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          • 2654 Trabecular cell monolayer culture 2011-9-2
            Trabecular cell monolayer cultureOriginally described in 1979 and more recently modified by Stamer et al primary trabecular monolayer cell culture has been a cornerstone for inves

          • 2430 Isolation of rodent pancreatic β cells 2011-8-1
            Isolation of rodent pancreatic β cells 1.Adult rats weighing 250-350g were anesthetized, sacrificed and immediately used for pancreas sampling.2.Rat islets were isolated from mal

          • 2500 Culture of human renal proximal tubule cells and renal cortical fibroblasts 2011-7-11
            Culture of human renal proximal tubule cells and renal cortical fibroblasts 1.The method for primary culture of human renal proximal tubule cells (PTC) and renal cortical fibrobla

          • 2243 Isolation of human colonic epithelial cells (EC) 2011-6-21
            Isolation of human colonic epithelial cells (EC)1.Human colonic epithelial cells (EC) were isolated from freshly resected colonic surgical specimens obtained. 2.All diagnoses were

          • 2430 Primary brain cell isolation and culture 2011-6-13
            Primary brain cell isolation and culture. 1.Cerebella were removed from 7-day-old mice and passed through Nitex nylon netting (80 μm pore size) into primary cell system containin

          • 4069 xCELLigence系統實時監測低毒性X-tremeGENE DNA轉染實驗 2011-6-10
            xCELLigence系統實時監測低毒性X-tremeGENE DNA轉染實驗前言X-tremeGENE DNA Transfection Reagent是一種非脂質體、多組分轉染試劑,已被證明可有效轉染多種細胞。X-tremeGENE 9和X-tremeGENE H

          • 3289 滲透脅迫后擬南芥根表皮細胞膨壓恢復中離子吸收的作用 2011-5-6
            滲透脅迫后擬南芥根表皮細胞膨壓恢復中離子吸收的作用 注:滲透脅迫誘導的細胞膨壓和K+離子流的動力學變化。高滲處理導致膨壓快速下降,同時K+內流增加,膨壓在40min時恢復,K+內流減小。 提高

          • 2412 Measurement of primary endothelial cell permeability to fluxes of dextran or albumin 2011-4-1
            Measurement of primary endothelial cell permeability to fluxes of dextran or albuminThe fluxes of albumin or dextran across vascular endothelial cell (ECs) were evaluated using Tra

          • 15282 Isolation and Culture of Human Brain Tumor Stem Cell 2011-4-1
            Isolation and Culture of Human Brain Tumor Stem CellThe isolation, culture, identification, and purification of stem cells from primary human brain tumors of different phenotypes h

          • 2534 Identification and expansion of the tumorigenic lung cancer stem cell population 2011-4-1
            Identification and expansion of the tumorigenic lung cancer stem cell populationLung cancer contains a rare population of CD133+ cancer stem-like cells able to self-renew and gener

          • 2545 Isolation and Culture of Human Liver Stem Cells 2011-4-1
            Isolation and Culture of Human Liver Stem CellsMaterials and Methods1.Human hepatocytes were isolated from fresh surgical specimens of patients undergoing hepatectomies. Healthy li

          • 2291 FITC標記抗體-Marsshall氏法 2010-10-13
            FITC標記抗體-Marsshall氏法材料:抗體球蛋白溶液、0.5mol/L pH9.0碳酸鹽緩沖液、無菌生理鹽水、異硫氰酸熒光素、1%硫柳汞水溶液、三角燒瓶(25—50ml)、冰及冰槽(或1000ml燒杯)、電磁攪拌器

          • 4150 xCELLigence 系統內源性GPCRs 細胞功能研究 2010-10-11
            xCELLigence系統實時評測內源性G-偶聯蛋白受體(GPCRs)功能Jeff Irelan 美國圣地亞哥ACEA Biosciences 公司Jonathan H. Morgan 美國弗吉尼亞州Manassas ATCC 產品經理前言 G-偶聯蛋白受體(GPC

          • 3134 原代細胞骨架的染色方法 2010-10-11
            原代細胞骨架的染色方法微絲的顯示方法步驟:1. 用PBS液漂洗蓋片培養的原代細胞3次,每次30s;2. 用2%的甲醛/PBS液固定原代細胞3min;3. 用0.5%的三硝基甲苯/PBS處理3次,每次10min;4. PBS漂洗

          • 3035 原代細胞富爾根(Feulgen)反應顯示DNA 2010-10-11
            原代細胞富爾根(Feulgen)反應顯示DNA基本原理:顯示DNA的傳統方法是富爾根(Feulgen)反應,切片先用稀鹽酸處理,DNA經弱酸(1mol/L HCL)水解后,在60℃條件下使DNA分子中脫氧核糖與嘌呤之間

          • 6634 xCELLigence系統實時檢測神經毒性 2010-10-11
            xCELLigence系統持續檢測神經細胞培養Sebastian Diemert, Julia Grohm, Svenja,Tobaben, Amalia Dolga, Carsten Culmsee德國,馬爾堡大學,藥理學與臨床藥學研究所 摘要:為了研究類神經元細胞H

          • 2742 原代細胞DNA與RNA的吖啶橙熒光染色法 2010-10-9
            原代細胞DNA與RNA的吖啶橙熒光染色法基本原理:吖啶橙(acridine orange,AO)是一種常用熒光染料,吖啶橙與原代細胞內的DNA、RNA都有親和力,但有一定的特異性,即結合后發不同顏色的熒光,DNA

          • 2359 原代細胞甲基綠-哌咯寧法顯示DNA和RNA 2010-10-9
            原代細胞甲基綠-哌咯寧法顯示DNA和RNA基本原理:甲基綠(methyl green)和哌咯寧(pyronin)均為堿性染料,因此可與帶負電荷的磷酸根形成鹽。甲基綠分子有2個正電荷,易與雙鏈DNA分子結合使原代

          • 3454 原代細胞的脂類染色方法蘇丹紅Ⅲ染色法 2010-9-26
            原代細胞的脂類染色方法蘇丹紅Ⅲ染色法原理: 蘇丹紅染料在脂類物質中的溶解度大于其在溶劑中的溶解度,如果染料與含有脂類的試樣接觸,便有大量染料進入脂類物質的結構內,使這些結構呈紅色。多

          • 4348 蘇木精-伊紅(HE)染色 2010-9-26
            蘇木精-伊紅(HE)染色染液制備:1. 蘇木精染液(1) 稱取0.5g蘇木精、5.0g銨礬或鉀礬和0.1g碘酸鈉加溫溶于70ml蒸餾水中;(2) 加入30ml甘油和2ml冰乙酸充分混勻后過濾即成母液;(3) 母液可長

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