The lab tracked the differentiating process using
fluorescent cell imaging, which tested for the necessary markers during each step.
Not exact matches
Huerta also calls attention to
fluorescent resonance energy transfer, which he says, «really allowed us to start
imaging processes in
cells as they occur.»
«The massive advantage with our stain-less laser - based
imaging approaches is that you can use the stem
cell sample without having to interrupt the developmental process in real time, you don't need to perform any
cell disruption and there is no photobleaching (fading) which is fairly common with
fluorescent material,» Catarina enthused.
To surmount this hurdle, Dr. Hodgson and his colleagues in the Gruss Lipper Biophotonics Center at Einstein devised a new
fluorescent protein biosensor that, combined with live -
cell imaging, revealed exactly when and where Rac1 is activated inside cancer
cells.
These infrared
fluorescent proteins are expressed well in mammalian
cells and mice, and can be used for whole - body
imaging.
Continuous measurement and
imaging of the intracellular free calcium ion concentration -LRB-[Ca2 +] i) of mitotic and interphase PtK1
cells was accomplished with the new
fluorescent Ca2 + indicator fura - 2.
Through the new
imaging technology, researchers use
fluorescent imaging to locate proteins and other molecules in
cells and tissues.
When the team inserted the new analogues into a living
cell and used high - definition, single
fluorescent - molecule
imaging, they were finally able to directly document the actions of specific gangliosides in a living
cell for the first time.
Imaging techniques that rely on light — such as taking pictures of
cells tagged with a «reporter gene» that codes for green
fluorescent protein — only work in tissue samples removed from the body.
«We hope it will ultimately do for ultrasound what green
fluorescent protein has done for light - based
imaging techniques, which is to really revolutionize the
imaging of
cells in ways there were not possible before.»
The group of
imaging specialists led by Prof. Michael Schäfers, Coordinator of the Cluster of Excellence, labelled the
cells thus obtained with various
fluorescent dyes in order to be able to study them in living organisms — initially with the optical method of fluorescence reflectance
imaging.
Advances in molecular biology, organic chemistry, and materials science have recently created several new classes of
fluorescent probes for
imaging in
cell biology.
Invaluable as markers for monitoring photosynthesis and other energy - related processes in living
cells, green
fluorescent proteins (GFPs), discovered in a species of jellyfish, are vital in extremely high - resolution
imaging studies.
«The high efficiency of the materials along with cheap, scalable synthesis makes them very attractive as next generation emitters for
fluorescent lamps, LEDs and for biological
imaging, for example for highlighting tumours or
cell division.»
Embryonic hemocytes lend themselves beautifully to live
imaging studies since
fluorescent probes can be expressed specifically in these
cells using hemocyte specific promoters and their movements subsequently imaged within living embryos using confocal timelapse microscopy.
They found that injecting into the carotid artery breast cancer
cells that express markers allowing them to enter the brain —
cells labelled with bioluminescent and
fluorescent markers to enable tracking by
imaging technologies — resulted in the formation of many metastatic tumors throughout the brain, mimicking what is seen in advanced breast cancer patients.
The injected
cells express markers that allow them to enter the brain and are labelled with bioluminescent and
fluorescent markers to enable tracking by
imaging technologies.
Johanna Spandl (Thiele, MPG)-- «
Cell biology of lipid droplets: The function of the lipid droplet protein AUP1 and establishment of the novel
fluorescent dye LD540 for improved staining and
imaging of lipid droplets» (2009)
Application to Living
Cell Fluorescent Imaging.
smFISH can be used to detect specific RNA sequences in a
cell based on their binding to a
fluorescent probe, but
imaging the «dots» corresponding to each RNA molecule requires high magnification and delicate
imaging settings.
The 1833 and SCP28 breast cancer
cells were engineered to express reporters with luciferase and green
fluorescent protein to monitor metastatic progression by bioluminescence
imaging (Fig. 2A).
Through clever biochemistry combined with superresolution
imaging techniques, Yao and colleagues introduced two EB proteins into
cells, one with half of a photoactivatable green
fluorescent protein (PAGFP), and one with the other half of PAGFP.
The optical contrast (measured as a ratio of the
fluorescent image amplitudes for C4 - 2B to HS - 5) of
fluorescent imaging for cancer versus stromal
cells was 2.3 (Figure 7B, D).
HeLa
cells were untreated or treated with 1mM Deferoxamine (DFO) for 24h and fixed with paraformaldehyde for
imaging by
fluorescent microscopy.