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paradigm shift in our fundamental understanding of the charge-lattice interactions that govern such effects. This PDRA role will utilize several state-of-the-art spectroscopic techniques, such as transient
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cancer biology, molecular biology, medicine, or neuroscience. Your expertise will include molecular biology techniques, advanced microscopy, quantitative image analysis, and primary tissue culture, all
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, stable isotope tracers, medical imaging). Experience with molecular biology techniques, stable isotope tracers methodologies, GCMS desirable. Familiarity with bioinformatics and computational biology
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imaging data - Developing new methods for inference of copy number alterations from single-cell DNA sequencing data - Analysing patterns of single-cell copy number variation to identify mechanistic
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frequency stabilisation and control, image analysis, data acquisition, optical design and Gaussian beam propagation. Desirable: 4. Experience · Demonstrable ability to develop research proposals
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a series of high-resolution FRET biosensors to track such dynamics for gibberellin, abscisic acid, auxin and salicylic acid in living plants. The Jones group combines imaging of FRET biosensors with
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/practicals. Experience with C. elegans (husbandry/genetics/transgenics) Experience in molecular cloning and genome editing Experience in microscopy, including confocal microscopy, live imaging and image
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cultures. Experience in molecular biology methodologies, following and adapting protocols and setting up cellular assays including image-based is essential for this role, and knowledge of neuroinflammation
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well as bioinformatics and bacterial imaging. Main Duties and Responsibilities Perform the following activities in conjunction with and under the guidance of the Principal Investigators (PI): 1. Plan and conduct assigned
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research, fundamental cell biology and cell signalling with excellent shared facilities including the Centre for Proteome Research, the Computational Biology Facility, the Liverpool Centre for Cell Imaging