Linde A, Persliden B, Rönnbäck L
Acta Odontol Scand. 1978;36(3):117-26. doi: 10.3109/00016357809004660.
Rat liver cathepsin D (EC 3.4.23.5) was purified using precipitation technique, ion exchange chromatography, molecular sieve chromatography and isoelectric focusing. Rabbit anti-rat cathepsin D IgG was prepared and rat incisor teeth were cross-sectioned in a cryostat. These sections were incubated with FITC-conjugated anti-rat cathepsin D IgG. Marked fluorescence, indicating the localization of cathepsin D, could be seen over the odontoblast and predentin area. No specific fluorescence could be dmonstrated in the pulp connective tissue proper nor in the dentin.
使用沉淀技术、离子交换色谱法、分子筛色谱法和等电聚焦法对大鼠肝脏组织蛋白酶D(EC 3.4.23.5)进行了纯化。制备了兔抗大鼠组织蛋白酶D IgG,并在低温恒温器中对大鼠切牙进行了横断面切片。将这些切片与异硫氰酸荧光素(FITC)偶联的抗大鼠组织蛋白酶D IgG一起孵育。在成牙本质细胞和前期牙本质区域可见明显的荧光,表明组织蛋白酶D的定位。在牙髓结缔组织本身和牙本质中未显示出特异性荧光。