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1)  immunostaining
免疫染色
1.
Assessment of retinal and choroidal neovascularization by in vivo immunostaining
活体免疫染色评估眼底新生血管实验研究
2.
A new method for titration of Porcine Reproductive and Respiratory Syndrome Virus (PRRSV) was developed utilizing immunostaining.
本文建立一种测定猪繁殖与呼吸综合征病毒(PRRSV)滴度的新方法-免疫染色法。
2)  immunoperoxidase staining
免疫酶染色
1.
Developmentof type and subtype-specific immunoperoxidase staining techniques for detection of avian influenza virus;
禽流感病毒型及亚型特异性免疫酶染色技术的研究
3)  immunofluorescence staining
免疫荧光染色
1.
Methods Cells were harvested at 0 day,the 3rd day and the 7th day after BGSCs differentiation,then the ratio of Hes-1 positive cells were counted by flow cytometry,and the expression intensity and cell types were detected by laser confocal microscopy after immunofluorescence staining with Hes-1 and GFAP,MAP2 or MBP.
方法对体外培养的人脑胶质瘤干细胞进行诱导分化,于未分化、分化第3、7d收集标本,行Hes-1蛋白免疫荧光染色后流式细胞术检测标本中阳性细胞比例;Hes-1分别与CD133、GFAP、MAP2、MBP蛋白双标免疫荧光染色后,激光共聚焦显微镜下观察Hes-1蛋白表达强度及细胞类型的变化。
2.
The nNOS neurons were detected by immunofluorescence staining.
用免疫荧光染色、RT-PCR和Western blot方法对nNOS神经元数量、nNOS基因和蛋白的表达量进行检测。
3.
The aim of this experiment was to study the effective method of fixation and penetration before immunofluorescence staining in oocytes and early embryos to raise the effect of immunofluorescence staining in them.
本实验旨在探索有效的染色前固定和渗透卵母细胞及早期胚胎的方法,以提高小鼠卵母细胞和早期胚胎免疫荧光染色的效果;同时检测RNA聚合酶Ⅱ(PolⅡ)在小鼠卵母细胞和早期胚胎的表达,探讨PolⅡ在卵母细胞和早期胚胎发育中的作用。
4)  immunohistochemistry stain
免疫组化染色
1.
Then frozen serial sections were made and the sections were treated with HE stain, immunohistochemistry stains including anti-Ezrin and anti-Neural cell adhesion molecule (NCAM) monoclonal antibodies.
方法取肌纤维再生活跃的假肥大型肌营养不良(DMD,9例)和多发性肌炎(PM,5例)患者的骨骼肌标本,冰冻连续切片,进行HE染色及抗-Ezrin、抗-神经细胞黏附分子(NCAM)单克隆抗体免疫组化染色,观察被检肌的病理改变和Ezrin蛋白的表达。
5)  Immunohistochemistry
免疫组化染色
1.
At 6h, 24h, 72h and 7d after operation, the rats were sacrificed and the brain tissues were made for immunohistochemistry analysis of Tf.
方法 采用立体定向技术注入自体不凝血建立实验性大鼠ICH模型 ,在不同时间断头取脑 ,免疫组化染色检测脑组织中Tf阳性细胞的表达并与对照组比较。
2.
We measured the area of the lesions on radiographs and detected the expression of TNF-α by immunohistochemistry 1 d,3 d,7 d,14 d,and 21 d after pulp exposure.
方法采用髓腔直接暴露法建立SD大鼠根尖周炎模型,分别通过X线测量法和免疫组化染色观察对照组、术后1、3、7、14、21d时根尖病损的大小和TNF-α免疫组化光密度值的变化。
3.
The expressions of Nogo-A and receptor (NgR protein) were detected by immunohistochemistry(IHC) staining on 4μm thickness of Formalin Fixed Paraffin-embedded(FFPE) and positive cells per each 0.
通过HE染色,观察各组大鼠脑组织的细胞形态学变化;利用免疫组化染色技术和图象分析的检测手段,检测Nogo-A及其受体NgR蛋白的阳性表达量,来探讨实验性变态反应性脑脊髓炎以及甲基强的松龙干预下的脑组织Nogo-A及其受体NgR蛋白的表达变化。
6)  indirect immunoenzymatic technique
间接免疫酶染色
1.
Indirect immunoenzymatic technique detecting TOXOPLASMA GONDII and its antigen in infected mice;
间接免疫酶染色检测小鼠组织内弓形虫及抗原
补充资料:染色与非染色剂量计
分子式:
CAS号:

性质:利用染色和非染色塑料光密度的辐射诱导变化测定剂量。目前它是一种流行、方便的常规剂量计,所测定的剂量范围在1kGy~1MGy之间。一些材料比如PMMA,PVC,PC等被用于该种剂量计。

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