CellASIC^® ONIX Microfluidic Platform Images and Videos

Y04C Cell Cycle Arrest and Release - S. Cerevisiae imaged with a 60x objective for 4hrs in SC Medium, followed by alpha-factor exposure and arrest. Cells expressing GFP-tubulin and SPC42 mCherry. Views taken every 10 min. Courtesy of Soni Lacefield, University of Indiana.

Y04C Fission Yeast Growth - Growth of S. japonicus in the yeast microfluidic plate. From Prof. Hironori Niki, National Institute of Genetics, Japan.

Y04C Fission Yeast Growth - Growth of S. pombe in the Y04C microfluidic plate with continuous perfusion of YES medium. Cells courtesy of Forsburg Lab, USC.

Y04C DIC Analysis - S.cerevisiae were grown in CSM medium in Y04C plate with 5psi perfusion flow at 24°C. Views taken every 60 sec. with 150x immersion objective. Courtesy of Jan Wisniewski, National Cancer Institute, NIH, Bethesda, MD

B04A E. coli Growth - Growth of E. coli (BL21) in the B04 microfluidic plate. Cells were perfused with LB medium and imaged on a 100X oil immersion phase contrast objective. Cells courtesy of Tim Lu, MIT.

B04A Mycobacteria Growth - Growth of Mycobacterium smegmatis in the B04 (0.9 um trap) under continous perfusion for 18 hours. Views taken with a 100X phase contrast objective. Cells courtesy of Travis Hartman, William Jacobs, Albert Einstein College of Medicine.

B04A Antibiotic Burst - E. coli cell growth in the presence of ampicillin to visualize antibiotic effects on the cell membrane. Cells grow and divide normally until ampicillin is added, causing them to burst. Views taken every 10 minutes over 5 hours on a Nikon Plan microscope and 100x objective lens. Courtesy of Sonia Singhal, Rob Egbert, Eric Klavins at the University of Washington, Seattle.

M04S 4-Color Switching: Switching between 4 fluorescent solutions - Solution exchange in the M04S microfluidic plate between PBS and 4 fluorescent dyes with a system set point of 4 psi. Note the rapid and uniform laminar exchange profile. Movie taken with a 4X objective lens, showing the entry portion of the 2.8 mm diameter culture chamber.

M04S Cell Loading - Cell loading using capillary flow - Loading of MCF-7 cells (2.5 million cells/ml) into the M04S microfluidic culture region via capillary flow. Note that as the cells enter the culture area, they settle onto the glass surface.

M04S Perfusion Culture - MCF-10A cells - Microfluidic culture of MCF10A human breast cancer cells using the CellASIC® ONIX2 microincubation system.

M04S Perfusion Culture - NIH3T3 cells - Microfluidic culture of NIH3T3 mouse fibroblasts using the ONIX2 microincubation system. Cells exposed to flow of DMEM at 1psi, 37C and 5% CO2, using a 40X objective lens.

M04S Perfusion Culture - HT-1080 cells - HT-1080 cancer cells cultured in the M04S plate with the micro-incubator system imaged with a 40X phase contrast objective for 1 hour.

M04L Solution Switching - Solution switching flow profile - Flow switching in the M04L microfluidic plate taken with a 4X objective. Solution swiching is shown between PBS and Texas Red conjugated dextran (red) at 4 psi. The chamber diameter is 2 mm.

M04G Gradient Switching - Creating and switching a stable concentration gradient - Switching of concentration gradients in the M04G microfluidic plate. Flow of Fluorescein conjugated dextran, 3kDa (green) and PBS at 1psi creates a stable diffusion gradient between the top and bottom channels. Views taken with a 4x objective lens.

M04G Neutrophil Migration - HL-60 cells migrating in response to a spatial gradient - Chemotaxis of differentiated neutrophil-like HL-60 cells in a stable gradient of formyl-Met-Leu-Phe, a potent chemoattractant for granulocytes. Note the cell movement downwards as the attractant was added midway through the movie. Courtesy Jason Park, Lim Lab, UCSF.

M04G HL-60 Migration - HL-60 cells responding to a gradient - HL-60 migration in response to a chemokine (traced with red fluorescence). Unattached cells flow out to the left. Courtesy of Jason Park, Lim Lab, UCSF.

M04S Transfection - HT-1080 cells in microfluidic culture tranfected with GFP-tubulin - HT-1080 cells cultured in the M04S microfluidic plate using the microincubation system. Cells were transfected with GFP-tubulin (Invitrogen CellLight) via continuous flow overnight, and imaged at 40X for 1 hour with flow at 1 psi.

M04L Perfusion Culture - Live cell analysis of MCF7 cells - Microfluidic culture of MCF7 human breast cancer cells the M04L with flow at 0.5 psi. 20X objective.

M04S Bacteria Infection - HT-29 cells exposed to an invasive strain of E. coli - The human HT-29 colorectal adenocarcinoma cell line infected with an invasive strain of E. coli. The cells were engineered to expressed mCherry during invasion. Cells courtesy of Tim Lu, MIT.

M04S Removal of Cells from Chamber - NIH3T3 Fibroblast cells grown to confluency in the M04S plate. The chamber is treated with trypsin and cells are flushed out by pneumatic pressure thereafter.

U87 cells with DAPI - Live cell transfected nuclei in the ONIX M04S microfluidic plate. Cells segmented using CY5 membrane dye image of the same frame and then merged with phase contrast views. GFP expression of non-targeted bacmam retrovirus increases over time. Time course: 20 hours, frame interval 10 min