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Images of CFP and YFP emission were acquired at a rate of 0.5 Hz, with exposure times ranging from 100 ms to 1 sec, determined by the baseline expression of indicators.
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Lower relative expression of key innate immune genes, including the Toll-like receptor 2 (TLR2) and TLR4 genes, lack of differential expression of indicator adaptive immune gene transcripts (IFNG, IL2, IL4), and lower BOLA major histocompatibility complex – class I (BOLA) and class II (BOLA-DRA) gene expression was consistent with innate immune gene repression in the BTB-infected animals.
Here we report on the design, synthesis, and characterization of a protein transduction domain mimic capable of efficiently delivering an antibody against phosphorylated PKCθ (Thr538) into human peripheral mononuclear blood cells and altering expression of downstream indicators of T cell activation and differentiation.
For most reporters in this work, the internalization of the Cre was monitored by genomic excision of a "floxed" cassette, allowing the expression of various indicator genes.
This process was retarded after stimulation in SM0, complying well with the delayed induction of the expression of our indicator genes in SM0.
The basal expression of the indicator gene in these cells stabilizes at approximately 50% of the initial level by 48 h and is not eliminated by long-term estrogen deprivation, but is abruptly blocked by the addition of ICI 182780.
Reduced expression of key indicator genes, with well established roles in the bovine immune response to BTB, associated with BTB-infection was particularly suggestive of innate immune gene repression in vivo.
The ranking of the expression levels of Indicator genes between samples was presented as the mean rank statistical difference.
Poly(A) PCR was used to globally amplify the RNA followed by measurement of the expression levels of Indicator genes by real-time PCR.
We argue that environmental quality assessment using gene expression profiles of indicator organisms exposed to test substrates is more sensitive, more toxicant specific and significantly faster than current risk assessment methods.
It was confirmed that sole treatment of VPA of 200 mk/ kg body weight) had no effect on the expression of the six indicators.
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