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In order to extend the dielectronic recombination (DR) experiments from the main cooler storage ring CSRm with intermediate charge state ions to the experimental cooler storage ring CSRe with highly charged ions and even radioactive ions, a test electron‐ion recombination experiment of B‐like Ar13+ ions was performed with a section of the new electron beam energy detuning system, which will be installed at the CSRe. We present the measured and also the calculated DR spectra for the ∆n = 0 resonances from 0 to 3 eV. The experimental results agree very well with the previous DR experimental data from CRYRING, and the energy resolution reached 30 meV full width at half maximum. This test experiment demonstrates that the reliability and stability of the newly developed electron beam energy detuning system are satisfactory for the upcoming DR experiments at the CSRe. However, we found large discrepancies between the experimental result and the calculation in both resonance positions and the intensities of the recombination spectrum below 0.7 eV, which indicate that precise calculation of the DR spectrum of multielectron ions is still a challenge. [ABSTRACT FROM AUTHOR]

A novel custom bead array technology is introduced, and it is applied to multiplexed analysis of highly polymorphic human leukocyte antigen (HLA) genetic loci. Our technology combines the construction of probe libraries on color-encoded microparticles (beads) with semiconductor chip processing to produce custom-designed high-density bead array chips in large quantities. Using this novel assay format, two modes of parallel molecular typing of the HLA complex were implemented, namely direct hybridization, illustrated here for class II HLA-DR, and a novel format of on-chip polymerase-mediated primer elongation, illustrated here for class I HLA-A, HLA-B, and HLA-DR using patient and reference cell-line DNA samples. Hybridization-mediated multiplexed analysis of polymorphism method was validated with 142 samples, resulting in 100% concordance with sequence-specific oligonucleotide typing results and a concomitant average of 40% less allele ambiguity. In addition, elongation and hybridization reactions were combined to identify multiple polymorphisms on the same phase of DNA for allele identification. [ABSTRACT FROM AUTHOR]