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Other Targets

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Cat. No. Product Name Field of Application Chemical Structure
DC35294 Methyltetrazine-DBCO
Methyltetrazine-DBCO is a TCO reactive reagent containing a methyltetrazine group and a DBCO moiety. DBCO is very reactive toward Azide through click chemistry.
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DC35273 2-hydroxyethyl disulfide mono-Tosylate
2-hydroxyethyl disulfide mono-Tosylate is a cleavable PEG Linker. PEG Linkers may be useful in the development of antibody drug conjugates.
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DC35272 THP-SS-PEG1-Tos
THP-SS-PEG1-Tos is a cleavable PEG Linker. PEG Linkers may be useful in the development of antibody drug conjugates.
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DC35271 THP-SS-PEG1-t-butyl ester
THP-SS-PEG1-t-butyl ester is a cleavable PEG Linker. PEG Linkers may be useful in the development of antibody drug conjugates.
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DC35262 Acid-PEG2-SS-PEG2-acid
Acid-PEG2-SS-PEG2-acid is a cleavable PEG Linker. PEG Linkers may be useful in the development of antibody drug conjugates.
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DC35261 Propargyl-PEG1-SS-PEG1-t-butyl ester
Propargyl-PEG1-SS-PEG1-t-butyl ester is a cleavable PEG Linker. PEG Linkers may be useful in the development of antibody drug conjugates.
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DC35259 Propargyl-PEG1-SS-PEG1-PFP ester
Propargyl-PEG1-SS-PEG1-PFP ester is a cleavable PEG Linker. Cleavable PEG Linkers may be useful in the development of antibody drug conjugates.
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DC35258 Propargyl-PEG1-SS-PEG1-acid
Propargyl-PEG1-SS-PEG1-acid is a cleavable PEG Linker. PEG Linkers may be useful in the development of antibody drug conjugates.
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DC35253 Azidoethyl-SS-ethylamine
Azidoethyl-SS-ethylamine is a cleavable PEG linker. PEG Linkers may be useful in the development of antibody drug conjugates.
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DC35252 Azidoethyl-SS-ethylalcohol
Azidoethyl-SS-ethylalcohol is a cleavable PEG Linker. PEG Linkers may be useful in the development of antibody drug conjugates.
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DC35241 Bromoacetamido-PEG4-t-butyl ester
Bromoacetamido-PEG4-t-butyl ester is a PEG derivative containing a bromide group and a t-butyl protected carboxyl group. The hydrophilic PEG spacer increases solubility in aqueous media. The bromide (Br) is a very good leaving group for nucleophilic substitution reactions. The t-butyl protected carboxyl group can be deprotected under acidic conditions.
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DC35240 Bromoacetamido-PEG3-t-butyl ester
Bromoacetamido-PEG3-t-butyl ester is a PEG derivative containing a bromide group and a t-butyl protected carboxyl group. The bromide (Br) is a very good leaving group for nucleophilic substitution reactions. The t-butyl protected carboxyl group can be deprotected under acidic conditions.
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DC35232 Bromoacetamido-PEG4-acid
Bromoacetamido-PEG4-acid is a PEG derivative containing a bromide group and a terminal carboxylic acid. The bromide (Br) is a very good leaving group for nucleophilic substitution reactions. The terminal carboxylic acid can be reacted with primary amine groups in the presence of activators (e.g. EDC, or DCC) to form a stable amide bond.
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DC35231 Bromoacetamido-PEG3-acid
Bromoacetamido-PEG3-acid is a PEG derivative containing a bromide group and a terminal carboxylic acid. The bromide (Br) is a very good leaving group for nucleophilic substitution reactions. The terminal carboxylic acid can be reacted with primary amine groups in the presence of activators (e.g. EDC, or DCC) to form a stable amide bond.
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DC35209 Bromo-PEG4-CH2CO2tBu
Bromo-PEG4-CH2CO2tBu is a PEG derivative containing a bromide group and a t-butyl protected carboxyl group. The hydrophilic PEG spacer increases solubility in aqueous media. The bromide (Br) is a very good leaving group for nucleophilic substitution reactions. The t-butyl protected carboxyl group can be deprotected under acidic conditions.
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DC35207 Bromo-PEG2-CH2CO2tBu
Bromo-PEG2-CH2CO2tBu is a PEG derivative containing a bromide group and a t-butyl protected carboxyl group. The hydrophilic PEG spacer increases solubility in aqueous media. The bromide (Br) is a very good leaving group for nucleophilic substitution reactions. The t-butyl protected carboxyl group can be deprotected under acidic conditions.
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DC35197 Bromo-PEG5-acid
Bromo-PEG5-acid is a PEG derivative containing a bromide group and a terminal carboxylic acid. The bromide (Br) is a very good leaving group for nucleophilic substitution reactions. The terminal carboxylic acid can be reacted with primary amine groups in the presence of activators (e.g. EDC, or DCC) to form a stable amide bond.
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DC35194 Bromo-PEG2-acid
Bromo-PEG2-acid is a PEG derivative containing a bromide group and a terminal carboxylic acid. The bromide (Br) is a very good leaving group for nucleophilic substitution reactions. The terminal carboxylic acid can be reacted with primary amine groups in the presence of activators (e.g. EDC, or DCC) to form a stable amide bond.
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DC35190 t-Boc-N-amido-PEG3-sulfonic acid
t-Boc-N-amido-PEG3-sulfonic acid is a biochemical. PEG Linkers may be useful in the development of antibody drug conjugates.
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DC35178 Bromoacetamido-PEG2-Boc-amine
Bromoacetamido-PEG2-Boc-amine is a PEG derivative. PEG Linkers and derivatives may be useful in the development of antibody drug conjugates.
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DC35116 TAMRA-Azide-PEG-Biotin
TAMRA-Azide-PEG-Biotin is a Biotin PEG Linker. PEG Linkers may be useful in the development of antibody drug conjugates.
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DC35108 Biotin-PEG3-oxyamine HCl
Biotin-PEG3-oxyamine HCl salt is an aldehyde-reactive biotinylation reagent. It reacts with an aldehyde to form an oxime bond. If a reductant is used, it will form a hydroxylamine linkage. The hydrophilic PEG spacer arm imparts water solubility that is transferred to the biotinylated molecule.
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DC35104 Biotin-PEG2-NH-Boc
Biotin-PEG2-NH-Boc is a Biotin PEG Linker. PEG Linkers may be useful in the development of antibody drug conjugates (ADCs).
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DC35098 Dde Biotin-PEG4-DBCO
Dde Biotin-PEG4-DBCO is a cleavable reagent for introduction of a biotin moiety to azide-containing biomolecules using copper-free Click Chemistry. Dde protecting group allows efficient release of captured biotinylated molecules from streptavidin under mild conditions with hydrazine. PEG Linkers may be useful in the development of antibody drug conjugates.
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DC35087 Dde Biotin-PEG4-alkyne
Dde Biotin-PEG4-alkyne is useful for introducing a biotin moiety to azide-containing biomolecules using Cu(I)-catalyzed Click Chemistry. The hydrophilic spacer arm provides better solubility to the labeled molecules in aqueous media. Dde protecting group allows efficient release of captured biotinylated molecules from streptavidin under mild conditions with hydrazine. PEG Linkers may be useful in the development of antibody drug conjugates.
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DC35078 Dde Biotin-PEG4-azide
Dde Biotin-PEG4-azide is useful for introducing a biotin moiety to alkyne-containing biomolecules using Cu(I)-catalyzed Click Chemistry. The Dde protecting group allows efficient release of captured biotinylated molecules from streptavidin under mild conditions with hydrazine.
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DC35037 Benzyl-PEG6-Ms
Benzyl-PEG6-Ms is a Benzyl PEG Linker. PEG Linkers may be useful in the development of antibody drug conjugates.
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DC35035 Benzyl-PEG6-CH2CO2tBu
Benzyl-PEG6-CH2CO2tBu is a Benzyl PEG Linker. PEG Linkers may be useful in the development of antibody drug conjugates.
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DC35034 Benzyl-PEG5-CH2CO2tBu
Benzyl-PEG5-CH2CO2tBu is a Benzyl PEG Linker. PEG Linkers may be useful in the development of antibody drug conjugates.
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DC35013 t-Boc-Aminooxy-PEG4-Tos
t-Boc-Aminooxy-PEG4-Tos is an Aminooxy PEG Linker. Aminooxy-PEG can be used in bioconjugation. It reacts with an aldehyde to form an oxime bond. If a reductant is used, it will form a hydroxylamine linkage.
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