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Amplite 比色法Bradford蛋白定量分析试剂盒
货号 | 11118 | 存储条件 | Multiple |
规格 | 1000 Tests | 价格 | 1200 |
Ex (nm) | Em (nm) | ||
分子量 | 溶剂 | ||
产品详细介绍 |
简要概述
传统的Bradford蛋白质检测法广泛用于定量蛋白质浓度。但是,许多市场的许多操作说明非常复杂繁琐。 我们的Amplite 比色法Braford蛋白定量检测试剂盒是一种用于测定总蛋白浓度的包含两组分且与洗涤剂兼容的测定方法。该检测法基于与Bradford蛋白质测定法相同的考马斯亮蓝G-250蛋白指示剂,并提供相当的准确性。我们专有的配方使我们的试剂盒更加方便快捷。在600 nm附近检测蛋白质信号,并在30分钟内完成测定。 Amplite 比色Braford蛋白定量分析试剂盒可以以方便的96孔板进行操作,无需分离步骤即可轻松实现自动化。
适用仪器
光吸收酶标仪 | |
吸收: | 595nm |
推荐孔板: | 透明底板 |
产品说明书
样品分析方案
概述
准备Bradford工作溶液(50μL)
添加BSA标准品或检测样品(50μL)
在室温下孵育5-15分钟
读取595 nm处的吸光度
注:使用前,请在室温下解冻所有试剂盒组分。
标准溶液制备:
BSA标准溶液:
将20 µL的1 mg / mL BSA标准溶液(组分C)添加到480 µL的PBS(未提供)中,以生成40 µg / mL的BSA标准溶液(BS1)。然后在PBS中执行1:2连续稀释,以得到连续稀释的BSA标准BS2-BS7。注意:有必要为每个测定创建标准曲线。
操作步骤
表1.在透明的底96孔板中布置BSA标准品和测试样品。 BS = BSA标准品(BS1-BS7,40至0.625 µg / mL); BL =空白控件; TS =测试样品
BS1 | BS1 | TS | TS |
BS2 | BS2 | … | … |
BS3 | BS3 | ||
BS4 | BS4 | ||
BS5 | BS5 | ||
BS6 | BS6 | ||
BS7 | BS7 | ||
BL | BL |
表2:每个孔的试剂
孔 | 溶液体积 | 试剂 |
BS1-BS7 | 50 µL | 系列稀释液(40-0.625 µg / mL) |
BL | 50 µL | PBS |
TS | 50 µL | 测试样品 |
1.根据表1和表2提供的布局准备BSA标准(BS),空白对照(BL)和检测样品(TS)。
2.向BSA标准品,空白对照和测试样品的每个孔中添加50 µL的Bradford工作溶液,以使总测定体积为100 µL /孔。
3.将反应在室温下孵育5至15分钟。
4.用酶标仪在OD 595 nm处读取吸光度。
图示
图1.使用透明底96孔板,使用Amplite 比色法Bradford蛋白定量分析试剂盒测量BSA剂量响应。
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