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In this study, by using of near-field scanning optical microscopy (NSOM /immune-labeling quaNSOM /immune-labelingual-color imaging system, we achieved the direct visualization of nanoscale profiles for distribution and organization of CD4 and CD25 molecules in T cells.
In the current study, by using our homemade NSOM/QD-based dual-color imaging system, we achieved the direct visualization of the nanoscale profiles for distribution and organization of CD4 and CD25 in CD4+CD25high regulatory T cells or CD4+CD25low T cells.
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With this new inorganic artificial photosynthetic system, we achieve effective light utilization, fast photo-induced charge separation, high electron transfer, enhanced photocatalytic activity for dye degradation rate and improved H2 evolution efficiency.
With the automated method running on three parallel systems, we achieved an average throughput of approximately 1,200 samples per month (including maintenance of the system, and reanalysis of failed samples).
Utilizing this system, we have achieved 50 and 63% reductions, respectively, of the normal and CUG expanded repeat-containing transcripts.
Using a tetracycline-dependent gene regulation system [ 35] we achieved a tightly-controlled ccpA expression, leading to a wide range of CcpA amounts in the cells.
Using this pumping system, we can achieve chamber pressures as low as 10 -6 torr.
It can be seen that at BER = 10−4, for both the linear MMSE-based optimal relay system and the nonlinear MMSE DFE-based optiMMSE DFE-basedem, we can achieve approptimally 5-dB gain by increlayng from K=2 to K=5.
Importantly, by using this novel NSOM/QD-based dual-color imaging system, we can achieve the direct visualization of the nanoscale nanospatial relationship between cell-surface molecules, and this will provide more useful information for the research of distribution-function relationship of cell-surface molecules.
Using adenoviral vectors, the CRE/loxP system and hypomorphic mice, we achieved chronic expression of two levels of TNF-α in the SN of adult mice.
By using two complementary enrichment protocols (hydrazide chemistry and lectin resin) and two orbitrap-based and triple TOF-based double high LC-MS/MS systems, we have achieved an in-depth identification of 25 N-glycoproteins that mapped on to 53 sites on RJ proteins.
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