Instruments
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BD FACSAria-SORP Location: USA COM Medical Sciences Building & Mitchell Cancer Institute ![]() |
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Agilent NovoCyte Opteon Location: Mitchell Cancer Institute (MCI) |
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Agilent NovoCyte Quanteon
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Nexcelom CeligoS microplate based imaging cytometer
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Celsee Prep100 CTC isolation system Location: Mitchell Cancer Institute (MCI) |
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On-Chip Biotechnologies Microfluidic Cell Sorter (3 laser 6 color) Location: Mitchell Cancer Institute (MCI) |
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On-Chip Biotechnology SPiS Location: Mitchell Cancer Institute (MCI) |
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The ZetaView® TWIN - NTA Nanoparticle Tracking - Video Microscope PMX-220 Location: USA COM Medical Sciences Building (MSB) , Room 2264
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Agilent Seahorse XFe24 Analyzer Location: USA COM Medical Sciences Building, Room 2264
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10x Genomics Chromium iX Controller The controller combines a single cell with a single gel bead that is coated with a unique oligonucleotide barcode to form a single cell emulsion droplet, which is referred to as a “GEM” (Gel Bead-in-emulsion). Within each GEM the unique barcoded oligonucleotides are used as primers to generate cDNAs, which can be traced back to cell of origin. The barcoded amplified fragments from hundreds to thousands of cells are pooled to create short read sequencer compatible libraries. Sequencing of these libraries enables analysis of single cells for gene expression, cell surface proteins, immune clonotype, antigen specificity, and chromatin accessibility. There are currently no user fees associated with this system, but advanced scheduling is required. Location: USA COM Medical Sciences Building, Room 2264 |
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Miltenyi Biotech GentleMACS tissue disassociation system Location: USA COM Medical Sciences Building, Room 2264 |
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CellRad+ cabinet x-ray irradiator Location: Mitchell Cancer Institute (MCI) |
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Kimtron IC-320 X-ray irradiation system Location: USA COM Medical Sciences Building, Room 1045
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Finesse 325 Microtome Location: USA COM Medical Sciences Building
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Additional instrumentation available for use, but not managed by the Flow Cytometry Shared Resource Laboratories:
- Agilent BioTek Cytation 7 Imaging System (MSB 2264)
The Bioimaging facilities at the USA College of Medicine manage the Agilent BioTek Cytation 7, a versatile imaging system that combines digital upright microscopy, digital inverted microscopy, and multimode microplate detection in one unit. Its inverted widefield module supports fluorescence and brightfield imaging at magnifications ranging from 1.25x to 60x, making it ideal for everything from whole-organism studies to high-resolution intracellular analysis. Complementing this is an upright reflected light module designed for specialized tasks like ELISpot, colony counting, and rapid slide scanning. As a high-performance plate reader it utilizes quadruple monochromator-based optics. It supports multiple detection modes including fluorescence
intensity (top and bottom reading), UV-Vis absorbance (230 nm to 999 nm), luminescence, and time-resolved fluorescence (TRF) and TR-FRET.
For assistance contact:
Joel F. Andrews, Ph.D.
Associate Professor, Research
Department of Biochemistry and Molecular Biology
Manager, BioImaging Core Facility
Frederick P. Whiddon College of Medicine
USA Mitchell Cancer Institute
University of South Alabama
jandrews@southalabama.edu
(251) 410-4927 - Beckman Coulter Multisizer 4e (Earth and Life Sciences Building)
Dr. Nathan Chasen has graciously made his instrument available to other investigators. The Beckman Coulter Multisizer 4e is a high-resolution automated particle analyzer used for counting and characterizing particles and cells. It utilizes the Coulter Principle, also known as electrical sensing zone technology, which measures the change in electrical resistance as particles suspended in a conductive electrolyte pass through a small aperture. The Multisizer 4e provides comprehensive particle and cell analysis using the accurate, "direct" Coulter method, which measures true volume regardless of optical properties. Key specifications include the detection of particles from 200 nm to 1,600 μm, delivering precise data on sample cell number, size, and concentration. The instrument analyzes particles individually, allowing for real-time detection of average cell size changes and identification of individual particles or cell aggregates that deviate from the sample mean.
For assistance contact:
Nathan Chasen, PhD
Assistant Professor of Biology
Department of BIology
ELSB 123
University of South Alabama
nchasen@southalabama.edu
(251) 460-7533






