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In patient samples from the field of CRC the run length increased from 228 nm to 305 nm, and in rat samples of early CRC the run length increased from 141 to 173 nm.
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Wild-type samples yielded an amplicon of 131 bp, Tp53 Δ11/+ rat samples yielded amplicons of 131 bp and 120 bp, and Tp53 Δ11/Δ11 rat samples yielded an amplicon of 120 bp.
The average sizes of nuclei of patient samples were 60% larger than that of rat samples, which explains the difference in the run length values between two models.
Figure 2 shows the Differential Reference and the terahertz reflection measurements from the normal and burned skin of one of the rat samples.
This list was derived from 5,361 IPI-identified Rat proteins observed in the LC-MS/MS experiment of all Rat samples.
Fresh pieces of whole rat and human skin were cleared of subcutaneous fat and connective tissue, and hair in the case of the rat samples, and mounted onto glass slides in PBS buffer.
In addition, in order to determine the amount of fat in rat AT, samples of inguinal, epididymal, mesenteric, omental and retroperitoneal AT from 3 male Long Evans rats were resected, combined and subjected to chemical analysis in the same run as the female samples.
To learn more about the skin-specific functions of GS we have investigated in detail the distribution of GS in different cell types and structures in human and rat skin samples of different age.
A significant learning impairment was documented in rats administered samples of P. piscicida that were recently frozen.
The principle of the rat LH assay is based on competition between the LH of the rat sample and a I-labeled rat LH tracer for binding to a highly specific rabbit polyclonal antibody.
Data is presented as mean values±SEM (n = number of rats, samples, or experiments).
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