Coupling Reagents

DescriptionAir- and moisture-tolerant, this (+)-PSI Reagent was developed in theBaran lab for stereocontrolled synthesis of phosphorothioate oligonucleotides. The enantiomer, (−)-PSI Reagent, is also available (cat#ALD00602).The PSI Reagents open

DescriptionAir- and moisture-tolerant, this (+)-PSI Reagent was developed in theBaran lab for stereocontrolled synthesis of phosphorothioate oligonucleotides. The enantiomer, (−)-PSI Reagent, is also available (cat#ALD00602).The PSI Reagents open

DescriptionAir- and moisture-tolerant, this (+)-PSI Reagent was developed in theBaran lab for stereocontrolled synthesis of phosphorothioate oligonucleotides. The enantiomer, (−)-PSI Reagent, is also available (cat#ALD00602).The PSI Reagents open

DescriptionAir- and moisture-tolerant, this (-)-PSI Reagent was developed in theBaran lab for stereocontrolled synthesis of phosphorothioate oligonucleotides. The enantiomer, (+)-PSI Reagent, is also available (cat#ALD00604).The PSI Reagents open

DescriptionAir- and moisture-tolerant, this (-)-PSI Reagent was developed in theBaran lab for stereocontrolled synthesis of phosphorothioate oligonucleotides. The enantiomer, (+)-PSI Reagent, is also available (cat#ALD00604).The PSI Reagents open

DescriptionAir- and moisture-tolerant, this (-)-PSI Reagent was developed in theBaran lab for stereocontrolled synthesis of phosphorothioate oligonucleotides. The enantiomer, (+)-PSI Reagent, is also available (cat#ALD00604).The PSI Reagents open

DescriptionAir- and moisture-tolerant, this (-)-PSI Reagent was developed in theBaran lab for stereocontrolled synthesis of phosphorothioate oligonucleotides. The enantiomer, (+)-PSI Reagent, is also available (cat#ALD00604).The PSI Reagents open

A probe for DNA synthesis in vivo that is less toxic than both EdU and BrdU. Ideally suited for metabolic DNA labeling when prolonged cell survival and undisturbed cell cycle progression are required.Application：F-ara-EdU

A probe for DNA synthesis in vivo that is less toxic than both EdU and BrdU. Ideally suited for metabolic DNA labeling when prolonged cell survival and undisturbed cell cycle progression are required.Application：F-ara-EdU

(−)-2-Amino-6-mercaptopurine riboside hydrate.

1,10-Phenanthroline Maleimide is used in the synthesis of hybrid transition-metalloproteins via thiol-selective covalent anchoring of Rh-phosphine and Ru-phenanthroline complexes.

2′-Deoxyadenosine 5′-monophosphate.