酶蛋白

Ingredients: Electrodialyzed Deep Sea Water, Disodium Laureth sulfosuccinate, Coco-Betaine, Mink Oil, Emu Oil, Jojoba Oil, Calendula Officinalis Flower Oil, Lavandula Angustifolia Fiower Oil, Rosmarinus Officinalis Oil, Rose Hip Oil, Borage Seed Oil, Daucus Carota Sativa Seed Oil, Eucalyptus Globulus Leaf Oil, Pelargonium Graveolens Oil, Lecithin, Tocopherol, Hydrolyzed Collagen, Hydrolyzed Elastin, Ubiquinone Ferment, Squalene, Sodium Hyaluronate, Retinol, Glycine Soya Phytoplacenta Extract, Ceramide, Panthenol, Allantoin, Melaleuca Alternifolia Extract, Rosa Damascena Flower Extract, Propolis Extract, Morus alba L.

主要成分：含海洋深层水， Disodium Laureth sulfosuccinate，可可甜菜碱，水貂油， Emu Oil， Borage Seed Oil，金盏菊花油，薰衣草油，迷迭香精油，玫瑰果油，胡萝卜素油，蓝桉叶油，天竹葵香薰精油，卵磷脂，维生素E，水解胶原蛋白，弹性蛋白水解，辅酶Q10，角鲨烯，透明质酸钠，视黄醇，甘氨酸大豆提取物，神经酰胺，D-L泛醇，尿囊素，互叶白千层提取物，突厥蔷薇，蜂胶，薄荷，芝麻，何首乌，银杏叶，枸杞，荨麻腿子属，洋甘菊，葛根等提取物

The expression of Bcl-2, Bcl-xL and ICAD was reduced time dependently,whereas the expression of Bax was increased.

细胞内抑制凋亡蛋白Bcl 2 ，Bcl xL和caspase激活的DNA酶抑制物表达量时间依赖性地减少，而促凋亡蛋白Bax表达量增加。

Taking Shewanella and Geobacter as examples, this paper reviewed three kinds of possible mechanisms of microbial enzyme-catalyzed dissimilatory Fe reduction and its molecular regulation, i.e., direct contact between microbial cell and Fe oxides, siderrophores, and electron shuttling compounds. Many membrane-bound cytochrome proteins are involved in the dissimilatory Fe reduction, forming a complicated regulation network.

以希瓦氏菌和地杆菌为例，本文综述了3种异化Fe还原的酶促反应机制及其分子调控机理：异化Fe还原菌与Fe氧化物直接接触机制、电子穿梭体的作用机制、铁载体作用机制，多种膜蛋白特别是多血红素的细胞色素蛋白参与微生物的异化Fe还原过程，并形成复杂的调控网络。

To investigate the expression, location and function, long distance PCR was used to expand the targets containing open reading frame. The expressive vectors of prokaryotic and eukaryotic cells were constructed after product purification and connecting with vectors. The prokayotic vectors were induced to express the protein by IPTG and the protein was seen by denaturalization PAG electrophoresis and dyeing. The eukayotic expressive vectors were transfected into culture cells and the protein was found in the nulceolus under the observation of the confocal microscope. The transfected cells were chosen by the geneticin (G418). The cell cyele was examined by flow cytometer and the cell numbers were reduced obviously in the stage of G〓-G〓 and G〓-M, but increased distinguishably in the S stage.

为研究磷酸化应激诱导蛋白的表达、定位和功能，采用了长距离聚合酶链反应扩增含有开放阅读框架的靶片段，经产物纯化、与载体连接，分别构建了STIP1基因的原核表达载体和真核表达载体；IPTG诱导原核表达载体，变性聚丙酰胺凝胶电泳与染色后，可见相应大小的蛋白质表达；STIP1基因的真核表达载体转染细胞系后，共聚焦显微镜下观察STIP1蛋白主要分布于细胞核内；用药物筛选STIP1基因转染的细胞后，流式细胞仪检测细胞周期，可见G〓-G〓期和G〓-M期的细胞明显降低，S期细胞明显增多。

As a constituent of selenoproteins, selenium has structural and enzymic roles.

晒是含硒蛋白的一个组份，某些含硒蛋白具有重要的酶催化功能。

Mammary gland epithetical cells were taken to analyze the phospholipids ingredients. SDS-Polyacrylamide gel electrophoresis was used for analyzing the membrane protein ingredients. ATPase activities which have important function in mammary protein were also tested.

同时提取乳腺上皮细胞膜，检测了乳腺上皮细胞膜磷脂组分的相对百分含量，并对膜蛋白进行了SDS-PAGE电泳，蛋白质凝胶成像系统对电泳条带进行定性定量分析，对膜蛋白中具有重要功能的ATP酶的活性进行了测定。

RESULTS: Cells in neurospheres expressed nestin and differentiated into neuro-specific enolase and glial fibrillary acidic protein.

结果：培养的神经球细胞表达巢蛋白，可分化为神经元特异性烯醇化酶、胶质纤维酸性蛋白阳性细胞。

To explore the expression of neuron specific enolaes, S protein(S100) and glial fibrillary acidic protein in retinoblastoma and its clinical significance.

目的探讨神经元特异性烯醇化酶、酸性钙结合蛋白(S100)及胶质纤维酸性蛋白在视网膜母细胞瘤中的表达及临床意义。

Neuron specific enolase,neurofilament,glial fibrillary acidic protein were detected by immunohistochemistry.

免疫组化鉴定神经元烯醇化酶、神经丝蛋白、胶质纤维酸性蛋白的表达。

The PCR based assay was tested on 19 strains isolated in throats from patients with guttate psoriasis. The results demonstrated that 6 strains were positive in 15 streptococus strains among which there were 3 streptococus pyogenes, 1.S.agalactiae, 1 S. eguisimilis and 1 S. uberis, and 4 non- streptococus strains were negative. Emm6 was found not only in suppurative hemolytic streptococus, but also in S.uberis.

应用聚合酶链式反应方法对点滴型银屑病患者咽部培养出的19株细菌中的M6蛋白基因进行检测，结果，15株链球菌中6株为阳性，其中化脓链球菌3株，无乳链球菌、似马链球菌和乳房链球菌各1株，4株非链球菌均为阴性。M6蛋白基因不仅存在化脓性溶血链球菌中，在其它链球菌如乳房链球菌中也存在。

This one mode pays close attention to network credence foundation of the businessman very much.

这一模式非常关注商人的网络信用基础。

Cell morphology of bacterial ghost of Pasteurella multocida was observed by scanning electron microscopy and inactivation ratio was estimated by CFU analysi.

扫描电镜观察多杀性巴氏杆菌细菌幽灵和菌落形成单位评价遗传灭活率。