A scalable scanning transfer cavity laser stabilization scheme based on the Red Pitaya STEMlab platform.

Many experiments in atomic and molecular physics require simultaneous frequency stabilization of multiple lasers. We present a stabilization scheme based on a scanning transfer cavity lock that is simple, stable, and easily scalable to many lasers at minimal cost. The scheme is based on the Red Pitaya STEMlab platform, with custom software developed and implemented to achieve up to 100 Hz bandwidth. As an example demonstration, we realize simultaneous stabilization of up to four lasers and a reduction of long-term drifts to well below 1 MHz/h. This meets typical requirements, e.g., for experiments on laser cooling of molecules.

Native protein blotting after isoelectric focusing in fabric reinforced polyacrylamide gels in carrier ampholyte generated or immobilized pH gradients.

An optimized procedure for the preparation of fabric reinforced polyacrylamide gels for native protein blotting is described. The gels, typically 5% T, 3% C, were internally stabilized with the aid of an AcrylAide-pretreated, hydrophilized polyester fabric, preferably with a 60 microns mesh opening. Ultrathin (120-180 microns) gels were prepared with the flap technique and 500 microns gels with the cassette technique; 500 microns gels with immobilized pH gradients were cast using precision molds and a computer controlled mixing device of four burettes. The fabric reinforced gels could be used either wet or after drying and rehydration. Isoelectric focusing was performed in carrier ampholyte pH gradients or hybrid immobilized pH gradients, supplemented with 1-3% w/v carrier ampholytes. Incorporation of 40-60% w/v glycerol into the gels decisively improved their operational properties. The high glycerol gels, which tolerated field strengths of 900-1700 V/cm for extended periods under steady state focusing conditions, were not afflicted by liquid exudation on the gel surface and showed retarded diffusion of the separated proteins on termination of focusing. By unidirectional capillary blotting, with an intermediate dialysis membrane eliminating bidirectional protein transfer, proteins were blotted to 0.1-0.2 micron pore size nitrocellulose membranes in 10-20 min from ultrathin gels and in 30-60 min from 500 microns gels. Based on quantification of residual protein in the gels after blotting, a transfer efficiency of 60-87% was found for the ultrathin and 53-69% for the 500 microns gels. Semidry electrophoretic blotting was carried out in a modified setup with cooled graphite electrodes. In a continuous Tris-glycine buffer system electrophoretic blotting required only 2-5 min with ultrathin gels and 20 min with 500 microns gels. Marker proteins, including horse spleen ferritin (Mr465,000), could be transferred with 91-96% efficiency.

[Results of immunotherapy in 244 children with asthma or allergic rhinitis (author's transl)]. / Ergebnisse der Hyposensibilisierungsbehandlung im Kindesalter.

The results of immunotherapy in 244 children with asthma or allergic rhinitis have been evaluated by means of a questionaire directed at the parents. 86,9% of the children showed improvement. Additional information has been obtained about the side-effects of therapy--2,9% regularily showed dyspnoea--, the severity of symptoms before treatment and the influence of age on the above mentioned parameters. The results are discussed, compared with similar studies in adults and possible consequences for future diagnostic measures and therapy are proposed.