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首页> 外文期刊>Journal of immunoassay and immunochemistry >Effects of red blood cell lysing solutions on the detection of peripheral basophils of healthy normals and sle patients by flow cytometry
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Effects of red blood cell lysing solutions on the detection of peripheral basophils of healthy normals and sle patients by flow cytometry

机译:流式细胞仪检测红细胞裂解液对健康人和正常人外周血嗜碱性粒细胞检测的影响

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摘要

To evaluate the effect of four widely used red blood cell lysing solutions on counting and measurement of activation marker of peripheral basophils in normals and systemic lupus erythematosus (SLE) patients by flow cytometry. Our results showed that the light scatter properties including FS and SS value of leukocytes in whole blood were preserved when whole blood samples were lysed in RBC Lysis Buffer and FACS Lysing Solution, while were affected when lysed in distilled water or ACK. By counting basophils, RBC Lysis Buffer and FACS Lysing Solution were almost the same level, while were significantly lower when lysed in distilled water or ACK. The expressions of CD203c on peripheral basophils of SLE patients were significantly higher than those of normals. Comparing the data of CD203c expression obtained demonstrated that there were no significant differences among them, while FACS Lysing Solution treatment leads to a slightly lower staining intensity of CD203c. We provide a solid description that the widely used red blood cell lysing reagents may influence the light scatter properties of leukocytes, the accuracy of quantity of absolute number of the existence of basophil subsets and the quantity of staining intensity of cell-activated marker CD203c fluorescence when measured by flow cytometry.
机译:通过流式细胞术评估四种广泛使用的红细胞裂解液对正常人和系统性红斑狼疮(SLE)患者外周嗜碱性粒细胞活化标记的计数和测量的效果。我们的结果表明,当全血样品在RBC裂解缓冲液和FACS裂解液中裂解时,包括全血中白细胞的FS和SS值在内的光散射特性得以保留,而在蒸馏水或ACK中裂解时则受到影响。通过对嗜碱性粒细胞计数,RBC裂解缓冲液和FACS裂解液的水平几乎相同,而在蒸馏水或ACK中裂解则明显降低。 SLE患者外周嗜碱性粒细胞CD203c的表达明显高于正常人。比较获得的CD203c表达数据表明,它们之间没有显着差异,而FACS裂解液处理导致CD203c的染色强度稍低。我们提供了扎实的描述,即广泛使用的红细胞裂解试剂可能会影响白细胞的光散射特性,嗜碱性粒细胞亚群存在的绝对数量的准确度以及细胞活化的标记CD203c荧光的染色强度的数量。通过流式细胞仪测量。

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