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以Wistar大鼠肝为材料,确立了一个简便的纯化鼠肝DNA甲基化酶的程序,包括:细胞的超声破碎、去内源核酸、硫酸铵盐析、磷酸纤维素亲和层析、DEAE-SephadexA-50柱层析及SephadexG-150凝胶过滤。用不同浓度聚丙烯酰胺凝胶电泳和孔梯度凝胶电泳检测,纯化后的酶已达电泳均一,且酶的比活力提高112倍。以聚丙烯酰胺孔梯度凝胶电泳测得其天然酶的分子量为365kD,以SDS-聚丙烯酰胺凝胶电泳测得该酶有两种亚基,大亚基为95kD,小亚基为85kD,推测该酶由两个大亚基和两个小亚基组成。  相似文献   
2.
以蛋白质双向凝胶电泳(2-DE)比较了不同中和抗体效价的SARS康复患者血浆样本(试验组)与正常人单采血浆样本(对照组)蛋白谱的异同。结果显示:对照组9份样本的2-DE 图谱出现蛋白斑点338±24个,试验组9份样本出现蛋白斑点348±45个,二者主要斑点的位置与数量基本一致;对照组中少量蛋白斑点的出现频度不同,且有4个蛋白点群的灰度值存在明显的差异;试验组有6个蛋白点群与对照组出现差异,并在相同区域Ⅲ内有4个蛋白斑点的灰度值出现变化,且灰度值与样本的中和抗体效价呈正相关性。结果表明,试验组与对照组的蛋白谱存在差异,且与SARS病毒中和抗体效价呈现相关性。  相似文献   
3.
点带石斑鱼的亲鱼培育、产卵受精和胚胎发育   总被引:28,自引:0,他引:28  
在水泥池人工养殖条件下,对人工诱导性逆转的“功能性雄性”、天然雄性及天然雌性点带石斑鱼(Epinephelus malabaricus)亲鱼进行强化培育,自然产卵受精。2002年繁殖季节,共获3cm以上的点带石斑鱼苗145万尾。亲鱼培育、产卵受精和胚胎发育的程序:(1)经过强化培育的亲鱼,自然产卵受精,受精率平均81%,最高97%;(2)成熟的“人工变性雄鱼”的精子头部呈球型,精子头径约3.7—6.1gm,尾长12.4~44.5μm;在水温26℃、盐度3%、pH7.9条件下,精子游动时间最长超过58min,精液中90%精子在31min停止游动,与天然雄亲鱼的精子无异,可作为生产雄亲鱼的来源;(3)在东山岛,产卵期由4月初持续到11月中旬,产卵高潮集中在4月底至5月底、9月底至10月初。在24h内,自然产卵通常从16:30持续到次日1:30;(4)产卵适宜水温为23.5—28.6℃,最适产卵水温为25.5—26.5℃;(5)水温26℃时,受精卵在盐度2.82%~2.96%,的海水中呈悬浮状态,盐度2.82%以下时下沉,盐度2.96%以上时上浮;(6)在水温24.9—27.6℃、盐度3%—3.3%、pH7.6—8.2的情况下,胚胎发育时间为21h。  相似文献   
4.
This study was to explore whether repeated non-invasive limb ischemic pre-conditioning (NLIP) can confer an equivalent cardioprotection against myocardial ischemia-reperfusion (I/R) injury in acute diabetic rats to the extent of conventional myocardial ischemic pre-conditioning (MIP) and whether or not the delayed protection of NLIP is mediated by reducing myocardial oxidative stress after ischemia-reperfusion. Streptozotocin-induced diabetic rats were randomized to four groups: Sham group, the I/R group, the MIP group and the NLIP group. Compared with the I/R group, both the NLIP and MIP groups showed an amelioration of ventricular arrhythmia, reduced myocardial infarct size, increased activities of total superoxide dismutase (SOD), manganese-SOD and glutathione peroxidase, increased expression of manganese-SOD mRNA and decreased xanthine oxidase activity and malondialdehyde concentration (All p < 0.05 vs I/R group). It is concluded that non-invasive limb ischemic pre-conditioning reduces oxidative stress and attenuates myocardium ischemia-reperfusion injury in diabetic rats.  相似文献   
5.
Exploring novel chemotherapeutic agents is a great challenge in cancer medicine. To that end, 2-substituted benzimidazole copper(II) complex, [Cu(BMA)Cl2]·(CH3OH) (1) [BMA = N,N′-bis(benzimidazol-2-yl-methyl)amine], was synthesized and its cytotoxicity was characterized. The interaction between complex 1 and calf thymus DNA was detected by spectroscopy methods. The binding constant (K b = 1.24 × 10M?1) and the apparent binding constant (K app = 6.67 × 10M?1) of 1 indicated its moderate DNA affinity. Complex 1 induced single strand breaks of pUC19 plasmid DNA in the presence of H2O2 through an oxidative pathway. Cytotoxicity studies proved that complex 1 could inhibit the proliferation of human cervical carcinoma cell line HeLa in both time- and dose-dependent manners. The results of nuclei staining by Hoechst 33342 and alkaline single-cell gel electrophoresis proved that complex 1 caused cellular DNA damage in HeLa cells. Furthermore, treatment of HeLa cells with 1 resulted in S-phase arrest, loss of mitochondrial potential, and up-regulation of caspase-3 and -9 in HeLa cells, suggesting that complex 1 was capable of inducing apoptosis in cancer cells through the intrinsic mitochondrial pathway.  相似文献   
6.
A new cytotoxic copper(II) complex with Schiff base ligand [CuII(5-Cl-pap)(OAc)(H2O)]·2H2O (1) (5-Cl-pap = N-2-pyridiylmethylidene-2-hydroxy-5-chloro-phenylamine), was synthesized and structurally characterized by X-ray diffraction. Single-crystal analysis revealed that the copper atom shows a 4 + 1 pyramidal coordination, a water oxygen appears in the apical position, and three of the basal positions are occupied by the NNO tridentate ligand and the fourth by an acetate oxygen. The interaction of Schiff base copper(II) complex 1 with DNA was investigated by UV-visible spectra, fluorescence spectra and agarose gel electrophoresis. The apparent binding constant (Kapp) value of 6.40 × 105 M− 1 for 1 with DNA suggests moderate intercalative binding mode. This copper(II) complex displayed efficient oxidative cleavage of supercoiled DNA, which might indicate that the underlying mechanism involve hydroxyl radical, singlet oxygen-like species, and hydrogen peroxide as reactive oxygen species. In addition, our present work showed the antitumor effect of 1 on cell cycle and apoptosis. Flow cytometric analysis revealed that HeLa cells were arrested in the S phase after treatment with 1. Fluorescence microscopic observation indicated that complex 1 can induce apoptosis of HeLa cells, whose process was mediated by intrinsic mitochondrial apoptotic pathway owing to the activation of caspase-9 and caspase-3.  相似文献   
7.
以5-氮-2'-脱氧胞苷(5-aza-CdR)为诱导物,在0.5μmol/L的最佳浓度下,可诱导HL-60细胞分化达15%左右。同时,用[ ̄3H]-methyl-s-adenosylmethionine( ̄3H-SAM)为底物,通过同位素参入法,测定了不同浓度诱导物对HL-60细胞DNA甲基化酶活力的影响,发现在最佳诱导物浓度下,可使HL-60细胞DNA甲基化酶活力明显下降,此外,也比较了不同分化水平的HL-60细胞中具有不同甲基化水平的DNA在体外接受甲基的能力,从而证明5-aza-CdR诱导HL-60细胞分化与其DNA甲基化状态密切相关。  相似文献   
8.
目的:研究雷米普利对糖尿病大鼠心肌缺血/再灌注损伤的保护作用,并从超微结构的角度初步探讨其作用机制。方法:链脲佐菌素致糖尿病大鼠被随机分为3组(n=16):缺血/再灌注(I/R)、缺血预适应(IPC)和雷米普利(RAM)组。RAM组每天用雷米普利(1mg/kg)灌胃,I/R和IPC组用等体积生理盐水灌胃。4周后各组动物均经历心肌缺血/再灌注损伤,IPC组于缺血前行心肌缺血预适应。连续监测心电图变化,测定心肌梗死面积,光、电镜下观察心肌形态学改变。结果:与I/R组比较,RAM及IPC组缺血期心脏ST-段抬高幅度降低,室早出现时间推迟,持续时间缩短,室速、室颤发生率降低,心肌梗死面积缩小,形态学观察心肌损伤减轻,心肌纤维及线粒体特征性结构保持清晰,血管通畅,内皮损伤减轻。结论:连续4周使用RAM对实验性糖尿病大鼠具有与IPC相似的心脏保护效应,机制可能与保护心肌细胞及线粒体、改善内皮功能等有关。  相似文献   
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