Catalog No.
Product Name
Application
Product Information
Citations
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PROTAC linker
N-(Azide-PEG3)-N'-(PEG4-acid)-Cy5 is a PEG-based linker designed for the synthesis of PROTACs, functioning primarily through click chemistry mechanisms. It features an azide group that facilitates copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules. Additionally, this compound is capable of participating in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN moieties, making it useful for selective protein degradation studies and related applications in chemical biology. -
PROTAC linker
N-(m-PEG4)-N'-(azide-PEG4)-Cy7 is a PEG-based linker designed for use in PROTAC (proteolysis targeting chimeras) synthesis. This compound features an azide functional group, allowing it to participate in copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing partners, as well as strain-promoted alkyne-azide cycloaddition (SPAAC) with DBCO or BCN groups. Its biological activity in forming stable linkages facilitates targeted proteolysis research applications, making it a valuable tool for molecular biology and drug development studies. -
PROTAC Linkers
Boc-N-Amido-PEG3-azide is a PEG-based linker designed for use in the synthesis of PROTACs (Proteolysis Targeting Chimeras). This compound features an azide group, enabling it to participate in copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with alkyne-containing molecules. Additionally, it can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) with dibenzocyclooctyne (DBCO) or bicyclo[6.1.0]nonyne (BCN) groups, making it a versatile tool for chemical research and development in targeted protein degradation studies. -
PROTAC Linkers
Pyrene azide 3 is a PEG-based PROTAC linker designed for the synthesis of PROTACs. It features an azide group that enables copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with alkyne-bearing molecules. Additionally, it can participate in strain-promoted alkyne-azide cycloaddition (SPAAC) with DBCO or BCN-containing compounds, making it versatile for targeted protein degradation applications in chemical biology research. -
PROTAC Linker
Boc-NHCH2CH2-PEG1-azide is a PEG-based linker specifically designed for use in synthesizing PROTACs (Proteolysis Targeting Chimeras). This compound features an azide group that enables it to participate in copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules. Additionally, it can engage in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with entities containing DBCO or BCN groups, facilitating the development of targeted protein degradation strategies in chemical research. -
PROTAC Linker
Boc-NH-PEG6-azide is a PEG-based linker designed for use in PROTAC (proteolysis-targeting chimera) synthesis. This compound features an azide group, enabling it to participate in copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with alkyne-containing molecules. Additionally, Boc-NH-PEG6-azide is capable of undergoing strain-promoted alkyne-azide cycloaddition (SPAAC) with constructs containing DBCO or BCN groups. Its applications are pivotal in the development of targeted protein degradation strategies. -
PROTAC Linkers
Boc-N-Amido-PEG2-C2-azide is a PEG-based PROTAC linker designed for the synthesis of targeted protein degradation agents. This compound contains an azide group that facilitates copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-functionalized molecules, enhancing conjugation efficiency. Additionally, it can participate in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN groups, making it suitable for diverse bioconjugation applications in chemical biology and drug discovery. -
PROTAC Linker
5-(Biotinamido)pentylazide is a versatile PROTAC linker that facilitates the synthesis of proteolysis-targeting chimeras (PROTACs). This reagent features an azide functional group, enabling it to participate in copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with alkynes. Additionally, it can engage in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN moieties, making it a valuable tool for chemical research in targeted protein degradation and related applications. -
PROTAC Linkers
m-PEG8-azide is a PEG-based linker specifically designed for PROTAC synthesis. This compound features an azide functional group, enabling it to participate in copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with alkyne-containing molecules. Additionally, m-PEG8-azide is suitable for strain-promoted alkyne-azide cycloaddition (SPAAC) when used with DBCO or BCN groups. Its versatile reactivity makes it a valuable tool for researchers engaged in targeted protein degradation studies. -
PROTAC Linker
Azide-PEG3-C1-Ala is a PEG-based linker designed for PROTAC (proteolysis-targeting chimera) synthesis. This compound features an azide group that facilitates copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules. Additionally, it can participate in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with dibenzocyclooctyne (DBCO) or bicyclononyne (BCN) compounds. This versatile linker is essential for studying targeted protein degradation and enhancing the efficacy of therapeutic agents. -
PROTAC Linker
Amino-PEG8-hydrazide-Boc is a PEG-based linker designed for use in the synthesis of PROTACs (proteolysis-targeting chimeras). Its primary mechanism targets the recruitment of E3 ubiquitin ligases, facilitating the ubiquitination and degradation of specific proteins. This reagent is essential for developing novel therapeutic strategies aimed at modulating protein levels and has significant applications in chemical biology and drug discovery research. -
PROTAC Linkers
Propargyl-PEG3-azide is a PEG-based linker specifically designed for the synthesis of PROTACs. This compound features an azide group that participates in copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with alkyne-containing molecules. Additionally, it is capable of undergoing strain-promoted alkyne-azide cycloaddition (SPAAC) with DBCO or BCN-functionalized compounds. Its versatility makes it a valuable tool in chemical biology and therapeutic research applications involving targeted protein degradation. -
PROTAC linker
N-methyl-N'-(azide-PEG3)-Cy3 is a PEG-based linker designed for use in the synthesis of PROTACs, facilitating targeted protein degradation. This compound acts as a click chemistry reagent due to the presence of an azide group, enabling copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules. Additionally, it can participate in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN functionalized compounds, making it a versatile tool in chemical biology and medicinal chemistry research applications. -
PROTAC linker
N-(azide-PEG3)-N'-(Amine-C3-Amide-PEG4)-Cy5 is a PEG-based linker designed for the synthesis of PROTACs, functioning primarily through the azide group. This compound participates in click chemistry, specifically through copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules. It is also capable of undergoing strain-promoted alkyne-azide cycloaddition (SPAAC) with DBCO or BCN functionalized entities, making it a versatile tool for targeted protein degradation studies and other bioconjugation applications. -
PROTAC Linker
Azide-PEG5-Boc is a PEG-based linker designed for use in the synthesis of PROTACs, functioning primarily as a click chemistry reagent. Its azide group enables efficient copper-catalyzed azide-alkyne cycloaddition reactions with alkyne-containing compounds, as well as strain-promoted alkyne-azide cycloaddition (SPAAC) with DBCO or BCN-functionalized molecules. This versatility makes Azide-PEG5-Boc a valuable tool in the development of targeted protein degradation strategies in chemical biology research. -
PROTAC linker
N-Boc-N-bis(C2-PEG1-azide) is a PROTAC linker designed to facilitate the synthesis of proteolysis-targeting chimeras (PROTACs). This compound features an azide functional group that enables it to participate in copper-catalyzed azide-alkyne cycloaddition (CuAAC) when paired with alkyne-containing moieties. Additionally, it can engage in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN functionalized molecules, providing versatile coupling options for bioconjugation and targeting studies in chemical biology. -
PROTAC linker
Boc-Aminooxy-PEG4-azide is a PEG-based PROTAC linker that facilitates the synthesis of PROTACs through its unique azide functionality. This compound participates in copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with alkyne-containing molecules, as well as strain-promoted alkyne-azide cycloaddition (SPAAC) with DBCO or BCN moieties. Its versatile click chemistry capabilities make it an essential tool for researchers studying targeted protein degradation and other innovative therapeutic approaches. -
PROTAC Linker
Methyltetrazine-Ph-PEG4-azide is a PEG-based linker specifically designed for the synthesis of PROTACs, functioning as a vital component in targeted protein degradation strategies. This compound features a Tetrazine moiety that enables inverse electron-demand Diels-Alder reactions (iEDDA) with TCO-containing partners, enhancing the efficiency of linkage in complex biomolecular assemblies. Additionally, the azide functionality facilitates copper-catalyzed azide-alkyne cycloaddition (CuAAc) and can engage in strain-promoted alkyne-azide cycloaddition (SPAAC) with DBCO or BCN derivatives. This dual reactivity expands its utility in bioconjugation and chemical biology applications. -
PROTAC Linkers
N-(Boc-PEG2)-N-bis(PEG3-azide) is a PEG-based PROTAC linker designed for the synthesis of proteolysis-targeting chimeras (PROTACs). This compound features an azide functional group, enabling copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules, as well as strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN groups. It is valuable for researchers focusing on targeted protein degradation and expanding the applications of PROTAC technology. -
PROTAC Linker
m-PEG9-azide serves as a PEG-based PROTAC linker that facilitates the synthesis of proteolysis-targeting chimeras (PROTACs). This compound features an azide functionality that enables it to participate in copper-catalyzed azide-alkyne cycloaddition reactions (CuAAc) with alkynyl compounds. Additionally, it can engage in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN derivatives, making it a versatile tool for chemical biology applications, particularly in targeted protein degradation research. -
PROTAC linker
Azido-PEG2-hydrazide-Boc is a PEG-based linker designed for use in the synthesis of PROTACs. Functioning as a click chemistry reagent, it features an azide group that facilitates copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules. Additionally, it can participate in strain-promoted azide-alkyne cycloaddition (SPAAC) reactions with compounds containing DBCO or BCN groups. This linker is essential for developing targeted protein degradation strategies and enhances the versatility of bioconjugation in chemical biology research. -
PROTAC linker
N-methyl-N'-methyl-O-(m-PEG4)-O'-(azide-PEG4)-Cy5 functions as a PEG-based PROTAC linker, facilitating the synthesis of heterobifunctional protein-targeting chimeras. This compound features an azide group, enabling its use in click chemistry through copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-bearing molecules. Additionally, it can participate in strain-promoted alkyne-azide cycloaddition (SPAAC) with DBCO or BCN groups, making it suitable for advanced applications in chemical biology and targeted protein degradation research. -
PROTAC Linker
Amino-PEG4-hydrazide-Boc is a PEG-based linker specifically designed for use in the synthesis of Proteolysis Targeting Chimeras (PROTACs). This compound features a hydrazide functional group, facilitating the conjugation of large biomolecules to induce targeted protein degradation. Its unique structure enhances solubility and stability, making it suitable for a variety of applications in chemical biology and drug discovery. -
PROTAC linker
Methyltetrazine-amido-PEG7-azide is a PEG-based linker designed for the synthesis of PROTACs, facilitating targeted protein degradation. This compound features an azide functional group, enabling it to participate in copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with alkyne-containing molecules. Additionally, it is suitable for strain-promoted azide-alkyne cycloaddition (SPAAC) with molecules that have dibenzocyclooctyne (DBCO) or bicyclononyne (BCN) groups, making it a versatile tool in chemical biology and drug development. -
PROTAC Linker
Fmoc-N-amido-PEG3-azide is a PEG-based linker designed for use in the synthesis of PROTACs, functioning primarily through click chemistry. This compound features an azide group that allows for efficient copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules. Additionally, it can participate in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN-modified compounds, making it a versatile tool in chemical biology research and therapeutic development. -
PROTAC linker
Boc-Aminooxy-PEG1-azide is a PEG-based PROTAC linker that facilitates the synthesis of proteolysis-targeting chimeras (PROTACs). Featuring an azide group, it participates in copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules and can engage in strain-promoted alkyne-azide cycloaddition (SPAAC) with DBCO or BCN-functionalized compounds. This reagent is pivotal for studies in targeted protein degradation, providing a versatile tool for advancing research in cell biology and therapeutic development. -
PROTAC Linker
1,1,1-Trifluoroethyl-PEG4-azide is a PEG-based PROTAC linker designed for the synthesis of PROTACs. Functioning as a click chemistry reagent, it features an azide group that enables copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules. Additionally, it can participate in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN derivatives, making it valuable for the development of targeted protein degradation strategies in chemical biology research. -
PROTAC linker
m-PEG10-azide is a PEG-based linker designed for use in the synthesis of PROTACs (Proteolysis Targeting Chimeras). Featuring an azide functional group, it participates in copper-catalyzed azide-alkyne cycloaddition (CuAAc) and strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with alkyne-containing molecules, as well as those with DBCO or BCN groups. This versatile reagent is essential for the assembly of complex bioconjugates, facilitating targeted protein degradation research and advancing drug discovery applications. -
PROTAC Linker
Azide-PEG3-Sulfone-PEG3-azide is a PEG-based linker designed for use in PROTAC synthesis, facilitating the creation of targeted protein degraders. This compound features an azide functional group, enabling it to engage in copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules. Additionally, it is capable of participating in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules possessing DBCO or BCN groups, making it versatile for various bioconjugation applications in chemical research. -
PROTAC Linkers
Fmoc-N-amido-PEG5-azide is a PEG-based PROTAC linker designed for use in the synthesis of PROTAC compounds. This reagent features an azide moiety that enables it to participate in copper-catalyzed azide-alkyne cycloaddition reactions (CuAAc) with alkyne-containing molecules. Additionally, it is capable of undergoing strain-promoted alkyne-azide cycloaddition (SPAAC) with DBCO or BCN-modified entities, making it a versatile tool for bioconjugation and chemical biology applications. -
PROTAC linker
N-Methyl-N'-methyl-O-(m-PEG4)-O'-(azide-PEG4)-Cy3 is a PEG-based PROTAC linker designed for the assembly of PROTAC molecules. Its azide functionality allows for copper-catalyzed azide-alkyne cycloaddition (CuAAC) reactions with alkyne-bearing compounds. Additionally, it is suitable for strain-promoted azide-alkyne cycloaddition (SPAAC) with dibenzocyclooctyne (DBCO) or bicyclononynes (BCN), facilitating precise biomolecular conjugation. This reagent is pivotal for advancing drug development and targeted protein degradation research. -
PROTAC Linker
Fluorescein-thiourea-PEG2-azide is a PEG-based linker designed for use in the synthesis of PROTACs, functioning primarily through click chemistry. This reagent contains an azide group capable of participating in copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with alkyne-containing molecules. Additionally, it can perform strain-promoted alkyne-azide cycloaddition (SPAAC) with DBCO or BCN groups, making it a versatile tool for bioconjugation applications in chemical biology and drug development. -
PROTAC Linker
Azido-PEG3-S-PEG3-azide is a PEG-based linker designed for targeted protein degradation applications via PROTAC technology. This compound features an azide group that facilitates copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules. Additionally, it can participate in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN-bearing compounds, making it a versatile tool for bioconjugation and drug development research. -
PROTAC Linker
Ald-C2-PEG4-azide serves as a PEG-based PROTAC linker, facilitating the synthesis of PROTAC compounds. This compound features an azide functional group enabling its participation in copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with alkyne-containing molecules. Additionally, it can engage in strain-promoted alkyne-azide cycloaddition (SPAAC) with DBCO or BCN groups, making it a versatile tool for bioconjugation and targeted protein degradation studies. -
PROTAC Linker
Trityl-PEG8-azide is a PEG-based linker specifically designed for PROTAC synthesis, facilitating targeted protein degradation. This compound features an azide group, enabling its use in copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-functionalized molecules. Additionally, it supports strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN functionalized compounds, making it a versatile tool in chemical biology and drug development research. -
PROTAC Linker
Benzyl-PEG6-azide is a polyethylene glycol (PEG)-based reagent designed as a PROTAC linker, facilitating the synthesis of proteolysis-targeting chimeras (PROTACs). This compound features an azide functional group which enables copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with alkyne-containing molecules. Additionally, it can participate in strain-promoted alkyne-azide cycloaddition (SPAAC) with dibenzocyclooctyne (DBCO) or bicyclo[6.1.0]non-4-yne (BCN) derivatives, making it a versatile tool in chemical biology for targeted protein degradation studies. -
PROTAC linker
N-(m-PEG4)-N'-(m-PEG4)-O-(m-PEG4)-O'-(azide-PEG4)-Cy5 functions as a PEG-based PROTAC linker, facilitating the synthesis of proteolysis-targeting chimeras (PROTACs). This compound is equipped with an azide group, enabling it to participate in copper-catalyzed azide-alkyne cycloaddition reactions (CuAAc) with alkyne-containing molecules. Additionally, it supports strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN groups, making it a versatile tool for chemical biology applications in targeted protein degradation research. -
PROTAC Linker
m-PEG3-Sulfone-PEG3-azide is a PEG-based linker specifically designed for PROTAC synthesis. Featuring an azide functional group, this compound enables efficient copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing substrates. Additionally, it can participate in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN moieties, facilitating the development of innovative targeted protein degradation strategies in chemical biology research. -
PROTAC Linker
m-PEG4-Hydrazide is a polyethylene glycol (PEG)-based linker designed for use in the synthesis of PROTACs (proteolysis-targeting chimeras). Its unique hydrazide functionality facilitates the conjugation of target proteins with E3 ubiquitin ligases, thereby promoting targeted protein degradation. This compound is an essential tool for researchers exploring targeted therapy and studying protein regulation mechanisms. -
PROTAC linker
N-(m-PEG4)-N'-(azide-PEG4)-Cy3 is a PEG-based linker designed for use in the synthesis of PROTAC (Proteolysis Targeting Chimeras). This molecule features an azide group that facilitates copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing substrates, as well as strain-promoted alkyne-azide cycloaddition (SPAAC) with DBCO or BCN functionalities. Its efficient coupling capabilities make it valuable for advancing research in targeted protein degradation and the development of therapeutic modalities. -
PROTAC Linkers
Boc-NH-PEG4-azide is a polyethylene glycol (PEG)-based PROTAC linker designed for the synthesis of PROTACs. This compound features an azide functional group, enabling it to participate in copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules. Additionally, Boc-NH-PEG4-azide can engage in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with donors like DBCO or BCN. Its versatile reactivity makes it a valuable tool in chemical biology and drug discovery research applications. -
PROTAC Linkers
N-(Boc-PEG3)-N-bis(PEG3-azide) serves as a polyethylene glycol (PEG)-based linker for PROTAC (proteolysis targeting chimeras) synthesis, facilitating the development of targeted protein degradation strategies. This compound contains an azide group, allowing it to participate in copper-catalyzed azide-alkyne cycloaddition (CuAAC) and strain-promoted azide-alkyne cycloaddition (SPAAC) reactions with alkyne-containing partners, such as DBCO and BCN groups. Its versatile reactivity makes it valuable in chemical biology research for constructing novel PROTACs. -
PROTAC Linkers
m-PEG16-azide is a polyethylene glycol (PEG)-based linker designed for the synthesis of proteolysis-targeting chimeras (PROTACs). This compound features an azide functional group that facilitates copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-bearing compounds. Additionally, m-PEG16-azide can participate in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with dibenzocyclooctyne (DBCO) or bicyclononyne (BCN) tagged molecules, making it a valuable tool for bioconjugation and targeted protein degradation studies. Its versatile reactivity enhances the development of novel therapeutic strategies in chemical biology and drug discovery. -
PROTAC linker
m-PEG5-azide is a PEG-based PROTAC linker that facilitates the synthesis of proteolysis-targeting chimeras (PROTACs). Featuring an azide group, it participates in copper-catalyzed azide-alkyne cycloaddition (CuAAc) as well as strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN-containing molecules. This versatile reagent is essential for advancing research in targeted protein degradation and related fields. -
Non-natural Amino Acid
(Rac)-Azide-phenylalanine is a non-natural amino acid featuring an azide functional group, allowing for selective incorporation into proteins for labeling purposes. This compound serves as a valuable tool in click chemistry, participating in copper-catalyzed azide-alkyne cycloaddition (CuAAc) and strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with alkyne-containing molecules. Its applications extend to bioconjugation strategies, facilitating the study of protein interactions and dynamics in chemical biology and biochemical research. -
Click Chemical Reagent
Biotin-azide (N-(3-Azidopropyl)biotinamide) serves as a versatile click chemical reagent featuring a terminal azide moiety. This compound facilitates the synthesis of biotinylated conjugates through copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules. Additionally, Biotin-azide is capable of undergoing strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with dibenzocyclooctyne (DBCO) or bicyclo[6.1.0]nonyne (BCN) functional groups. Its applications span various fields, including bioconjugation and visualization studies in chemical biology. -
Cross-Linked Peptide
Azide-A-DSBSO crosslinker is a homobifunctional, azide-labeled crosslinking reagent that targets lysine residues through an NHS ester reaction. This membrane-permeable and acid-cleavable compound is particularly useful in cross-linking mass spectrometry (XL-MS) to investigate protein-protein interactions. Its mass spectrometry-cleavable properties enable efficient analysis of cross-linked complexes, facilitating deeper insights into protein dynamics and interactions in biological systems. -
Click Chemistry Reagent
Cyclo[Arg-Gly-Asp-D-Phe-Lys(Azide)] is a click chemistry reagent featuring an azide functional group. This compound facilitates the efficient and specific labeling of biomolecules, including nucleic acids, lipids, and proteins, making it valuable in various research applications. Its properties allow for high-yield reactions and straightforward conjugation processes, enabling advancements in drug development, bioconjugation, and materials science. -
Long Chain Protein Modification Reagent
Biotin LC hydrazide is a long chain protein modification reagent that specifically targets periodate-oxidized glycoproteins. It facilitates the biotinylation of these proteins, enhancing their detection and isolation in various biological assays. This reagent is widely used in research applications that require the study of glycoprotein functionality and interactions. -
Azide
Cholesteryl-Teg azide is a cholesterol-modified azide that facilitates bioconjugation reactions. It serves as a valuable ligand for tagging and modifying biomolecules, particularly RNA strands, enabling advanced studies in molecular biology and drug development. Its properties support research in areas such as gene delivery and the synthesis of cholesterol-based therapeutics.
