Athens Research/Cambio - Excellence in Molecular Biology/100µmoles/10-1072-90

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Oligo Synthesis

Oligo Synthesis : CEPs

Prices quoted are for single packs only. For multiples of the same product please request a quote. Some of Glen"sproductsarehazardousandmay be subject to additional shipping charges. Full product information is available onGlen Research"s website.

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  • Description
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  • Applications & Benefits

6-thio-dG-CE Phosphoramidite

6-thio-dG-CE Phosphoramidite

Glen Research

Catalogue No.DescriptionPack SizePriceQty
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10-1072-026-thio-dG-CE Phosphoramidite0.25g£780.00£741.00Offer until : 31-Mar-2021Offer Code : GLEN55% off all Glen productsView OfferQuantityAdd to Order
10-1072-906-thio-dG-CE Phosphoramidite100µmoles£284.00£269.80Offer until : 31-Mar-2021Offer Code : GLEN55% off all Glen productsView OfferQuantityAdd to Order
10-1072-956-thio-dG-CE Phosphoramidite50µmoles£142.00£134.90Offer until : 31-Mar-2021Offer Code : GLEN55% off all Glen productsView OfferQuantityAdd to Order

6-thio-dG-CE Phosphoramidite

6-thio-dG-CE Phosphoramidite

Glen Research

Structure

Catalog Number: 10-1072-xx

Description: 6-thio-dG-CE Phosphoramidite

5"-Dimethoxytrityl-N2-trifluoroacetyl-2"-deoxy-6-(2-cyanoethyl)thio-Guanosine,3"-[(2-cyanoethyl)-(N,N-diisopropyl)]-phosphoramidite
Formula: C45H50F3N8O7PSM.W.: 934.97F.W.: 345.26

Diluent: Anhydrous Acetonitrile
Coupling: Standard coupling time.Use 0.02 M Iodine for Oxidation.
Deprotection: Deprotect with1.0M DBU in anhydrous acetonitrile at Room Temperature for 5hrs to remove the cyanoethyl protection. Complete the deprotection with 50mM NaSH in concentrated NH4OH at Room Temperature for 24hrs.
Storage: Refrigerated storage, maximum of 2-8°C, dry

Stability in Solution: 24 hours

The C-nucleoside2’-deoxypseudouridine, in contrast to dU, forms stable C:pseudoU-A triplets.2-Aminopurine lacks groups critical for hydrogen bonding and is a mildlyfluorescent base.

Demand for sulfur modified bases continues to expand forinvestigations of oligonucleotide structure, but primarily for cross-linkingpurposes. 6-Thio-dG, 4-Thio-dT and 4-thio-dU are very useful modifications forphoto cross-linking and photoaffinity labelling experiments. Oligos containing2-thio-dT are useful in examining protein-DNA interaction by acting asphotosensitizing probes. The thiocarbonyl group in 2-thio-dT is especiallyinteresting in that it is available to react with compounds associating with theminor groove of DNA. 2-Amino-A forms a very stable base pair with T containingthree hydrogen bonds but the stability of the base pair with 2-thio-T is greatlydiminished. Due to steric interactions between the 2-thio group of thymidine andthe 2-amino group of 2-amino-A, the base pair contains only a single hydrogenbond. Oligos containing 2-amino-dA and 2-thio-dT exhibit high affinity fornatural oligonucleotides but show little affinity for other similar oligos evenof a complementary sequence.

If you cannot find the answer to your problem below then please contact us or telephone 01954 210 200

6-thio-dG-CE Phosphoramidite

6-thio-dG-CE Phosphoramidite

Glen Research

MSDS

Glen Report 11.1: MORE NOVEL MONOMERS

If you cannot find the answer to your problem below then please contact us or telephone 01954 210 200

6-thio-dG-CE Phosphoramidite

6-thio-dG-CE Phosphoramidite

Glen Research

6-thio-dG-CE Phosphoramidite

5"-Dimethoxytrityl-N2-trifluoroacetyl-2"-deoxy-6-(2-cyanoethyl)thio-Guanosine,3"-[(2-cyanoethyl)-(N,N-diisopropyl)]-phosphoramidite
Formula: C45H50F3N8O7PSM.W.: 934.97F.W.: 345.26

Diluent: Anhydrous Acetonitrile
Coupling: Standard coupling time. Use 0.02 M Iodine for Oxidation.
Deprotection: Deprotect with1.0M DBU in anhydrous acetonitrile at Room Temperature for 5hrs to remove the cyanoethyl protection. Complete the deprotection with 50mM NaSH in concentrated NH4OH at Room Temperature for 24hrs.
Storage: Refrigerated storage, maximum of 2-8°C, dry
Stability in Solution: 24 hours
Material Safety Data Sheet

Literature Highlights

Glen Report 11.1: MORE NOVEL MONOMERS

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.PackSizeGrams/Pack0.1M Dil.(mL)LV40LV20040nm0.2µm1µm10µm
Approximate Number of Additions
10-1072-020.25grams.25grams2.6775.6745.428.3820.6415.133.78
10-1072-90100µmoles.093grams120127.55.4541
10-1072-9550µmoles.047grams.53.3321.25.91.67.17
Expedite
Cat.No.PackSizeGrams/PackDilution(mL)Molarity50nm0.2µm1µm15µm
Approximate Number of Additions
10-1072-020.25grams.25grams3.99.06773.445.8833.364.59
10-1072-90100µmoles.093grams1.5.06723.614.7510.731.48
10-1072-9550µmoles.047grams.75.0678.65.383.91.54
Beckman
Cat.No.PackSizeGrams/PackDilution(mL)Molarity30nm200nm1000nm
Approximate Number of Additions
10-1072-020.25grams.25grams3.99.0677546.8834.09
10-1072-90100µmoles.093grams1.5.06725.215.7511.45
10-1072-9550µmoles.047grams.75.06710.26.384.64
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If you cannot find the answer to your problem below then please contact us or telephone 01954 210 200

6-thio-dG-CE Phosphoramidite

6-thio-dG-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. Please link for more detailed usage information with the various synthesizers.

ABI 392/394
Cat.No.PackSizeGrams/Pack0.1M Dil.(mL)LV40LV20040nm0.2µm1µm10µm
Approximate Number of Additions
10-1072-020.25grams.25grams2.6775.6745.428.3820.6415.133.78
10-1072-90100µmoles.093grams120127.55.4541
10-1072-9550µmoles.047grams.53.3321.25.91.67.17
Expedite
Cat.No.PackSizeGrams/PackDilution(mL)Molarity50nm0.2µm1µm15µm
Approximate Number of Additions
10-1072-020.25grams.25grams3.99.0773.445.8833.364.59
10-1072-90100µmoles.093grams1.5.0723.614.7510.731.48
10-1072-9550µmoles.047grams.75.078.65.383.91.54
Beckman
Cat.No.PackSizeGrams/PackDilution(mL)Molarity30nm200nm1000nm
Approximate Number of Additions
10-1072-020.25grams.25grams3.99.077546.8834.09
10-1072-90100µmoles.093grams1.5.0725.215.7511.45
10-1072-9550µmoles.047grams.75.0710.26.384.64

If you cannot find the answer to your problem below then please contact us or telephone 01954 210 200

Myeloperoxidase Enzyme Immunoassay Kit 髓过氧化物酶 免疫分析试剂盒 Human MPO EIA KIT FEATURES: USE - Measure human MPO in a variety of matrices SAMPLE -Serum, Platelet-Poor Heparin Plasma, Saliva, Urine or Tissue Culture Media SAMPLES / KIT - 40 in duplicate SENSITIVITY - 0.068 ng/mL STABILITY - liquid reagents stable at 4°C QUICK RESULTS - 2.5 HOURS Myeloperoxidase (MPO) is a tetrameric heme-containing protein abundantly produced in neutrophil granulocytes where it plays an important anti-microbial role. During degranulation MPO is released into the extracellular space. There, as part of the neutrophils “respiratory burst”, it produces hypochlorous acid from hydrogen peroxide and Cl–. MPO also uses hydrogen peroxide to oxidize tyrosine to the tyrosyl radical. Both hypochlorous acid and tyrosyl are cytotoxic and when present can kill bacteria and other pathogens. Hereditary deficiency of myeloperoxidase predisposes individuals to immune deficiency. Studies have shown an association between elevated MPO levels and coronary artery disease, and in 2003 it was suggested that MPO may serve as a sensitive predictor of myocardial infarction in patients complaining of chest pain. Since that time the clinical utility of MPO testing in cardiac patients has been solidly established in the literature with well over 100 papers published. In 2010 this clinical application was further refined by additional studies which determined that measuring both MPO and C-reactive protein (CRP) provided more accurate prediction of mortality risk than measuring just CRP alone.