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Nasal swabs that were processed for confirmatory influenza testing by polymerase chain reaction testing were confirmed by panel (xTAG) or specific influenza A and B PCR (Luminex Molecular Diagnostics, Toronto, CA).[16] Positive tests were confirmed as being caused by H1N1 using the Prodesse ProFlu-ST, Influenza A [2009] real-time PCR (H1N1 subtyping) assay (Focus Diagnostics, Cypress, CA).
However, it has been shown that AQP5 showed more robust oncogenic potential than AQP1 as well as AQP3 in soft agar assay, focus formation assay, and cell proliferation (MTT) assay [13] [15], leading us to choose AQP5 for its role in lung carcinogenesis not only for clinical validation study but also for studies in its underlying molecular mechanisms.
Chlamydia IgG and IgM antibodies were measured by using a microimmunofluorescent antibody assay (Focus Technologies, Cypress, CA).
For herpes simplex virus 2, we used the Focus HerpeSelect HSV-2 ELISA IgG assay (Focus Technologies, Cypress, California, USA) to detect serum antibodies.
Anti-dsDNA antibodies and ANAs were measured by Farr assay (Specialty Laboratories, Santa Monica, CA, USA) and indirect fluorescent antibody assay (FOCUS Diagnostics, Herndon, VA, USA), respectively.
The SCL-90 is a reliable and valid instrument [ 40]. (3) C. burnetii serology (immunofluorescence assay; Focus Diagnostics, Inc., Cypress, CA, USA) and serum PCR.
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In the first approach, we used a CD4-TLR assay focusing on an NFκB-driven luciferase reporter.
Consequently, this form of the dual reporter assay focuses on the assessment of BTR not influenced by specific cis-elements.
So far, only several studies about Xpert MTB/RIF assay focused on the application of Xpert MTB/RIF in children.
Another explanation relates to the NMR assay, which, in contrast to a radioactive incorporation assay, focuses exclusively on the detection of the predominant product.
The first assay focused on the capacity of the WS types to invade, from rare, a numerically dominant population of ancestral SM types marked with GFP.
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