Next,
the researchers labeled cells in 3 - day - old embryos and followed where they wound up in the chick.
Not exact matches
Meanwhile,
researchers at Columbia University in New York are working on a way to add dozens of color
labels to Raman - imaged
cells.
In experiments in human
cells grown in a lab dish, the
researchers showed that they could accurately
label mRNA molecules and determine how frequently they are being translated.
After initiating photoreceptor loss in the fish retinas, the
researchers monitored the immune system's response by tracking the activity of three types of fluorescently
labeled immune
cells in and around the eye: neutrophils, microglia and peripheral macrophages.
By developing a new technique for
labeling the gene segments of influenza viruses,
researchers now know more about how influenza viruses enter the
cell and establish
cell co-infections — a major contributing factor to potential pandemic development.
The Max Planck
researchers found that H3K27me3 modifications
labeling chromatin DNA in the mother's egg
cells were still present in the embryo after fertilization, even though other epigenetic marks are erased.
The
researchers solved this problem by developing markers to
label the
cells of interest and then testing different enzymes and other reagents to draw them out of tissues.
Using quantitative mass spectrometry to search for proteins that contained these stable isotope
labels,
researchers were able to determine the
cell of origin of both intracellular and secreted proteins identified in multicellular culture.
Using this, the
researchers performed 3D super-resolution imaging of stained structures in the
cells, and combined it with 3D
label - free phase imaging.
To
label individual
cells,
researchers use a very thin violet laser beam aimed at small blood vessels.
Now, a new approach developed by Dr. Ekaterina Galanzha of the University of Arkansas for Medical Sciences in Little Rock and her colleagues allows for
labeling and tracking of individual circulating cancer
cells throughout the body, thereby helping
researchers elucidate the pathways of single
cells from start to finish.
To better understand what happens during immune reactions in the body,
researchers at Tübingen University have developed a new way of
labeling T -
cells, allowing them to track the T -
cell movement in mice using non-invasive positron emission technology (PET).
Now,
researchers reporting in the
Cell Press journal Chemistry & Biology have developed a new method that allows investigators to
label and track single tumor
cells circulating in the blood.
To find out what's going on inside a
cell,
researchers expose the chip to fluorescently
labeled genetic material that's being shipped around inside the
cell.
The
researchers used CRISPR gene editing technology to engineer stem
cells that produced fluorescently
labeled inner ear sensory
cells.
The
researchers then attempted to see if the
cells, which they
labeled multipotent adult germline stem
cells (maGSC), would differentiate into specific types of body
cells.
Labeled antibodies, which bind to specific
cell types, allowed the
researchers to determine which types of neuron were being created at which times.
To see if Narp played a role in making these new
cells in mice, the
researchers injected a synthetic molecule, BrdU, to
label and allow detection of newly created
cells that would become neurons in the hippocampus.
The
researchers injected a compound normally used to
label tumor
cell division into patients who had agreed to have their brains examined after death.
In the current study, the
researchers used high - affinity antibodies to «
label» the cannabinoid receptors so they could be seen using various microscopy techniques, including electron microscopy, which allowed very detailed visualization at individual synapses, or gaps between nerve
cells.
Two days later, the
cells assembled into a 5 - millimetre - long, three - dimensional tissue that the
researchers labelled a liver bud — an early stage of liver development.
During fear conditioning,
researchers used a virus to deliver a gene into the dentate gyrus, which
labeled active engram
cells.
Researchers used this approach to
label memory
cells during a fear - conditioning event that involved a mild electric shock to the mouse and then used light to artificially reactive memories at different times.
The ClonTracer library allows a
researcher to
label individual members of a starting population of
cells with specifc, easily read sequences that can be used to measure their clonal abundance before and after a treatment.
Researchers at Columbia University have made a significant step toward breaking the so - called «color barrier» of light microscopy for biological systems, allowing for much more comprehensive, system - wide
labeling and imaging of a greater number of biomolecules in living
cells and tissues than is currently attainable.
A novel study from
researchers at Karolinska Institutet shows that by using so called random sequence
labels, working as barcodes for tracing genetically altered
cells, during CRISPR / Cas9 gene knock - outs it is possible to generate more comprehensive data from a smaller number of
cells.
At times, those
labels can be incompatible with live
cells, or unavailable to
researchers.
By mimicking the intricate visual system of a butterfly,
researchers have created a camera that provides surgeons with both a traditional color image as well as a near - infrared image that makes fluorescently
labeled cancerous
cells visible even under bright surgical lighting.
Flow cytometry is a powerful technique that allows
researchers to examine multiple proteins on
cell populations using fluorescently
labeled antibodies.
Researchers from University of Massachusetts Medical School has used CRISPR / Cas9 gene editing tool to track and
label chromosomes in live
cells.
Researchers at SciLifeLab / Uppsala University headed by Johan Elf have used a combination of microfluidics and image analysis of E. coli with fluorescent
labels on the replication machinery to study how the replication and division cycles are coupled in individual
cells.
«Brainbow,» a multi-color
labeling system, is helping
researchers study the brains of animals such as the mouse
cell by
cell.
Results The
researchers were able to estimate the amount of growth that took place in the participants» muscle
cells by looking at the amount of
labelled phenylalanine that they absorbed.