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  2. Safety data sheet - Wikipedia

    en.wikipedia.org/wiki/Safety_data_sheet

    An example SDS, including guidance for handling a hazardous substance and information on its composition and properties. A safety data sheet (SDS), [1] material safety data sheet (MSDS), or product safety data sheet (PSDS) is a document that lists information relating to occupational safety and health for the use of various substances and products.

  3. Sodium thiosulfate - Wikipedia

    en.wikipedia.org/wiki/Sodium_thiosulfate

    Some analytical procedures exploit the oxidizability of thiosulfate anion by iodine. The reaction produces tetrathionate: 2 S 2 O 2− 3 + I 2 → S 4 O 2− 6 + 2 I −. Due to the quantitative nature of this reaction, as well as because Na 2 S 2 O 3 ·5H 2 O has an excellent shelf-life, it is used as a titrant in iodometry.

  4. FLUKA - Wikipedia

    en.wikipedia.org/wiki/FLUKA

    FLUKA (FLUktuierende KAskade) is a fully integrated Monte Carlo simulation package for the interaction and transport of particles and nuclei in matter. [2] [3] ...

  5. Polyacrylamide gel electrophoresis - Wikipedia

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

    The gel mobility is defined as the rate of migration traveled with a voltage gradient of 1V/cm and has units of cm 2 /sec/V. [3]: 161–3 For analytical purposes, the relative mobility of biomolecules, R f, the ratio of the distance the molecule traveled on the gel to the total travel distance of a tracking dye is plotted versus the molecular ...

  6. SDS-PAGE - Wikipedia

    en.wikipedia.org/wiki/SDS-PAGE

    Proteins of the erythrocyte membrane separated by SDS-PAGE according to their molecular masses. SDS-PAGE (sodium dodecyl sulfate–polyacrylamide gel electrophoresis) is a discontinuous electrophoretic system developed by Ulrich K. Laemmli which is commonly used as a method to separate proteins with molecular masses between 5 and 250 kDa.

  7. Analytical quality control - Wikipedia

    en.wikipedia.org/wiki/Analytical_quality_control

    Validation of analytical procedures is imperative in demonstrating that a drug substance is suitable for a particular purpose. [5] Common validation characteristics include: accuracy, precision (repeatability and intermediate precision), specificity, detection limit, quantitation limit, linearity, range, and robustness.