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Keyboard macro software that helps you create your own custom shortcuts. Make your mouse work for you.
Keyboard Macro Editor Description:
A program to create your own keyboard macros.
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Free for home and educational use. Paid versions are available.
Keyboard Macro Editor License:
Free to non-commercial and free to commercial use.
Keyboard Macro Professional License Description:
Professional version with support for faster undo and undo file groups.
This version also includes an improved user interface.
Keyboard Macro Professional License:
You can use it for free non-commercial use.
Source: parallel use of CFU-C and CFU-S assays with EIA and EMA to measure granulopoiesis in mice and humans.
The colony-forming unit-granulocyte-macrophage (CFU-GM) assay and colony-forming unit-spleen (CFU-S) assay are the classic methods used to measure granulopoiesis in mice and humans. The limitations of these assays include a lack of standardized experimental conditions and the use of a variety of clonogenic assays which are inherently more time-consuming than agar plating and results in a poor reproducibility. Recently, cell-surface phenotyping using flow cytometry has been applied to determine the relative contributions of specific hematopoietic lineages in the murine bone marrow. As a part of this effort, a three-color flow cytometric assay was developed to simultaneously detect and quantitate the progenitor cell populations (erythroid, granulocyte/macrophage, and multipotent [CFU-GEMM]) in murine bone marrow in real time and in a more standardized fashion than that which is possible using colony assay methods. The results of the simultaneous detection and quantitation of these hematopoietic lineages were used to calculate absolute numbers of the progenitor cell populations present in the mouse bone marrow. In order to determine the applicability of this new approach to quantitate murine granulopoiesis in the EIA and EMA models, the CFU-GM and CFU-S assays were simultaneously performed using similar marrow from both models. The results showed a substantial correlation between the CFU-GM and CFU-S assays d82f892c90

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