Modification : Maleimide (5')
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
26-6574
Conjugation Chemistry
[Mal]
Y
N
N
203.09
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PS26-6574.pdf
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Catalog No | Scale | Price |
26-6574-05 | 50 nmol | $113.00 |
26-6574-02 | 200 nmol | $113.00 |
26-6574-01 | 1 umol | $147.00 |
26-6574-03 | 2 umol | $221.00 |
26-6574-06 | 5 umol | $661.50 |
26-6574-10 | 10 umol | $881.00 |
26-6574-15 | 15 umol | $1,477.00 |
Discounts are available for Maleimide (5')! |
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
|
MW Note: The molecular weight of 203.09 for maleimide is for the completely deprotected form after retro-Diels Alder reaction. Prior to retro-Diels Alder reaction the MW is 299.22. Gene Link provides maleimide modified oligos that requires retro-Diels Alder reaction by the user. See protocol below.
Maleimide Modifier (5') can be used to directly incorporate an active maleimide moiety onto the 5'-end of an oligonucleotide. The maleimide is separated from the 5'-end nucleotide base by a 2-carbon spacer arm to reduce steric interaction between it and the oligo. Maleimide-labeled oligos are typically used to form conjugates with thiol-labeled moieties, or Diels-Alder cycloaddition products.
As the maleimide moiety itself is not stable over the long-term, Gene Link provides lyophilized maleimido-oligos with all base protecting groups removed and as a maleimide-2,5-dimethylfuran cycloadduct.The cycloadduct serves to protect the maleimide from degradation. The customer then converts the cycloadduct to the active maleimide via a retro-Diels-Alder reaction using toluene and heat. The conversion protocol is provided with the modified oligo. If required the protected oligo should be aliquoted in smaller portions and stored dry.The retro-Diels-Alder reaction should be performed immediately prior to conjugation.
Deprotection by heating in Toluene
Gene Link provides the oligo in a dried lyophilized form. The maleimide is provided in a protected state and deprotection by Retro Diels-Alder reactions is required before use by the end user for conjugation.
The Retro Diels-Alder reactions involves dehydration by co-evaporation with anhydrous acetonitrile and anhydrous toluene. The Retro Diels-Alder reaction requires anhydrous conditions and any significant level of moisture can cause incomplete deprotection, hydrolysis, and/or addition of water to the maleimide. The evaporation of the toluene leaves a white residue ready for conjugation. A detailed procedure is shipped with the product. An abbreviated procedure is described below.
1. Suspend lyophilized oligo in 1 mL anhydrous Acetonitrile. It will be a suspension as oligo will NOT dissolve.
2. Evaporate using a speedvac.
3. Resuspend oligo in 1.5 mL Toluene.
4. Incubate for 4 hrs at 90
o C.
5. Cool to room temperature.
6. Evaporate toluene using a speedvac.
7. The oligonucleotide is now ready for conjugation.
Detailed deprotection Retro Diels-Alder reactions protocol
Retro Diels-Alder Reaction protocol.
- Maleimide-Modifier (5')