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One week after arrival, rats were inoculated subcutaneously with 107 cells48 cells in 0.5 ml HBSS.
On the second day after burn, four groups of rats were inoculated with P. aeruginosa and one group was left as negative control.
Male Lewis rats were inoculated intradermally with Mycobacterium butyricum into the hind paw and the arthritic responses were evaluated by measuring the changes in paw volume.
Female athymic rats were inoculated with HeLa or Ace-1 cancer cells lines producing osteolytic or mixed (osteolytic & osteoblastic) metastases respectively (N=17 per group).
When cotton rats were inoculated with the vaccine, high-titer RSV-binding and neutralizing antibodies as well as interferon-γ-producing T-cells were induced.
Thirty immunocompetent rats were inoculated with syngeneic rat colon carcinoma cells and 13 14 days later 21 of these rats were treated with 400 MBq/kg of 177Lu-DOTA-BR96 monoclonal antibodies.
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Bacteria were not detectable in the 10 male Sprague-Dawley rathathat were inoculated with 1 × 10 CFU, while all 10 rats inoculated with 1 × 10 and greater had bacteria detectable on both hardware and bone samples (Fig. 2).
Female Lewis rats (n=72) were inoculated with an emulsion of spinal cord and complete Freund's adjuvant.
However, in our previous twin tumour study, the same effect was obtained in rats that were inoculated with a pure tumour cell suspension at two different sites in the liver (Tranberg et al, 2002), a model that carries a reduced risk of transplantation antigen involvement.
Four rats per group were inoculated with SCC-158 tumor cells (2 × 10) in the area of the skin incision, and the immuno-flap was overlaid on the inoculation site at the same time.
Three sets of male Lewis rats (Harlan Laboratories, the Netherlands) were inoculated on Day 0. First, a set of 30 animals was injected with guinea pig myelin basic protein (MBP), complete Freund adjuvant H37 RA (CFA, Difco Laboratories, Detroit, MI, USA) and Mycobacterium tuberculosis type H37RA (Difco).
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