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  2. Tris - Wikipedia

    en.wikipedia.org/wiki/Tris

    Tris, or tris (hydroxymethyl)aminomethane, or known during medical use as tromethamine or THAM, is an organic compound with the formula (HOCH 2) 3 CNH 2. It is extensively used in biochemistry and molecular biology as a component of buffer solutions [2] such as in TAE and TBE buffers, especially for solutions of nucleic acids.

  3. TE buffer - Wikipedia

    en.wikipedia.org/wiki/TE_buffer

    10 mM Tris, bring to pH 8.0 with HCl; 1 mM EDTA, bring to pH 8.0 with NaOH; TE buffer is also known as T 10 E 1 buffer, which can be read as "T ten E one 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 ...

  4. Tris-buffered saline - Wikipedia

    en.wikipedia.org/wiki/Tris-Buffered_Saline

    Tris-buffered saline (TBS) is a buffer used in some biochemical techniques to maintain the pH within a relatively narrow range. Tris (with HCl) has a slightly alkaline buffering capacity in the 7–9.2 range. The conjugate acid of Tris has a pK a of 8.07 at 25 °C. The pK a declines approximately 0.03 units per degree Celsius rise in temperature.

  5. TBE buffer - Wikipedia

    en.wikipedia.org/wiki/TBE_buffer

    TBE or Tris/Borate/EDTA, is a buffer solution containing a mixture of Tris base, boric acid and EDTA. In molecular biology, TBE and TAE buffers are often used in procedures involving nucleic acids, the most common being electrophoresis. Tris -acid solutions are effective buffers for slightly basic conditions, which keep DNA deprotonated and ...

  6. Lysis buffer - Wikipedia

    en.wikipedia.org/wiki/Lysis_buffer

    Lysis buffer usually contains one or more salts. The function of salts in lysis buffer is to establish an ionic strength in the buffer solution. Some of the most commonly used salts are NaCl, KCl, and (NH 4) 2 SO 4. They are usually used with a concentration between 50 and 150 mM. [4] Sodium dodecyl sulfate (SDS) structure

  7. TAE buffer - Wikipedia

    en.wikipedia.org/wiki/TAE_buffer

    TAE buffer. TAE buffer is a buffer solution containing a mixture of Tris base, acetic acid and EDTA. In molecular biology, it is used in agarose electrophoresis typically for the separation of nucleic acids such as DNA and RNA. [1] It is made up of Tris-acetate buffer, usually at pH 8.3, and EDTA, which sequesters divalent cations.

  8. Acid strength - Wikipedia

    en.wikipedia.org/wiki/Acid_strength

    Acid strength is the tendency of an acid, symbolised by the chemical formula , to dissociate into a proton, , and an anion, . The dissociation or ionization of a strong acid in solution is effectively complete, except in its most concentrated solutions. Examples of strong acids are hydrochloric acid , perchloric acid , nitric acid and sulfuric ...

  9. TSE buffer - Wikipedia

    en.wikipedia.org/wiki/TSE_buffer

    TSE buffer. TSE or Tris/Saline/EDTA, is a buffer solution containing a mixture of Tris base, Sodium chloride and EDTA. In molecular biology, TSE buffers are often used in procedures involving nucleic acids. Tris-acid solutions are effective buffers for slightly basic conditions, which keep DNA deprotonated and soluble in water.

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