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用酶清除阿尔辛蓝染色的小型脊椎动物整体标本以显示软骨。

Enzyme clearing of alcian blue stained whole small vertebrates for demonstration of cartilage.

作者信息

Dingerkus G, Uhler L D

出版信息

Stain Technol. 1977 Jul;52(4):229-32. doi: 10.3109/10520297709116780.

Abstract

Preparation of small vertebrates cleared after alcian blue staining of cartilage is facilitated by trypsin digestion. Specimens are fixed in formation, washed, skinned, and eviscerated. After staining in a solution of alcian blue in acetic acid-alcohol for 24-48 hours, they are transferred to water through graded alcohols. Excess alcian blue is removed over a period of up to three weeks by changes every 2-3 days of 1% trypsin in approximately one-third-saturated sodium borate. Bony tissues may be stained after this in a solution of alizarin red S in 0.5% KOH. Specimens are bleached if necessary and dehydrated through graded KOH-glycerine mixtures for storage in glycerine. Since alcohol treatment in addition to formalin fixation does not affect results with this method, it should be useful to researchers who want to study the cartilage or cartilaginous skeletons in museum specimens, which are routinely fixed in formalin and stored in alcohol.

摘要

通过胰蛋白酶消化有助于制备经阿尔辛蓝染色软骨后透明的小型脊椎动物。标本固定成型、冲洗、去皮并取出内脏。在乙酸 - 酒精的阿尔辛蓝溶液中染色24 - 48小时后,通过梯度酒精转移至水中。通过每2 - 3天更换一次约三分之一饱和硼酸钠中的1%胰蛋白酶,在长达三周的时间内去除多余的阿尔辛蓝。此后,骨组织可在0.5%氢氧化钾的茜素红S溶液中染色。如有必要,标本进行漂白处理,并通过梯度氢氧化钾 - 甘油混合物脱水,以便保存在甘油中。由于除甲醛固定外的酒精处理不影响该方法的结果,对于想要研究博物馆标本中软骨或软骨骨骼的研究人员来说应该是有用的,这些标本通常用甲醛固定并保存在酒精中。

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