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19 Sentences With "passaging"

How to use passaging in a sentence? Find typical usage patterns (collocations)/phrases/context for "passaging" and check conjugation/comparative form for "passaging". Mastering all the usages of "passaging" from sentence examples published by news publications.

Yacht transport is the shipping of a yacht to a destination instead of sailing or motoring it. Yacht transport is an alternative to the traditional passaging (sailing or motoring) to reach desired destinations around the globe. Transport when compared to passaging is cost-effective, safer and improves availability. For many dedicated sailors, passaging or an ocean crossing is a rite of passage, but it comes with many risks and expenses.
Among more than 1,200 products for stem cell research, the company offered an engineered stem cell line (BG01v/hOG) and various STEMPRO products for manual passaging of human embryonic stem cells (hESC), to promote hESC growth and expansion, and to allow scientists to ascertain hESC pluripotency.
In biology, a subculture is a new cell or microbiological culture made by transferring some or all cells from a previous culture to fresh growth medium. This action is called subculturing or passaging the cells. Subculture is used to prolong the life and/or expand the number of cells or microorganisms in the culture.
Among the common manipulations carried out on culture cells are media changes, passaging cells, and transfecting cells. These are generally performed using tissue culture methods that rely on aseptic technique. Aseptic technique aims to avoid contamination with bacteria, yeast, or other cell lines. Manipulations are typically carried out in a biosafety cabinet or laminar flow cabinet to exclude contaminating micro-organisms.
The same year, former Los Angeles Auxiliary Bishop Gabino Zavala, who did not resign from either his post as Auxiliary Bishop or from the Catholic clergy until revelations that he fathered two children were made public, was implicated by the Los Angeles Times for having "more than a passaging relationship" with the mother of his two children, who also had two separate pregnancies.
The replicative form of SpV1 has been attempted to be used as a vector to express foreign genes in S. citri R8A2. The goal is to allow foreign genes to be transcribed, translated into proteins, and maintained in a stable form for generations. However, the recombinant viral DNA can prove to be unstable after passaging. SpV1-R8A2 B can be isolated from its host.
There are several challenges that scientists face when developing or using PDX models in research. For instance, not all tumor samples will successfully engraft in an immunodeficient mouse. When engraftment does occur, clinical study protocols are difficult to standardize if engraftment rates vary. It is also expensive to house mice, maintain histopathological cores for frequent testing, and perform ex vivo passaging of tumors in mice with high tumor burdens.
For many serious cruisers, financial, business and family considerations argue against the long-term full-time dedication that ocean crossings require. Yacht transport becomes an alternative when the destination and cruising (maritime) is more important than the passaging. Yacht transport generally eliminates costly, time-consuming, and dangerous difficult ocean crossings, opening up cruising to more people. Container cruising, one approach to yacht transport, is significantly less expensive and has greater flexibility with respect to timing and destinations.
VCaP are an adherent, epithelial cell line with high Androgen receptor and Prostate specific antigen expression. VCaP are the only prostate cancer cell model that express the Androgen receptor splice variant, AR-V7, and the TMPRSS2-ERG gene fusion. The cells have an approximate doubling time of 53 hours, and require more specific culture conditions than other prostate cancer cell lines. VCaP cells are XMRV virus positive and produce the mouse xenotropic retrovirus Bxv-1, likely acquired during passaging in infected mice.
Originating from a mouse, the N2a cell line has a neuronal and amoeboid stem cell morphology, allowing it to differentiate in response to environmental factors. The differentiated cells have many properties of neurons, including neurofilaments. The cells, due to passaging since initial collection, can exhibit responses to toxins that differ from those of neuronal cells in a live organism. Synthesizing large amounts of microtubules, N2a cells are susceptible to viruses (such as herpes simplex and poliovirus) that can alter cell morphology and physiology.
Specific strains of each serotype are used to prepare vaccines against polio. Inactive polio vaccine is prepared by formalin inactivation of three wild, virulent reference strains, Mahoney or Brunenders (PV-1), MEF-1/Lansing (PV-2), and Saukett/Leon (PV-3). Oral polio vaccine contains live attenuated (weakened) strains of the three serotypes of poliovirus. Passaging the virus strains in monkey kidney epithelial cells introduces mutations in the viral IRES, and hinders (or attenuates) the ability of the virus to infect nervous tissue.
For sexually reproducing populations, studies have shown that single-celled bottlenecks are beneficial for resisting mutation build-up. Passaging a population through a single-celled bottleneck involves the fertilization event occurring with haploid sets of DNA, forming one fertilized cell. For example, humans undergo a single-celled bottleneck in that the haploid sperm fertilizes the haploid egg, forming the diploid zygote, which is unicellular. This passage through a single cell is beneficial in that it lowers the chance of mutations from being passed on through multiple individuals.
There are advantages and disadvantages in utilizing either discrete tumor fragments or single-cell suspensions. Tumor fragments retain cell-cell interactions as well as some tissue architecture of the original tumor, therefore mimicking the tumor microenvironment. Alternatively, a single-cell suspension enables scientists to collect an unbiased sampling of the whole tumor, eliminating spatially segregate subclones that are otherwise inadvertently selected during analysis or tumor passaging. However, single- cell suspensions subject surviving cells to harsh chemical or mechanical forces that may sensitize cells to anoikis, taking a toll on cell viability and engraftment success.
Pulp stones generally do not have significant clinical implications as they are usually not a source of pain, discomfort or any form of pulpitis. However, when the tooth concerned will undergo endodontic treatment such as root canal treatment, presence of large pulp stones will be clinically significant. Large pulp stones in the pulp chamber might block the access to canal orifices and prevent the exploring dental instruments from passaging down the canal. In these cases, burs or even ultrasonic instrumentation can be used to remove the blocking pulp stones.
Passaging (also known as subculture or splitting cells) involves transferring a small number of cells into a new vessel. Cells can be cultured for a longer time if they are split regularly, as it avoids the senescence associated with prolonged high cell density. Suspension cultures are easily passaged with a small amount of culture containing a few cells diluted in a larger volume of fresh media. For adherent cultures, cells first need to be detached; this is commonly done with a mixture of trypsin- EDTA; however, other enzyme mixes are now available for this purpose.
Gain-of-function (GoF) experiments aim to increase the virulence and/or transmissibility of pathogens, in order to better understand them and inform public health preparedness efforts. This includes targeted genetic modification (to create hybrid viruses), the serial passaging of a virus through a host animal (to generate adaptive mutations), and targeted mutagenesis (to introduce mutations). Lipkin is a listed “supporter” of GoF advocate group, Scientists for Science, which was co-founded by Columbia colleague Vincent Racaniello. The US National Institutes of Health placed a moratorium on GoF research in October 2014, and lifted the moratorium in December 2017, after the implementation of stricter controls.
However useful the neurosphere culture has been for biological studies of developmental processes and the functional assay for testing neuronal characteristics, there are several limitations to the method. First, the neurosphere culture formation is highly sensitive to the procedure, as the creation is contingent on the system used to create the culture. Variation in cell density, different constituents or concentrations of factors in the media and method, method and frequency of passaging, and whether the neurosphere is dissociated before differentiation can lead to differences in both the composition of cell types and properties within each neurosphere. This poses a problem for consolidating and interpreting data, even within the same study.
Although ascospore development is very unique, it is very hard to identify A. aggregata because the spore balls and conidia tend to resemble other species. Recent investigations by James and Skinner (2005) have discovered that PCR of the ITS domain of ribosomal DNA with species specific primer sets allows the detection of fungal DNA (working, even, in asymptomatic individuals). The PCR technique can also be used on hair and honey samples to avoid the difficulty of culturing spores, as spore were shown before to only germinate well in lipids. Storage of the fungus has also proven to be difficult as it collapses after 1–2 months during normal culture passaging.
As is common with tumor cells and other pathogens, the invasive hyphae of A. fumigatus encounters hypoxic (low oxygen levels, ≤ 1%) micro-environments at the site of infection in the host organism. Current research suggests that upon infection, necrosis and inflammation cause tissue damage which decreases available oxygen concentrations due to a local reduction in perfusion, the passaging of fluids to organs. In A. fumigatus specifically, secondary metabolites have been found to inhibit the development of new blood vessels leading to tissue damage, the inhibition of tissue repair, and ultimately localized hypoxic micro- environments. The exact implications of hypoxia on fungal pathogenesis is currently unknown, however these low oxygen environments have long been associated with negative clinical outcomes.

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