Words in blue were inserts. Digested from our proofread manuscripts.
To determine whether the constructed plasmid was efficient
works well, we first transfected the plasmid with liposomes into cultured SH-SY5Y cells for 24 hours and analyzed the expression of corresponding proteins by usedwestern blot analysis using an withantibody against EGFP to check the expression of corresponding proteins.
We screened aA pool of
Arabidospislines transformed with the activation vector for short hypocotyl mutants under dim far-red light . Consequently we isolatedthree mutant lines designated chibi1-3 (chi) .
killedat different time point ofreperfusion. Frontal and parietal lobe cortex o n the left hemisphere(6 to 11 mm tothe tip of olfactory bulb) were separated and saved in li guid nitrogen.
whichwere supplemented with further injections as necessary during experiments to sustain a level of acceptable anesthesia. Body temperature was maintained at 36-37C using a heating pad placed underneath the rat. . Each ratsThe head s waswas erefixed horizontally in a stereotaxic instrument (Narishige, Japan). The skull was exposed ,and a small burr hole was made at the appropriate coordinates drilledto enable vertical penetration by the stimulating and recording electrodes. All electrodes were zeroed on theat bregma ,and all coordinates were calculated from this point.
WeThese experiments demonstrated a distinctive localization of OMPFC neurons, which revealed excitatory responses to BLA stimulation, although Prez-Jaranay and Vivesa previous study did not demonstrate this apparent distribution of the excitatory responses (Prez-Jaranay and Vives, 1991).
Here we suggest thata comprehensive molecular genetic study involving a large number of NF2 is encouragedto build up our Chinese gene mutation database not only for the benefit forof theclinical practice, but also for genetic counseling purposes s.
highreasonable to believesuggest that these NATs are critical for the life of humans, mousemice and rats, justbecause they are stillremain in the transcriptome after tens of million years of evolution.
A total of 570 NATs were selected,
tripled ofthree times the number lehnerreported earlierin a previous study (8), andwith most of them are thebeing reported for the first time to be reported.
It was noted that the onset of SWS1 expression in our study was earlier than
thethat onereported previously  where the expression initiated sbetween 55 and 60 hpf andwith about half of the embryos showing expression at 60 hpf but are stillremaining in stage 1. In theirThe aforementioned study differed from ours in that only fish that had achieved certain developmental characteristics at certain time points were examined for opsin expression to minimize the individual variation , while we did not perform any such selection. The time differencediscrepancy between the two studies is most likely to be due to this difference originate from it.
By constructing DB2GO, the entries in the BioDW member databases
of BioDWare linked organically to the terms of Gene Ontology Database. organically. In the DB2GO table,I it is quite easy to find entries in the DB2GO table from different databases as they whichall are allannotated by the same GO term, from different databases.
[Author: You should mention the 3 treatment groups here since this is really part of the study design (like you did in the \’Methods\’ section but in less detail).]