Laboratory production of 100 base pair DNA molecular weight markers.

[1]  Han-Jung Lee,et al.  An intracellular delivery method for siRNA by an arginine-rich peptide. , 2007, Journal of biochemical and biophysical methods.

[2]  Microsugar Chang,et al.  Noncovalent protein transduction in plant cells by macropinocytosis. , 2007, The New phytologist.

[3]  Microsugar Chang,et al.  Arginine-rich intracellular delivery peptides noncovalently transport protein into living cells. , 2006, Biochemical and biophysical research communications.

[4]  H. Hsu,et al.  Dye‐free protein molecular weight markers , 2005, Electrophoresis.

[5]  Microsugar Chang,et al.  Gradient polymerase chain reaction performance using regular thermal cycle machine. , 2005, Analytical Biochemistry.

[6]  Microsugar Chang,et al.  Cellular internalization of fluorescent proteins via arginine-rich intracellular delivery peptide in plant cells. , 2005, Plant & cell physiology.

[7]  S. Polyarush,et al.  Preparation of DNA Markers Based on E. Coli Plasmid DNA , 2003, Chemistry of Natural Compounds.

[8]  R. Rigler,et al.  Fluorescent high-density labeling of DNA: error-free substitution for a normal nucleotide. , 2001, Journal of biotechnology.

[9]  M. Amills,et al.  Primer-directed synthesis of a molecular weight marker. , 1996, Genetic analysis : biomolecular engineering.

[10]  C. Cooney.  Techniques and high resolution DNA size markers for pulsed field gel electrophoresis , 1994, Molecular biotechnology.

[11]  K. Sullivan,et al.  Automated DNA profiling by fluorescent labeling of PCR products. , 1992, PCR methods and applications.

[12]  R. Watson,et al.  Mapping of closed circular DNAs by cleavage with restriction endonucleases and calibration by agarose gel electrophoresis. , 1977, Proceedings of the National Academy of Sciences of the United States of America.