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Proteins & Peptides Kits on ZAGENO

N2 - A system was established for the parallel synthesis of peptide library arrays in a fully automated manner. Synthesis takes place in blocks made of polyoxymethylene that hold during all synthesis steps a polypropylene membrane of 8 x 12 cm. Yields are in the nanomole range, obtained at a low consumption of reagents. The current setup is based on a commercially available pipetting robot and supports the generation of 1536 different oligomers/run. Much higher array densities are possible because the membranes are amicable to spot diameters of down to 200 μm, naturally at a cost of the absolute amount produced of each oligomer. The method was put to use for the creation of arrayed libraries of peptide nucleic acids (PNAs). These can be employed both as a source of PNA molecules applied individually in experimentation subsequent to their release or as intact oligomer arrays in hybridization analyses.

Genetics Real-Time PCR Homepage
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AB - A system was established for the parallel synthesis of peptide library arrays in a fully automated manner. Synthesis takes place in blocks made of polyoxymethylene that hold during all synthesis steps a polypropylene membrane of 8 x 12 cm. Yields are in the nanomole range, obtained at a low consumption of reagents. The current setup is based on a commercially available pipetting robot and supports the generation of 1536 different oligomers/run. Much higher array densities are possible because the membranes are amicable to spot diameters of down to 200 μm, naturally at a cost of the absolute amount produced of each oligomer. The method was put to use for the creation of arrayed libraries of peptide nucleic acids (PNAs). These can be employed both as a source of PNA molecules applied individually in experimentation subsequent to their release or as intact oligomer arrays in hybridization analyses.

GLOSSARY OF REAL-TIME PCR TERMS

20/06/2017 · Synthesis of a C-linked glycosylated thymine-based PNA monomer and its incorporation into a PNA oligomer
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A system was established for the parallel synthesis of peptide library arrays in a fully automated manner. Synthesis takes place in blocks made of polyoxymethylene that hold during all synthesis steps a polypropylene membrane of 8 x 12 cm. Yields are in the nanomole range, obtained at a low consumption of reagents. The current setup is based on a commercially available pipetting robot and supports the generation of 1536 different oligomers/run. Much higher array densities are possible because the membranes are amicable to spot diameters of down to 200 μm, naturally at a cost of the absolute amount produced of each oligomer. The method was put to use for the creation of arrayed libraries of peptide nucleic acids (PNAs). These can be employed both as a source of PNA molecules applied individually in experimentation subsequent to their release or as intact oligomer arrays in hybridization analyses.

Stabilization of Insulin by Adsorption on a …

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