Michael A Jensen

Summary

Affiliation: Stanford University
Country: USA

Publications

  1. doi request reprint Next generation 1536-well oligonucleotide synthesizer with on-the-fly dispense
    Michael Jensen
    Stanford Genome Technology Center, Stanford University, Palo Alto, CA 94304, USA Electronic address
    J Biotechnol 171:76-81. 2014
  2. pmc Direct oligonucleotide synthesis onto super-paramagnetic beads
    Michael A Jensen
    Stanford Genome Technology Center, Stanford University, Palo Alto, CA 94304, USA Electronic address
    J Biotechnol 167:448-53. 2013
  3. pmc A rapid, cost-effective method of assembly and purification of synthetic DNA probes >100 bp
    Michael A Jensen
    Stanford Genome Technology Center, Palo Alto, California, United States of America
    PLoS ONE 7:e34373. 2012
  4. pmc DMSO and betaine greatly improve amplification of GC-rich constructs in de novo synthesis
    Michael A Jensen
    Stanford Genome Technology Center, Stanford University, Palo Alto, California, USA
    PLoS ONE 5:e11024. 2010
  5. doi request reprint Gas-phase cleavage and dephosphorylation of universal linker-bound oligodeoxynucleotides
    Michael A Jensen
    Stanford Genome Technology Center, Stanford University, 855 S California Ave, Palo Alto, CA 94304, USA
    Nucleosides Nucleotides Nucleic Acids 29:867-78. 2010
  6. ncbi request reprint A novel catechol-based universal support for oligonucleotide synthesis
    Keith M Anderson
    Stanford Genome Technology Center, Stanford University, Palo Alto, California 94304, USA
    J Org Chem 72:9875-80. 2007
  7. ncbi request reprint Targeted and highly multiplexed detection of microorganisms by employing an ensemble of molecular probes
    Weihong Xu
    Stanford Genome Technology Center, Palo Alto, California, USA
    Appl Environ Microbiol 80:4153-61. 2014

Collaborators

Detail Information

Publications7

  1. doi request reprint Next generation 1536-well oligonucleotide synthesizer with on-the-fly dispense
    Michael Jensen
    Stanford Genome Technology Center, Stanford University, Palo Alto, CA 94304, USA Electronic address
    J Biotechnol 171:76-81. 2014
    ..53/717 bases. Furthermore, mass spectral analysis on strands synthesized up to 80 bases showed high purity with an average coupling efficiency of 99.5%...
  2. pmc Direct oligonucleotide synthesis onto super-paramagnetic beads
    Michael A Jensen
    Stanford Genome Technology Center, Stanford University, Palo Alto, CA 94304, USA Electronic address
    J Biotechnol 167:448-53. 2013
    ..In addition to direct synthesis of oligodeoxynucleotides (DNA) onto SPMBs, this platform also has the potential for RNA and peptide nucleic acid synthesis...
  3. pmc A rapid, cost-effective method of assembly and purification of synthetic DNA probes >100 bp
    Michael A Jensen
    Stanford Genome Technology Center, Palo Alto, California, United States of America
    PLoS ONE 7:e34373. 2012
    ....
  4. pmc DMSO and betaine greatly improve amplification of GC-rich constructs in de novo synthesis
    Michael A Jensen
    Stanford Genome Technology Center, Stanford University, Palo Alto, California, USA
    PLoS ONE 5:e11024. 2010
    ..Furthermore, we believe either additive will allow for the production of a wide variety of GC-rich gene constructs without the need for expensive and time-consuming sample extraction and purification prior to downstream application...
  5. doi request reprint Gas-phase cleavage and dephosphorylation of universal linker-bound oligodeoxynucleotides
    Michael A Jensen
    Stanford Genome Technology Center, Stanford University, 855 S California Ave, Palo Alto, CA 94304, USA
    Nucleosides Nucleotides Nucleic Acids 29:867-78. 2010
    ..Finally, performance between the two linkers was similar enough to conclude each fulfills the desired requirements for mainstream, high-throughput oligodeoxynucleotide cleavage/deprotection and dephosphorylation in the gas phase...
  6. ncbi request reprint A novel catechol-based universal support for oligonucleotide synthesis
    Keith M Anderson
    Stanford Genome Technology Center, Stanford University, Palo Alto, California 94304, USA
    J Org Chem 72:9875-80. 2007
    ..The flexibility of the universal support and the efficiency of 3'-dephosphorylation are expected to increase the use of universal supports in oligonucleotide synthesis...
  7. ncbi request reprint Targeted and highly multiplexed detection of microorganisms by employing an ensemble of molecular probes
    Weihong Xu
    Stanford Genome Technology Center, Palo Alto, California, USA
    Appl Environ Microbiol 80:4153-61. 2014
    ..In addition, we employed molecular probes to identify the bacteria from vaginal swabs and demonstrate how a deliberate selection of molecular probes can identify less abundant bacteria even in the presence of much more abundant species. ..