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Oligo Synthesis

Oligo Synthesis : CEPs

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2'-dX-CE Phosphoramidite

2'-Deoxyxanthosine phosphoramidite

Glen Research

Catalogue No.DescriptionPack SizePriceQty
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10-1537-022'-dX-CE Phosphoramidite0.25g €1,080.00 Quantity Add to Order
10-1537-902'-dX-CE Phosphoramidite100umole €469.20 Quantity Add to Order
10-1537-952'-dX-CE Phosphoramidite50umole €246.00 Quantity Add to Order

Description

Structure

Catalog Number: 10-1537-xx

Description: dX-CE Phosphoramidite

5'-(4,4'-Dimethoxytrityl)-2,6-O-bis(2-(4-nitrophenyl)ethyl)-2'-deoxyXanthosine,
3Õ-[(2-cyanoethyl)-N,N-diisopropyl)]-phosphoramidite
Formula: C56H61N8O12P M.W.: 1069.10 F.W.: 330.19

Diluent: Anhydrous Acetonitrile
Coupling: No changes needed from standard method recommended by synthesizer manufacturer.
Deprotection: With the oligonucleotide still attached to the support, treat with 1 M DBU in anhydrous ACN for 2-3 minutes, followed by 17 hours using fresh 1 M DBU at room temperature. Rinse support with ACN and then deprotect as required by nucleobases. Note, the dX nucleoside is susceptible to depurination though short exposure to acid is tolerated - e.g. Glen-Pak purification.
Storage: Freezer storage, -10 to -30°C, dry
Stability in Solution: 1-2 days

2’-DeoxyXanthosine (dX) is a naturally occurring nucleoside that may be derived from oxidative deamination of 2’-deoxyGuanosine (dG). dX has a similar bonding pattern to thymidine and it may base pair with dA, with such purine-purine interactions causing duplex distortion. dX also featured in attempts to extend the genetic alphabet with a new base pair of dX and pyrimidine-2,4-diamine nucleoside. dX has also interested researchers in the field of DNA damage and repair since it is a product of nitric oxide-induced mutagenesis.

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Protocols

MSDS

Glen Report 22.2

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References

  1. R Eritja, et al., Nucleic Acids Res., 1986, 14, 8135-53
  2. M J Lutz, H A Held, M Hottiger, U Hubscher, and S A Benner, Nucleic Acids Res., 1996, 24, 1308-13
  3. G E Wuenschell, T R O'Connor, and J Termini, Biochemistry, 2003, 42, 3608-16
  4. S C Jurczyk, J Horlacher, K G Devined, S A Benner, and T R Battersby, Helv Chim Acta, 2000, 83, 1517-1524

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Applications & Benefits

DILUTION/COUPLING DATA

The table below shows pack size data and, for solutions, dilutions and approximate couplings based on normal priming procedures.

ABI 392/394
Cat.No. Pack
Size
Grams/
Pack
0.1M Dil.
(mL)
LV40 LV200 40nm 0.2µm 1µm 10µm
Approximate Number of Additions
10-1537-02 0.25grams .25grams 2.34 64.67 38.8 24.25 17.64 12.93 3.23
10-1537-90 100µmoles .107grams 1 20 12 7.5 5.45 4 1
10-1537-95 50µmoles .053grams .5 3.33 2 1.25 .91 .67 .17
Expedite
Cat.No. Pack
Size
Grams/
Pack
Dilution
(mL)
Molarity 50nm 0.2µm 1µm 15µm
Approximate Number of Additions
10-1537-02 0.25grams .25grams 3.49 .07 63.4 39.63 28.82 3.96
10-1537-90 100µmoles .107grams 1.5 .07 23.6 14.75 10.73 1.48
10-1537-95 50µmoles .053grams .75 .07 8.6 5.38 3.91 .54
Beckman
Cat.No. Pack
Size
Grams/
Pack
Dilution
(mL)
Molarity 30nm 200nm 1000nm

Approximate Number of Additions
10-1537-02 0.25grams .25grams 3.49 .07 65 40.63 29.55

10-1537-90 100µmoles .107grams 1.5 .07 25.2 15.75 11.45

10-1537-95 50µmoles .053grams .75 .07 10.2 6.38 4.64

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Related products

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