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To identify new regulatory genes released from the dental epithelium, gene expression profiling of dental epithelium was analysed.
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Glucagon-like peptide-1 (GLP-1) is a peptide product of the proglucagon gene, released from the L cells of the small intestine in response to food ingestion (Drucker, 2006).
Since sexual-stage genes are released from purifying selection in asexual culture (experienced by several of the isolates under study) [ 43] genes with no evidence of asexual expression in transcriptomic surveys [ 44, 45] were also excluded.
Previous studies have indicated that bacteria bearing a combination of antimicrobial and heavy-metal resistance genes are released from poorly treated wastewater treatment plants (27, 28).
Antibiotic resistance genes (ARGs) released from dead microorganisms can persist in the environment for an extended period of time (Pote et al. 2003) and spread among bacteria through vertical transfer (generation) or horizontal transfer (conjugation, transduction, transformation, and transposition).
When Ds moves, the aleurone-color gene is released from the suppressing effect of the Ds and transformed into the active form, which initiates the pigment synthesis in cells.
The construct was purified by the CsCl2 gradient method, and the mutated rod opsin gene was released from its vector by BamHI digestion.
b) Construction of pTP248 To create a His/GST double tagged destination vector, a SalI NheI fragment containing the GST gene was released from pDEST24 by restriction enzyme digestion, and then inserted into pDEST17 between the SalI and NheI sites.
L1 gene was released from pBSK after double-digestion with XhoI and NotI and employed for creating the expression vectors.
Like GLP-1, oxyntomodulin (OXM) is also produced from the proglucagon gene and released from the small intestine in response to a meal.
For probe synthesis, the L. braziliensis α-tubulin gene was released from clone pTOLb α tub-B by BamHI/ PstI cutting, excised from gel, purified using Wizard® SV Gel and PCR Clean-Up System (Promega, Inc., Madison, WI, USA), and finally labeled with digoxigenin by randomly primed synthesis using the DIG High Prime DNA Labeling kit (Roche, Inc., Mannheim, Germany).
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