| 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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| DC35099 |
PC DBCO-PEG3-biotin |
PC DBCO-PEG3-biotin is useful for introducing a biotin moiety to azide-containing biomolecules using copper-free Click Chemistry. The hydrophilic spacer arm provides better solubility to the labeled molecules in aqueous media. Captured biomolecules can be efficiently photoreleased using near-UV, low intensity lamp (e.g. 365 nm lamp at 1-5 mW/cm2). |
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| DC35100 |
WSPC Biotin-PEG3-DBCO |
WSPC Biotin-PEG3-DBCO is useful for introducing a biotin moiety to azide-containing proteins and cell surfaces using copper-free Click Chemistry. This biotin compound is membrane-impermeable due to its water soluble sulfonate group. Captured biomolecules can be efficiently photoreleased using near-UV, low intensity lamp (e.g. 365 nm lamp at 1-5 mW/cm2). |
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| DC35102 |
Biotin-PEG6-hydrazide |
Biotin-PEG6-hydrazide is a hydrazide-activated biotinylation reagent used to label glycoproteins, carbohydrate-containing compounds that have oxidizable sugars or aldehydes. Hydrazine moiety reacts with an aldehyde to form semi-permanent hydrazone bonds. The hydrophilic PEG spacer arm imparts water solubility that is transferred to the biotinylated molecule. |
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| DC35103 |
Biotin-PEG12-hydrazide |
Biotin-PEG12-hydrazide is a hydrazide-activated biotinylation reagent used to label glycoproteins, carbohydrate-containing compounds that have oxidizable sugars or aldehydes. Hydrazine moiety reacts with an aldehyde to form semi-permanent hydrazone bonds. 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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| DC35105 |
Biotin-PEG5-NH-Boc |
Biotin-PEG5-NH-Boc is a Biotin PEG Linker. PEG Linkers may be useful in the development of antibody drug conjugates. |
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| DC35106 |
Biotin-EDA-PEG5-NHS |
Biotin-EDA-PEG5-NHS enables efficient biotinylation of antibodies, proteins and other primary amine-containing biomolecules. NHS-activated biotin compound can react with primary amino groups (-NH2) to form stable, irreversible amide bonds. The hydrophilic PEG spacer arm imparts water solubility that is transferred to the biotinylated molecule. |
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| DC35107 |
Biotin-EDA-PEG4-PFP |
Biotin-EDA-PEG4-PFP is a Biotin PEG Linker. This biochemical will react with primary amino groups (-NH2) to form stable, irreversible amide bonds. 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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| DC35109 |
Biotin-PEG11-oxyamine HCl |
Biotin-PEG11-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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| DC35110 |
Biotin-PEG4-SS-NH-PEG3-oxyamine HCl |
Biotin-PEG4-SS-NH-PEG3-oxyamine HCl salt is a cleavable, 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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| DC35111 |
Biotin-PEG4-methyltetrazine |
Biotin-PEG4-methyltetrazine reacts with TCO-containing compounds via an Inverse-Electron-Demand Diels-Alder reaction to form a stable covalent bond and does not require Cu-catalyst or elevated temperatures. The inverse-electron demand Diels-Alder cycloaddition reaction of TCO with tetrazines is a bioorthogonal reaction. |
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| DC35112 |
Azide-SS-biotin |
Azide-SS-biotin is a cleavable biotinylation reagent for labeling alkyne-containing biomolecules using click chemistry. The azide group reacts with alkynes to form a stable triazole linkage. The hydrophilic PEG spacer arm imparts water solubility that is transferred to the biotinylated molecule. The disulfide bond in this linker can be cleaved using reducing agents such as DTT, BME and TCEP to remove the biotin label. |
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| DC35113 |
Biotin-PEG3-SS-azide |
Biotin-PEG3-SS-azide is a Biotinylating reagent and PEG Linker. PEG Linkers may be useful in the development of antibody drug conjugates (ADCs). |
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| DC35114 |
PC-Biotin-PEG4-NHS carbonate |
PC-Biotin-PEG4-NHS carbonate is a unique amine reactive, photocleavable biotin reagent that is useful for introducing a biotin moiety to amine-containing biomolecules. The NHS carbonate portion of this compound reacts specifically with primary amine groups on the target molecule(s) to form a carbamate linkage. Captured biomolecules can be efficiently photoreleased using an inexpensive, near-UV, low intensity lamp (e.g. 365 nm lamp at 1-5 mW/cm2). |
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| DC35115 |
Fmoc-Lys (biotin-PEG4)-OH |
Fmoc-Lys (biotin-PEG4)-OH is a Lysine embedded biotin PEG derivatives containing a carboxylic group and Fmoc-protected amine. Reaction of carboxylic with primary amino (-NH2) forms stable, irreversible amide bonds. The Fmoc group can be deprotected under basic condition to obtain the free amine which can be used for further conjugations. |
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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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| DC35117 |
TAMRA-Azide-PEG-Desthiobiotin |
TAMRA-Azide-PEG-Desthiobiotin is a Biotin PEG Linker. PEG Linkers may be useful in the development of antibody drug conjugates. |
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| DC35118 |
N-(Biotin)-N-bis(PEG1-alcohol) |
N-(Biotin)-N-bis(PEG1-alcohol) is a PEG Linker. PEG Linkers may be useful in the development of antibody drug conjugates. |
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| DC35119 |
N-(Biotin-PEG4)-N-bis(PEG4-acid) HCl |
N-(Biotin-PEG4)-N-bis(PEG4-acid) HCl salt is a PEG Linker. PEG Linkers may be useful in the development of antibody drug conjugates. |
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| DC35120 |
2-(Biotin-amido)-1,3-bis(carboxylethoxy)propane |
2-(Biotin-amido)-1,3-bis(carboxylethoxy)propane is a Biotin PEG Linker. PEG Linkers may be useful in the development of antibody drug conjugates. |
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| DC35121 |
N-(Azido-PEG3)-N-Biotin-PEG4-methyl ester |
N-(Azido-PEG3)-N-Biotin-PEG4-methyl ester is a Biotin PEG Linker. PEG Linkers may be useful in the development of antibody drug conjugates. |
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| DC35122 |
Bis-PEG1-acid |
Bis-PEG1-acid is a PEG derivative containing two terminal carboxylic acid groups. The terminal carboxylic acids can be reacted with primary amine groups in the presence of activators (e.g. EDC, or DCC) to form a stable amide bond. PEG Linkers may be useful in the development of antibody drug conjugates. |
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| DC35123 |
Bis-PEG2-acid |
Bis-PEG2-acid is a PEG derivative containing two terminal carboxylic acid groups. The hydrophilic PEG spacer increases solubility in aqueous media. The terminal carboxylic acids can be reacted with primary amine groups in the presence of activators (e.g. EDC, or DCC) to form a stable amide bond. PEG Linkers may be useful in the development of antibody drug conjugates. |
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| DC35124 |
Bis-PEG3-acid |
Bis-PEG3-acid is a PEG derivative containing two terminal carboxylic acid groups. The terminal carboxylic acids can be reacted with primary amine groups in the presence of activators (e.g. EDC, or DCC) to form a stable amide bond. PEG Linkers may be useful in the development of antibody drug conjugates. |
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| DC35125 |
Bis-PEG7-acid |
Bis-PEG7-acid is a PEG derivative containing two terminal carboxylic acid groups. The terminal carboxylic acids can be reacted with primary amine groups in the presence of activators (e.g. EDC, or DCC) to form a stable amide bond. PEG Linkers may be useful in the development of the antibody drug conjugates. |
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| DC35126 |
Bis-PEG8-acid |
Bis-PEG8-acid is a PEG derivative containing two terminal carboxylic acid groups. The terminal carboxylic acids can be reacted with primary amine groups in the presence of activators (e.g. EDC, or DCC) to form a stable amide bond. PEG Linkers may be useful in the development of antibody drug conjugates. |
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| DC35127 |
Bis-PEG9-acid |
Bis-PEG9-acid is a PEG derivative containing two terminal carboxylic acid groups. The terminal carboxylic acids 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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| DC35128 |
Bis-PEG10-acid |
Bis-PEG10-acid is a PEG derivative containing two terminal carboxylic acid groups. The terminal carboxylic acids can be reacted with primary amine groups in the presence of activators (e.g. EDC, or DCC) to form a stable amide bond. PEG Linkers may be useful in the development of antibody drug conjugates (ADCs). |
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