DSS (disuccinimidyl suberate), No-Weigh™ Format
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DSS (disuccinimidyl suberate), No-Weigh™ Format
Thermo Scientific™

DSS (disuccinimidyl suberate), No-Weigh™ Format

Thermo Scientific Pierce DSS, also called disuccinimidyl suberate, is noncleavable and membrane permeable crosslinker that contains an amine-reactive N-hydroxysuccinimide (NHS)Read more
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Catalog NumberQuantity
2165550 mg
A3926710 x 2 mg
215551 g
Catalog number 21655
Price (CNY)
1,425.00
Each
Add to cart
Quantity:
50 mg
Price (CNY)
1,425.00
Each
Add to cart
Thermo Scientific Pierce DSS, also called disuccinimidyl suberate, is noncleavable and membrane permeable crosslinker that contains an amine-reactive N-hydroxysuccinimide (NHS) ester at each end of an 8-carbon spacer arm.

NHS esters react with primary amines at pH 7-9 to form stable amide bonds, along with release of the N-hydroxysuccinimide leaving group. Proteins, including antibodies, generally have several primary amines in the side chain of lysine (K) residues and the N-terminus of each polypeptide that are available as targets for NHS-ester crosslinking reagents. DSS is first dissolved in an organic solvent such as DMF or DMSO, then added to the aqueous crosslinking reaction. BS3, the water soluble analog of DSS is also available for applications that require a hydrophilic crosslinker (e.g. to effect cell-surface crosslinking). DSS and BS3 have essentially identical crosslinking activity toward primary amines.

Features of disuccinimidyl suberate:

Reactive groups: NHS ester (both ends)
Reactive towards: amino groups (primary amines)
• Amine reactive sulfo-NHS ester reacts rapidly with any primary amine-containing molecule
• Membrane-permeable, allowing for intracellular crosslinking
• High purity, crystalline reagent can be used to create high-purity conjugates
• Non-cleavable
• Water-insoluble (dissolve first in DMF or DMSO); compare to BS3 (Sulfo-DSS)

Applications:
• Chemical crosslinking of intracellular proteins prior to cell lysis and immunoprecipitation
• 'Fix' protein interactions to allow identification of weak or transient protein interactions
• Protein crosslinking to create bioconjugates via single-step reactions
• Immobilize proteins onto amine-coated surfaces

Properties of DSS
• Alternative names: Disuccinimidyl suberate
• Molecular formula: C16H20N2O8
• Molecular weight: 368.35
• Spacer arm length: Å (8 atoms)
• CAS number: 68528-80-3
• Reactive groups: NHS esters, react with primary amines at pH 7.0–9.0

DSS Specifications
We manufacture DSS to the highest specifications to produce the most specific bioconjugates, ensure the integrity of your data and to provide you with the highest degree of consistency. Each lot of DSS crosslinker is tested to meet the following minimum specifications:
Identity: IR scan shows only peaks characteristic of the structure and functional groups of DSS
Purity: > 90% by quantitative NMR (the highest standard in crosslinking purity)
Solubility: > 9.2 mg/mL in DMF and DMSO, clear and colorless solution

Product References
Crosslinker Application Guide -- search for recent literature references for this product

Related Products
BS3 (bis(sulfosuccinimidyl)suberate)
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Cell PermeabilityYes
DescriptionDSS
FormPowder
Labeling MethodChemical Labeling
Molecular Weight (g/mol)368.35
PEGylatedNo
Product LinePierce
Quantity50 mg
Reactive MoietyNHS Ester
Shipping ConditionAmbient
SolubilityDMF, DMSO
Spacer Arm Length11.4 Å
Water SolubleNo
Chemical ReactivityAmine-Amine
CleavableNo
Crosslinker TypeHomobifunctional
FormatStandard, Single-use
Product TypeCrosslinker
SpacerMedium (10 to 30 Å)
Unit SizeEach
Contents & Storage
Upon receipt store desiccated at 4°C.

Frequently asked questions (FAQs)

Will the DSS crosslinked product become unlinked as a result of boiling, incubation with SDS, high salt, high or low pH or any other means?

No. DSS crosslinks are amide bonds (same as peptide bonds).

Find additional tips, troubleshooting help, and resources within our Protein Assays and Analysis Support Center.

What is the recommended buffer for optimal DSS crosslinking?

We recommend the following buffers: 20 mM sodium phosphate, 0.15 M NaCl, PBS, pH 7.5. Or HEPES, bicarbonate-carbonate and borate buffers may be substituted for PBS. Nearly any non-amine buffer pH 7-8 can be used.

Find additional tips, troubleshooting help, and resources within our Protein Assays and Analysis Support Center.

What is the difference between DSS and BS3 crosslinkers?

BS3 is the water-soluble analogue of DSS (i.e., DSS is the membrane-permeable analog of BS3). DSS is water-insoluble and membrane-permeable, so it can be used for both intracellular and cell surface crosslinking. BS3 is water-soluble and membrane-impermeable, so it can be used for cell-surface crosslinking.

Find additional tips, troubleshooting help, and resources within our Protein Assays and Analysis Support Center.

What buffers are not recommended for DSS crosslinking?

Any buffer containing primary amines (Tris, glycine, lysine, and ethanolamine) will not work. Glutathione- and imidazole-containing buffers are also not recommended.

Find additional tips, troubleshooting help, and resources within our Protein Assays and Analysis Support Center.

What are the reactive groups in the DSS crosslinking reagent and what are they reactive toward?

The reactive groups are NHS esters that are reactive toward primary amines.

Find additional tips, troubleshooting help, and resources within our Protein Assays and Analysis Support Center.

Citations & References (7)

Citations & References
Abstract
Anti-human activin receptor-like kinase 1 (ALK1) antibody attenuates bone morphogenetic protein 9 (BMP9)-induced ALK1 signaling and interferes with endothelial cell sprouting.
Authors:van Meeteren LA, Thorikay M, Bergqvist S, Pardali E, Stampino CG, Hu-Lowe D, Goumans MJ, ten Dijke P
Journal:J Biol Chem
PubMed ID:22493445
'Genetic and molecular studies suggest that activin receptor-like kinase 1 (ALK1), a transforming growth factor ß (TGF-ß) type I receptor, and endoglin, a TGF-ß co-receptor, play an essential role in vascular development and pathological angiogenesis. Several agents that interfere with ALK1 and endoglin function are currently in clinical trials for ... More
The MUC1-C oncoprotein binds to the BH3 domain of the pro-apoptotic BAX protein and blocks BAX function.
Authors:Ahmad R, Alam M, Rajabi H, Kufe D
Journal:J Biol Chem
PubMed ID:22544745
'The pro-apoptotic BAX protein contains a BH3 domain that is necessary for its dimerization and for activation of the intrinsic apoptotic pathway. The MUC1 (mucin 1) heterodimeric protein is overexpressed in diverse human carcinomas and blocks apoptosis in the response to stress. In this study, we demonstrate that the oncogenic ... More
Crossveinless 2 regulates bone morphogenetic protein 9 in human and mouse vascular endothelium.
Authors:Yao Y, Jumabay M, Ly A, Radparvar M, Wang AH, Abdmaulen R, Boström KI,
Journal:Blood
PubMed ID:22474252
The importance of morphogenetic proteins (BMPs) and their antagonists in vascular development is increasingly being recognized. BMP-4 is essential for angiogenesis and is antagonized by matrix Gla protein (MGP) and crossveinless 2 (CV2), both induced by the activin receptor like-kinase 1 (ALK1) when stimulated by BMP-9. In this study, however, ... More
Crosslinking-MS analysis reveals RNA polymerase I domain architecture and basis of rRNA cleavage.
Authors:Jennebach S, Herzog F, Aebersold R, Cramer P
Journal:Nucleic Acids Res
PubMed ID:22396529
RNA polymerase (Pol) I contains a 10-subunit catalytic core that is related to the core of Pol II and includes subunit A12.2. In addition, Pol I contains the heterodimeric subcomplexes A14/43 and A49/34.5, which are related to the Pol II subcomplex Rpb4/7 and the Pol II initiation factor TFIIF, respectively. ... More
Binding of calmodulin to the D2-dopamine receptor reduces receptor signaling by arresting the G protein activation switch.
Authors:Bofill-Cardona E, Kudlacek O, Yang Q, Ahorn H, Freissmuth M, Nanoff C
Journal:J Biol Chem
PubMed ID:10926927
Signaling by D(2)-dopamine receptors in neurons likely proceeds in the presence of Ca(2+) oscillations. We describe here the biochemical basis for a cross-talk between intracellular Ca(2+) and the D(2) receptor. By activation of calmodulin (CaM), Ca(2+) directly inhibits the D(2) receptor; this conclusion is based on the following observations: (i) ... More