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Oligo Synthesis

Oligo Synthesis : CEPs

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Asymmetric Doubler (Lev) Phosphoramidite

Asymmetric Doubler (Lev) Phosphoramidite

Glen Research

Catalogue No.DescriptionPack SizePriceQty
10-1981-02Asymmetric Doubler (Lev) Phosphoramidite0.25g £227.00 Quantity Add to Order
10-1981-90Asymmetric Doubler (Lev) Phosphoramidite100 umoles £95.00 Quantity Add to Order

Description

Description: Asymmetric Doubler (Lev) Phosphoramidite

1-[5-(4,4’-dimethoxytrityloxy)pentylamido]-3-[5-levulinyloxypentylamido]-propyl- 2-[(2-cyanoethyl)-(N,N-diisopropyl)]-phosphoramidite

Formula: C48H67N4O10
M.W.: 891.04 
F.W.: 352.32 

Diluent: Anhydrous Acetonitrile

Coupling: 6 minute coupling time recommended.

Deprotection: Levulinyl Deprotection: The levulinyl protecting group can be selectively removed without cleavage of the oligonucleotide from the CPG by treatment with 0.5M Hydrazine hydrate in 1:1 pyridine/acetic acid. [Note hydrazine hydrate is a violent poison that is both volatile and readily absorbed through skin] Fit the column with syringes and push the solution back and forth across the column. Let sit for 15 minutes at room temperature. Rinse the column with 1.5 mL of 1:1 pyridine/acetic acid (3x) and then 1.5 mL of ACN (3x). Dry CPG under a stream of argon and proceed with the synthesis of the branching sequence. If a non-branching control is desired, simply deprotect in ammonium hydroxide as required by the nucleobases.

Storage: Freezer storage, -10 to -30°C, dry

Stability in Solution: 1-2 Days

Click here for more information on Olignucleiotide Dendrimers

 

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