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A large number of Y. pestis strains with clear background were isolated from different plague foci since the year of 1943.
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NK cells from CD45−/− mice 15 on the B6 background were isolated and cultured using the same method.
To perform the analysis in an isogenic background, RNA and DNA were isolated from SCC, AK and normal (unexposed) epidermis (NS) from each of 13 OTRs.
Step 5. Significant radiotracer uptake regions were isolated from background noise and tissue through segmentation.
Using the threshold colour plugin, FVIII- and αSMA-positive cells were isolated from background staining and the resulting images converted to binary.
The suppressors were isolated from each background separately.
To analyze the expression pattern of the E spl -CD2 carE spl -CD2hin the Dcarefullysoma withinsolathe from the backgrounDCNsing ImageJ.
Viable suppressors were isolated from the prkaca-F327A background (Table 2 and Figure 5).
In this report, we identify suppressor mutations that were isolated from two discrete genetic backgrounds.
Cortical GFP− cells were isolated from Tie2GFP+ mice with gating based on background GFP fluorescence from wild type FvB mice.
To identify shmt2 protein products expressed from alternative shmt2 transcripts, liver and kidney were isolated from SHMT1+/+ mice on a C57Bl/6 background.
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