPA buffer is a commonly used lysis buffer for immunoprecipitation and general protein extraction from cells and tissues. The buffer can be stored without vanadate at 4 °C for up to 1 year. [10] RIPA buffer releases proteins from cells as well as disrupts most weak interactions between proteins. [9] Recipe: [10] 1% (w/w) Nonidet P-40 (NP-40)

  6. Calcium chloride transformation - Wikipedia

    en.wikipedia.org/wiki/Calcium_Chloride...

    It enhances plasmid DNA incorporation by the bacterial cell, promoting genetic transformation. Plasmid DNA can attach to LPS by being added to the cell solution together with CaCl 2. [12] Thus, when heat shock is applied, the negatively charged DNA backbone and LPS combine, allowing plasmid DNA to enter the bacterial cell. [13]

  7. Agarose gel electrophoresis - Wikipedia

    en.wikipedia.org/wiki/Agarose_gel_electrophoresis

    After the experiment is finished, the resulting gel can be stored in a plastic bag in a refrigerator. Electrophoresis is performed in buffer solutions to reduce pH changes due to the electric field, which is important because the charge of DNA and RNA depends on pH, but running for too long can exhaust the buffering capacity of the solution.

  8. Notre Dame vs. Army has special meaning for Irish ... - AOL

    www.aol.com/notre-dame-vs-army-special-111414067...

    Download for award-winning coverage, crosswords, audio storytelling, the eNewspaper and more. This article originally appeared on USA TODAY: Notre Dame vs. Army has special meaning for Irish ...

  9. Vector (molecular biology) - Wikipedia

    en.wikipedia.org/wiki/Vector_(molecular_biology)

    The pBR322 plasmid is one of the first plasmids widely used as a cloning vector. Plasmids with specially-constructed features are commonly used in laboratory for cloning purposes . These plasmid are generally non-conjugative but may have many more features, notably a " multiple cloning site " where multiple restriction enzyme cleavage sites ...