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  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

    Guanidine exists protonated, as guanidinium, in solution at physiological pH. Guanidinium chloride (also known as guanidine hydrochloride) has chaotropic properties and is used to denature proteins. Guanidinium chloride is known to denature proteins with a linear relationship between concentration and free energy of unfolding.

  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. 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

  6. 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.

  7. 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]

  8. 1,1,3,3-Tetramethylguanidine - Wikipedia

    en.wikipedia.org/wiki/1,1,3,3-Tetramethylguanidine

    Print/export Download as PDF; Printable version; In other projects Wikimedia Commons; Wikidata item; Appearance. move to sidebar hide. 1,1,3,3-Tetramethylguanidine ...

  9. Avidin - Wikipedia

    en.wikipedia.org/wiki/Avidin

    The monomeric avidin is created by treatment of immobilized native avidin with urea or guanidine HCl (6–8 M), giving it a lower dissociation K D ≈ 10 −7 M. [19] This allows elution from the avidin matrix to occur under milder, non-denaturing conditions, using low concentrations of biotin or low pH conditions. For a single high affinity ...