Learn More about our other offerings:
Biosearch Technologies Oligo Synthesis
|
Lucigen Reagent Components
|
Rapid Genomics Genotyping Solutions
|
SeraCare
In sequencing applications, the design of primers can be complicated by the degeneracy of the genetic code (there are 64 possible 3-base codon configurations and only 21 amino acids, and therefore the third base in a sequence codon is often unknown). The problem of degeneracy can also be tackled by the use of universal bases.(1) Deoxyinosine is often used as a degenerate base in an oligonucleotide to alleviate this problem.(2) This is possible since its 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 occurring bases. The overall preferential order of base-pairing is: dI-dC > dI-dA > dI-dG = dI-dT. We provide both dI phosphoramidite and CPGs. 2'-Deoxynebularine(3) is another example.
In a true universal nucleoside, the base analogue 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'-deoxynucleosides were 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.
Ref:
|
Synthesizer
|
Column
|
Type/Description
|
Notes
|
|---|---|---|---|
|
MerMade 6,12
|
MerMade, syringe (all scales)
|
Pipette type column
|
A MerMade column is also known as a Supercolumn
|
|
MerMade 4, 48X, 96E, 192E, 192X
|
MerMade, Syringe (up to 1.3 mL)
|
Pipette type column
|
A MerMade column is also known as a Supercolumn
|
|
ABI 384 / 394
|
Luer
|
Barrel column with luer fitting at either end
|
Also known as ALL-FIT or Standard
|
|
Expedite 8909
|
Luer
|
Barrel column with luer fitting at either end
|
Also known as ALL-FIT or Standard
|
|
ABI3900
|
MerMade
|
Pipette type column
|
A MerMade column is also known as a Supercolumn
|
|
K&A H4, H8, H8SE, H2, H32, H64
|
Luer
|
Barrel column with luer fitting at either end
|
Also known as ALL-FIT or Standard
|
|
K&A S4CL/S8CL
|
Luer
|
Barrel column with luer fitting at either end
|
Also known as Standard. For this instrument, we recommend the Luer (Standard) column as the ALL-FIT columns have a wider barrel.
|
|
Dr Oligo 48
|
MerMade
|
Pipette type column
|
A MerMade column is also known as a Supercolumn
|
|
Dr Oligo 192XLc, 768XLc just plates
|
MerMade, Syringe (up to 1.3 mL)
|
Pipette type column
|
A MerMade column is also known as a Supercolumn
|
|
OligoMaker X12, 48, 192, X192, X96
|
MerMade, Syringe (up to 1.3 mL)
|
Pipette type column
|
A MerMade column is also known as a Supercolumn
|
| LK2013 | dU-CE Phosphoramidite |
| LK2016 | dI-CE Phosphoramidite |
| LK2017 | 5-Me-dC(Bz)-CE Phosphoramidite |
| LK2145 | 2-Amino-dA-CE Phosphoramidite |
| LK2164 | 2'-Deoxyxanthosine-CE Phosphoramidite |
| LK2287 | dU SynBase™ CPG 1000/110 |
| LK2293 | dI SynBase™ CPG 1000/110 |
| LK2323 | 5-Me-dC SynBase™ CPG 1000/110 |
| LK2529 | 5-Me-dC(Ac)-CE Phosphoramidite |
Dilution volumes (in ml) are for 0.1M solutions in dry acetonitrile (LK4050). Adjust accordingly for other concentrations. For µmol pack sizes, products should be diluted as 100µmol/ml to achieve 0.1M, regardless of molecular weight.
Item |
Mol. Formula |
Mol. Wt. |
Unit Wt. |
250mg |
500mg |
1g |
| LK2013 | C39H47N4O8P | 730.80 | 290.17 | 3.42 | 6.84 | 13.68 |
| LK2016 | C40H47N6O7P | 754.83 | 314.19 | 3.31 | 6.62 | 13.25 |
| LK2017 | C47H54N5O8P | 847.90 | 303.21 | 2.95 | 5.90 | 11.79 |
| LK2145 | C58H83N10O6P | 1047.33 | 328.22 | 2.39 | 4.77 | 9.55 |
| LK2164 | C56H61N8O12P | 1069.12 | 330.20 | 2.34 | 4.68 | 9.35 |
| LK2287 | - | - | 290.17 | - | - | - |
| LK2293 | - | - | 314.19 | - | - | - |
| LK2323 | - | - | 303.21 | - | - | - |
| LK2529 | C42H52N5O8P | 785.88 | 303.21 | 3.18 | 6.36 | 12.72 |
Couple the phosphoramidites LK2013, LK2016 and LK2017 using the standard method as recommended by synthesiser manufacturer with coupling times as per standard bases. 90s is recommended for 2529. A coupling time of 15min is recommended for LK2145. A coupling time of 3min is recommended for LK2164. The solid supports are used as per standard nucleoside supports.
For LK2013, LK2016, LK2017 and LK2529 standard oligonucleotide deprotection conditions can be applied when deprotecting an oligo containing these modifications, however LK2013, LK2016 and LK2529 are also compatible with AMA deprotection; typically 10min at 55oC.
LK2145 - Use AMA deprotection in conjunction with Ac-dC, rather than Bz-dC, or transamidation will occur. The supports are cleaved and deprotection carried out using the protocols required by the nucleobases.
LK2164 - Cleavage from support and primary deprotection is accomplished by treatment with ammonium hydroxide solution at room temperature for 24h.
After removing the solution1, the NPE groups are removed by treatment with 0.3M tetramethylguanidinium 2-nitrobenzaldoximate solution in water/dioxan (1:1) at 70°C for 48h. We find that this extended treatment is necessary to ensure complete removal of both of the NPE protecting groups.
It should be noted that this treatment generates a variety of low molecular weight by-products which are observed in the HPLC. Satisfactory results are obtained by de-salting the deprotection mixture into water using a NAP or G25 column before HPLC, from which the final oligonucleotide product can then be isolated.
Refrigerate dry compounds. Stability of phosphoramidites in solution is similar to standard dA, dC, dG and dT monomers.
Need some support with placing an order, setting up an account, or finding the right protocol?
Contact us| Europe, Middle East, and Africa | |
|---|---|
| UK | +44 1992 470 757 |
| Germany | +49 30 1663 54600 |
| North America, Latin America | |
| Wisconsin, USA | +1 888 575 9695 |
| Asia Pacific | |
| China | +8621-22509000 |
| Singapore | +65 6734 4800 |