enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Guanidinium chloride - Wikipedia

    en.wikipedia.org/wiki/Guanidinium_chloride

    At high concentrations of guanidinium chloride (e.g., 6 M), proteins lose their ordered structure, and they tend to become randomly coiled, i.e. they do not contain any residual structure. However, at concentrations in the millimolar range in vivo, guanidinium chloride has been shown to "cure" prion positive yeast cells (i.e. cells exhibiting a ...

  3. Guanidine - Wikipedia

    en.wikipedia.org/wiki/Guanidine

    The general structure of a guanidine. Guanidines are a group of organic compounds sharing a common functional group with the general structure (R 1 R 2 N)(R 3 R 4 N)C=N−R 5. The central bond within this group is that of an imine, and the group is related structurally to amidines and ureas.

  4. Category:Guanidines - Wikipedia

    en.wikipedia.org/wiki/Category:Guanidines

    Download QR code; Print/export Download as PDF; Printable version; ... Help. The general structure of a guanidine Subcategories. This category has the following 8 ...

  5. Guanidinium thiocyanate - Wikipedia

    en.wikipedia.org/wiki/Guanidinium_thiocyanate

    Guanidinium thiocyanate can be used to deactivate a virus, such as the influenza virus that caused the 1918 "Spanish flu", so that it can be studied safely.. Guanidinium thiocyanate is also used to lyse cells and virus particles in RNA and DNA extractions, where its function, in addition to its lysing action, is to prevent activity of RNase enzymes and DNase enzymes by denaturing them.

  6. File:Guanidin.svg - Wikipedia

    en.wikipedia.org/wiki/File:Guanidin.svg

    The following other wikis use this file: Usage on az.wikipedia.org Quanidin; Usage on bn.wikipedia.org গুয়ানিডিন; Usage on ca.wikipedia.org

  7. Native chemical ligation - Wikipedia

    en.wikipedia.org/wiki/Native_chemical_ligation

    It involves the reaction of an unprotected peptide thioester with a second, unprotected peptide that has an N-terminal cysteine residue. It is carried out in aqueous solution at neutral pH, usually in 6 M guanidine.hydrochloride, in the presence of an arylthiol catalyst and typically gives near-quantitative yields of the desired ligation product.

  8. Latino men voted for Trump in large numbers. Here’s what they ...

    www.aol.com/news/latino-men-voted-trump-large...

    Latino men vaulted into the spotlight with their greater-than-expected support for President-elect Donald Trump.Soon, they’ll be looking for returns on their votes. U.S. Hispanics, who are ...

  9. 7-Methyl-1,5,7-triazabicyclo (4.4.0)dec-5-ene - Wikipedia

    en.wikipedia.org/wiki/7-methyl-1,5,7...

    7-Methyl-1,5,7-triazabicyclo[4.4.0]dec-5-ene (mTBD) is a bicyclic strong guanidine base (pK a = 25.43 in CH 3 CN and pK a = 17.9 in THF). [3] mTBD, like 1,5,7-triazabicyclo[4.4.0]dec-5-ene and other guanidine super bases, can be used as a catalyst in a variety of chemical reactions. [4]