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Effects of prolonged water washing of tissue samples fixed in formalin on histological staining

机译:长时间水洗固定在福尔马林中的组织样品对组织学染色的影响

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摘要

The effects of prolonged water washing after fixation for 48 h in 10% (v/v) phosphate-buffered neutral formalin on the quality of representative histological staining methods were evaluated using samples of liver, kidney, spleen and thymus collected from three male Crl:CD(SD)(IGS) rats and one male beagle dog. Because door-to-door courier services in Japan prohibit handling formalin, our goal was to confirm that formalin fixed wet tissue samples could be stored in tap water rather than formalin during transportation of the samples without decreasing the quality of their staining or immunohistochemistry. Each tissue sample was allocated randomly to one of three groups: 12 min, 3 days and 7 days of washing in running tap water; samples then were routinely embedded in paraffin and sectioned. The sections were stained with hematoxylin and eosin, perio-dic acid-Schiff, azan, and the TdT-mediated dUTP-biotin nick end labeling (TUNEL) method. Immunohistochemical staining for Factor VIII, ED-1 and CD3 also was assessed. Prolonged water washing for up to 7 days did not affect the morphology or stainability by standard histological methods, or the intensity and frequency of positive reactions using the TUNEL method. Only immunohistochemical staining of Factor VIII was altered in both the rat and dog sections after 7 days of water washing. The intensity of positive reactions of Factor VIII immunohistochemistry after 7 days water washing was still strong enough to detect microscopically. Therefore, prolonged water washing for up to 7 days after formalin fixation does not have seriously detrimental effects on the quality and characteristics of paraffin sections stained by various methods, including immunohistochemistry.
机译:使用从三个雄性Crl采集的肝脏,肾脏,脾脏和胸腺样品评估了在10%(v / v)磷酸盐缓冲的中性福尔马林溶液中固定48小时后长时间水洗对代表性组织学染色方法质量的影响: CD(SD)(IGS)大鼠和一只雄性比格犬。由于日本的门到门快递服务禁止处理福尔马林,因此我们的目标是确认福尔马林固定的湿组织样品可以在样品运输过程中而不是福尔马林中保存在自来水中,而不会降低其染色或免疫组织化学的质量。将每个组织样本随机分配至以下三组之一:在自来水中清洗12分钟,3天和7天;然后在3分钟内清洗。然后将样品常规地包埋在石蜡中并切片。切片用苏木精和曙红,碘酸-席夫(Schiff),阿赞(Azan)和TdT介导的dUTP-生物素缺口末端标记(TUNEL)方法染色。还评估了因子VIII,ED-1和CD3的免疫组织化学染色。延长的水洗时间长达7天不会影响标准组织学方法的形态或可染色性,也不会影响使用TUNEL方法的阳性反应的强度和频率。水洗7天后,在大鼠和狗切片中仅改变了因子VIII的免疫组织化学染色。水洗7天后,因子VIII免疫组化的阳性反应强度仍然足够强,可以在显微镜下检测到。因此,福尔马林固定后长时间水洗长达7天不会对用各种方法(包括免疫组织化学)染色的石蜡切片的质量和特性产生严重的不利影响。

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