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  2. Agarose gel electrophoresis - Wikipedia

    en.wikipedia.org/wiki/Agarose_gel_electrophoresis

    For a standard agarose gel electrophoresis, a 0.8% gel gives good separation or resolution of large 5–10kb DNA fragments, while 2% gel gives good resolution for small 0.2–1kb fragments. 1% gels is often used for a standard electrophoresis. [25]

  3. YEPD - Wikipedia

    en.wikipedia.org/wiki/YEPD

    It may be made as a broth, or made into an agar gel by adding 1.5 to 2% agar. [2] [3] References This page was last edited on 29 December 2024 ...

  4. Gel electrophoresis of nucleic acids - Wikipedia

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

    For a standard agarose gel electrophoresis, 0.7% gel concentration gives good separation or resolution of large 5–10kb DNA fragments, while 2% gel concentration gives good resolution for small 0.2–1kb fragments.

  5. 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.

  6. Southern blot - Wikipedia

    en.wikipedia.org/wiki/Southern_blot

    Agarose gel Tray with a stack consisting top down of a weight, paper towels, membrane of nitrocellulose or nylon, gel, salt solution and a slab of glass. Southern blot membrane after hybridization and rinsing. Southern blot agarose gel under ultraviolet illumination. Southern blot autoradiogram.

  7. Electrophoretic mobility shift assay - Wikipedia

    en.wikipedia.org/wiki/Electrophoretic_mobility...

    A mobility shift assay is electrophoretic separation of a protein–DNA or protein–RNA mixture on a polyacrylamide or agarose gel for a short period (about 1.5-2 hr for a 15- to 20-cm gel). [4] The speed at which different molecules (and combinations thereof) move through the gel is determined by their size and charge, and to a lesser extent ...

  8. Affinity electrophoresis - Wikipedia

    en.wikipedia.org/wiki/Affinity_electrophoresis

    This technique utilizes a high voltage (≥ 20 V/cm) with a 0.5× Tris-borate buffer run across an agarose gel. [9]This method differs from the traditional agarose gel electrophoresis by utilizing a higher voltage to facilitate a shorter run time as well as yield a higher band resolution.

  9. Simmons' citrate agar - Wikipedia

    en.wikipedia.org/wiki/Simmons'_citrate_agar

    Simmons’ citrate agar was developed by James S. Simmons in 1926 by adding 1.5% agar and bromothymol blue as a pH indicator to Koser’s citrate agar to observe changes in pH as a result of oxidative reactions from citrate metabolism. [5]

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