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Oligo Synthesis

Oligo Synthesis : CEPs

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Asymmetric Doubler Phosphoramidite

Asymmetric Doubler Phosphoramidite

Glen Research

Description

Asymmetric Doubler Phosphoramidite

Structure

Catalog Number: 10-1921-xx

Description: Asymmetric Doubler Phosphoramidite

1-[5-(4,4'-dimethoxytrityloxy)pentylamido]-3-[5-fluorenomethoxycarbonyloxy
pentylamido]-propyl-2-[(2-cyanoethyl)-(N,N-diisopropyl)]-phosphoramidite
Formula: C57H69N4O10P M.W.: 1001.17 F.W.: 351.31

Diluent: Anhydrous Acetonitrile
Coupling: Synthesis should be carried out on 1000 support. A 15 minute coupling time is recommended for the doubler addition.
Deprotection: - Complete the synthesis of the first branch, remove the final DMT, and terminate by capping for 30 min.- Remove the Fmoc group using 1M DBU in anhydrous acetonitrile for 5 minutes at room temperature.- Resume normal oligonucleotide synthesis to complete the second branch.
Storage: Freezer storage, -10 to -30°C, dry
Stability in Solution: 2-3 days
Please Note: This product is supplied under license from ISIS Innovation Limited.

Dendrimers

Dendrimers are discrete, highly branched, monodispersed polymers that possess patterns reminiscent of the branching of trees. Plain and mixed oligonucleotide dendrimers can be synthesized using novel doubling and trebling phosphoramidite synthons.1,2 Dendrimers offer the following advantages. Incorporation of label using γ-32P-ATP and polynucleotide kinase increases in proportion to the number of 5’-ends. Fluorescent signal also increases in proportion to the number of 5’-ends, if spacers are incorporated between the labels and the ends of the branches. When using a dendrimeric oligonucleotide as a PCR primer, the strand bearing the dendrimer is resistant to degradation by T7 Gene 6 exonuclease making it easy to convert the double-stranded product of the PCR to a multiply labelled, single-stranded probe. Enhanced stability of DNA dendrimers makes them useful as building blocks for the ‘bottom up’ approach to nano-assembly. These features also suggest applications in DNA chip technology when higher temperatures are required, for example, to melt secondary structure in the target

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Protocols

MSDS

Glen Report 12.1: OLIGONUCLEOTIDE DENDRIMERS: FROM POLY-LABELLED DNA PROBES TO STABLE NANO-STRUCTURES

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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
10-1921-02 0.25grams .25grams 2.5 70 42 26.25 19.09 14 3.5
10-1921-90 100µmoles .1grams 1 20 12 7.5 5.45 4 1
Expedite
Cat.No. Pack
Size
Grams/
Pack
Dilution
(mL)
Molarity 50nm 0.2µm 1µm 15µm  
Approximate Number of Additions
10-1921-02 0.25grams .25grams 3.73 .07 68.2 42.63 31 4.26  
10-1921-90 100µmoles .1grams 1.5 .07 23.6 14.75 10.73 1.48  
Beckman
Cat.No. Pack
Size
Grams/
Pack
Dilution
(mL)
Molarity 30nm 200nm 1000nm    
Approximate Number of Additions
10-1921-02 0.25grams .25grams 3.73 .07 69.8 43.63 31.73    
10-1921-90 100µmoles .1grams 1.5 .07 25.2 15.75 11.45  

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Related products

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