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Furthermore, immunostaining and Western blot analyses show that expression of α-SMA, a marker for HSC activation, was higher in livers from TIMP-1-/ mice compared with wild-type animals.
For each genotype, Western blot analyses show that these tissues contain similar levels of SMN when normalized per cell number (Figure 2A).
Also, their western blot analyses show that neither A-RIFIN antisera are cross-reactive.
Western blot analyses show that pretreatment with z-LEHD-fmk significantly abrogates the effect of etoposide on wtCD26 Jurkat transfectants.
Subsequently, confocal and western blot analyses show that nNOS/Nox4 translocates to the nucleus, suggesting that nNOS/Nox4 may directly regulate nuclear signaling.
Western blot analyses show that transfection with mimic miR-542-3p miR-542-3p miR-542-3ps of BMP-7 and inhibited the phosphoreducedn of Akt and survivin.
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Microarray and northern blot analyses showed that beyond miR-122, miRNA levels were globally decreased.
Western and dot blot analyses showed that Rhigh as well as Rlow are able to adsorb horse fibronectin and plasminogen present in the growth medium.
Western blot analyses showed that HqL07 and HqL09 had immunogenicity.
Immunoblotting and dot blot analyses showed that XIE62-1004 and XIE2008 reduced the levels of GFP-HDQ103 aggregates in the insoluble fraction (Fig. 6a, c).
Attenuated systemic symptoms were observed after particle bombardment on B. perviridis and Western blot analyses showed that both foreign proteins were produced.
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