Sassen A, Vander Plaetse F
Med Microbiol Immunol. 1980;168(2):129-37. doi: 10.1007/BF02121761.
Smears of cell suspensions from murine lymphoid organs were prepared on slides, air dried, and processed for detection of immunoglobulin (Ig) and theta (Thy-1) antigens by the unlabeled antibody peroxidase-antiperoxidase (PAP) technique. Satisfactory results were obtained for both antigens on recently made smears. However, slides kept at room temperature showed a progressive decrease in staining of the two antigens with time. Various fixatives and preservation procedures were tested to prevent this alteration. Good conservation of smears was obtained when slides were kept at -18 degrees C and/or air isolated before or after fixation with alcohols. A similar degradation of Ig and/or Thy-1 antigens occurred also in histological tissue sections or in serum spots dried on slides. The major cause for this degradation is thought to be contact with air, residual enzymatic hydrolysis playing a less important role.
将来自小鼠淋巴器官的细胞悬液涂片制备在载玻片上,空气干燥,然后通过未标记抗体过氧化物酶-抗过氧化物酶(PAP)技术处理以检测免疫球蛋白(Ig)和θ(Thy-1)抗原。在最近制备的涂片上,两种抗原均获得了满意的结果。然而,保存在室温下的载玻片显示,随着时间的推移,两种抗原的染色逐渐减少。测试了各种固定剂和保存程序以防止这种改变。当载玻片在-18℃保存和/或在用酒精固定之前或之后进行空气隔离时,涂片得到了良好的保存。在组织学组织切片或载玻片上干燥的血清斑点中也发生了类似的Ig和/或Thy-1抗原降解。这种降解的主要原因被认为是与空气接触,残留的酶促水解起的作用较小。