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  2. Triethylammonium acetate - Wikipedia

    en.wikipedia.org/wiki/Triethylammonium_acetate

    This page was last edited on 8 September 2024, at 15:40 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  3. Sigma-Aldrich - Wikipedia

    en.wikipedia.org/wiki/Sigma-Aldrich

    Supelco is the chromatography products branch of Sigma-Aldrich. It provides chromatography columns and related tools for environmental , government , food and beverage, pharmaceutical , biotechnology , medical and chemical laboratories; sample preparation products and chemical reference standards.

  4. Diethylaminoethyl cellulose - Wikipedia

    en.wikipedia.org/wiki/Diethylaminoethyl_cellulose

    Schematic structure of DEAE-C: positively charged diethylaminoethanol groups can bind negative ions. Diethylaminoethyl cellulose (DEAE-C) is a positively charged resin used in ion-exchange chromatography, a type of column chromatography, for the separation and purification of proteins and nucleic acids.

  5. 4-Anisaldehyde - Wikipedia

    en.wikipedia.org/wiki/4-Anisaldehyde

    A solution of para-anisaldehyde in acid and ethanol is a useful stain in thin layer chromatography. [4] Different chemical compounds on the plate can give different colors, allowing easy distinction. DNA breakage

  6. Triton X-100 - Wikipedia

    en.wikipedia.org/wiki/Triton_X-100

    it is an ingredient in Photo-Flo, a solution used in photographic processing to prevent minerals from water being deposited on the film after drying. Apart from laboratory use, Triton X-100 can be found in several types of cleaning compounds, [ 7 ] ranging from heavy-duty industrial products to gentle detergents.

  7. Phthalaldehyde - Wikipedia

    en.wikipedia.org/wiki/Phthalaldehyde

    OPA is used in a very sensitive fluorogenic reagent for assaying amines or sulfhydryls in solution, [6] notably contained in proteins, peptides, and amino acids, by capillary electrophoresis and chromatography. OPA reacts specifically with primary amines above their isoelectric point Pi in presence of thiols.

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