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- For binding assays, sufficient recombinant homodimeric, chimeric proteins containing a siglec domain and a Fc domain per subunit
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- For determining drug-like ligands to protein targets of known 3D structure
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- For experiments cells were grown in either 100 mm culture dishes, or gelatin-coated glass coverslips and used for experiments
- For factor Xa the NH2-terminal peptide of PCI was found to impact the inhibition charges the two in the absence
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- For further adaptation and tests in vivo plasminogen activators development of PCI complexes
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- For iNOS immunoblots, the key antibody employed was rabbit polyclonal anti-iNOS and secondary antibody was goat anti-rabbit IgG conjugated with biotin
- For illustration the SDHDD129T substitution shown in the direction of Isopyrazam in comparison to the in vitro values can differ notably
- For immunofluorescence examination, cells were set with 4% paraformaldehyde in PBS for 30 min
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- For simple estimation of binding affinities the variety in which the RBA-benefit of a presented compound
- For sonication with the regular, tapped tip, the end of the probe was placed in the water bath
- For statistical analysis of Ki-67 immunostaining and TUNEL results the ANOVA test and Tukey HSD post-test were applied
- For straightforward estimation of binding affinities the variety inside which the RBA-value of a offered compound
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- For the description of genotype effects, a co-dominant genetic model was fitted to each locus and contrasts were evaluated with a Wald test under the most general model
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- For this goal, independent triplicate experiments were performed and RNA isolated. RTPCR confirmed the induction on the Rv Function of the sH/sH/sB network in defending Mtb in the stress generated by THZ In Mtb
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