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Organometallic compounds contain direct bonds between carbon atoms and metal atoms/ions and play roles as homogeneous catalysts and stoichiometric reagents in reactions; available in various chemical compositions, quantities, purities, and reagent grades.
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NH2-PEG3-C6-Cl is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
Contains two different ligands connected by a linker
One is a ligand for an E3 ubiquitin ligase
The other is for the target protein
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Ribosomal protein L3 peptide (202-222) amide is a synthetic peptide corresponding to residues 202 to 222 of ribosomal protein L3 with the sequence Met-Ser-His-Arg-Lys-Tyr-Glu-Ala-Pro-Arg-His-Gly-His-Leu-Gly-Phe-Leu-Pro-Arg-Lys-Arg-amide and a molecular formula of C114H182N42O25S (Mw 2573) Ribosomal protein L3 is an integral component of the large ribosomal subunit (60S) interacting with 23S rRNA to constitute the ribosome s peptidyl transferase center This particular peptide segment can bind to HIV-1 TAR RNA suggesting its role in studying TAR-mediated transcriptional activation and RNA-protein interactions in molecular virology research
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Azido-PEG5-alcohol is a polyethylene glycol (PEG) linker bearing a terminal azide and a terminal hydroxyl group. It functions as a non-cleavable, five-unit PEG spacer for bioconjugation and click chemistry applications.
Contains azide (-N3) and terminal alcohol (-OH) functional groups.
Water-soluble PEG linker suitable for click chemistry and PROTAC/ADC assembly.
Molecular weight ~263.29 g/mol; formula C10H21N3O5.
High purity, typically ≥97.0% by manufacturer specification.
Available in multiple pack sizes, including 10 g.
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Azido-PEG5-CH2CO2H is a cleavable, azide-functionalized polyethylene glycol (PEG) linker with a terminal carboxylic acid that provides a hydrophilic spacer and a reactive azide handle for bioconjugation and linker synthesis.
Cleavable 5-unit PEG linker suitable for linker-based conjugation.
Azide functional group for copper-catalyzed or strain-promoted click reactions.
Terminal carboxylic acid enables further derivatization or coupling.
Hydrophilic spacer increases solubility in aqueous media.
High purity suitable for chemical synthesis and bioconjugation.
Available in 250 MG pack size.
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N-(Amino-PEG5)-N-bis(PEG4-acid) is a PEG derivative that contains an amino group and two terminal carboxylic acids. The amino group is reactive with carboxylic acids and activated NHS esters. The terminal carboxylic acids can react with primary amine groups in the presence of activators to form a stable amide bond. This compound is useful in the development of antibody drug conjugates (ADCs).
Contains an amino group and two terminal carboxylic acids
Amino group is reactive with carboxylic acids and activated NHS esters
Terminal carboxylic acids can react with primary amine groups
Forms a stable amide bond
Useful in the development of antibody drug conjugates (ADCs)
For research use only
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