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  2. Maleimide - Wikipedia

    en.wikipedia.org/wiki/Maleimide

    Maleimide-mediated methodologies are among the most used in bioconjugation. [5] [6] Due to fast reactions and high selectivity towards cysteine residues in proteins, a large variety of maleimide heterobifunctional reagents are used for the preparation of targeted therapeutics, assemblies for studying proteins in their biological context, protein-based microarrays, or proteins immobilisation. [7]

  3. Xenu's Link Sleuth - Wikipedia

    en.wikipedia.org/wiki/Xenu's_Link_Sleuth

    Link Sleuth runs on Microsoft Windows. Link verification is performed on links which appear in <a> tags, as well as images, frames, plug-ins, backgrounds, local image maps, style sheets, scripts, and Java applets. The program follows links to other pages, and checks the links on those pages also, so it is possible to check an entire site for ...

  4. Bisindolylmaleimide - Wikipedia

    en.wikipedia.org/wiki/Bisindolylmaleimide

    This core structure includes a central maleimide group with two indole groups attached. Examples of bisindolylmaleimide derivatives include: Bisindolylmaleimide I

  5. Succinimidyl 4-( N -maleimidomethyl)cyclohexane-1-carboxylate

    en.wikipedia.org/wiki/Succinimidyl_4-(N-maleimi...

    Succinimidyl 4-(N-maleimidomethyl)cyclohexane-1-carboxylate (SMCC) is a heterobifunctional amine-to-sulfhydryl crosslinker, which contains two reactive groups at opposite ends: N-hydroxysuccinimide-ester and maleimide, reactive with amines and thiols respectively.

  6. Category:Maleimides - Wikipedia

    en.wikipedia.org/wiki/Category:Maleimides

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  7. N-Ethylmaleimide - Wikipedia

    en.wikipedia.org/wiki/N-Ethylmaleimide

    The MEROPS online database for peptidases and their inhibitors: NEM [permanent dead link ‍]; The bifunctional analogues such as p-NN′-phenylenebismaleimide can be used as cross-linking reagent for cystine residues.

  8. N-Methylmaleimide - Wikipedia

    en.wikipedia.org/wiki/N-Methylmaleimide

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  9. Site-directed spin labeling - Wikipedia

    en.wikipedia.org/wiki/Site-directed_spin_labeling

    At neutral pH, protein thiol groups specifically react with the functional groups methanethiosulfonate, maleimide, and iodoacetamide, creating a covalent bond with the amino acid Cys. [4] Spin labels are a unique molecular reporter, in that they are paramagnetic (contain an unpaired electron).