The expression of Ksp-cadherin mRNA and the absence of the intact protein were also observed in RCC tissue, whereas in normal kidney tissue the mRNA was present and a strong specific signal at 130 kDa could be detected by immunoblotting, indicating that the used anti-human Ksp-cadherin antibody is successfully applicable for this method.
However, the applicable conditions of this method remain disputable and unclear.
The mechanism and applicable conditions for this method have been studied.
Thus, the simplicity and versatility of this method applicable to any type of cell may increase the application of gene targeting.
Online monitoring of an on-state collector emitter voltage (υce,on) and a junction temperature is necessary to ensure the design performance within a safe limit and also to make this method applicable for derating/uprating power.
Compared to existing protocols based on cryosections [13], [35], working on embedded cell monolayers and sectioning them at room temperature make this method applicable on a routine basis.
To make this method applicable for the analyses of biological fluids of PhIP-exposed human subjects, it is now being improved by using immunoaffinity chromatography.
Furthermore, the broad phylogenetic utility of the probe set employed here makes this method applicable for plastome-based evolutionary studies across not only eudicots, but also monocots and potentially all angiosperms.
This method is applicable to various applications including speech enhancement, source separation, direction of arrival (DOA) estimation, and dereverberation by beamformers and has high versatility.
This method is applicable for clinical applications aiming at the validation of the impact of highly physiologically and pathophysiologically active angiotensin II.
