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三种脱钙液对骨组织免疫组化染色的影响 被引量:6

The effect of bone tissue by immunohistochemical staining under three decalcifying solutions
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摘要 目的探讨三种脱钙液对骨组织免疫组化染色的影响。方法选择12例骨组织,随机分为3组。A组用14%硝酸脱钙液进行处理,B、C组分别用EDTA脱钙液、PLANK脱钙液进行处理,同时对CD3、CD68、Ki-67和TTF-1染色。结果室温条件下,硝酸脱钙液的脱钙时间最短,但对组织损伤最大。PLANK脱钙液和EDTA脱钙液脱钙效果较好,组织结构完整,形态清晰,免疫组化染色较好。结论室温条件下,三种脱钙液中PLANK脱钙液和EDTA脱钙液对骨组织脱钙及免疫组化染色效果较好。但由于EDTA脱钙液脱钙时间过长,PLANK脱钙液脱钙均匀,速度快,更适合用于临床病理检查。硝酸脱钙液脱钙最快,但是免疫组化染色效果较差。 Objective To explore effect of three different decalcifying solutions on the bone tissue immunohistoehemical staining. Methods Twelve cases of bone samples were randomly divided into three groups. The bones had been decalcified with three kinds of decalcifying solutions(including 14% nitric acid, EDTA and PLANK decalcifcation fluid). The immuno histochemieal staining included CD3,CD68,Ki-67 and TI'F-1. Results In room temperature, 14% nitric acid could decal cify strongly and rapidly. But it has the maximum damage level of bone tissues. PLANK and EDTA could not destroy bone tissues and the effect of immunohistochemieal staining was good. Conclusion The effect of decalcification and immunohis tochemical staining of PLANK and EDTA decalcify fluid is nice, but EDTA fluid decalcify cycle is excessively long. PLANK decalcify fluid is even, the decalcify speed is quick, suits for clinical pathological examination. The decalcify effect of nitric acid group is so fast but immunohistochemical staining effect is not too good.
出处 《中国现代医生》 2012年第24期101-103,共3页 China Modern Doctor
关键词 脱钙液 骨组织 免疫组化染色 Decalcification solutions Bone tissue Immunohistochemieal staining
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  • 1许燕云,姜汉国,吴艳霞.不同抗原修复方法对cyclin B1在肿瘤中表达的比较[J].诊断病理学杂志,2004,11(3):201-201. 被引量:4
  • 2关凯,张立仁,郑永军,吴霞,皋岚湘.改良非脱钙骨塑料包埋、切片、染色方法[J].诊断病理学杂志,2004,11(4):280-280. 被引量:8
  • 3赵刚,杨海贤,白景文,曾嘉,沈伟,郭小红.不脱钙骨组织标本超薄切片的制作方法[J].临床与实验病理学杂志,2005,21(3):360-361. 被引量:18
  • 4杨传红,赖晃文,唐赓云,姜秀英.微波快速脱钙及其脱钙液的选择[J].临床与实验病理学杂志,1996,12(4):357-358. 被引量:18
  • 5王珏,朱礼国,张健.影响骨组织切片质量的原因分析[J].江西医学检验,2007,25(2):175-175. 被引量:9
  • 6Yamamoto-Fukud T, Shibata Y, Hishikawa Y, et al. Effects of var-ious decalcification protocolson detection of DNAstrand breaksbyterminal dUTP nick end labeling[J]. Histochem J, 2000,32(11):697-702,.
  • 7Weisberg E C, Hilburn M, Johnson B, et al. Intraoperative Microwave processing of bone margins during resection of head and neck cancer[J]. Arch Otolaryngol Head Neck Surg, 2001,127(7):790-3.
  • 8Cunningham C D, Schulte B A, Bianchi L M, et al. Microwave decacification of human temporal bones[J]. Laryngoscope, 2001,111(2):278-82.
  • 9Walsh L, Freemont A J, Hoylland J A. The effect of tissue decalcifcation on mRNAretentionwithin bone for in-situ hybridization studies[J]. Int J Exp Pathol, 1993,74(3):237-41.
  • 10Shibata Y, Fujita S, Takahashi H, et al. Assessment of decalcifying protocols for detection of specific RNA by non-radioactive in situ hybridization in calcified tissues[J]. Histochem Cell Biol, 2000,113(3):153-9.

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