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  2. Radioimmunoprecipitation assay buffer - Wikipedia

    en.wikipedia.org/wiki/Radioimmunoprecipitation...

    Radioimmunoprecipitation assay buffer (RIPA buffer) is a lysis buffer used to lyse cells and tissue for the radio immunoprecipitation assay (RIPA). [1] [2] This buffer is more denaturing than NP-40 or Triton X-100 because it contains the ionic detergents SDS and sodium deoxycholate as active constituents and is particularly useful for disruption of nuclear membranes in the preparation of ...

  3. 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

  4. Deoxycholic acid - Wikipedia

    en.wikipedia.org/wiki/Deoxycholic_acid

    Sodium deoxycholate, the sodium salt of deoxycholic acid, is often used as a biological detergent to lyse cells and solubilise cellular and membrane components. [11] Sodium deoxycholate mixed with phosphatidylcholine , is used in mesotherapy injections to produce lipolysis, and has been used as an alternative to surgical excision in the ...

  5. Hanks' salts - Wikipedia

    en.wikipedia.org/wiki/Hanks'_salts

    Hanks' salts is a collective group of salts rich in bicarbonate ions, formulated in 1940 by the microbiologist John H. Hanks. [1] Typically, they are used as a buffer system in cell culture media and aid in maintaining the optimum physiological pH (roughly 7.0–7.4) for cellular growth.

  6. Protein precipitation - Wikipedia

    en.wikipedia.org/wiki/Protein_Precipitation

    The relationship between the solubility of a protein and increasing ionic strength of the solution can be represented by the Cohn equation: ⁡ = S = solubility of the protein, B is idealized solubility, K is a salt-specific constant and I is the ionic strength of the solution, which is attributed to the added salt.

  7. TE buffer - Wikipedia

    en.wikipedia.org/wiki/TE_buffer

    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 amounts of high molarity HCl to lower the pH to 8.

  8. Hoagland solution - Wikipedia

    en.wikipedia.org/wiki/Hoagland_solution

    The main difference between solution (1) and solution (2) is the different use of nitrate-nitrogen and ammonium-nitrogen based stock solutions to prepare the respective Hoagland solution of interest. Accordingly, the original 1933 and the modified concentrations of 1938 and 1950 for each essential element and sodium are shown below, the ...

  9. TBST - Wikipedia

    en.wikipedia.org/wiki/TBST

    The following is a sample recipe for TBST: 20 mM Tris; 150 mM NaCl; 0.1% Tween 20; Adjust pH with HCl to pH 7.4–7.6 The simplest way to prepare a TBS-Tween solution is to use TBS-T tablets. They are formulated to give a ready to use TBST solution upon dissolution in 500 ml of deionized water. [1]