“Thermo Fisher Scientific Snags Finnzymes for High-Performance PCR ... - Genetic Engineering News” plus 3 more |
- Thermo Fisher Scientific Snags Finnzymes for High-Performance PCR ... - Genetic Engineering News
- Mechanism Behind miRNAs Ability to Shut Down Protein Production ... - Genetic Engineering News
- For Bonobos, Sharing Is Caring - Softpedia
- Glial cells can protect or kill neurons in retina - The Gaea Times
Thermo Fisher Scientific Snags Finnzymes for High-Performance PCR ... - Genetic Engineering News Posted: 02 Feb 2010 07:11 AM PST Feb 2 2010, 10:16 AM EST Thermo Fisher Scientific Snags Finnzymes for High-Performance PCR SolutionsGEN News Highlights Thermo Fisher Scientific is acquiring Finnzymes, a provider of integrated tools for molecular biology analysis, including reagents, instruments, consumables, and kits. Headquartered in Espoo, Finland, Finnzymes has 90 employees and generated revenue of $20 million in 2009. Finnzymes provides solutions for high-performance PCR, RT-PCR, and real-time qPCR. The company's expertise in DNA polymerases has led to significant increases in the performance of these enzymes, making the PCR process faster and more accurate, according to Thermo Fisher Scientific. The acquisition of Finnzymes expands Thermo Fisher's portfolio of reagents and other consumables for the molecular biology research and diagnostics markets through the addition of its DNA polymerases Phire™ and Phusion™ as well as high-speed miniaturized thermal cyclers and plastic tubes and plates. These products complement the recently launched Thermo Scientific Solaris qPCR gene-expression assays. Combining the gene-specific MGB®-based probes from Thermo Scientific with the advanced enzyme performance from Finnzymes will further enhance qPCR assay technology, Thermo Fisher believes. "The addition of Finnzymes' innovative enzyme portfolio and unique PCR instrument platform strengthens our broad range of life science reagents and consumables as well as our specialty diagnostics product offering," notes Marc N. Casper, president and CEO of Thermo Fisher Scientific. "This combination brings together key complementary technologies for molecular biology and diagnostics, allowing us to create significant value for our customers." Finnzymes will be integrated primarily into Thermo Fisher Scientific's analytical technologies segment, with some equipment and consumable product lines being added to the laboratory products and services segment. The transaction is expected to close during the first quarter of this year. The company does not expect this transaction to have a material impact on its 2010 financial results. Comment on this News:Five Filters featured article: Chilcot Inquiry. Available tools: PDF Newspaper, Full Text RSS, Term Extraction. |
Mechanism Behind miRNAs Ability to Shut Down Protein Production ... - Genetic Engineering News Posted: 02 Feb 2010 07:18 AM PST Feb 2 2010, 10:19 AM EST Mechanism behind miRNA's Ability to Shut Down Protein Production RevealedGEN News Highlights Johns Hopkins scientists believe they may have figured out how miRNAs are able to stop the production of some proteins. In both computer and test-tube studies using fruit-fly protein, the team found that miRNAs direct Argonaute proteins to specific target mRNAs to repress protein expression. The research appeared in the January edition of Nature Structural & Molecular Biology in a paper titled "MicroRNA assassins: factors that regulate the disappearance of miRNAs." The Johns Hopkins group studied Argonaute because it is known to bind to miRNA and ultimately shut down protein production. Previous studies have been inconclusive about the mechanism by which miRNAs bound to Argonautes prevented the production of protein from a given gene. The team set out to characterize Argonautes first using computers to compare their shapes and structures with other proteins. They found striking similarities between Argonaute structures and proteins that happened to exhibit allostery, a condition in which the binding of one molecule stimulates the binding of a second. By chopping up Argonaute proteins from fruit flies and testing each piece individually, the team showed that allostery stimulated 10-fold the binding of the Argonaute and miRNA complex to mRNA. The scientists speculate that as a result of being bound, the mRNA was prevented from doing its job of delivering a gene's instructions to the ribosome that translates them and manufactures proteins. "MicroRNAs are all the rage," points out Rachel Green, Ph.D., a Howard Hughes Medical Institute investigator and professor of molecular biology and genetics in the Johns Hopkins University School of Medicine. "Suddenly, in the last 10 years there's this whole set of genes and cellular components that we had no idea existed, and they're ubiquitous. They play roles in all manner of development, and Argonautes are the main class of protein involved in regulating them." Comment on this News:Five Filters featured article: Chilcot Inquiry. Available tools: PDF Newspaper, Full Text RSS, Term Extraction. |
For Bonobos, Sharing Is Caring - Softpedia Posted: 02 Feb 2010 05:59 AM PST Bonobos are very peculiar animals. In addition to their bizarre mating rituals, they also tend to share things. But that would in itself be nothing of significant importance, had researchers not discovered that there is basically nothing you can do to stop the primates from doing so. While human kindergarten teachers struggle to implement the values of sharing and cooperation in our youngsters, bonobos have this ability built in, so deep that they cannot seem to be able to shake it. Details of the recent investigation appear in the latest issue of the respected scientific journal Current Biology. When compared to these primates, chimpanzees, and even humans, fall very short. While our species tends to get past its natural impulses to hoard stuff through long years of education, chimps never really learn to do it. In fact, they are notorious for keeping as much food to themselves as possible, sometimes protecting it from others via physical violence. The only times when chimps share is when they produce offspring, but they quickly grow out of it. According to experts at the Duke and Harvard universities, the differences that occur between bonobos and chimps may be rooted in developmental patterns. This means that the behaviors could be used to discover more data on the historical lifestyles of these two closely related ape species. Bonobos live in "a sort of Peter Pan world. They never grow up, and they share," Duke Assistant Professor of Evolutionary Anthropology Brian Hare explains. He has been involved in both Current Biology papers. Hare and Richard Wrangham, the Harvard Ruth Moore professor of anthropology, believe that one of the main reasons why bonobos developed this type of cooperative behavior was the fact that their environments were plentiful, which entailed less competition. Additionally, these primates do not have to fight gorillas for access to food, as chimps do, which may also be a contributing factor to this. It was also discovered that bonobos didn't really get past their childhood-style behaviors, even after they went well into adulthood. "It seems like some of these adult differences might actually derive from developmental differences. Evolution has been acting on the development of their cognition," Victoria Wobber, a Harvard graduate student, says. She has been the lead author of one of the journal entries. Five Filters featured article: Chilcot Inquiry. Available tools: PDF Newspaper, Full Text RSS, Term Extraction. |
Glial cells can protect or kill neurons in retina - The Gaea Times Posted: 01 Feb 2010 05:25 AM PST WASHINGTON - Scientists from University of Montreal and McGill University's Montreal Neurological Institute have discovered that glial cells, which normally protect neurons in the retina can also kill them, resulting in vision loss and blindness.
They found that a molecule, called proNGF, activates glial cells that kill neurons. "We found that glial cells attack and kill neurons after being triggered by proNGF," said coauthor Dr. Philip Barker, a neuroscientist at the Montreal Neurological Institute and a professor at the McGill Department of Neurology and Neurosurgery. "Since glial cells normally protect neurons, we were surprised to find that proNGF can convert glial cells into killers that cause neuron death in the retina." The researchers compared the proNGF molecule to a cell hijacker. "Before this study, we didn't know what physiological role the proNGF molecule played in the eye," said coauthor Dr. Adriana Di Polo, a professor at the Universite de Montreal Department of Pathology and Cell Biology. "We now propose that, following brain damage or neurodegenerative diseases, proNGF alters the glial cell network to change its function. Rather than protecting neurons, proNGF makes the glial cells attack neurons," she added. Scientists must now pay more attention to the damage proNGF can trigger. "Once retinal neurons die, they are gone forever and the permanent loss of these cells causes blindness," said Di Polo. "The next step for researchers is to explore whether proNGF signals can be controlled", said Frederic Lebrun-Julien, first author and a PhD student at the Universite de Montreal's Department of Pathology and Cell Biology. Dr. Barker concurs. "If we can block factors induced by proNGF, we can protect neurons that would normally be lost. We think these findings may eventually translate into clinical benefits in diseases such as glaucoma." The findings are published in the journal Proceedings of the National Academy of Sciences (PNAS). (ANI) Five Filters featured article: Chilcot Inquiry. Available tools: PDF Newspaper, Full Text RSS, Term Extraction. |
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