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Oligo Synthesis

Oligo Synthesis : CEPs

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8-Aza-7-deaza-A-CE Phosphoramidite

8-Aza-7-deaza-A-CE Phosphoramidite

Glen Research

Description

8-Aza-7-deaza-A-CE Phosphoramidite

Structure

Catalog Number: 10-3083-xx

Description: 8-Aza-7-deaza-A-CE Phosphoramidite

5'-Dimethoxytrityl-N6-dimethylaminomethylidene-8-aza-7-deaza-Adenosine,
2'-O-TBDMS-3'-[(2-cyanoethyl)-(N,N-diisopropyl)]-phosphoramidite
Formula: C49H67N8O7PSi M.W.: 939.16 F.W.: 329.21

Diluent: Anhydrous Acetonitrile
Coupling: 12 minute coupling time recommended.
Deprotection: RNA Deprotection-see bulletin. Technical Bulletin
Storage: Freezer storage, -10 to -30°C, dry
Stability in Solution: 2-3 days

7-Deaza-Adenosine is lacking nitrogen at the 7-position, which is replaced by carbon. The N7 position in adenosine takes part in non-Watson and Crick hydrogen bonding, which may be relevant to RNA folding and subsequent activity. This Adenosine analogue is also known as Tubercidin. 8-Aza-7-deaza-Adenosine is an isomer of Adenosine with virtually identical electron density. Again, the N7 nitrogen is not available for hydrogen bonding. Nebularine or Purine Nucleoside can be viewed as an Adenosine derivative that is lacking the exocyclic amino group. This molecule allows researchers to determine the relevance of the exocyclic amine of Adenosine to RNA structure and function. Ribozyme activity is substantially affected by the substitution of modified pyrimidine bases. Zebularine (pyrimidin-2-one ribonucleoside) may be regarded as a Cytidine derivative lacking the exocyclic amino group. Zebularine and Pyridin-2-one Ribonucleoside, the 3-deaza analogue of Zebularine, are prime candidates for use in evaluating ribozyme activity and function. It should be noted that Zebularine is mildly fluorescent, absorbing at 298nm and emitting at 367nm. PseudoUridine is one of the most common modified nucleosides found in RNA. The availability of a phosphoramidite will allow detailed research into the effects of this modified base on RNA structure and activity.

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Protocols

MSDS

Glen Report 19.1: Modified RNA Phosphoramidites Useful In Sirna Research And Biologically Significant 1-Methy-Adenosine

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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. Please link for more detailed usage information with the various synthesizers.

ABI 392/394
Cat.No. Pack
Size
Grams/
Pack
0.1M Dil.
(mL)
LV40 LV200 40nm 0.2µm 1µm 10µm
Approximate Number of Additions
10-3083-95 50µmoles .047grams .5 3.33 2 1.25 .91 .67 .17
10-3083-90 100µmoles .094grams 1 20 12 7.5 5.45 4 1
10-3083-02 0.25grams .25grams 2.66 75.33 45.2 28.25 20.55 15.07 3.77
Expedite
Cat.No. Pack
Size
Grams/
Pack
Dilution
(mL)
Molarity 50nm 0.2µm 1µm 15µm
Approximate Number of Additions
10-3083-95 50µmoles .047grams .75 .07 N/A N/A 1.79 N/A
10-3083-90 100µmoles .094grams 1.5 .07 N/A N/A 4.92 N/A
10-3083-02 0.25grams .25grams 3.97 .07 N/A N/A 15.21 N/A
Beckman
Cat.No. Pack
Size
Grams/
Pack
Dilution
(mL)
Molarity 30nm 200nm 1000nm

Approximate Number of Additions
10-3083-95 50µmoles .047grams .75 .07 N/A 1.65 1.55

10-3083-90 100µmoles .094grams 1.5 .07 N/A 4.06 3.82

10-3083-02 0.25grams .25grams 3.97 .07 N/A 12.03 11.3

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Related products

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