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Thiol SS-C3

picture of Thiol SS-C3

Modification : Thiol SS-C3

Catalog Reference Number
Category
Modification Code
5 Prime
3 Prime
Internal
Molecular Weight (mw)
Extinction Coeficient (ec)
Technical Info (pdf)
Absorbance MAX
Emission MAX
Absorbance EC



26-6482
End Modifiers
SS-C3
N
Y
N
154.12
-
PS26-6482.pdf
-
-
-


Catalog NoScalePrice
26-6482-0550 nmol$210.00
26-6482-02200 nmol$210.00
26-6482-011 umol$290.00
26-6482-032 umol$395.00
26-6482-1010 umol$2,127.00
26-6482-1515 umol$2,450.00
Discounts are available for Thiol SS-C3!
Modification* Discount Price Structure
1 site/order List price
2 sites/order 10% discount
3 sites/order 20% discount
4 sites/order 30% discount
5-9 sites/order 50% discount
10+ sites/order 60% discount
*Exceptions apply

Thiol-SS-C3 is a disulfide-containing modifier designed to functionalize an oligonucleotide with a reactive thiol (sulfhydryl) group at the 5- or 3-end. This modification is incorporated into the oligonucleotide as a disulfide during oligonucleotide synthesis, in order to protect the thiol group from undesired side reactions. The oligo is supplied as a disulfide and the customer has to reduce it with TCEP or DTT or other reducing agent to generate the reduced thiol group. The thiol group is separated from the oligo by a three-carbon spacer arm, to reduce steric interactions with the end of the oligo.


See Gene Link thiol reduction technical sheet for details Thiol Reduction Protocol

Thiolated oligonucleotides can be labeled with thiol-reactive dye / happen iodoacetamides or maleimides (for example, lucifer yellow iodoacetamide or fluorescein maleimide) for use as hybridization or PCR-based detection probes (1). They also can be conjugated to enzymes (for example, alkaline phosphatase or horseradish peroxidase), through bifunctional linkers (2). Finally, thiolated oligos can be attached to glass slides or gold surfaces for use in various microarray or nanoelectronic applications (3,4). However, because oligos labeled with only one thiol slowly dissociate from a gold surface at the temperatures (60C to 90C) and high salt concentrations commonly used to denature DNA duplexes (5), Gene Link recommends that researchers who plan to use such conditions to repeatedly strip and re-probe oligo arrays based on thiol-gold surface conjugation modify the oligos with DTPA, which incorporates two thiol groups into the oligo, thereby allowing for a more stable attachment to gold. For further information on DTPA, please see its technical sheet.



References
1. Connolly, B.A., Rider, P. Chemical synthesis of oligonucleotides containing a free sulphydryl group and subsequent attachment of thiol specfic probes. Nucleic Acids Res. (1985), 13: 4485-4502.
2. Ghosh, S.S, Kao, P.M., McCue, A.W., Chappelle, H.L. Use of maleimide-thiol coupling chemistry for efficient syntheses of oligonuclotide-enzyme conjugate hybridization probes. Bioconjugate Chem. (1990), 1: 71-76.
3. Roger, Y-H., Jiang-Baucom, P., Huang, Z-J., Bogdanov, V., Anderson, S., Boyce-Jacino, M.T. Immobilization of oligonucleotides onto a glass support via disulfide bonds: A method for preparation of DNA microarrays. Anal. Biohem. (1999), 266: 23-30.
4. Ackerson, C.J., Sykes, M.T., Kornberg, R.D. Defined DNA/nanoparticle conjugates. Proc. Natl. Acad. Sci. USA (2005), 102: 13383-13385.
5. Li, Z., Jin, R., Mirkin, C.A., Letsinger, R.L. Multiple thiol-anchor capped DNA-gold nanoparticle conjugates Nucleic Acids Res. (2002), 30: 1558-1562.
- Thiol SS-C3

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