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Ac-dC-CE Phosphoramidite - (10-1015)

5'-Dimethoxytrityl-N-acetyl-2'-deoxyCytidine,3'-[(2-cyanoethyl)-(N,N-diisopropyl)]-phosphoramidite
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10-1015
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Product Specifications

Formula:
C41H50N5O8P
M.W.:
771.85
F.W.:
289.18
CAS Number:
154110-40-4
5'-Dimethoxytrityl-N-acetyl-2'-deoxyCytidine,3'-[(2-cyanoethyl)-(N,N-diisopropyl)]-phosphoramidite
Description
Glen Research CE (B-cyanoethyl) Phosphoramidites are produced and packaged to ensure the highest performance on DNA synthesizers. Every Glen Research product is accompanied by a Certificate of Analysis and HPLC trace, showing the results of our QC testing. Every Glen Research monomer vial is specially cleaned to eliminate particulate contamination, and each vial type is thoroughly tested or inspected to ensure a tight fit on synthesizers.
Details

Usage

  • Coupling: No changes needed from standard method recommended by synthesizer manufacturer.
  • Deprotection: No changes needed from standard method recommended by synthesizer manufacturer.
Specifications
Diluent Anhydrous Acetonitrile
Recommended Storage Controlled room temperature or lower, dry
Stability In Solution Similar to dA,C,G,T-CE Phosphoramidites
Dilution/Coupling Data

The table below show pack size data and, for solutions, dilution and approximate coupling based on normal priming procedures.

ABI 392/394

Catalog # Pack Size Grams/Pack 0.1M Dil. (mL) Approximate Number of Additions
LV40 LV200 40nm 0.2μm 1μm 10μm
10-1015-02 0.25 g .25grams 3.24 94.67 56.8 35.5 25.82 18.93 4.73
10-1015-05 0.5 g .5grams 6.48 202.67 121.6 76 55.27 40.53 10.13
10-1015-10 1.0 g 1grams 12.96 418.67 251.2 157 114.18 83.73 20.93
10-1015-20 2.0 g 2grams 25.91 850.33 510.2 318.88 231.91 170.07 42.52
10-1015-40 4.0 g 4grams 51.82 1714 1028.4 642.75 467.45 342.8 85.7

Expedite

Catalog # Pack Size Grams/Pack Dilution (mL) Approximate Number of Additions
Molarity 50nm 0.2μm 1μm 15μm
10-1015-C2 0.25 g .25grams 4.83 0.07 93.4 58.38 42.45 5.84
10-1015-C5 0.5 g .5grams 9.67 0.07 190.2 118.88 86.45 11.89
10-1015-1C 1.0 g 1grams 19.34 0.07 383.6 239.75 174.36 23.98
10-1015-2C 2.0 g 2grams 38.67 0.07 770.2 481.38 350.09 48.14
Certificate of analysis

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References

Chemical synthesis of oligodeoxyribonucleotides containing the Dewar valence isomer of the (6-4) photoproduct and their use in (6-4) photolyase studies Junpei Yamamoto, Kenichi Hitomi, Takeshi Todo,and Shigenori Iwai

New approach to real-time nucleic acids detection: folding polymerase chain reaction amplicons into a secondary structure to improve cleavage of Förster resonance energy transfer probes in 5'-nuclease assays. Igor V. Kutyavin

Solid-Phase Synthesis of Oligodeoxyribonucleotides without Base Protection Utilizing O-Selective Reaction of Oxazaphospholidine Derivatives N. Oka, Y. Maizuru, M. Shimizu, and T. Wada

Thrombin binding aptamer G-quadruplex stabilized by pyrene-modified nucleotides Matic Kovačič, Peter Podbevšek, Hisae Tateishi-Karimata, Shuntaro Takahashi, Naoki Sugimoto, Janez Plavec,

Development of decoy oligonucleotide-warheaded chimeric molecules targeting STAT3 Po-Chang Shih, Miyako Naganuma, Genichiro Tsuji, Yosuke Demizu, and Mikihiko Naito

A unified Watson-Crick geometry drives transcription of six-letter expanded DNA alphabets by E.coli RNA polymerase Juntaek Oh, Zelin Shan, Shuichi Hoshika, Jun Xu, Jenny Chong, Steven A. Benner, Dmitry Lyumkis, and Dong Wang

Oligodeoxynucleotide Synthesis Under Non-Nucleophilic Deprotection Conditions Shiyue Fang, Komal Chillar, Yipeng Yin, Alexander Apostle, Dhananjani N. A. M. Eriyagama, Shahien Shahsavari, Bhaskar Halami, and Yinan Yuan

Multiplexed Assay for Small-Molecule Quantification via Photo-cross-linking of Structure Switching Aptamers Sharon S. Newman, Brandon Wilson, Liwei Zheng, Michael Eisenstein, Tom Soh

Selection of DNA aptamers that prevent the fibrillization of a-synuclein protein in cellular and mouse models Erin M. McConnell, Dennis Chan, Katelyn Ventura, Joshua P. Callahan, Kathryn Harris, Vernon H. Hunt, Spencer Boisjoli, Daniel Knight, Evan T. Monk, Matthew R. Holahan, and Maria C. DeRose.

Products FAQS
dC when protected as an amide linkage is susceptible to transamination or displacement of the amide with the deprotecting amine. Normally, the deprotecting amine is ammonia and displacement leads to the same product as hydrolysis. However, if methylamine is used for the deprotection step with a benzoyl protected dC, approximately 10% of the product is from the displacement reaction to give N-methyl-dC residues, while the remaining 90% is the desired product formed by hydrolysis. A more labile protecting group on dC is isobutyryl which is also commercially available. This group is displaced by methylamine to about 5% - an improvement but still a mutation. Ac-dC, on the other hand, is hydrolyzed virtually instantaneously by the AMA reagent and none of the slower displacement reaction gets a chance to occur.||REFERENCE(S):M.P. Reddy, Beckman Instruments, personal communication.||
Yes. Store tightly sealed in a glass bottle in the refrigerator. The reagent does not decompose but routine opening will lose some of the volatile bases. Dispose properly after 4-6 weeks.||REFERENCE(S):Candy Lee, Dartmouth