Pierce™ SATA (N-succinimidyl S-acetylthioacetate)
Pierce™ SATA (N-succinimidyl S-acetylthioacetate)
Thermo Scientific™

Pierce™ SATA (N-succinimidyl S-acetylthioacetate)

Thermo Scientific Pierce SATA is a short-chain (2.8 angstrom spacer arm) reagent for covalent modification of primary amines and additionRead more
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Catalog NumberQuantity
2610250 mg
Catalog number 26102
Price (USD)
107.00
Each
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Quantity:
50 mg
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Price (USD)
107.00
Each
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Thermo Scientific Pierce SATA is a short-chain (2.8 angstrom spacer arm) reagent for covalent modification of primary amines and addition of a protected yet exposable sulfhydryl group, enabling heterobifunctional crosslinking strategies.

Features of SATA:

• Adds a protected sulfhydryl that can be deprotected by hydroxylamine
• Allows long-term storage of the sulfhydryl-modified molecule
• Forms cleavable disulfide bonds with other sulfhydryl-containing molecules
• Reacts with primary amines (e.g., lysine residues proteins) to form stable amide bonds
• Preserves protein activity with its mild, non-denaturing reaction conditions

SATA (N-succinimidyl S-acetylthioacetate) adds sulfhydryl groups to proteins and other amine-containing molecules in a protected form. The modified molecule can be stored indefinitely and treated with hydroxylamine to expose the labile sulfhydryl group when needed for conjugation reactions. SATA contains an N-hydroxysuccinimide (NHS) ester, which forms a stable, covalent amide bond with primary amines (i.e., lysine residues and the amino termini of proteins) and releases NHS as a by-product. De-protection (deacylation) to generate a free sulfhydryl is accomplished using hydroxylamine-HCl.

Sulfhydryl groups present on proteins, peptides and other compounds are important in protein chemistry/modification reactions. Frequently, thiols are unavailable or absent within the molecules of interest. Several reagents and techniques are available for introducing sulfhydryl groups or disulfides into proteins and peptides, including Traut's Reagent, variants of SPDP, and variants of SATA.

Related Products
Pierce™ Sulfhydryl Addition Kit
Pierce™ SATP
Pierce™ SAT(PEG)4
For Research Use Only. Not for use in diagnostic procedures.
Specifications
FormPowder
Label TypeConjugating Groups
Label or DyeSulfhydryl Group
Product LinePierce™
Quantity50 mg
Reactive MoietyActive Ester, Succinimidyl Ester, NHS Ester
Reagent TypeSATA
SolubilityDMF, DMSO
Chemical ReactivityAmine
Crosslinker TypeHeterobifunctional
Product TypeCrosslinker
SpacerShort (<10 Å)
Unit SizeEach
Contents & Storage
Upon receipt store desiccated at -20°C. Product is shipped at ambient temperature.
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Frequently asked questions (FAQs)

What is the best way to remove unreacted SATA (Cat. No. 26102) after peptide modification?

The best way for removing unreacted SATA (Cat. No 26102) would be HPLC. Another possibility would be to use desalting columns. In case the peptide is bigger than 1.8 kDa, you would like to use the Pierce Polyacrylamide Desalting Columns, 1.8K MWCO, 5 mL (Cat. No 43426).

Find additional tips, troubleshooting help, and resources within our Protein Dialysis, Desalting, and Concentration Support Center.

Documents & Downloads

Certificates

Lot #Certificate TypeDateCatalog Number(s)
3230844Certificate of AnalysisJun 17, 202526102
AB400207Certificate of AnalysisFeb 25, 202526102
ZL396768Certificate of AnalysisFeb 12, 2025DNU-26102, 26102
AA399927Certificate of AnalysisFeb 04, 2025DNU-26102, 26102
ZI379035Certificate of AnalysisOct 24, 202426102
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Safety Data Sheets

Citations & References (1)

Citations & References
Abstract
The lipid A moiety of Porphyromonas gingivalis lipopolysaccharide specifically mediates the activation of C3H/HeJ mice.
Authors:Tanamoto K, Azumi S, Haishima Y, Kumada H, Umemoto T,
Journal:J Immunol
PubMed ID:9127008
The lipid A preparation isolated from Porphyromonas gingivalis was found to induce splenocyte mitogenicity and TNF-alpha release from peritoneal macrophages in LPS-unresponsive C3H/HeJ mice to the same extent as in LPS-responsive mice. In order to clarify whether the activation of C3H/HeJ mice was specifically caused by the lipid A and ... More
1 total citations

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