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Corrigendum
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《Neural Regeneration Research》 2026年第3期922-922,共1页
Corrigendum:Epalrestat protects against diabetic peripheral neuropathy by alleviating oxidative stress and inhibiting polyol pathway https://doi.org/10.4103/NRR.NRR-D-25-00562 In the article titled“Epalrestat protect... Corrigendum:Epalrestat protects against diabetic peripheral neuropathy by alleviating oxidative stress and inhibiting polyol pathway https://doi.org/10.4103/NRR.NRR-D-25-00562 In the article titled“Epalrestat protects against diabetic peripheral neuropathy by alleviating oxidative stress and inhibiting polyol pathway,”published on pages 345-351 in Issue 2,Volume 11 of Neural Regeneration Research(Li et al.,2016),the Western blot bands in Figure 2A are incorrect. 展开更多
关键词 western blot bands diabetic peripheral neuropathy alleviating oxidative stress oxidative stress polyol pathway EPALRESTAT
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Retraction:miR-641 functions as a tumor suppressor by targeting MDM2 in human lung cancer
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作者 Oncology Research Editorial Office 《Oncology Research》 2025年第3期737-737,共1页
Following the publication,concerns have been raised about a number of figures in this article.The western blots in this article were presented with atypical,unusually shaped and possibly anomalous protein bands in man... Following the publication,concerns have been raised about a number of figures in this article.The western blots in this article were presented with atypical,unusually shaped and possibly anomalous protein bands in many cases. 展开更多
关键词 western blots protein bands protein band human lung cancer tumor suppressor MDM MIR western blot
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Retraction:Inhibition of Proliferation,Migration,and Invasion by Knockdown of Pyruvate Kinase-M2(PKM2)in Ovarian Cancer SKOV3 and OVCAR3 Cells
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作者 Oncology Research Editorial Office 《Oncology Research》 2025年第7期1801-1801,共1页
Following the publication,concerns have been raised about a number of figures in this article.The western blots in this article were presented with atypical,unusually shaped and possibly anomalous protein bands in man... Following the publication,concerns have been raised about a number of figures in this article.The western blots in this article were presented with atypical,unusually shaped and possibly anomalous protein bands in many cases. 展开更多
关键词 western blots protein bands RETRACTION ovarian cancer MIGRATION INVASION SKOV PROLIFERATION
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Retraction:MicroRNA-221-3p Plays an Oncogenic Role in Gastric Carcinoma by Inhibiting PTEN Expression
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作者 Oncology Research Editorial Office 《Oncology Research》 2025年第9期2598-2598,共1页
The published article titled“MicroRNA-221-3p Plays an Oncogenic Role in Gastric Carcinoma by Inhibiting PTEN Expression”has been retracted from Oncology Research,Vol.25,No.4,2017,pp.523–536.DOI:10.3727/096504016X14... The published article titled“MicroRNA-221-3p Plays an Oncogenic Role in Gastric Carcinoma by Inhibiting PTEN Expression”has been retracted from Oncology Research,Vol.25,No.4,2017,pp.523–536.DOI:10.3727/096504016X14756282819385 URL:https://www.techscience.com/or/v25n4/56833 Following the publication,concerns have been raised about a number of figures in this article.An unexpected area of similarity was identified in terms of the cellular data,where the results from differently performed experiments were intended to have been shown,although the areas immediately surrounding this area featured comparatively different distributions of cells.In addition,the western blots in this article were presented with atypical,unusually shaped and possibly anomalous protein bands in many cases. 展开更多
关键词 cellular datawhere microrna p PTEN western blots inhibiting pten expression gastric carcinoma cellular data RETRACTION
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Retraction: MYBL2 is targeted by miR-143-3p and regulates breast cancer cell proliferation and apoptosis
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作者 Oncology Research Editorial Office 《Oncology Research》 2025年第3期739-739,共1页
Following the publication,concerns have been raised about a number of figures in this article.An unexpected area of similarity was identified in terms of the cellular data,where the results from differently performed ... Following the publication,concerns have been raised about a number of figures in this article.An unexpected area of similarity was identified in terms of the cellular data,where the results from differently performed experiments were intended to have been shown,although the areas immediately surrounding this area featured comparatively different distributions of cells.In addition,the western blots in this article were presented with atypical,unusually shaped and possibly anomalous protein bands in many cases. 展开更多
关键词 western blots cellular datawhere protein bands performed experiments RETRACTION cellular data
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Retraction:miR-135a confers resistance to gefitinib in non-small cell lung cancer cells by upregulation of RAC1
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作者 Oncology Research Editorial Office 《Oncology Research》 2025年第3期733-733,共1页
Following the publication,concerns have been raised about a number of figures in this article.The western blots in this article were presented with atypical,unusually shaped and possibly anomalous protein bands in man... Following the publication,concerns have been raised about a number of figures in this article.The western blots in this article were presented with atypical,unusually shaped and possibly anomalous protein bands in many cases. 展开更多
关键词 non small cell lung cancer western blots protein bands RETRACTION GEFITINIB MIR
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Retraction:Knockdown of Rap1b Enhances Apoptosis and Autophagy in Gastric Cancer Cells via the PI3K/Akt/mTOR Pathway
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作者 Oncology Research Editorial Office 《Oncology Research》 2025年第8期2177-2177,共1页
The published article titled“Knockdown of Rap1b Enhances Apoptosis and Autophagy in Gastric Cancer Cells via the PI3K/Akt/mTOR Pathway”has been retracted from Oncology Research,Vol.24,No.5,2016,pp.287–293.DOI:10.37... The published article titled“Knockdown of Rap1b Enhances Apoptosis and Autophagy in Gastric Cancer Cells via the PI3K/Akt/mTOR Pathway”has been retracted from Oncology Research,Vol.24,No.5,2016,pp.287–293.DOI:10.3727/096504016X14648701447779 URL:https://www.techscience.com/or/v24n5/56977 Following the publication,concerns have been raised about a number of figures in this article.An unexpected area of similarity was identified in terms of the cellular data,where the results from differently performed experiments were intended to have been shown,although the areas immediately surrounding this area featured comparatively different distributions of cells.In addition,the western blots in this article were presented with atypical,unusually shaped and possibly anomalous protein bands in many cases. 展开更多
关键词 gastric cancer cells cellular datawhere western blots AUTOPHAGY RETRACTION rap b APOPTOSIS pi k akt mtor pathway
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蔬菜病毒不同检测技术灵敏度的比较研究
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作者 陈伟 姚洁 +4 位作者 冯明峰 李帅 蒋西子 蒋磊 江彤 《浙江农业学报》 北大核心 2025年第5期1072-1081,共10页
为了明确蔬菜病毒种类,探索快速、灵敏、低成本、高通量的病毒检测方法。将10种蔬菜病毒,烟草花叶病毒(Tobacco mosaic virus,TMV)、黄瓜花叶病毒(Cucumber mosaic virus,CMV)、黄瓜绿斑驳花叶病毒(Cucumber green mottle mosaic virus,... 为了明确蔬菜病毒种类,探索快速、灵敏、低成本、高通量的病毒检测方法。将10种蔬菜病毒,烟草花叶病毒(Tobacco mosaic virus,TMV)、黄瓜花叶病毒(Cucumber mosaic virus,CMV)、黄瓜绿斑驳花叶病毒(Cucumber green mottle mosaic virus,CGMMV)、番茄花叶病毒(Tomato mosaic virus,ToMV)、蚕豆萎蔫病毒(Broad bean wilt virus,BBWV)、芜菁花叶病毒(Turnip mosaic virus,TuMV)、小西葫芦黄花叶病毒(Zucchini yellow mosaic virus,ZYMV)、番茄褪绿病毒(Tomato chlorosis virus,ToCV)、马铃薯Y病毒(Potato virus Y,PVY)和番茄环纹斑点病毒(Tomato zonate spot virus,TZSV)的cp基因质粒DNA顺次固定在同一张硝酸纤维素膜(NC膜)上,根据10种蔬菜病毒的cp基因序列制备地高辛(DIG)标记的特异性探针,利用dot-Southern blot方法一次性检测10种病毒。再采用dot-Southern blot、dot-Northern blot、PCR和ELISA方法检测TMV,比较不同检测方法的灵敏度。结果发现,dot-Southern blot方法可在同一张NC膜上一次性检出10种病毒的cp基因质粒DNA。dot-Southern blot检测TMV cp基因质粒DNA和cp基因cDNA的最低浓度分别为5×10^(-2)ng·μL^(-1)和5×10^(-1)ng·μL^(-1),dot-Northern blot检测感染TMV蔬菜样本总RNA的最低浓度为5×10^(-2)ng·μL^(-1),PCR检测TMV cp基因质粒DNA的最低浓度为5×10-3ng·μL^(-1),RT-PCR检测TMV cDNA的最低浓度为5×10^(-2)ng·μL^(-1),dot-ELISA和TAS-ELISA检测感染TMV蔬菜病汁液的最低浓度为9.8 ng·μL^(-1)和78 ng·μL^(-1)。说明dot-Southern blot能够一次性检出多种病毒,可用于蔬菜病毒复合侵染检测。dot-Southern blot、dot-Northern blot、RT-PCR和PCR等核酸检测方法的灵敏度相对较高,而ELISA检测方法的灵敏度相对较低。 展开更多
关键词 蔬菜病毒 检测方法 灵敏度 dot-Southern blot
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自体黄韧带干预TGF-β1/Smad3信号通路抑制兔硬膜外纤维瘢痕形成的实验研究
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作者 王鹏 张德宝 +5 位作者 张杨 张海斌 时嘉 张少杰 李树文 吴一民 《中国临床解剖学杂志》 北大核心 2025年第1期69-75,共7页
目的通过对不同组别的兔分别行椎板切除术,对比其各组术后3、6周TGF-β1、Smad3蛋白表达量以及两者相应的mRNA表达水平,从而探讨自体黄韧带抑制腰椎术后硬膜外纤维瘢痕形成与TGF-β1/Smad3信号通路的关系。方法将于内蒙古医科大学实验... 目的通过对不同组别的兔分别行椎板切除术,对比其各组术后3、6周TGF-β1、Smad3蛋白表达量以及两者相应的mRNA表达水平,从而探讨自体黄韧带抑制腰椎术后硬膜外纤维瘢痕形成与TGF-β1/Smad3信号通路的关系。方法将于内蒙古医科大学实验动物中心购买的48只6~8月龄的日本大白兔,分为保留黄韧带组,自体脂肪回置组,不保留黄韧带组,对不同组别进行手术造模。术后对每组间的实验动物分别饲养3、6周后进行处死(3、6周各处死8只)。采用Western blot蛋白定量分析、RTPCR技术测定各组样本中的TGF-β1、Smad3蛋白含量及mRNA表达水平,并将以上数据分别进行组间比较,分析其差异性。结果①Western blot检测结果:3、6周保留组TGF-β1、Smad3蛋白表达量小于不保留组和脂肪组(P<0.05),不保留组和脂肪组之间并未发现明显差异。②RT-PCR结果显示:对于TGF-β1、Smad3两者的mRNA表达量而言,3、6周保留组明显小于不保留组和脂肪组(P<0.05),不保留组和脂肪组之间并未见明显差异。结论腰椎手术术后,会形成不同程度的硬膜外纤维瘢痕。若在术中保留自体黄韧带,可减少硬膜外成纤维细胞的形成,其机制与TGF-β1/Smad3信号通路有关。 展开更多
关键词 黄韧带 纤维瘢痕 TGF-β1/Smad3信号通路 Western blot RT-PCR技术
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条件性胰岛β细胞HLF基因敲除小鼠构建与鉴定
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作者 侯梦龙 齐心语 +4 位作者 吴建凤 廖启超 马杰 周磊 李一星 《安徽医科大学学报》 北大核心 2025年第8期1432-1439,共8页
目的为了探究肝白血病因子(HLF)在糖尿病中的作用机制,构建条件性胰岛β细胞HLF基因敲除小鼠动物模型。方法在细胞水平上,通过CCK-8试验验证HLF抑制或过表达对MIN6细胞增殖的影响。通过RT-qPCR和Western blot,分别在mRNA水平和蛋白水平... 目的为了探究肝白血病因子(HLF)在糖尿病中的作用机制,构建条件性胰岛β细胞HLF基因敲除小鼠动物模型。方法在细胞水平上,通过CCK-8试验验证HLF抑制或过表达对MIN6细胞增殖的影响。通过RT-qPCR和Western blot,分别在mRNA水平和蛋白水平检测HLF抑制或过表达效果。将HLF flox/flox转基因小鼠与Pdx1-Cre+/-小鼠(C57BL/6J)杂交繁育,获得子代小鼠。利用PCR方法鉴定小鼠基因型,通过RT-qPCR技术和Western blot检测HLF基因在胰岛β细胞敲除小鼠(HLF flox/flox Cre+/-)和对照小鼠(HLF flox/flox)中的mRNA水平和蛋白水平表达差异,验证敲除效果。同时取2组小鼠的胰岛组织制作石蜡切片并进行苏木精-伊红(HE)染色分析。结果HLF基因抑制或过表达对MIN6细胞增殖无显著影响。在MIN6细胞中抑制HLF基因,其mRNA表达水平较对照组下降了74%,蛋白表达水平较对照组下降了60%;过表达HLF基因后,其mRNA表达水平为对照组的2.13倍,蛋白表达水平为对照组的1.8倍。敲除小鼠的HLF基因mRNA表达水平较对照组下降了89%,蛋白表达水平较对照组下降了65%。HE染色结果显示:敲除小鼠胰岛组织内细胞形态与对照小鼠无明显差异。抑制HLF使MIN6细胞中糖原含量提高约20%。结论成功构建HLF基因敲除小鼠,为研究HLF在糖尿病发病机制中的作用提供了动物模型。 展开更多
关键词 肝白血病因子 条件性胰岛β细胞 RT-QPCR Western blot 基因敲除 C57BL/6J小鼠
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CSF1R^(+/-)小鼠的构建和基因鉴定
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作者 周园园 刘崇 +4 位作者 王安琪 张慧茹 邱佳琪 朱梦娟 涂佳杰 《安徽医科大学学报》 北大核心 2025年第5期884-889,共6页
目的构建集落刺激因子1受体杂合(CSF1R^(+/-))小鼠并分析其基因型,为疾病病理机制及药物靶点提供动物模型基础。方法根据Cre/Loxp系统设计一种线性化的靶向载体,在集落刺激因子1受体(CSF1R)基因第5外显子上游插入一个Loxp位点,在第5外... 目的构建集落刺激因子1受体杂合(CSF1R^(+/-))小鼠并分析其基因型,为疾病病理机制及药物靶点提供动物模型基础。方法根据Cre/Loxp系统设计一种线性化的靶向载体,在集落刺激因子1受体(CSF1R)基因第5外显子上游插入一个Loxp位点,在第5外显子下游插入一个双侧有Loxp位点的新霉素抗性盒(PGK-neo)。将线性化的靶向载体电穿孔至胚胎干细胞(ES)。将正确靶向的ES注射到C57BL/6J小鼠的胚泡中得到嵌合小鼠,与透明带3-Cre(Zp3-Cre)小鼠进行繁殖。新生小鼠出生后9~14天编号并剪鼠尾,提取小鼠的DNA,通过聚合酶链式反应(PCR)和琼脂糖凝胶电泳鉴定小鼠基因型,筛选出CSF1R^(+/-)小鼠。应用流式细胞术检测小鼠巨噬细胞中CSF1R的表达;Western blot检测小鼠组织中CSF1R的蛋白表达。结果琼脂糖凝胶电泳结果显示,野生小鼠(WT)扩增出453 bp的条带,CSF1R^(+/-)小鼠扩增出453 bp和650 bp的条带。流式细胞术结果显示,与WT组比较,CSF1R^(+/-)组小鼠的腹腔来源巨噬细胞(PM)和骨髓来源巨噬细胞(BMDM)中的CSF1R低表达(P<0.05)。Western blot结果显示,与WT组比较,CSF1R^(+/-)组小鼠脾脏、肾脏、脑组织中的CSF1R蛋白低表达(P<0.05)。结论成功构建、繁育和鉴定CSF1R^(+/-)小鼠,为进一步揭示CSF1R在免疫调节中的潜在机制研究提供动物模型基础。 展开更多
关键词 CSF1R PCR Western blot 流式细胞术 Cre/Loxp 动物模型
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ODF1单克隆、多克隆抗体的制备及特异性检测
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作者 瞿成龙 向雨欣 +3 位作者 明胜利 曾磊 王江 褚贝贝 《山西农业科学》 2025年第6期159-165,共7页
为探究ODF1蛋白的生物学功能,制备并鉴定其特异性抗体工具,采用原核表达系统表达重组ODF1蛋白,将高纯度的重组ODF1蛋白作为免疫原,利用杂交瘤技术制备鼠源单克隆抗体,通过免疫新西兰兔制备多克隆抗体。采用Western blot和免疫荧光(IFA)... 为探究ODF1蛋白的生物学功能,制备并鉴定其特异性抗体工具,采用原核表达系统表达重组ODF1蛋白,将高纯度的重组ODF1蛋白作为免疫原,利用杂交瘤技术制备鼠源单克隆抗体,通过免疫新西兰兔制备多克隆抗体。采用Western blot和免疫荧光(IFA)对抗体性能进行系统评价。结果成功筛选出1A1-7、5C6-4等2株稳定分泌抗ODF1单克隆抗体的杂交瘤细胞株,亚型均为IgM,同时获得了高效价的兔源多克隆抗体。Western blot和免疫荧光分析结果表明,单克隆、多克隆抗体均能特异性识别内源性、外源性ODF1蛋白,表现出良好的特异性和应用潜力。综上,该试验成功制备了特异性良好的ODF1单克隆、多克隆抗体。 展开更多
关键词 原核表达 ODF1蛋白 单克隆抗体 Western blot 多克隆抗体 杂交瘤技术 免疫荧光
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短链脂肪酸异戊酸对痘苗病毒体外活性的影响
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作者 杜梦华 李云洁 +6 位作者 郭亚迪 梅航天 邵弓宇 尚雨欣 王江 褚贝贝 明胜利 《山西农业科学》 2025年第6期127-134,共8页
为探究短链脂肪酸异戊酸对痘苗病毒(VACV)体外增殖的抑制作用及其机制,采用直接免疫荧光法筛选5种短链脂肪酸的抗病毒效应;通过CCK-8法评估异戊酸(30~3000μmol/L)对BHK-21、Vero细胞活力的影响;PI染色结合流式细胞术分析异戊酸(10~100... 为探究短链脂肪酸异戊酸对痘苗病毒(VACV)体外增殖的抑制作用及其机制,采用直接免疫荧光法筛选5种短链脂肪酸的抗病毒效应;通过CCK-8法评估异戊酸(30~3000μmol/L)对BHK-21、Vero细胞活力的影响;PI染色结合流式细胞术分析异戊酸(10~100μmol/L)对细胞周期的干预作用。利用流式细胞术定量异戊酸处理细胞中VACV-GFP的增殖水平;采用Western blotting检测VACV结构蛋白A27L、GFP表达变化;采用实时荧光定量PCR分析病毒关键基因F17R、E9L的mRNA转录水平。结果表明,异戊酸显著抑制VACV增殖,且在30~3000μmol/L浓度下对细胞活力无显著影响,在10~100μmol/L浓度时未干扰细胞周期;West⁃ern blotting结果显示,异戊酸剂量依赖性抑制A27L、GFP蛋白表达;qPCR证实,其显著下调F17R、E9L的mRNA水平。综上,异戊酸通过抑制病毒蛋白合成及基因转录,有效阻断VACV体外增殖。 展开更多
关键词 短链脂肪酸 异戊酸 痘苗病毒 Western blotting 流式细胞术 抗病毒
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猪衣原体ompA基因的原核表达与纯化及其蛋白功能预测
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作者 李宁倩 禹思宇 +6 位作者 李桐菲 李文超 魏颖 谭建锡 胡忆文 唐连飞 刘伟 《湖南畜牧兽医》 2025年第5期29-33,共5页
为了将猪衣原体ompA基因作为目标抗原,为后续建立间接ELISA检测方法提供理论依据,开展了该基因的原核表达与纯化工作,并利用生物信息学方法对ompA蛋白的理化性质、亲疏水性、跨膜区域和抗原表位等进行了分析与预测。结果显示:该研究成... 为了将猪衣原体ompA基因作为目标抗原,为后续建立间接ELISA检测方法提供理论依据,开展了该基因的原核表达与纯化工作,并利用生物信息学方法对ompA蛋白的理化性质、亲疏水性、跨膜区域和抗原表位等进行了分析与预测。结果显示:该研究成功构建了重组质粒,并通过SDS-PAGE和Western blot确认该蛋白以包涵体形式表达,分子量约为27 kDa;该蛋白的预测分子质量为23.31921 kDa,理论等电点为4.37,不含跨膜区,属于亲水性蛋白,含有7个抗原决定簇,平均抗原倾向值为1.0316。结果表明:ompA蛋白具备良好的免疫反应性,是免疫反应中的关键成分,适合作为间接ELISA的包被抗原。该研究为深入理解猪衣原体的致病机制及开发相应的防控技术提供了理论基础。 展开更多
关键词 猪衣原体ompA基因 重组质粒 表达及纯化 Western blot验证 生物信息学预测 间接ELISA
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基于网络药理学和实验验证探究杏贝止咳祛痰口服液治疗儿童支气管炎的作用机制
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作者 杨子烨 谭征 +4 位作者 刘洁 刘润花 杨畅 关晶 张建民 《中南药学》 2025年第8期2165-2172,共8页
目的运用网络药理学、分子对接以及体外细胞实验探究杏贝止咳祛痰口服液治疗儿童支气管炎的作用机制。方法检索TCMSP、BATMAN-TCM、PubChem、SwissTargetPrediction等数据库,获得杏贝止咳祛痰口服液活性成分、相关作用靶点以及儿童支气... 目的运用网络药理学、分子对接以及体外细胞实验探究杏贝止咳祛痰口服液治疗儿童支气管炎的作用机制。方法检索TCMSP、BATMAN-TCM、PubChem、SwissTargetPrediction等数据库,获得杏贝止咳祛痰口服液活性成分、相关作用靶点以及儿童支气管炎相应疾病靶点,并将杏贝止咳祛痰口服液作用靶点与疾病靶点的交集作为潜在作用靶点;利用Cytoscape软件构建成分-疾病网络及蛋白互作网络,分析其网络拓扑结构,筛选关键成分及核心靶点,并进行分子对接验证;采用R语言对交集靶点进行GO功能及KEGG富集分析。最后,基于香烟烟雾提取物(CSE)诱导人正常支气管上皮细胞16-HBE构建体外细胞模型,采用Western blot技术进行相关通路靶点的验证。结果杏贝止咳祛痰口服液关键成分包括光甘草定、槲皮素、山柰酚等,主要通过调控TNF-α、STAT3、EGFR、PTGS2等在内的核心靶点介导的AGE-RAGE等信号通路发挥治疗儿童支气管炎的作用。Western blot实验结果显示,与空白组相比,模型组TNF-α、STAT3、MAPK3、ICAM1和PIK3CD蛋白的表达显著上调(P<0.01);与模型组相比,杏贝止咳祛痰口服液给药组对应蛋白显著下调(P<0.01)。结论杏贝止咳祛痰口服液可通过多成分、多靶点、多途径改善儿童支气管炎临床症状,其作用机制可能与抑制AGE-RAGE信号传导通路的活化有关。 展开更多
关键词 儿童支气管炎 杏贝止咳祛痰口服液 网络药理学 Western blot AGE-RAGE信号通路
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Studies on the antioxidant properties of Staphylococcus epidermidis fermentation broth
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作者 Wenlin Geng Ming Li Yuhua Cao 《日用化学工业(中英文)》 北大核心 2025年第10期1275-1283,共9页
In this work, Staphylococcus epidermidis (S. epidermidis) was used to prepare the fermentation broths with antioxidant activity. Through the optimization of the carbon source, three kinds of S. epidermidis fermentatio... In this work, Staphylococcus epidermidis (S. epidermidis) was used to prepare the fermentation broths with antioxidant activity. Through the optimization of the carbon source, three kinds of S. epidermidis fermentation broth were obtained and designated as SFB, Gly-SFB, and Glu-SFB, which were cultivated in beef protein medium and the beef protein medium supplemented with glycerol or glucose, respectively. The differences in antioxidant efficacy of SFB, Gly-SFB and Glu-SFB were investigated by evaluating intracellular ROS fluorescence intensity, SOD enzyme activity and MDA concentration. Gly-SFB and Glu-SFB exhibited a greater capacity to eliminate ROS as compared to that of SFB. The intracellular SOD enzyme activity increased as the concentrations of SFB and Gly-SFB increased. Nevertheless, the intracellular SOD enzyme activity was the highest after the treatment with Glu-SFB at the low concentrations. The intracellular MDA content reached a lower value after the treatment with Gly-SFB and Glu-SFB at lower concentrations, which was opposite to the case after the treatment with SFB. WB indicated that the S. epidermidis fermentation broth regulated the expression of relevant proteins in the Nrf2-Keap1 signaling pathway to exhibit the antioxidant effects. This indicates that the S. epidermidis fermentation broth promotes the expression of relevant proteins in the Nrf2-Keap1 signaling pathway, consequently, antioxidant benefits were exerted. The fermentation broth that were prepared by incorporating glycerol or glucose into the culture medium can augment their antioxidant activity. 展开更多
关键词 S.epidermidis fermentation broth ANTIOXIDANT Western Blotting
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Evogene子公司发现一系列针对小麦叶枯病的新型杀菌化合物
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《农药》 北大核心 2025年第3期210-210,共1页
近日,Evogene子公司AgPlenus宣布,成功发现一种针对小麦叶枯病(Septoria tritici blotch, STB)的病原菌——Zymoseptoria tritici的新型作用机制。通过大规模化合物库的虚拟筛选和试验测试,该公司已鉴定出一系列具有杀菌活性的化合物,... 近日,Evogene子公司AgPlenus宣布,成功发现一种针对小麦叶枯病(Septoria tritici blotch, STB)的病原菌——Zymoseptoria tritici的新型作用机制。通过大规模化合物库的虚拟筛选和试验测试,该公司已鉴定出一系列具有杀菌活性的化合物,这些化合物能够有效抑制真菌生长。 展开更多
关键词 虚拟筛选 化合物库 杀菌活性 BLOT 有效抑制 病原菌 子公司
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Photosystem Development in Dark-grown Lotus (Nelumbo nucifera) Seedlings 被引量:5
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作者 季宏伟 唐崇钦 +1 位作者 李良璧 匡廷云 《Acta Botanica Sinica》 CSCD 2001年第11期1129-1133,共5页
It is well known that no chlorophyll synthesis and photosystem biogenesis have been detected in dark-grown angiosperm seedlings. However, in this report, we showed that both PS II and PS I could be formed in dark-grow... It is well known that no chlorophyll synthesis and photosystem biogenesis have been detected in dark-grown angiosperm seedlings. However, in this report, we showed that both PS II and PS I could be formed in dark-grown lotus (Nelumbo nucifera Gaertn.) seedlings. Lots of evidence were given: First I during the dark-grown period, the single fluorescence emission peak at 679 nm in lotus embryo red-shifted and transformed into the normal PS II fluorescence emission; Simultaneously, PS I fluorescence emission at 730 nm appeared and increased obviously; Second, with partial denaturing SDS-PAGE method, PS I chlorophyll-protein complex could be clearly separated from 10 days dark-grown lotus seedlings; Third, the existence of Lhca1 was also proved by Western blots. Moreover, measurements of electron transfer rate demonstrated that both PS II and PS I core in dark-grown lotus seedlings were photochemically active. 展开更多
关键词 LOTUS photosystem development dark-grown Western blots
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Reverse-normal immunopurification:An effective approach for purifying recombinant erythropoietin from its analogues in doping analysis
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作者 Sen He Die Wu +7 位作者 Chengshuai Niu Xinchao Liu Jie Zhang Liangzhi Xie Laurent Martin Kaifeng Liu Xinmiao Zhou Lisi Zhang 《Journal of Sport and Health Science》 2025年第6期107-116,共10页
Background Recombinant erythropoietin(rEPO)is commonly used in therapy but may be abused in sports to enhance endurance.In doping analysis,rEPO can be detected in human urine or blood samples at picogram(pg)levels bas... Background Recombinant erythropoietin(rEPO)is commonly used in therapy but may be abused in sports to enhance endurance.In doping analysis,rEPO can be detected in human urine or blood samples at picogram(pg)levels based on its slightly higher molecular weight(MW)than that of endogenous EPO using western blotting(WB).However,a type of variant erythropoietin(VAR-EPO)encoded by the EPO c.577del variant has a similar MW to rEPO,and these 2 molecules cannot be distinguished using conventional analytical methods.A fit-for-purpose method needs to be developed immediately.Methods In this study,we introduced a reverse–normal immunopurification technique for sample pretreatment to remove VAR-EPO from samples to eliminate its interference with rEPO detection.Firstly,a rabbit monoclonal antibody(mAb)that can specifically recognize trace amounts of VAR-EPO with high affinity was generated.Then,using this antibody to enrich VAR-EPO,we developed reverse–normal immunopurification coupled with WB on the purpose of analyzing rEPO in urine and serum samples.Next,the method was fully validated and evaluated using blank samples,spiked samples and rEPO excreted samples.Finally,the identification criteria of rEPO was established.Results A specific anti-VAR mAb with high affinity was developed.Using it,we developed the doping analytical method for rEPO.Our method effectively detects and removes VAR-EPO,enabling accurate rEPO detection.Conclusion A method has already been applied for rEPO confirmation in routine doping analyses. 展开更多
关键词 ERYTHROPOIETIN Doping analysis IMMUNOPURIFICATION Western blotting
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Identification and molecular docking mechanism of novel anti-inflammatory peptides from Lactobacillus paraplantarum fermented Cannabis sativa L.(hemp)seeds
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作者 Lingyue Shan Akanksha Tyagi +1 位作者 Hun Ju Ham Deog Hwan Oh 《Food Science and Human Wellness》 2025年第7期2656-2667,共12页
The inflammatory response is a crucial physiological process that can lead to tissue damage and is considered a causative factor for various chronic diseases,such as rheumatoid arthritis.Recent research has focused on... The inflammatory response is a crucial physiological process that can lead to tissue damage and is considered a causative factor for various chronic diseases,such as rheumatoid arthritis.Recent research has focused on exploring valuable nutrients derived from Cannabis sativa L.(hemp)seeds,particularly hemp seed proteins.Therefore,this study aimed to investigate the release of anti-inflammatory peptides from Lactobacillus paraplantarum-fermented hemp seed proteins.To confirm the complete hydrolysis of hemp seed proteins during the fermentation process,sodium dodecyl sulfate-polyacrylamide gel electrophoresis(SDS-PAGE)was employed.Further,the isolation and purification of peptides were achieved through ultrafiltration.The identity of peptides was nextly established using ultra-high performance liquid chromatography coupled with hybrid quadrupole time-of-flight mass spectrometry(UHPLC-QTOF-MS).The results revealed a total of 39 identified peptides in fermented hemp seeds,with 9 peptides selected based on their relative quantity.Notably,AAELIGVP(P1),AAVPYPQ(P2),VFPEVAP(P4),DVIGVPLG(P6),and PVPKVL(P9)demonstrated strong anti-inflammatory abilities in lipopolysaccharide(LPS)-induced RAW264.7 macrophage cells.Molecular docking was used to understand the potential anti-inflammatory mechanism of these 5 peptides,and in silico results indicated that P1,P2,P4,P6,and P9 could bind to the active sites of toll-like receptor 4(TLR-4),nuclear factor-κB(NF-κB),and inhibitor of NF-κB kinase(IKK)with higher binding energies.Overall,these findings indicate that hemp seeds have potential to be a source of bioactive peptides for functional foods with anti-inflammatory properties. 展开更多
关键词 Hemp seeds ANTI-INFLAMMATION UHPLC-QTOF-MS Western blotting Molecular docking
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