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Following extraction, sample quality was confirmed using a Bioanalyzer 2100 (Agilent Technologies, CA, US).
Leaks are confirmed using a dye test and then patched.
These results were also confirmed using a co-sibling design.
This activity was then confirmed using a panel of myelomas with various MCL1 dependencies.
This was also confirmed using a probe for Slug, another neural crest-specific marker (Supplementary Fig. 2f).
Robustness was confirmed using a three level resolution IV fractional factorial design.
The developed solutions have to be confirmed using a DT burning plasma in ITER.
The analysis methodology is confirmed using a detailed ANSYS nonlinear finite element model.
However, the results obtained should be confirmed using a larger sample.
Bone union was also confirmed using a follow-up CT scan (10 months postoperatively).
Genomic insertion was confirmed using a polymerase chain reaction-based method and Southern blots.
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