

Oligo Synthesis : CEPs
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Amino-Modifier C6 dA
Amino-Modifier C6 dA
Glen Research
Catalogue No. | Description | Pack Size | Price | Qty |
|
---|---|---|---|---|---|
10-1089-02 | Amino-Modifier C6 dA | 0.25g | £364.00£345.80Offer until : 31-Mar-2021Offer Code : GLEN5View Offer | Quantity | Add to Order |
10-1089-90 | Amino-Modifier C6 dA | 100µmoles | £164.00£155.80Offer until : 31-Mar-2021Offer Code : GLEN5View Offer | Quantity | Add to Order |
Related products
Amino-Modifier C6 dA
Amino-Modifier C6 dA
Glen Research
Amino-Modifier C6 dA |
Catalog Number: 10-1089-xx
Description: Amino-Modifier C6 dA
5"-Dimethoxytrityl-N6-benzoyl-N8-[6-(trifluoroacetylamino)-hex-1-yl]-8-amino-2"-deoxyAdenosine-3"-[(2-cyanoethyl)-(N,N-diisopropyl)]-phosphoramidite | ||
Formula: C55H65F3N9O8P | M.W.: 1068.14 | F.W.: 427.40 |
Diluent: Anhydrous Acetonitrile |
Coupling: Amino-Modifier C6 dA reacts in a manner identical to normal phosphoramidites.To prevent side reactions, synthesize using acetyl-protected dC. See Deprotection for futher details. |
Deprotection:No changes needed from standard method recommended by synthesizer manufacturer. The TFA protecting group is removed during standard ammonium hydroxide deprotection.A minor side reaction during ammonia deprotection can lead to irreversibly capping 2-5% of the amine. This could be significant if multiple additions of the modifier are made. To prevent the reaction, synthesize using acetyl-protected dC and deprotect in 30% ammonia/40% methylamine 1:1 (AMA) at 65°C for 15 minutes. |
Storage: Refrigerated storage, maximum of 2-8°C, dry |
Stability in Solution: 2-3 days |
SEQUENCE MODIFIERS
Sequence Modifiers are designed for use in automated synthesis.The carboxy-dT is hydrolyzed during deprotection and can be coupled directly toa molecule containing a primary amino group by a standard peptide coupling orvia the intermediate N-hydroxysuccinimide (NHS) ester. Amino-Modifier dA,Amino-Modifier dC, Amino-Modifier dG and both Amino-Modifier dT products can beadded in place of a dA, dC, dG and dT residue, respectively, duringoligonucleotide synthesis. Corresponding Amino-Modifier supports can replacetheir respective deoxynucleoside supports. After deprotection, the primary amineon the C6 analogues is separated from the oligonucleotide by a spacer arm with atotal of 7 -10 atoms and can be labelled or attached to an enzyme. The C2analogue is more suitable for the attachment of molecules designed to react withthe oligonucleotide.
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Amino-Modifier C6 dA
Amino-Modifier C6 dA
Glen Research
MSDS
Glen Report 16.1: Minor Base and Related Novel Phosphoramidites
Techinical Notes
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Amino-Modifier C6 dA
Amino-Modifier C6 dA
Glen Research
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. | PackSize | Grams/Pack | 0.1M Dil.(mL) | LV40 | LV200 | 40nm | 0.2µm | 1µm | 10µm |
Approximate Number of Additions | |||||||||
10-1089-02 | 0.25grams | .25grams | 2.34 | 64.67 | 38.8 | 24.25 | 17.64 | 12.93 | 3.23 |
10-1089-90 | 100µmoles | .107grams | 1 | 20 | 12 | 7.5 | 5.45 | 4 | 1 |
Expedite | |||||||||
Cat.No. | PackSize | Grams/Pack | Dilution(mL) | Molarity | 50nm | 0.2µm | 1µm | 15µm | |
Approximate Number of Additions | |||||||||
10-1089-02 | 0.25grams | .25grams | 3.49 | .07 | 63.4 | 39.63 | 28.82 | 3.96 | |
10-1089-90 | 100µmoles | .107grams | 1.5 | .07 | 23.6 | 14.75 | 10.73 | 1.48 | |
Beckman | |||||||||
Cat.No. | PackSize | Grams/Pack | Dilution(mL) | Molarity | 30nm | 200nm | 1000nm | ||
Approximate Number of Additions | |||||||||
10-1089-02 | 0.25grams | .25grams | 3.49 | .07 | 65 | 40.63 | 29.55 | ||
10-1089-90 | 100µmoles | .107grams | 1.5 | .07 | 25.2 | 15.75 | 11.45 |
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