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METHODS: The collagen type Ⅰ gene was cloned by the improved subtractive hybridization, and the fragment of collagen type Ⅰ cDNA was labeled by digoxin and was hybrided by in situ hybridization on the section of capsule of normal and cataractous lens.

用改良的消减杂交法克隆Ⅰ型胶原基因,地高辛标记Ⅰ型胶原cDN####段制作探针,用原位杂交法研究其在晶状体前囊膜切片上的表达,并作统计学处理。

Methods: A 5ml bone marrow was extracted from the lilac of human volunteers. By Percoll fluid and density gradient centrifugation, the MSC was obtained; after the cells filled the bottom of vessel, subcultured them, when they subculture in third generation, redigested them, 500 R/min centrifugate, alter the completed medium to chemical definition medium, examined the form change and prolifration of cells by invert microscope, toluidine blue stain、immunocytochemical stain and RT-PCR to test the type Ⅱ collagen mRNA and proteoglycan.

取健康成人髂后上棘处骨髓5ml,经percoll液分离后密度梯度离心,〓/ml密度接种培养,观察原代细胞的贴壁、增殖状况,细胞长满瓶底后进行传代培养;传至第三代细胞,重新消化后以500转/分钟轻度离心5分钟,〓/ml接种,改用化学限定培养基代替完全培养基培养,倒置显微镜观察细胞生长情况及形态变化,甲苯胺蓝染色观察诱导细胞合成细胞外基质中的蛋白多糖,免疫细胞化学染色检测ECM中Ⅱ胶原的蛋白合成,RT-PCR鉴定诱导细胞Ⅱ胶原mRNA的表达。

The aim are:lTo examine the proliferation ability and potential chondroblast differentiation ;2To find an ideal condition stimulated BMSC differentiate into chondroblast;3To examine the chondroblast proliferation in porous scaffolds and to explore the interaction between cells and materials;4To examine the release of cytokine in vitro.

取健康成人略后上棘处骨髓 5ml,经 percoll液分离后密度梯度离心,10'砌l密度接种培养,观察原代细胞的贴壁、增殖状况,细胞长满瓶底后进行传代培养;传至第三代细胞,重新消化后以500转/分钟轻度离心 5分钟,10V加 l接种,改用化学限定培养基代替完全培养基培养,倒置显微镜观察细胞生长情况及形态变化,甲苯胺蓝染色观察诱导细胞合成细胞外基质QCM)中的蛋白多糖,免疫细胞化学染色检测ECM中*胶原的蛋白合成,RT干CR鉴定诱导细胞*胶原mRNA的表达。

In this study, immunohistochemical staining was performed with antibodies against D2-40, S100, pankeratin, epithelial membrane antigen, brachyury, and glial fibrillary acidic protein in 4 cases of chordoid glioma, 6 skeletal myxoid chondrosarcomas, 10 chordoid meningiomas, 16 extraskeletal myxoid chondrosarcoma, 18 chordomas, 22 low-grade chondrosarcomas, and 27 enchondromas.

本研究中,我们给4例脊索样胶质瘤、6例骨的黏液样软骨肉瘤、10脊索样脑膜瘤、16例骨外黏液样软骨肉瘤、18例脊索瘤、22例低级别软骨肉瘤和27例内生性软骨瘤做了D2-40、S100、pankeratin、上皮膜抗原、brachyury和胶质纤维酸性蛋白的免疫组化染色。

In this study, Polyurethane/hydrogel composites were fabricated for wound repair applications. The hydrogel was copolymer of thermosensitive N-isopropyl acrylamide and acrylic acid.γ-ray irradiation was employed to copolymerize NIPAAm with AAc and to graft hydrogel onto porous PU simultaneously.

本研究以聚胺基甲酸酯为基材,将感温性异丙基丙烯醯胺(N-isopropyl acrylamide, NIPAAm)和丙烯酸(Acrylic acid, AAc)以γ-ray照射聚合法进行聚合,并同时将水胶接枝在多孔PU上,制备出PU/水胶复材之人工敷料,应用於伤口修复。

CIK cells are highly efficient cytolytic effector cells which have a stronger significant suppression against growth of glioma in vitro and in vivo.

CIK细胞是一种新型和高效的免疫活性细胞,具有较强的体内外抑制胶质瘤生长的作用,有可能用于临床上脑胶质瘤的过继性免疫治疗。

Adhesive chemical gel State so that the viscosity and liquidity decreases and the loss of business card printing and membership card making performance, while still in tuhung on deink.

油不朱胶化不败冻胶状况,使粘度和流动性贬矮,获得制卡和会员卡制作本能机能,而遨游在不朱斗上引起脱不朱。

Methods The NGF, BDNF, and NT3 genes of rats were cloned, the eukaryote expression vectors were established, the three kind of recombinant vectors were used to transfect astrocytes, the positive cloned cells were cultured dilatedly after G418 sifting; using supernates of culture liquid of astrocytes modified by gene to culture PC12 or TrkB-PC12, the expression and its level of gene target cells aimed genes were measured by Western blotting or immunohistochemical method.

克隆大鼠NGF、BDNF和NT3基因,构建真核表达载体;3种重组载体分别转染星形胶质细胞,G418筛选后获得阳性克隆细胞进行扩大培养;取基因修饰星形胶质细胞培养液上清培养PC12细胞或TrkB-PC12细胞;用Western blotting杂交或免疫组织化学方法检测基因靶细胞目的基因的表达及其水平。

So the electrical conductive adhensive is costliness at the present market. On the other hand, the silver particles were easy sinking down in the polymer matrix because it's density are more bigger than the polymer matrix which made the transportation and preservation of the conductive adhensive being very discommodiousness.

一方面银粉的价格比较昂贵,一般都要添加质量分数为60%以上才能达到良好的导电性,因此目前市场上的导电胶价格很高,另一方面银粉与聚合物树脂密度相差很大,在聚合物基体中容易产生沉降,给导电胶的储存和运输带来极大的不便。

Results In control group, AQP4 protein and its mRNA were expressed in subpial astrocytes, choroid plexus, ependyma and perivascular astrocytes.

结果AQP4及其mRNA在软脑膜下星形胶质细胞、脉络膜丛、室管膜及血管周围星形胶质细胞胞膜上均有表达。

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