Oligo Synthesis : CEPs
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2-Aminopurine-TBDMS-CE Phosphoramidite
2-Aminopurine-TBDMS-CE Phosphoramidite
Glen Research
| Catalogue No. | Description | Pack Size | Price | Qty |
|
|---|---|---|---|---|---|
| 10-3070-02 | 2-Aminopurine-TBDMS-CE Phosphoramidite | 0.25g | £780.00£741.00Offer until : 31-Mar-2021Offer Code : GLEN5View Offer | Quantity | Add to Order |
| 10-3070-90 | 2-Aminopurine-TBDMS-CE Phosphoramidite | 100µmoles | £340.00£323.00Offer until : 31-Mar-2021Offer Code : GLEN5View Offer | Quantity | Add to Order |
| 10-3070-95 | 2-Aminopurine-TBDMS-CE Phosphoramidite | 50µmoles | £170.00£161.50Offer until : 31-Mar-2021Offer Code : GLEN5View Offer | Quantity | Add to Order |
Related products
2-Aminopurine-TBDMS-CE Phosphoramidite
2-Aminopurine-TBDMS-CE Phosphoramidite
Glen Research
| 2-Aminopurine-TBDMS-CE Phosphoramidite |
Catalog Number: 10-3070-xx
Description: 2-Aminopurine-TBDMS-CE Phosphoramidite
| 5"-Dimethoxytrityl-N2-isobutyryl-2-aminopurine riboside, 2"-O-TBDMS-3"-[(2-cyanoethyl)-(N,N-diisopropyl)]- phosphoramidite | ||
| Formula: C50H68N7O8PSi | M.W.: 954.19 | F.W.: 329.21 |
Diluent: Anhydrous Acetonitrile |
| Coupling: 12 minute coupling time recommended.See Technical Bulletin |
| Deprotection: RNA deprotaction using Ammonium Hydroxide:MethylAmine (AMA) 1:1 at 65°C for 10 minutes.See Technical Bulletin for details (www.glenresearch.com/Technical/TB_RNA_TBDMS_Deprotection.pdf). Technical Bulletin |
| Storage: Freezer storage, -10 to -30°C, dry |
| Stability in Solution: 2-3 days |
minor rna phosphoramidites (TBDMS PROTECTED)
Inosine and 5-Methyl-Uridine are useful for analyzing RNAstructure and activity relationships. 5-Bromo-Uridine and 5-Iodo-Uridine havebeen used for crystallography studies and cross-linking experiments.6-Thioguanosine (6-thio-G) has applications in ribozyme and siRNA research, aswell as in RNA-protein interactions. The removal of the silyl protecting groupwithout interfering with the sulfur is critical. This is removed1 cleanly by triethylamine trihydrofluoride in DMSO but t-butylammonium fluoride(TBAF) leads to degradation of the thio-nucleotide analogue and should not beused. 2-Aminopurine riboside is useful for analyzing RNA structure and activityrelationships, for example, in ribozyme studies.
If you cannot find the answer to your problem below then please contact us or telephone 01954 210 200
2-Aminopurine-TBDMS-CE Phosphoramidite
2-Aminopurine-TBDMS-CE Phosphoramidite
Glen Research
MSDS
Glen Report 19.1
If you cannot find the answer to your problem below then please contact us or telephone 01954 210 200
2-Aminopurine-TBDMS-CE Phosphoramidite
2-Aminopurine-TBDMS-CE Phosphoramidite
Glen Research
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. | PackSize | Grams/Pack | 0.1M Dil.(mL) | LV40 | LV200 | 40nm | 0.2µm | 1µm | 10µm |
| Approximate Number of Additions | |||||||||
| 10-3070-02 | 0.25grams | .25grams | 2.62 | 74 | 44.4 | 27.75 | 20.18 | 14.8 | 3.7 |
| 10-3070-90 | 100µmoles | .095grams | 1 | 20 | 12 | 7.5 | 5.45 | 4 | 1 |
| 10-3070-95 | 50µmoles | .048grams | .5 | 3.33 | 2 | 1.25 | .91 | .67 | .17 |
| Expedite | |||||||||
| Cat.No. | PackSize | Grams/Pack | Dilution(mL) | Molarity | 50nm | 0.2µm | 1µm | 15µm | |
| Approximate Number of Additions | |||||||||
| 10-3070-02 | 0.25grams | .25grams | 3.91 | .07 | N/A | N/A | 14.96 | N/A | |
| 10-3070-90 | 100µmoles | .095grams | 1.5 | .07 | N/A | N/A | 4.92 | N/A | |
| 10-3070-95 | 50µmoles | .048grams | .75 | .07 | N/A | N/A | 1.79 | N/A | |
| Beckman | |||||||||
| Cat.No. | PackSize | Grams/Pack | Dilution(mL) | Molarity | 30nm | 200nm | 1000nm | ||
| Approximate Number of Additions | |||||||||
| 10-3070-02 | 0.25grams | .25grams | 3.91 | .07 | N/A | 11.84 | 11.12 | ||
| 10-3070-90 | 100µmoles | .095grams | 1.5 | .07 | N/A | 4.06 | 3.82 | ||
| 10-3070-95 | 50µmoles | .048grams | .75 | .07 | N/A | 1.65 | 1.55 | ||
If you cannot find the answer to your problem below then please contact us or telephone 01954 210 200
