Sub Cat. No. |
Molecular Weight |
Glycan Name |
Functional Group |
Inquiry |
X25-04-ZQ361-1 |
PEG 350 Da |
Lactosyl |
Iodoacetate |
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|
X25-04-ZQ361-2 |
PEG 550 Da |
Lactosyl |
Iodoacetate |
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|
X25-04-ZQ361-3 |
PEG 750 Da |
Lactosyl |
Iodoacetate |
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|
X25-04-ZQ361-4 |
PEG 1 kDa |
Lactosyl |
Iodoacetate |
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|
X25-04-ZQ361-5 |
PEG 2 kDa |
Lactosyl |
Iodoacetate |
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|
X25-04-ZQ361-6 |
PEG 3 kDa |
Lactosyl |
Iodoacetate |
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|
X25-04-ZQ361-7 |
PEG 4 kDa |
Lactosyl |
Iodoacetate |
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|
X25-04-ZQ361-8 |
PEG 5 kDa |
Lactosyl |
Iodoacetate |
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|
X25-04-ZQ361-9 |
PEG 10 kDa |
Lactosyl |
Iodoacetate |
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|
X25-04-ZQ361-10 |
PEG 20 kDa |
Lactosyl |
Iodoacetate |
Inquiry
|
Properties
Description
This meticulously synthesized thiol-reactive reagent features a highly reactive iodoacetate moiety covalently linked via a hydrophilic and biocompatible polyethylene glycol (PEG) spacer to lactosyl, a galactose-glucose disaccharide known for its interactions with specific lectins. This high-purity conjugate enables precise and stable alkylation of thiol groups on biomolecules under mild conditions, facilitating the creation of tailored bioconjugates with potential for targeted delivery or surface modification mediated by lactosyl-lectin interactions.
Source
Chemical synthesis
Solubility
Iodoacetate-PEG-lactosyl is soluble in a wide range of organic solvents, such as DCM, DMF, and DMSO, and shows excellent solubility in water.
Identity
Confirmed by NMR.
Applications
Iodoacetate-PEG-lactosyl allows for alkylation of thiol groups with a lactosyl scaffold for potential lectin interactions.