- 更多网络例句与组蛋白抗体相关的网络例句 [注：此内容来源于网络，仅供参考]
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Dentritic cell and expression of agglutinin were studied in 87 cases of transitional cell bladder carcinoma by immunohistochemistry using 4 kinds of bio-agglutinin and anti-S-100 protein antibodies.
为探讨凝集素染色与树突细胞的关系，在膀胱癌发生、发展过程中的作用，选取二种凝集素和抗S-100蛋白抗体，对87例膀胱癌进行免疫组化染色。
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It was interesting that positive perc entage of the autoantibody against histone proteins was higher than that of autoantibody against ds-DNA or ss-DNA in the early stage of the chronic C.jejuni infection, too.
在慢性肠道感染早期小鼠抗组蛋白抗体的阳性率也高于抗ds-DNA和ss-DNA抗体。
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Results The patients in ACI group had a 38.07± 32.14 ku/L ox-LDL antibody level and in TIA group had a 25.18±9.17 ku/L ox-LDL antibody level. A significant difference as compared with the patients in the two group (P.05). The other biochemics index had no dependability in the two groups.
结果 急性脑梗死组血清氧化型低密度脂蛋白抗体为38.07±32.14 ku/L，短暂脑缺血组为25.18±9.17 ku/L，二组比较有显著性差异(P.05)；而与其它生物化学学指标无相关性。
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The study showed the recombinant wt/mCREG protein depressed the VSMC proliferation depending on dose and the optimal concentration was 400nM;2biologic function of CREG protein and the membrance receptor mechanism:①effect on VSMC migration: the wound healing experiment showed the OB2 cells migration was slower significantly after added wt/mCREG(400Nm) in supernatant. The HITASY cells migration were very slowly and no remarkable change. The gelatinase digestion and Western blot analysis showed the matrix metalloproteinase was decreased and TIMPs was increased;②effect on differentiation: after added wt/mCREG(400nM), the expression of myocardin, SMα-actin, MHC and caldesmin were increased and that of LM-1 and FN were decreased in OB2 cells. These effects were more significant when adding wtCREG.;③effect on VSMC proliferation: Cell cycle assay and BrDU stain showed: after added the wtCREG and mCREG protein, the ratio of cell in G0/G1 phase increased to 0.5773 and 0.5572 from 0.5308 respectively in OB2 group, which increased to 0.7369 and 0.7034 respectively from 0.6297 in HITASY group;3Role of M6P/IGF2R in CREG biologic function:①ELISA and co-immunoprecipitation showed the wt/mCREG binding to M6P/IGF2R directly.②antibody blocking test: when the anti-IGF2R was added to medium at the same time with wt/mCREG at different concentration(2μg/mL、4μg/mL、8μg/mL),the effects of CREG protein which depressing proliferation, migration, secretion and promoting differentiation were blocked, which had the positive correlation to the concentration of added anti body. The studies showed two combinant CREG promoted VSMC switch to differentiation phaenotype, at the same time, depress VSMC proliferation, migration and secreting extracellular matrix.
上述实验结果证实：两种重组CREG蛋白对VSMC增殖均有剂量依赖性的抑制作用，并且相同浓度的糖基化的CREG蛋白对细胞增殖的抑制效应更为显著，最佳效应浓度为400nM；2两种重组CREG蛋白添加后对HITASY和OB2细胞生物学行为的影响：①CREG蛋白对VSMC迁移的影响：刮伤实验发现，加入最佳效应浓度的wtCREG和mCREG蛋白24h后，OB2组迁移能力下降，HITASY组无明显变化；细胞外基质金属蛋白酶-2，9(Matrix metallo-proteinase 2，9，MMP2 ，9)明胶酶电泳检测和Western blot检测结果证实，两种CREG蛋白均可以使OB2细胞合成细胞外基质MMP2，9减少，而组织金属蛋白酶抑制物(Tissue Inhibitors of Metalloproteinases，TIMPs)增加；②CREG蛋白对VSMC分化的影响：加入400nM的wtCREG和mCREG蛋白12h后，OB2细胞myocardin、SMα-actin、MHC、caldesmin表达增加，LM-1、FN表达减少；③流式细胞仪分析细胞周期和BrDU染色分析证实，加入400nM的wtCREG和mCREG蛋白后，OB2组G0/G1期细胞由0.5308分别增加至0.5773和0.5572，HITASY组G0/G1期细胞由0.6297分别增加至0.7369和0.7034；3M6P/IGF2R在重组CREG蛋白的生物学功能中的调控作用：①免疫共沉淀和免疫荧光双染色分析结果显示，CREG蛋白与M6P/IGF2R存在直接结合；②应用抗体阻断实验：将不同浓度的anti- M6P/IGF2R(2、4、8μg /mL)与两种CREG蛋白同时加入培养液中，CREG蛋白抑制VSMC增值、迁移和合成细胞外基质、促进分化的效应减弱，而且与加入anti- M6P/IGF2R浓度正相关。
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We have cloned three novel histone genes using antibodies that recognize onlynuclei of the male gametic cells of Lilium longiflorum.
我们已克隆了3个新的组蛋白基因，利用抗体确认onlynuclei的雄性配子细胞的铁炮百合。
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We examined RPE by microscopic observation and immmunohistochemical analysis with antibodies against cytokeratin, an epithelial marker, and α-smooth muscle actin, a marker of myoid differentiation.
自成人供体眼获取RPE培养传代，显微镜下观察原代RPE的形态以及传代(3、9)RPE的去分化改变，免疫组化法(角蛋白抗体和平滑肌肌动蛋白抗体)检测传代后RPE免疫标记的改变。
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Methods Seral anti-P 53 antibody was detected with immuno-PCR.The expression of P 53 in tissue was detected with enzyme imunohisto-chemistry technique.
采用免疫PCR方法检测血清抗P 53 蛋白抗体，酶免疫组化方法检测组织P 53 蛋白表达。
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Objective To present a new serological method for diagnosis of breast cancer. Methods Seral anti-P 53 antibody was detected with immuno-PCR.The expression of P 53 in tissue was detected with enzyme imunohisto-chemistry technique.
目的 探讨乳腺癌患者P 53 蛋白及抗体表达情况方法采用免疫PCR方法检测血清抗P 53 蛋白抗体，酶免疫组化方法检测组织P 53 蛋白表达。
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The coverslip with differentiated cells were fixed at different timepoints and used for toludine blue or inmunohistochemical dying Meanwhile, different doses of antibody to Fibronectin were added to observe aggregating phenomenon.
用2，3传代细胞按一定比例种植于24孔板内，加入TGF-β1 1，5，10ng／mL，分别于不同时间点取材固定，用于甲苯胺兰组织学染色及抗纤维连接蛋白抗体免疫组化染色。
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As an adjuvant for the protein vaccine,PoIFN-αinduced strong inflammatory cytokine production in vivo and the results denoted that IFN-adjuvant and our vaccines could drive the immune response toward Th1 type responses.The data of ELISA suggests that the recombinant protein vaccine synergizes with the IFN-adjuvant to produce endogenous IFN in vivo.
在病毒攻击实验中，所有的对照组动物均出现口蹄疫临床症状；然而佐剂和疫苗联合注射组的动物均得到保护，没有发现病毒血症和口蹄部水疱，对该组的病毒非结构蛋白抗体检测表明，攻毒14天后没有发现病毒在动物体内复制。
- 更多网络解释与组蛋白抗体相关的网络解释 [注：此内容来源于网络，仅供参考]
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AFC：抗体形成细胞
还是MΦ组产生的抗体效价均较高于对照组.过继转移白蛋白时,DCs组产生抗体水平较MΦ组低;过继转移SRBC时,DCs组产生的抗体水平较MΦ组稍高, 但无统计学意义,而血清中的抗体水平与抗体形成细胞(AFC)水平发生分离.
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myosin：肌球蛋白
3.2 肌球蛋白(myosin) 肌球蛋白与肌动蛋白一样是构成肌纤维的基本蛋白,可以维持肌纤维的结构和功能. 肌球蛋白的免疫组化可说明肌纤维分化的类型,在石蜡包埋和冰冻肌组织中,通过抗肌球蛋白重链Ⅱ抗体可以鉴别Ⅱ型肌纤维[9].
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speckled：斑点
颗粒( particle) 型或斑点(speckled)型 此型相关抗体为抗UlnRNP、抗S队抗5cl-70 、抗5SB、抗SS-A 、抗Ki 、抗Ku 及抗其他非组蛋白的抗体. 最多见于MCTD ,且滴度甚高. 也见于SLE 和60%以上的PS5 患者.
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lamin：核层蛋白
此荧光染色型与抗核层蛋白(Lamin)抗体相关. 抗dsDNA抗体亦呈核膜型,或呈周边型. 须经过特殊处理才能鉴别. 免疫印迹法证明,抗核层蛋白分三型:LaminA、B、C,LaminA和C常见于自身免疫性肝炎;LaminB见于SLE. 英利昔单抗治疗组,
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AEC 3-amino-9-ethyl-carbazole：3-氨-9-乙基咔唑
ADH antidiuretic hormone 抗利尿激素 | AEC 3-amino-9-ethyl-carbazole 3-氨-9-乙基咔唑 | AHA anti-histone antibody 抗组蛋白抗体