Oligo Synthesis : CEPs
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dI-CE Phosphoramidite
dI-CE Phosphoramidite
Glen Research
| Catalogue No. | Description | Pack Size | Price | Qty |
|
|---|---|---|---|---|---|
| 10-1040-02 | dI-CE Phosphoramidite | 0.25g | £100.00£95.00Offer until : 31-Mar-2021Offer Code : GLEN5View Offer | Quantity | Add to Order |
| 10-1040-90 | dI-CE Phosphoramidite | 100µmoles | £50.00£47.50Offer until : 31-Mar-2021Offer Code : GLEN5View Offer | Quantity | Add to Order |
Related products
dI-CE Phosphoramidite
dI-CE Phosphoramidite
Glen Research
| dI-CE Phosphoramidite |
Catalog Number: 10-1040-xx
Description: dI-CE Phosphoramidite
| 5"-Dimethoxytrityl-2"-deoxyInosine,3"-[(2-cyanoethyl)-(N,N-diisopropyl)]-phosphoramidite | ||
| Formula: C40H47N6O7P | M.W.: 754.79 | F.W.: 314.19 |
Diluent: Anhydrous Acetonitrile |
| Coupling: No changes needed from standard method recommended by synthesizer manufacturer. |
| Deprotection: No changes needed from standard method recommended by synthesizer manufacturer. |
| Storage: Refrigerated storage, maximum of 2-8°C, dry |
| Stability in Solution: Similar to dA,C,G,T-CE Phosphoramidites |
duplex effects
The design of primers is frequently complicated by the degeneracy of the genetic code. Three strategies are now available to confront this problem. In the first, a mixed base addition (N) is used to form the degenerate site. This approach is best if the number of degenerate sites is small. A second option is the use of 2’-deoxyInosine or 2’-deoxyNebularine which exhibit low, but unequal, hydrogen bonding to the other four bases. The third option is the use of a universal nucleoside. In this strategy, the base analog does not hybridize significantly to the other four bases and makes up some of the duplex destabilization by acting as an intercalating agent. 3-Nitropyrrole 2’-deoxynucleoside (M) is the first example of a set of universal bases. Subsequently, 5-nitroindole was determined to be an effective universal base and to be superior to 3-nitropyrrole, based on duplex melting experiments.
The modified bases designated P and K show considerable promise as degenerate bases. The pyrimidine derivative P, when introduced into oligonucleotides, base pairs with either A or G, while the purine derivative K base pairs with either C or T. A dP dK mix also can serve as a mixed base with much less degeneracy than dA dC dG dT (N).
If you cannot find the answer to your problem below then please contact us or telephone 01954 210 200
dI-CE Phosphoramidite
dI-CE Phosphoramidite
Glen Research
Material Safety Data Sheet
If you cannot find the answer to your problem below then please contact us or telephone 01954 210 200
dI-CE Phosphoramidite
dI-CE Phosphoramidite
Glen Research
The design of primers is frequently complicated by the degeneracy of the genetic code. Three strategies are now available to confront this problem.
- A mixed base addition (N) is used to form the degenerate site. This approach is best if the number of degenerate sites is small.
- The use of 2"-deoxyInosine or 2"-deoxyNebularine which exhibit low, but unequal, hydrogen bonding to the other 4 bases.
- The use of a universal nucleotide. In this strategy, the base analog does not hybridise significantly to the other 4 bases and makes up some of the duplex destabilisation by acting as an intercalating agent.
EXTINCTION DATA
| Item | Nucleoside | λMax-1 | Emax-1 | λMax-2 | Emax-2 | E260 |
| (nm) | (ml/µmole) | nm | (ml/µmole) | (ml/µmole) | ||
| 10-1040 | dI (Inosine) | 249 | 12.5 | 7.5 |
Frequently Asked Technical Question
QUESTION: What is the base-pairing specificity of dI in an oligonucleotide?
RESPONSE:Deoxy-Inosine is often used as a degenerate base in an oligonucleotide probe or primer. This is possible since the structure allows it to base pair with all four bases in various wobble structures. However the base-pairing is not equivalent with each of the 4 naturally occuring bases. The overall preferential order of base-pairing is.
dI-dC > dI-dA > dI-dG = dI-dT
REFERENCE(S):Martin,F.H. et.al., (1985), Nucleic Acids Res., 13, 8927-8938.Case-Green,S. C., Southern, E.M., (1994), Nucleic Acids Res., 22, 131-136.
DILUTION/COUPLING DATA
The table below shows pack size data and, for solutions, dilutions and approximate couplings based on normal priming procedures. Please link for more detailed usage information with the various synthesizers.
| ABI 392/394 | |||||||||
| Cat.No. | PackSize | Grams/Pack | 0.1M Dil.(mL) | LV40 | LV200 | 40nm | 0.2µm | 1µm | 10µm |
| Approximate Number of Additions | |||||||||
| 10-1040-02 | 0.25grams | .25grams | 3.31 | 97 | 58.2 | 36.38 | 26.45 | 19.4 | 4.85 |
| 10-1040-90 | 100µmoles | .075grams | 1 | 20 | 12 | 7.5 | 5.45 | 4 | 1 |
| Expedite | |||||||||
| Cat.No. | PackSize | Grams/Pack | Dilution(mL) | Molarity | 50nm | 0.2µm | 1µm | 15µm | |
| Approximate Number of Additions | |||||||||
| 10-1040-02 | 0.25grams | .25grams | 4.94 | .07 | 92.4 | 57.75 | 42 | 5.78 | |
| 10-1040-90 | 100µmoles | .075grams | 1.5 | .07 | 23.6 | 14.75 | 10.73 | 1.48 | |
| Beckman | |||||||||
| Cat.No. | PackSize | Grams/Pack | Dilution(mL) | Molarity | 30nm | 200nm | 1000nm | ||
| Approximate Number of Additions | |||||||||
| 10-1040-02 | 0.25grams | .25grams | 4.94 | .07 | 94 | 58.75 | 42.73 | ||
| 10-1040-90 | 100µmoles | .075grams | 1.5 | .07 | 25.2 | 15.75 | 11.45 | ||
If you cannot find the answer to your problem below then please contact us or telephone 01954 210 200
