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characterization techniques such as scanning electron microscopy (SEM, HRTEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and chemisorption techniques (TPD, TPR) is needed. Your contribution
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of immunocompromised mice. These lesions can then be studied over time using intravital microscopy to elucidate immune cell interactions, vascularization, and growth. In addition, the effects of drug candidates
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spectrometry, X-ray diffraction, X-ray photoelectron spectroscopy, vibrational spectroscopy, and electron microscopy. Documented experience in photophysical characterization, including UV–Vis absorption
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-electron microscopy (cryo-EM) and tomography (cryo-ET) are performed. The group values a collegial and supportive research environment, with open communication, structured mentoring, and a strong emphasis on
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and molecular genetics as well as hands-on experience with cloning, live-cell fluorescence microscopy, image analysis, and sample preparation for sequencing and multi-omics analyses. The main model
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fluorescence microscopy, image analysis, and sample preparation for sequencing and multi-omics analyses. The main model organism will be Bacillus subtilis, but other bacteria as well as fungal species including