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Oligo Synthesis

Oligo Synthesis : CEPs

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Amino-Modifier Serinol Phosphoramidite

Amino-Modifier Serinol Phosphoramidite

Glen Research

Catalogue No.DescriptionPack SizePriceQty
10-1997-02Amino-Modifier Serinol Phosphoramidite 0.25g £541.00 Quantity Add to Order
10-1997-90Amino-Modifier Serinol Phosphoramidite 100µmoles £205.00 Quantity Add to Order
10-1997-95Amino-Modifier Serinol Phosphoramidite 50µmoles £114.00 Quantity Add to Order

Description

Amino-Modifier Serinol Phosphoramidite

Structure

Catalog Number: 10-1997-xx

Description: Amino-Modifier Serinol Phosphoramidite

3-Dimethoxytrityloxy-2-(3-(fluorenylmethoxycarbonylamino)propanamido)propyl-1-O-
(2-cyanoethyl)-(N,N-diisopropyl)-phosphoramidite
Formula: C51H59N4O8P M.W.: 887.01 F.W.: 224.15
Diluent: Anhydrous Acetonitrile
Coupling: 6 minute coupling time recommended.
Deprotection: No changes needed from standard method recommended by synthesizer manufacturer.
Storage: Freezer storage, -10 to -30°C, dry

Stability in Solution: 2-3 days

Our repertoire of NHS ester derivatives has been expanded to include the NHS-Carboxy-dT-CE Phosphoramidite. By making a dT analog of the Carboxy-Modifier C10, it is possible to label one or multiple sites within an oligonucleotide. This opens up the possibility to label any number of different dyes or molecules within an oligonucleotide when the phosphoramidite is unavailable. Doing so is straightforward and may be done manually off the synthesizer or even in a fully-automated manner on the DNA synthesizer.

We have never found conditions which allow the TFA group to be removed from an amino-modifier while the oligonucleotide remains attached to the support. We are able to solve this problem by using a 9-fluorenylmethoxycarbonyl (Fmoc) protecting group. The Fmoc group is removed using a two step procedure, the first to remove the cyanoethyl protection groups and flush the formed acrylonitrile from the synthesis column using 1% diisopropylamine in acetonitrile, and the second to remove the Fmoc group using 10% piperidine in DMF. The amino group so formed on the column can be reacted with a variety of activated esters. We offer Fmoc-Amino-Modifier C6 dT Phosphoramidite as a nucleosidic option and Amino-Modifier Serinol Phosphoramidite as a non-nucleosidic alternative. We also offer S-Bz-Thiol-Modifier C6-dT to join the ranks of thiol-modifiers for oligonucleotide synthesis. Thiol-Modifier C6-dT can be added as usual at the desired locations within a sequence.

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Protocols

MSDS

Glen Report 20.2: Novel Reagents for Modification and Labelling

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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
10-1997-90 100µmoles .089grams 1 20 12 7.5 5.45 4 1
10-1997-02 0.25grams .25grams 2.82 80.67 48.4 30.25 22 16.13 4.03
10-1997-95 50µmoles .044grams .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
10-1997-90 100µmoles .089grams 1.5 .07 23.6 14.75 10.73 1.48
10-1997-02 0.25grams .25grams 4.21 .07 77.8 48.63 35.36 4.86
10-1997-95 50µmoles .044grams .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
10-1997-90 100µmoles .089grams 1.5 .07 25.2 15.75 11.45

10-1997-02 0.25grams .25grams 4.21 .07 79.4 49.63 36.09

10-1997-95 50µmoles .044grams .75 .07 10.2 6.38 4.64

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Related products

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