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Western blot quantification indicates that treatment with 0.4 µg/mL cyclohexamide reduced the expression of FLAG-tagged Ptc-ICD7 to less than half of that of "No cyclohexamide" control (Figure 1I).
Our western blot quantification indicates that TGFβ treatment in primary epithelial cells weakly induces NF-κB/RelA translocation at levels significantly less than the prototypical TNF monokine (Fig. 7a).
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A densitometry quantification indicated that the ubiquitin signal is increased by ∼ 3-fold following MMS treatment.
Relative quantification indicated that reduced levels of SBEIIa led to increased representation of SBEI proteins.
Northern blot analysis indicates that human VIP1 is expressed in a variety of tissues and is enriched in skeletal muscle, heart, and brain.
Although it is not possible to exclude that the presence of autoantibodies might affect the correct quantification of LGALS3BP by ELISA, the identification of anti-LGALS3BP IgG in western blot indicates that the epitopes recognized by these autoantibodies are different from those recognized by the antibody used in ELISA.
Accordingly, quantification by western blot indicated that EVL/Ena levels were four times higher in wing discs extracts overexpressing Src and p35 under Scalloped-Gal4 (Sd-Gal4) control, compared to discs expressing p35 and GFP (Fig. 4f,g).
The quantification of the blotting data indicated that insulin induced a 2.8-fold increase in the level of NHE1 present in the cell surface of cardiomyocytes.
Western blot results indicated that BMP-6 obviously inhibited c-Fos and c-Jun expression.
Western blot analysis indicated that compound 12g potently inhibited the PAK4/LIMK1/cofilin signalling pathways.
Northern blot analysis indicated that pSTMVGFPRIB synthesized more genomic and sub-genomic RNAs in the protoplasts.
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