Molecular Biotechnology Programme Uppsala University School of Engineering

It showed large dynamic range, no measureable non-specific binding and high sensitivity (with linear range around 0.1 – 10 µg/ml depending on the proteins). The method

Escherichia coli, 23S rRNA, Post-transcriptional modification, In vitro, Peptidyl transferase centre, domain V, Methylation, Pseudouridine, Reverse

The fibrinolytic enzyme tissue type plasminogen activator (t-PA) is released by the vascular endothelium to limit the growth of blood clots and ultimately prevent the occurrence of

investigate the presence of P4 in the brain, in neuromuscular junctions and in adrenal glands, the colocation between P4 and VAChT respectively P4 and VMAT and the possibility that P4

The information obtained by using these algorithms could contribute to the development of new drugs by generating new ligands that target specific high-energy , unfavorable

Results from the project shows that when multiplexing there are differences in measured IgE- levels between an existing singleplex method and the multiplex prototype. The project also

A method for measuring cell concentration and identity based on flow cytometry (FCM) and fluorescent marking is developed and subsequently compared with traditional plating based

Here we have attempted to produce the serine proteases rat mast cell protease 2 and mouse mast cell protease 5 in a culture of HEK 293 cells; and mouse mast cell protease 4,