Method: Immunohistochemical analysis was performed on 45 human SCC samples.
方法：用免疫组化方法分析45例鳞癌标本。
Immunohistochemical analysis of frozen mouse heart tissue, using Connexin 43 Antibody.
使用Connexin43抗体对冷冻的小鼠心脏组织进行免疫组化分析。
Immunohistochemical analysis of paraffin-embedded human renal cell carcinoma, using 53bp1 Antibody.
免疫组织化学方法检测石蜡包埋的人肾细胞癌组织，使用的抗体为53bp1。
Immunohistochemical analysis of paraffin-embedded human breast carcinoma using Connexin 43 Antibody.
使用Connexin43抗体对石蜡包埋的人乳腺癌组织进行免疫组化分析。
Although immunohistochemical analysis was negative for complement components and immune complexes, it was positive for fibrin.
虽然对补体成分和免疫复合物的免疫组化分析是阴性的，纤维蛋白原是阳性的。
Immunohistochemical analysis of paraffin-embedded human breast carcinoma, showing nuclear localization, using 53bp1 Antibody.
免疫组织化学方法检测石蜡包埋的人乳腺癌组织，图示为核定位。使用的抗体为53bp1。
Methods: NT-3 was examined by immunohistochemical analysis in 32 cases of salivary ACC, 7 normal parotid glands and 3 acinic cell carcinoma tissue samples.
方法：以3 2例ACC、7例正常腮腺及3例腺泡细胞癌标本为研究对象，采用免疫组化法对NT -3进行检测。
Conclusion The polyclonal antibody against ARIP1 has been successfully prepared and can be used to do immunohistochemical analysis for ARIP1 protein expression.
结论：成功地制备了抗arip1多克隆抗体，该抗体可用于ARIP1成熟蛋白表达的免疫组织化学染色分析。
Immunohistochemical analysis of paraffin-embedded human lung carcinoma, using FAK Antibody in thre presence of control peptide (left) or antigen-specific peptide (right).
在对照肽(左)或抗原特异性多肽(右)存在的条件下使用FAk抗体对石蜡包埋的人肺癌组织进行免疫组化分析。
Immunohistochemical analysis of paraffin-embedded human breast carcinoma using c-Rel Antibody in the presence of control peptide (left) or antigen-specific peptide (right).
免疫组织化学染色分析石蜡包埋人乳腺癌组织。在对照多肽(左图)或抗原特异性封闭多肽(右图)的存在下所用抗体为c - RelAntibody。
Immunohistochemical analysis of paraffin-embedded human colon carcinoma, using 53bp1 Antibody in the presence of control peptide (left) or antigen-specific peptide (right).
免疫组织化学方法检测石蜡包埋的人结肠癌组织，使用的抗体为53bp1。左图是对照组，右图是抗原特异性肽段组。
Immunohistochemical analysis of paraffin-embedded human colon carcinoma using Wee1 (D10D2) Rabbit mAb in the presence of control peptide (left) or antigen-specific peptide (right).
在对照肽段(左)和抗原特异性肽段(右)存在的前提下，使用Wee1 (D10D2)RabbitmAb对石蜡包埋的人结肠癌组织进行免疫组化分析。
Immunohistochemical analysis of paraffin-embedded human breast carcinoma using Jak1 (6G4) Rabbit mAb #3344, in the presence of control peptide (left) or Jak1 Blocking Peptide (right).
免疫组织化学染色分析石蜡包埋人乳腺癌组织。在对照多肽（左图）或Jak1 封闭多肽（右图）存在下所用抗体为 Jak1 （6G4）Rabbit mAb#3344。
Immunohistochemical analysis of paraffin-embedded human breast carcinoma, using Phospho-YAP (Ser127) Antibody in the presence of control peptide (left) or antigen specific peptide (right).
在对照多肽(左)和抗原特异性多肽(右)存在的条件下使用Phospho -YAP (Ser127)对石蜡包埋的人乳腺癌进行免疫组化分析。
We report a case of leukemoid reaction resulting from granulocyte colony-stimulating factor producing urothelial carcinoma of the renal pelvis as evidenced on immunohistochemical analysis.
我们报告一个类白血病反应粒细胞集落刺激因子生产肾盂尿路上皮癌的，证明免疫组化分析。
Immunohistochemical method and zymogram analysis method, etc. were adopted to observe the change of microvessel structure, gelatinase and its inhibitor expression.
采用免疫组化和酶谱分析等方法，观察各组微血管结构、明胶酶及其抑制物的变化。
Methods Immunohistochemical staining combined with the micro-image analysis and immunofluorescence histochemical double-staining technique were used.
方法免疫组织化学染色结合显微图像定量分析和免疫荧光双重染色。
Immunohistochemical techniques and computer-imaging analysis were used to localize and observe the expression of AQP1 in lens subcapsule epithelial cells.
应用免疫组织化学方法和计算机图像分析技术对前囊膜下晶状体上皮细胞AQP1进行检测。
Methods Immunohistochemical technique and image analysis were used.
方法免疫组织化学染色和图像分析技术。
Method Immunohistochemical(IHC), transmission electron microscopy(TEM) and imaging analysis were used.
方法采用免疫组化、透射电镜及图象分析的方法。
Methods Immunohistochemical technique, image analysis, radioimmunoassay and Western blotting were used.
方法采用免疫组织化学技术、图像分析、放射免疫和免疫印迹法。
ObjectiveTo put forward an automatic extraction and analysis method based on HSV dimension in immunohistochemical positive objects.
目的提出一种基于HSV空间的免疫组化阳性目标自动提取分析方法。
Methods SP microwave immunohistochemical technique and statistical analysis were practiced.
方法应用SP微波免疫组化技术和统计学分析。
The neurite outgrowth of motor neurons was detected by NF-200 immunohistochemical staining and computer image analysis system to measure the lengths of nervous process.
采用NF- 200免疫组织化学染色并进行图像分析，测定神经突起主干长度。
Immunohistochemical technique and imaging analysis technique were used to detect the temporal and spatial distributions and changes of the astrocyte in spinal cord in the animals of each group.
利用免疫组织化学方法及图像分析系统对各组动物脊髓内星形胶质细胞的时空分布和变化进行观察和分析。
Immunohistochemical staining and image analysis were used to detect the number of the positive neurons and the mean optical density and the percentages of SP positive cells in the DRG.
免疫组织化学方法结合图像分析检测各组脊神经节sp的阳性神经元数和平均光密度，并计算阳性细胞百分率。
Methods HE staining and immunohistochemical staining technology (S-P method) were used to do retrospective analysis for 52 cases of fibrous dysplasia, which had morphologic abnormalities.
方法用HE及SP法免疫组织化学染色对5 2例形态学变异的纤维结构不良作回顾性分析。
Methods Immunohistochemical SP method was used to detect the expression of HDGF in 158 NSCLC tissues and 12 normal control lung tissues. Survival analysis was further conducted.
方法应用SP法，检测158例手术切除NSCLC及12例正常对照肺组织中HDGF蛋白表达情况，进行生存分析、预后判定。
Proximal gastric mucosal 5-ht-positive cells were examined by immunohistochemical method and their integrated optical density (IOD) value measured by image analysis.
以免疫组化方法检测近端胃黏膜5 - HT阳性细胞，应用图像分析系统测定其积分光密度(IOD)值。
Methods: VEGF-C protein expression in benign and malignant oral lesions was investigated with an immunohistochemical staining assay, followed by light microscopic examination and image analysis.
方法：采用免疫组化染色，光镜及图像分析观察并确定VEGF - C在正常口腔粘膜、白斑及鳞癌等组织中的表达。
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