We will extend our HTS tests using
different cell assays and extended chemical components libraries.
Not exact matches
Professor Dianna Bowles, a plant biochemist and founding Director of CNAP, led the research with Professor Paul Kaye, the Director of CII, who developed the robust
assay system involving human
cells to assess the impacts of the
different structures.
By establishing an
assay system where free virus infection is restricted and infection can only occur through
cell -
cell transmission, the researchers could then test whether a large selection of Nabs could prevent
cell - to -
cell transmission of
different HIV strains.
Once developed, the
assays will be used to analyse in vitro cytokine and chemokine induction, e.g. to compare
different versions of a vaccine, or the same vaccine produced in
different host
cells, or
different batches of a vaccine to demonstrate batch - to - batch reproducibility.
This will include testing the mechanism of action of
different adjuvant and antigen formulations by measuring B - and T -
cell responses and by using various functional
assays (ELISA, FACS, cytokine profiles), transcriptomics and / or proteomics.
«By getting me involved in the project, not only could we do these biological,
cell - based functional
assays that Roy's lab carries out, but we could also purify the integrins or parts of (them) and do both structural and biophysical characterization of interactions — how the
different subunits stick together,» he said.
I completed my PhD as a
cell biology major in an engineering lab, where I established a new
assay to answer questions very
different from what the main part of the lab was working on.
After 24 h of irradiation, amount of
cell death in
different groups was measured using TUNEL
assay (EMD Millipore, Cat.
This allows for a one - step PCR reaction and pooling of amplicons from several
different samples and targets (generated with other LymphoTrack
Assays for the Illumina ® MiSeq ® instrument, sold separately), onto one MiSeq ® flow
cell allowing for up to 24 samples per target to be analyzed in parallel in a single run.
(B and C) Western blot and immunofluoresence
assay of Jurkat
cells transfected with wild - type (WT), KMT2D mutants (V5486M)(B) and EP300 mutants (H1377R)(C) upon treatment with
different HDAC inhibitors.
The overall score encompass several factors: reproducibility of the antibody staining in
different cell lines (and if signal strength correlates with RNA expression levels);
assays for enhanced antibody validation by using antibodies binding to
different epitopes on the same target protein (independent antibodies), by knockdown / knockout of the target protein (genetic methods) and by matching of the signal with a GFP - tagged protein (recombinant expression); experimental evidence for location described in literature.
Different in vitro
assays were carried out in order to test the specific effects of kahweol treatment on several key steps of the angiogenic process in both endothelial and tumor
cells.
The gelatinolytic
assays were carried out in two
different ways to obtain complementary information: firstly,
cells were treated or not with the test compound and samples from these were submitted to gelatinase zymography to detect the effects of the kahweol treatment on the expression of gelatinase activities; secondly, in some experiments, samples from control, untreated HT - 1080 fibrosarcoma
cells were submitted to zymography and, after electrophoresis,
different concentrations of kahweol were added to the substrate buffer to determine the potential direct effect of kahweol on gelatinase activity.
Data are given as percentage, taking the normalized levels of COX - 2 in control
cells as 100 %, and they are means ± S.D. of three
different assays.
(A) EC50 values from MTT
assay using silver nanoparticles with
different coatings and HepG2
cells; (B) Analogous with Neuro - 2
cells; (C) Detection of oxidative stress from Ag - NPs (concentration 5 pM) via formation of protein carbonyls incubated with HepG2
cells.
This suggests that our automatic screening
assay is specifically measuring the effect amiodarone HCL has on
different populations of
cells.
Prior research had developed a number of new compounds making use of a novel drug discovery paradigm which begins with natural products extracted from plants; it then entails selecting synthetic derivatives which demonstrate efficacy in multiple
assays testing protection against
different factors of the nerve
cell damage and death which take place in brain injuries and in age - associated neurodegenerative conditions.