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  2. Ion chromatography - Wikipedia

    en.wikipedia.org/wiki/Ion_chromatography

    Ion chromatography (or ion-exchange chromatography) is a form of chromatography that separates ions and ionizable polar molecules based on their affinity to the ion exchanger. [1] It works on almost any kind of charged molecule —including small inorganic anions, [ 2 ] large proteins , [ 3 ] small nucleotides , [ 4 ] and amino acids .

  3. Ion interaction chromatography - Wikipedia

    en.wikipedia.org/wiki/Ion_Interaction_Chromatography

    Ion interaction chromatography (ion-pair chromatography) is a laboratory technique for separating ions with chromatography. In this technique ions are mixed with ion pairing reagents (IPR). [ 1 ] The analyte combines with its reciprocal ion in the IPR, this corresponds to retention time .

  4. Inductively coupled plasma mass spectrometry - Wikipedia

    en.wikipedia.org/wiki/Inductively_coupled_plasma...

    Inductively coupled plasma mass spectrometry (ICP-MS) is a type of mass spectrometry that uses an inductively coupled plasma to ionize the sample. It atomizes the sample and creates atomic and small polyatomic ions, which are then detected.

  5. ROSE test - Wikipedia

    en.wikipedia.org/wiki/ROSE_test

    The resistivity of solvent extract (ROSE) test is a test for the presence and average concentration of soluble ionic contaminants, for example on a printed circuit board (PCB).

  6. His-tag - Wikipedia

    en.wikipedia.org/wiki/His-tag

    Proteins can coordinate metal ions on their surface and it is possible to separate proteins using chromatography by making use of the difference in their affinity to metal ions. This is termed as immobilized metal ion affinity chromatography (IMAC), as originally introduced in 1975 under the name metal chelate affinity chromatography. [ 3 ]

  7. Hydrophilic interaction chromatography - Wikipedia

    en.wikipedia.org/wiki/Hydrophilic_interaction...

    Modifying the polarity of a weakly ionic group (e.g. carboxyl) on the surface is easily accomplished by adjusting the pH to be within two pH units of that group's pKa. For strongly ionic functional groups of the surface (i.e. sulfates or phosphates) one could instead use a lower amount of buffer so the residual charge is not completely ion paired.