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  2. Sodium dodecyl sulfate - Wikipedia

    en.wikipedia.org/wiki/Sodium_dodecyl_sulfate

    Sodium dodecyl sulfate (SDS) or sodium lauryl sulfate (SLS), sometimes written sodium laurilsulfate, is an organic compound with the formula CH 3 (CH 2) 11 OSO 3 Na and structure H 3 C−(CH 2) 11 −O−S(=O) 2 −O − Na +. It is an anionic surfactant used in many cleaning and hygiene products. This compound is the sodium salt of the 12 ...

  3. Alkaline lysis - Wikipedia

    en.wikipedia.org/wiki/Alkaline_lysis

    Sodium dodecyl sulfate detergent (SDS) and Sodium Hydroxide are used to lyse the cells. Sodium Hydroxide establishes an alkaline environment that disrupts the phospholipid bilayer and breaks hydrogen bonds between double-stranded chromosomal DNA, making it single-stranded. Due to the supercoiled nature of plasmid DNA, strands of the circular ...

  4. 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

  5. SDS-PAGE - Wikipedia

    en.wikipedia.org/wiki/SDS-PAGE

    [1] [2] The combined use of sodium dodecyl sulfate (SDS, also known as sodium lauryl sulfate) and polyacrylamide gel eliminates the influence of structure and charge, and proteins are separated by differences in their size. At least up to 2012, the publication describing it was the most frequently cited paper by a single author, and the second ...

  6. Polyacrylamide gel electrophoresis - Wikipedia

    en.wikipedia.org/wiki/Polyacrylamide_gel...

    Sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) is a method of separating molecules based on the difference of their molecular weight. At the pH at which gel electrophoresis is carried out the SDS molecules are negatively charged and bind to proteins in a set ratio, approximately one molecule of SDS for every 2 amino acids.

  7. Lysis - Wikipedia

    en.wikipedia.org/wiki/Lysis

    Common lysis buffers contain sodium hydroxide (NaOH) and sodium dodecyl sulfate (SDS). Cell lysis is best done at a pH range of 11.5–12.5. Cell lysis is best done at a pH range of 11.5–12.5. Although simple, it is a slow process, taking anywhere from 6 to 12 hours.

  8. Gel electrophoresis of proteins - Wikipedia

    en.wikipedia.org/wiki/Gel_electrophoresis_of...

    SDS-PAGE, sodium dodecyl sulfate polyacrylamide gel electrophoresis, describes a collection of related techniques to separate proteins according to their electrophoretic mobility (a function of the molecular weight of a polypeptide chain) while in the denatured (unfolded) state. In most proteins, the binding of SDS to the polypeptide chain ...

  9. Pore-C - Wikipedia

    en.wikipedia.org/wiki/Pore-C

    Next, in order to isolate DNA for sequencing, proteins bound to the DNA have to be detached and degraded. [5] First, Proteinase K, sodium dodecyl sulfate (SDS; a detergent), Tween-20, and nuclease-free water are added. [2] Subsequently, the reaction is heated to 56 °C in a thermocycler for optimal reaction kinetics.

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