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Aladdin™ SAT(PEG)4(PEGylated N-succinimidyl S-acetylthioacetate) , CAS No.A638760

Item Number
A638760
Grouped product items
SKUSizeAvailabilityPrice Qty
A638760-100mg
100mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$1,088.90

Basic Description

Storage TempStore at -20°C,Desiccated
Shipped InIce chest + Ice pads
Product Description

Product introduction:

SAT(PEG)4 is a long-arm (18.2 angstroms), pegylated form of SATA, a sulfhydryl-addition reagent for covalent modification of primary amines to facilitate controlled, heterobifunctional crosslinking.

Features of SAT(PEG)4:

• Thiolate and PEGylate primary amines in one step
• Add sulfhydryl groups for heterobifunctional crosslinking without compromising protein solubility
• NHS-activated for efficient PEGylation of primary amines at pH 7-9; reaction of NHS-ester group results in formation of stable, irreversible amide bonds
• Pure compound with defined structure and molecular weight, ensuring reproducible protein-modification effects
• PEG spacer provides unique advantages, including increased stability, reduced tendency toward aggregation and reduced immunogenicity

SAT(PEG)4 is the abbreviation for N-Succinimidyl S-acetyl(thiotetraethylene glycol), an amine-reactive reagent for PEGylating and adding sulfhydryl groups to proteins and other amine-containing molecules. LikeSATA and other S-acetyl (SAT) reagents, SAT(PEG)4 is most frequently used in bioconjugation methods to incorporate sulfhydryl (—SH) groups into proteins as part of a two-step or heterobifunctional crosslinking strategy. The SAT group prevents oxidation of the sulfur atom but is easily removed by treatment withhydroxylamine when the unprotected sulfhydryl group is needed for conjugation. The polyethylene glycol (PEG) spacer arm in SAT(PEG)4 minimizes steric hindrance and provides added solubility to the modified and conjugated molecules.

Specific reactivity to primary amines (e.g., lysine residues in proteins) occurs via the NHS-ester group. Spontaneous reaction in phosphate or other non-amine buffer at pH 7-9 results in formation of stable, covalent, amide bonds. Upon deprotection of the sulfhydryl group withhydroxylamine, molecules that have been modified with SAT(PEG)4 can be reacted with other proteins or surfaces that have been maleimide-activated with heterobifunctional crosslinkers likeSulfo-SMCC orSM(PEG)n Reagents.

Reactive Moiety:Active Ester,Succinimidyl Ester,NHS Ester

Crosslinker Type:Heterobifunctional

Form:Liquid

Spacer:Long, Pegylated

Product Properties

ReactivityAmine

Certificates

Certificate of Analysis(COA)

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Chemical and Physical Properties

SolubilityDMF,DMSO

Related Documents

Solution Calculators