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  2. Ethanol precipitation - Wikipedia

    en.wikipedia.org/wiki/Ethanol_precipitation

    Ethanol precipitation is a method used to purify and/or concentrate RNA, DNA, and polysaccharides such as pectin and xyloglucan from aqueous solutions by adding salt and ethanol as an antisolvent. In DNA extraction, after separating DNA from other cell constituents in water, DNA is precipitated out of solution by neutralizing it with positively ...

  3. Acid guanidinium thiocyanate-phenol-chloroform extraction

    en.wikipedia.org/wiki/Acid_guanidinium...

    Phenol: The phenol used for biochemistry comes as a water-saturated solution with Tris buffer, as a Tris-buffered 50% phenol, 50% chloroform solution, or as a Tris-buffered 50% phenol, 48% chloroform, 2% isoamyl alcohol solution (sometimes called "25:24:1"). Phenol is naturally somewhat water-soluble, and gives a fuzzy interface, which is ...

  4. Salting out - Wikipedia

    en.wikipedia.org/wiki/Salting_out

    Salting out (also known as salt-induced precipitation, salt fractionation, anti-solvent crystallization, precipitation crystallization, or drowning out) [1] is a purification technique that utilizes the reduced solubility of certain molecules in a solution of very high ionic strength.

  5. DNA extraction - Wikipedia

    en.wikipedia.org/wiki/DNA_extraction

    The first isolation of deoxyribonucleic acid (DNA) was done in 1869 by Friedrich Miescher. [1] DNA extraction is the process of isolating DNA from the cells of an organism isolated from a sample, typically a biological sample such as blood, saliva, or tissue. It involves breaking open the cells, removing proteins and other contaminants, and ...

  6. DNA separation by silica adsorption - Wikipedia

    en.wikipedia.org/wiki/DNA_separation_by_silica...

    In order to separate DNA through silica adsorption, a sample is first lysed, releasing proteins, DNA, phospholipids, etc. from the cells. The remaining tissue is discarded. The supernatant containing the DNA is then exposed to silica in a solution with high ionic strength. The highest DNA adsorption efficiencies occur in the presence of buffer ...

  7. TE buffer - Wikipedia

    en.wikipedia.org/wiki/TE_buffer

    To make a 100 ml solution of T 10 E 1 buffer, 1 ml of 1 M Tris base (pH 10–11) and 0.2 ml EDTA (0.5 M) are mixed and made up with double distilled water up to 100ml. Add microliter amounts of high molarity HCl to lower the pH to 8. Based on nuclease studies from the 1980s, the pH is usually adjusted to 7.5 for RNA and 8.0 for DNA.

  8. Diethyl pyrocarbonate - Wikipedia

    en.wikipedia.org/wiki/Diethyl_pyrocarbonate

    C 6 H 10 O 5: Molar mass: 162.141 g·mol −1 Appearance Clear, colorless liquid Density: 1.101 g/mL at 25 °C 1.121 g/mL at 20 °C Boiling point: 93 to 94 °C (199 to 201 °F; 366 to 367 K) at 24 hPa Hazards Occupational safety and health (OHS/OSH):

  9. TBE buffer - Wikipedia

    en.wikipedia.org/wiki/TBE_buffer

    54 g of Tris base (CAS# 77-86-1, free base) 27.5 g of boric acid (CAS# 10043-35-3) 20 ml of 0.5 M EDTA (CAS# 60-00-4) (pH 8.0) Adjust pH to 8.3 by HCl. [2] TBE can be diluted to 1X prior to use in electrophoresis, 0.5x is acceptable as well. Higher concentrations will result in poor results due to excessive heat generation.