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Image and Video Gallery
This is a searchable collection of scientific photos, illustrations, and videos. The images and videos in this gallery are licensed under Creative Commons Attribution Non-Commercial ShareAlike 3.0. This license lets you remix, tweak, and build upon this work non-commercially, as long as you credit and license your new creations under identical terms.
2759: Cross section of a Drosophila melanogaster pupa lacking Draper
2759: Cross section of a Drosophila melanogaster pupa lacking Draper
In the absence of the engulfment receptor Draper, salivary gland cells (light blue) persist in the thorax of a developing Drosophila melanogaster pupa. See image 2758 for a cross section of a normal pupa that does express Draper.
Christina McPhee and Eric Baehrecke, University of Massachusetts Medical School
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2637: Activated mast cell surface
2637: Activated mast cell surface
A scanning electron microscope image of an activated mast cell. This image illustrates the interesting topography of the cell membrane, which is populated with receptors. The distribution of receptors may affect cell signaling. This image relates to a July 27, 2009 article in Computing Life.
Bridget Wilson, University of New Mexico
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3742: Confocal microscopy of perineuronal nets in the brain 2
3742: Confocal microscopy of perineuronal nets in the brain 2
The photo shows a confocal microscopy image of perineuronal nets (PNNs), which are specialized extracellular matrix (ECM) structures in the brain. The PNN surrounds some nerve cells in brain regions including the cortex, hippocampus and thalamus. Researchers study the PNN to investigate their involvement stabilizing the extracellular environment and forming nets around nerve cells and synapses in the brain. Abnormalities in the PNNs have been linked to a variety of disorders, including epilepsy and schizophrenia, and they limit a process called neural plasticity in which new nerve connections are formed. To visualize the PNNs, researchers labeled them with Wisteria floribunda agglutinin (WFA)-fluorescein. Related to image 3741.
Tom Deerinck, National Center for Microscopy and Imaging Research (NCMIR)
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3282: Mouse heart muscle cells
3282: Mouse heart muscle cells
This image shows neonatal mouse heart cells. These cells were grown in the lab on a chip that aligns the cells in a way that mimics what is normally seen in the body. Green shows the protein N-cadherin, which indicates normal connections between cells. Red indicates the muscle protein actin, and blue indicates the cell nuclei. The work shown here was part of a study attempting to grow heart tissue in the lab to repair damage after a heart attack. Image and caption information courtesy of the California Institute for Regenerative Medicine. Related to images 3281 and 3283.
Kara McCloskey lab, University of California, Merced, via CIRM
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6800: Magnetic Janus particle activating a T cell
6800: Magnetic Janus particle activating a T cell
A Janus particle being used to activate a T cell, a type of immune cell. A Janus particle is a specialized microparticle with different physical properties on its surface, and this one is coated with nickel on one hemisphere and anti-CD3 antibodies (light blue) on the other. The nickel enables the Janus particle to be moved using a magnet, and the antibodies bind to the T cell and activate it. The T cell in this video was loaded with calcium-sensitive dye to visualize calcium influx, which indicates activation. The intensity of calcium influx was color coded so that warmer color indicates higher intensity. Being able to control Janus particles with simple magnets is a step toward controlling individual cells’ activities without complex magnetic devices.
More details can be found in the Angewandte Chemie paper “Remote control of T cell activation using magnetic Janus particles” by Lee et al. This video was captured using epi-fluorescence microscopy.
Related to video 6801.
More details can be found in the Angewandte Chemie paper “Remote control of T cell activation using magnetic Janus particles” by Lee et al. This video was captured using epi-fluorescence microscopy.
Related to video 6801.
Yan Yu, Indiana University, Bloomington.
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2499: Cell cycle (with labels)
2499: Cell cycle (with labels)
Cells progress through a cycle that consists of phases for growth (G1, S, and G2) and division (M). Cells become quiescent when they exit this cycle (G0). See image 2498 for an unlabeled version of this illustration.
Crabtree + Company
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1333: Mitosis and meiosis compared
1333: Mitosis and meiosis compared
Meiosis is used to make sperm and egg cells. During meiosis, a cell's chromosomes are copied once, but the cell divides twice. During mitosis, the chromosomes are copied once, and the cell divides once. For simplicity, cells are illustrated with only three pairs of chromosomes. See image 6788 for a labeled version of this illustration.
Judith Stoffer
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3334: Four timepoints in gastrulation
3334: Four timepoints in gastrulation
It has been said that gastrulation is the most important event in a person's life. This part of early embryonic development transforms a simple ball of cells and begins to define cell fate and the body axis. In a study published in Science magazine, NIGMS grantee Bob Goldstein and his research group studied how contractions of actomyosin filaments in C. elegans and Drosophila embryos lead to dramatic rearrangements of cell and embryonic structure. In these images, myosin (green) and plasma membrane (red) are highlighted at four timepoints in gastrulation in the roundworm C. elegans. The blue highlights in the top three frames show how cells are internalized, and the site of closure around the involuting cells is marked with an arrow in the last frame. See related image 3297.
Bob Goldstein, University of North Carolina, Chapel Hill
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2333: Worms and human infertility
2333: Worms and human infertility
This montage of tiny, transparent C. elegans--or roundworms--may offer insight into understanding human infertility. Researchers used fluorescent dyes to label the worm cells and watch the process of sex cell division, called meiosis, unfold as nuclei (blue) move through the tube-like gonads. Such visualization helps the scientists identify mechanisms that enable these roundworms to reproduce successfully. Because meiosis is similar in all sexually reproducing organisms, what the scientists learn could apply to humans.
Abby Dernburg, Lawrence Berkeley National Laboratory
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3389: NCMIR Intestine-1
3389: NCMIR Intestine-1
The small intestine is where most of our nutrients from the food we eat are absorbed into the bloodstream. The walls of the intestine contain small finger-like projections called villi which increase the organ's surface area, enhancing nutrient absorption. It consists of the duodenum, which connects to the stomach, the jejenum and the ileum, which connects with the large intestine. Related to image 3390.
Tom Deerinck, National Center for Microscopy and Imaging Research (NCMIR)
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2727: Proteins related to myotonic dystrophy
2727: Proteins related to myotonic dystrophy
Myotonic dystrophy is thought to be caused by the binding of a protein called Mbnl1 to abnormal RNA repeats. In these two images of the same muscle precursor cell, the top image shows the location of the Mbnl1 splicing factor (green) and the bottom image shows the location of RNA repeats (red) inside the cell nucleus (blue). The white arrows point to two large foci in the cell nucleus where Mbnl1 is sequestered with RNA.
Manuel Ares, University of California, Santa Cruz
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1012: Lily mitosis 02
1012: Lily mitosis 02
A light microscope image of a cell from the endosperm of an African globe lily (Scadoxus katherinae). This is one frame of a time-lapse sequence that shows cell division in action. The lily is considered a good organism for studying cell division because its chromosomes are much thicker and easier to see than human ones. Staining shows microtubules in red and chromosomes in blue.
Related to images 1010, 1011, 1013, 1014, 1015, 1016, 1017, 1018, 1019, and 1021.
Related to images 1010, 1011, 1013, 1014, 1015, 1016, 1017, 1018, 1019, and 1021.
Andrew S. Bajer, University of Oregon, Eugene
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2746: Active site of sulfite oxidase
2746: Active site of sulfite oxidase
Sulfite oxidase is an enzyme that is essential for normal neurological development in children. This video shows the active site of the enzyme and its molybdenum cofactor visible as a faint ball-and-stick representation buried within the protein. The positively charged channel (blue) at the active site contains a chloride ion (green) and three water molecules (red). As the protein oscillates, one can see directly down the positively charged channel. At the bottom is the molybdenum atom of the active site (light blue) and its oxo group (red) that is transferred to sulfite to form sulfate in the catalytic reaction.
John Enemark, University of Arizona
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5855: Dense tubular matrices in the peripheral endoplasmic reticulum (ER) 1
5855: Dense tubular matrices in the peripheral endoplasmic reticulum (ER) 1
Superresolution microscopy work on endoplasmic reticulum (ER) in the peripheral areas of the cell showing details of the structure and arrangement in a complex web of tubes. The ER is a continuous membrane that extends like a net from the envelope of the nucleus outward to the cell membrane. The ER plays several roles within the cell, such as in protein and lipid synthesis and transport of materials between organelles. The ER has a flexible structure to allow it to accomplish these tasks by changing shape as conditions in the cell change. Shown here an image created by super-resolution microscopy of the ER in the peripheral areas of the cell showing details of the structure and the arrangements in a complex web of tubes. Related to images 5856 and 5857.
Jennifer Lippincott-Schwartz, Howard Hughes Medical Institute Janelia Research Campus, Virginia
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6983: Genetic mosaicism in fruit flies
6983: Genetic mosaicism in fruit flies
Fat tissue from the abdomen of a genetically mosaic adult fruit fly. Genetic mosaicism means that the fly has cells with different genotypes even though it formed from a single zygote. This specific mosaicism results in accumulation of a critical fly adipokine (blue-green) within the fat tissue cells that have reduced expression a key nutrient sensing gene (in left panel). The dotted line shows the cells lacking the gene that is present and functioning in the rest of the cells. Nuclei are labelled in magenta. This image was captured using a confocal microscope and shows a maximum intensity projection of many slices.
Related to images 6982, 6984, and 6985.
Related to images 6982, 6984, and 6985.
Akhila Rajan, Fred Hutchinson Cancer Center
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3627: Larvae from the parasitic worm that causes schistosomiasis
3627: Larvae from the parasitic worm that causes schistosomiasis
The parasitic worm that causes schistosomiasis hatches in water and grows up in a freshwater snail, as shown here. Once mature, the worm swims back into the water, where it can infect people through skin contact. Initially, an infected person might have a rash, itchy skin, or flu-like symptoms, but the real damage is done over time to internal organs.
This image was part of the Life: Magnified exhibit that ran from June 3, 2014, to January 21, 2015, at Dulles International Airport.
This image was part of the Life: Magnified exhibit that ran from June 3, 2014, to January 21, 2015, at Dulles International Airport.
Bo Wang and Phillip A. Newmark, University of Illinois at Urbana-Champaign, 2013 FASEB BioArt winner
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2315: Fly cells live
2315: Fly cells live
If a picture is worth a thousand words, what's a movie worth? For researchers studying cell migration, a "documentary" of fruit fly cells (bright green) traversing an egg chamber could answer longstanding questions about cell movement. Historically, researchers have been unable to watch this cell migration unfold in living ovarian tissue in real time. But by developing a culture medium that allows fly eggs to survive outside their ovarian homes, scientists can observe the nuances of cell migration as it happens. Such details may shed light on how immune cells move to a wound and why cancer cells spread to other sites. See 3594 for still image.
Denise Montell, Johns Hopkins University School of Medicine
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1290: Nucleus and rough ER
1290: Nucleus and rough ER
The nucleus contains the DNA of eukaryotic cells. The double membrane that bounds the nucleus flows into the rough endoplasmic reticulum, an organelle studded with ribosomes that manufacture membrane-bound proteins for the rest of the cell.
Judith Stoffer
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1166: Leptospira bacteria
1166: Leptospira bacteria
Leptospira, shown here in green, is a type (genus) of elongated, spiral-shaped bacteria. Infection can cause Weil's disease, a kind of jaundice, in humans.
Tina Weatherby Carvalho, University of Hawaii at Manoa
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6808: Fruit fly larvae brains showing tubulin
6808: Fruit fly larvae brains showing tubulin
Two fruit fly (Drosophila melanogaster) larvae brains with neurons expressing fluorescently tagged tubulin protein. Tubulin makes up strong, hollow fibers called microtubules that play important roles in neuron growth and migration during brain development. This image was captured using confocal microscopy, and the color indicates the position of the neurons within the brain.
Vladimir I. Gelfand, Feinberg School of Medicine, Northwestern University.
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1330: Mitosis - prophase
1330: Mitosis - prophase
A cell in prophase, near the start of mitosis: In the nucleus, chromosomes condense and become visible. In the cytoplasm, the spindle forms. Mitosis is responsible for growth and development, as well as for replacing injured or worn out cells throughout the body. For simplicity, mitosis is illustrated here with only six chromosomes.
Judith Stoffer
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1287: Mitochondria
1287: Mitochondria
Bean-shaped mitochondria are cells' power plants. These organelles have their own DNA and replicate independently. The highly folded inner membranes are the site of energy generation.
Judith Stoffer
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3727: Zinc levels in a plant leaf
3727: Zinc levels in a plant leaf
Zinc is required for the function of more than 300 enzymes, including those that help regulate gene expression, in various organisms including humans. Researchers study how plants acquire, sequester and distribute zinc to find ways to increase the zinc content of crops to improve human health. Using synchrotron X-ray fluorescence technology, they created this heat map of zinc levels in an Arabidopsis thaliana plant leaf. This image is a winner of the 2015 FASEB Bioart contest and was featured in the NIH Director's blog.
Suzana Car, Dartmouth College
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2607: Mouse embryo showing Smad4 protein
2607: Mouse embryo showing Smad4 protein
This eerily glowing blob isn't an alien or a creature from the deep sea--it's a mouse embryo just eight and a half days old. The green shell and core show a protein called Smad4. In the center, Smad4 is telling certain cells to begin forming the mouse's liver and pancreas. Researchers identified a trio of signaling pathways that help switch on Smad4-making genes, starting immature cells on the path to becoming organs. The research could help biologists learn how to grow human liver and pancreas tissue for research, drug testing and regenerative medicine. In addition to NIGMS, NIH's National Institute of Diabetes and Digestive and Kidney Diseases also supported this work.
Kenneth Zaret, Fox Chase Cancer Center
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3792: Nucleolus subcompartments spontaneously self-assemble 3
3792: Nucleolus subcompartments spontaneously self-assemble 3
What looks a little like distant planets with some mysterious surface features are actually assemblies of proteins normally found in the cell's nucleolus, a small but very important protein complex located in the cell's nucleus. It forms on the chromosomes at the location where the genes for the RNAs are that make up the structure of the ribosome, the indispensable cellular machine that makes proteins from messenger RNAs.
However, how the nucleolus grows and maintains its structure has puzzled scientists for some time. It turns out that even though it looks like a simple liquid blob, it's rather well-organized, consisting of three distinct layers: the fibrillar center, where the RNA polymerase is active; the dense fibrillar component, which is enriched in the protein fibrillarin; and the granular component, which contains a protein called nucleophosmin. Researchers have now discovered that this multilayer structure of the nucleolus arises from differences in how the proteins in each compartment mix with water and with each other. These differences let the proteins readily separate from each other into the three nucleolus compartments.
This photo of nucleolus proteins in the eggs of a commonly used lab animal, the frog Xenopus laevis, shows each of the nucleolus compartments (the granular component is shown in red, the fibrillarin in yellow-green, and the fibrillar center in blue). The researchers have found that these compartments spontaneously fuse with each other on encounter without mixing with the other compartments.
For more details on this research, see this press release from Princeton. Related to video 3789, video 3791 and image 3793.
However, how the nucleolus grows and maintains its structure has puzzled scientists for some time. It turns out that even though it looks like a simple liquid blob, it's rather well-organized, consisting of three distinct layers: the fibrillar center, where the RNA polymerase is active; the dense fibrillar component, which is enriched in the protein fibrillarin; and the granular component, which contains a protein called nucleophosmin. Researchers have now discovered that this multilayer structure of the nucleolus arises from differences in how the proteins in each compartment mix with water and with each other. These differences let the proteins readily separate from each other into the three nucleolus compartments.
This photo of nucleolus proteins in the eggs of a commonly used lab animal, the frog Xenopus laevis, shows each of the nucleolus compartments (the granular component is shown in red, the fibrillarin in yellow-green, and the fibrillar center in blue). The researchers have found that these compartments spontaneously fuse with each other on encounter without mixing with the other compartments.
For more details on this research, see this press release from Princeton. Related to video 3789, video 3791 and image 3793.
Nilesh Vaidya, Princeton University
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6967: Multinucleated cancer cell
6967: Multinucleated cancer cell
A cancer cell with three nuclei, shown in turquoise. The abnormal number of nuclei indicates that the cell failed to go through cell division, probably more than once. Mitochondria are shown in yellow, and a protein of the cell’s cytoskeleton appears in red. This video was captured using a confocal microscope.
Dylan T. Burnette, Vanderbilt University School of Medicine.
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6969: Snowflake yeast 1
6969: Snowflake yeast 1
Multicellular yeast called snowflake yeast that researchers created through many generations of directed evolution from unicellular yeast. Stained cell membranes (green) and cell walls (red) reveal the connections between cells. Younger cells take up more cell membrane stain, while older cells take up more cell wall stain, leading to the color differences seen here. This image was captured using spinning disk confocal microscopy.
Related to images 6970 and 6971.
Related to images 6970 and 6971.
William Ratcliff, Georgia Institute of Technology.
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6965: Dividing cell
6965: Dividing cell
As this cell was undergoing cell division, it was imaged with two microscopy techniques: differential interference contrast (DIC) and confocal. The DIC view appears in blue and shows the entire cell. The confocal view appears in pink and shows the chromosomes.
Dylan T. Burnette, Vanderbilt University School of Medicine.
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3333: Polarized cells- 02
3333: Polarized cells- 02
Cells move forward with lamellipodia and filopodia supported by networks and bundles of actin filaments. Proper, controlled cell movement is a complex process. Recent research has shown that an actin-polymerizing factor called the Arp2/3 complex is the key component of the actin polymerization engine that drives amoeboid cell motility. ARPC3, a component of the Arp2/3 complex, plays a critical role in actin nucleation. In this photo, the ARPC3-/- fibroblast cells were fixed and stained with Alexa 546 phalloidin for F-actin (red) and DAPI to visualize the nucleus (blue). In the absence of functional Arp2/3 complex, ARPC3-/- fibroblast cells' leading edge morphology is significantly altered with filopodia-like structures. Related to images 3328, 3329, 3330, 3331, and 3332.
Rong Li and Praveen Suraneni, Stowers Institute for Medical Research
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3783: A multicolored fish scale 2
3783: A multicolored fish scale 2
Each of the tiny colored specs in this image is a cell on the surface of a fish scale. To better understand how wounds heal, scientists have inserted genes that make cells brightly glow in different colors into the skin cells of zebrafish, a fish often used in laboratory research. The colors enable the researchers to track each individual cell, for example, as it moves to the location of a cut or scrape over the course of several days. These technicolor fish endowed with glowing skin cells dubbed "skinbow" provide important insight into how tissues recover and regenerate after an injury.
For more information on skinbow fish, see the Biomedical Beat blog post Visualizing Skin Regeneration in Real Time and a press release from Duke University highlighting this research. Related to image 3782.
For more information on skinbow fish, see the Biomedical Beat blog post Visualizing Skin Regeneration in Real Time and a press release from Duke University highlighting this research. Related to image 3782.
Chen-Hui Chen and Kenneth Poss, Duke University
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5852: Optic nerve astrocytes
5852: Optic nerve astrocytes
Astrocytes in the cross section of a human optic nerve head
Tom Deerinck and Keunyoung (“Christine”) Kim, NCMIR
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6550: Time-lapse video of floral pattern in a mixture of two bacterial species, Acinetobacter baylyi and Escherichia coli, grown on a semi-solid agar for 24 hours
6550: Time-lapse video of floral pattern in a mixture of two bacterial species, Acinetobacter baylyi and Escherichia coli, grown on a semi-solid agar for 24 hours
This time-lapse video shows the emergence of a flower-like pattern in a mixture of two bacterial species, motile Acinetobacter baylyi and non-motile Escherichia coli (green), that are grown together for 24 hours on 0.75% agar surface from a small inoculum in the center of a Petri dish.
See 6557 for a photo of this process at 24 hours on 0.75% agar surface.
See 6553 for a photo of this process at 48 hours on 1% agar surface.
See 6555 for another photo of this process at 48 hours on 1% agar surface.
See 6556 for a photo of this process at 72 hours on 0.5% agar surface.
See 6557 for a photo of this process at 24 hours on 0.75% agar surface.
See 6553 for a photo of this process at 48 hours on 1% agar surface.
See 6555 for another photo of this process at 48 hours on 1% agar surface.
See 6556 for a photo of this process at 72 hours on 0.5% agar surface.
L. Xiong et al, eLife 2020;9: e48885
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2418: Genetic imprinting in Arabidopsis
2418: Genetic imprinting in Arabidopsis
This delicate, birdlike projection is an immature seed of the Arabidopsis plant. The part in blue shows the cell that gives rise to the endosperm, the tissue that nourishes the embryo. The cell is expressing only the maternal copy of a gene called MEDEA. This phenomenon, in which the activity of a gene can depend on the parent that contributed it, is called genetic imprinting. In Arabidopsis, the maternal copy of MEDEA makes a protein that keeps the paternal copy silent and reduces the size of the endosperm. In flowering plants and mammals, this sort of genetic imprinting is thought to be a way for the mother to protect herself by limiting the resources she gives to any one embryo. Featured in the May 16, 2006, issue of Biomedical Beat.
Robert Fischer, University of California, Berkeley
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1285: Lipid raft
1285: Lipid raft
Researchers have learned much of what they know about membranes by constructing artificial membranes in the laboratory. In artificial membranes, different lipids separate from each other based on their physical properties, forming small islands called lipid rafts.
Judith Stoffer
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3574: Cytonemes in developing fruit fly cells
3574: Cytonemes in developing fruit fly cells
Scientists have long known that multicellular organisms use biological molecules produced by one cell and sensed by another to transmit messages that, for instance, guide proper development of organs and tissues. But it's been a puzzle as to how molecules dumped out into the fluid-filled spaces between cells can precisely home in on their targets. Using living tissue from fruit flies, a team led by Thomas Kornberg of the University of California, San Francisco, has shown that typical cells in animals can talk to each other via long, thin cell extensions called cytonemes (Latin for "cell threads") that may span the length of 50 or 100 cells. The point of contact between a cytoneme and its target cell acts as a communications bridge between the two cells.
Sougata Roy, University of California, San Francisco
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3772: The Proteasome: The Cell's Trash Processor in Action
3772: The Proteasome: The Cell's Trash Processor in Action
Our cells are constantly removing and recycling molecular waste. This video shows one way cells process their trash.
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1313: Cell eyes clock
3288: Smooth muscle from human ES cells
3288: Smooth muscle from human ES cells
These smooth muscle cells were derived from human embryonic stem cells. The nuclei are stained blue, and the proteins of the cytoskeleton are stained green. Image and caption information courtesy of the California Institute for Regenerative Medicine.
Alexey Terskikh lab, Burnham Institute for Medical Research, via CIRM
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3624: Fibroblasts with nuclei in blue, energy factories in green and the actin cytoskeleton in red
3624: Fibroblasts with nuclei in blue, energy factories in green and the actin cytoskeleton in red
The cells shown here are fibroblasts, one of the most common cells in mammalian connective tissue. These particular cells were taken from a mouse embryo. Scientists used them to test the power of a new microscopy technique that offers vivid views of the inside of a cell. The DNA within the nucleus (blue), mitochondria (green), and actin filaments in the cellular skeleton (red) are clearly visible.
This image was part of the Life: Magnified exhibit that ran from June 3, 2014, to January 21, 2015, at Dulles International Airport.
This image was part of the Life: Magnified exhibit that ran from June 3, 2014, to January 21, 2015, at Dulles International Airport.
Dylan Burnette, NICHD
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3457: Sticky stem cells
3457: Sticky stem cells
Like a group of barnacles hanging onto a rock, these human cells hang onto a matrix coated glass slide. Actin stress fibers, stained magenta, and the protein vinculin, stained green, make this adhesion possible. The fibroblast nuclei are stained blue.
Ankur Singh and Andrés García, Georgia Institute of Technology
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2684: Dicty fruit
2684: Dicty fruit
Dictyostelium discoideum is a microscopic amoeba. A group of 100,000 form a mound as big as a grain of sand. Featured in The New Genetics.
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3687: Hippocampal neuron in culture
3687: Hippocampal neuron in culture
Hippocampal neuron in culture. Dendrites are green, dendritic spines are red and DNA in cell's nucleus is blue. Image is featured on Biomedical Beat blog post Anesthesia and Brain Cells: A Temporary Disruption?
Shelley Halpain, UC San Diego
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3688: Brain cells in the hippocampus
3688: Brain cells in the hippocampus
Hippocampal cells in culture with a neuron in green, showing hundreds of the small protrusions known as dendritic spines. The dendrites of other neurons are labeled in blue, and adjacent glial cells are shown in red.
Shelley Halpain, UC San Diego
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1306: Vesicular shuttle model
1306: Vesicular shuttle model
Animation for the vesicular shuttle model of Golgi transport.
Judith Stoffer
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5882: Beta-galactosidase montage showing cryo-EM improvement--transparent background
5882: Beta-galactosidase montage showing cryo-EM improvement--transparent background
Composite image of beta-galactosidase showing how cryo-EM’s resolution has improved dramatically in recent years. Older images to the left, more recent to the right. Related to image 5883. NIH Director Francis Collins featured this on his blog on January 14, 2016.
Veronica Falconieri, Sriram Subramaniam Lab, National Cancer Institute
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3280: Motor neuron progenitors derived from human ES cells
3280: Motor neuron progenitors derived from human ES cells
Motor neuron progenitors (green) were derived from human embryonic stem cells. Image and caption information courtesy of the California Institute for Regenerative Medicine.
Hans Keirstead lab, University of California, Irvine, via CIRM
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6586: Cell-like compartments from frog eggs 3
6586: Cell-like compartments from frog eggs 3
Cell-like compartments that spontaneously emerged from scrambled frog eggs. Endoplasmic reticulum (red) and microtubules (green) are visible. Image created using epifluorescence microscopy.
For more photos of cell-like compartments from frog eggs view: 6584, 6585, 6591, 6592, and 6593.
For videos of cell-like compartments from frog eggs view: 6587, 6588, 6589, and 6590.
Xianrui Cheng, Stanford University School of Medicine.
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1282: Lysosomes
1282: Lysosomes
Lysosomes have powerful enzymes and acids to digest and recycle cell materials.
Judith Stoffer
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6971: Snowflake yeast 3
6971: Snowflake yeast 3
Multicellular yeast called snowflake yeast that researchers created through many generations of directed evolution from unicellular yeast. Here, the researchers visualized nuclei in orange to help them study changes in how the yeast cells divided. Cell walls are shown in blue. This image was captured using spinning disk confocal microscopy.
Related to images 6969 and 6970.
Related to images 6969 and 6970.
William Ratcliff, Georgia Institute of Technology.
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