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We next evaluated expression and secretion of the T3sVHHs by Western blot (WB).
Since there can be a considerable degree of cell-specificity in the transcriptional response to glucocorticoids, we harvested multiple organs and evaluated expression and regulation of the mRNAs using multiple tissue in situ hybridisation.
As Cav1 is related to lipid metabolism in macrophages, and the SREBP is known to be a major regulator of Cav1 expression, we evaluated expression and activity of SREBP in the AM with CFTR knockdown.
Here, we evaluated expression and function of ASB9 in detail.
We first evaluated expression and localization of the human CEP290 N- and C-terminal constructs in zebrafish.
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Here, we aimed to evaluate expression and function of human Asb-9 (ASB9).
Subsequently, we used the same antibody to evaluate expression and cellular distribution of Sema4A in five MS patient plaques and four control specimens containing normal human white matter.
Immunoblotting analyses were conducted to evaluate expression and activation of ADAM17 as well as the level of ERK1/2 phosphorylation after UDCA treatment.
Due to the limited occurrence of import in Bienertia with biolistics, to further evaluate expression and targeting using these constructs, protoplast transformation was used.
To evaluate expression and cellular localization of MUC5B protein in lung adenocarcinoma tissues, we performed IHC using mouse anti-MUC5B monoclonal antibody (clone19.4E), which reacts with MUC5B and does not react with MUC5A or MUC5C.
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CEO of Professional Science Editing for Scientists @ prosciediting.com