. Essentials of laboratory diagnosis; designed for students and practitioners. - red. EhrlicTrs Triacid Staining Method (for formula and prepa-ration see Appendix).—The smear is taken in the -glassforceps .and a few drops of the prepared stain placed upon itand allowed to remain for about five minutes. There is litdanger of overstaining. I - ::imen is next washed in dis-tilled water and thoroughly dried prior to mounting. If. Normal and Pathological Blood-cells. i, Normal red cell, or erythrocyte ; diameter, m. 2, Nucleatedred cell, or normoblast; diameter, m. 3, Megaloblast; diameter,


. Essentials of laboratory diagnosis; designed for students and practitioners. - red. EhrlicTrs Triacid Staining Method (for formula and prepa-ration see Appendix).—The smear is taken in the -glassforceps .and a few drops of the prepared stain placed upon itand allowed to remain for about five minutes. There is litdanger of overstaining. I - ::imen is next washed in dis-tilled water and thoroughly dried prior to mounting. If. Normal and Pathological Blood-cells. i, Normal red cell, or erythrocyte ; diameter, m. 2, Nucleatedred cell, or normoblast; diameter, m. 3, Megaloblast; diameter, 8to 12 m ; seen in pernicious anemia. 4, Small lymphocyte; diameter, 6to 8 m; average in normal blood, 20 to 26%. 5, Large lymphocyte;diameter, 8 to 13 /*; average in normal blood, 5 to 9 %. 6, Polymor-phonuclear leukocyte: diameter. 10 to 11 n; average in normal blood,65 to 70%. 7, Eosinophile; diameter. 19 to 12 m ; average in normalblood, Yi to 2%. 8, Large mononuclear leukocyte ; diameter, 12 to 18M ; average in normal blood, 1 to 2%. 9, Transitional; diameter, 12to 17 n : average in normal blood, 2 to 3%. 10, Neutrophilic myelocyte;diameter, 12 to 20 a*; seen in myelogenous leukemia. //, Eosinophilicmyelocyte; diameter, 10 to 16 a* ; seen in myelogenous leukemia. MICROSCOPIC EXAMINATION. 69 mounted in Canada balsam it is imperative that this shouldnot contain any chloroform; otherwise the colors will graduallybe


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