Cell viabilities were determined by

Cell viabilities were determined by 3-(4,5-dimethylthiazol)-2,5-diphenyl tetrazolium bromide (MTT; Sigma) assay. Briefly, 2.5 mg/ml of MTT in phosphate buffered saline was added to wells of 24-well plates and incubated at 37 C for 4 h, followed by theaddition of dimethyl sulfoxide (Duksan, Korea). The absorbance was measured at 570 nm. Absorbance readings were subtracted from the value of blank wells. Cell viabilities were calculated as a percentage of control absorbance.

結果 (繁體中文) 1:

測定;細胞活力，通過3-（4,5-二甲基）-2,5-二苯基溴化四唑（MTT Sigma公司）測定。簡言之，將2.5毫克/毫升的MTT在磷酸鹽緩衝鹽水被添加到24孔板的孔中，並在37℃4小時，隨後溫育
另外二甲基亞砜（Duksan，韓國）的。吸光度在570nm測定。吸光度讀數從空白孔的值中減去。細胞存活率計算為對照吸光度的百分比。

結果 (繁體中文) 2:

細胞活力由3-（4，5-二甲基硫二氮）-2，5-二苯四苯二甲苯溴化（MTT;西格瑪）測定。簡單地說，在24孔板的井中加入2.5mg/ml的MTT，在37°C下孵育4小時，然後
添加二甲基硫酸鹽（韓國杜克山）。吸光度測量在570nm。從空井值中減去吸收讀數。細胞vi值計算為控制吸收率的百分比。

結果 (繁體中文) 3:

用3-（4,5-二甲基噻唑）-2,5-二苯基四唑溴化銨（MTT；Sigma）法測定細胞活性。簡單地說，將2.5mg/ml的MTT在磷酸鹽緩衝液中加入24孔板的孔中，在37℃下孵育4h，然後
添加二甲基亞碸（Duksan，韓國）。在570nm處量測吸光度。從空白孔的值中减去吸光度讀數。計算細胞通過率作為對照吸光度的百分比。