产品介绍：
  6×DNA上样缓冲液（SDS）用于结合有大量蛋白的 DNA 样品的琼脂糖凝胶电泳。其中含有 1%SDS，SDS 可消除 DNA-蛋白质之间的相互作用，同时含有100mM EDTA，它可结合二价金属离子，抑制金属离子依赖的酶反应，从而保护DNA。6×DNA 上样缓冲液（SDS）含有两种示踪染料：溴酚蓝和二甲苯青 FF。在 1%琼脂糖凝胶电泳中，溴酚蓝可与~300bp 片段共同迁
移，二甲苯青 FF 可与~4000bp 片段共同迁移。
注意事项：
为了您的自身安全，使用试剂前，请做好防护，如穿实验服，戴手套等。
使用说明：
1. 在 37°C 下，使 6×DNA 上样缓冲液（SDS）融化；
2. 轻轻涡旋，确保溶液混合均匀；
3. 将 1 份 6×DNA 上样缓冲液（SDS）加到 5 份 DNA 样品中；
4. 充分混匀；
5. 上样后进行电泳。

Product Introduction:
6 × DNA loading buffer (SDS) is used for agarose gel electrophoresis of DNA samples with a large number of proteins. It contains 1% SDS, which can eliminate the interaction between DNA and proteins, and 100mM EDTA, which can bind to divalent metal ions, inhibit metal ion dependent enzyme reactions, and protect DNA. The 6 × DNA loading buffer (SDS) contains two tracer dyes: bromophenol blue and xylene blue FF. In 1% agarose gel electrophoresis, bromophenol blue could migrate with~300bp fragment, and xylene green FF could migrate with~4000bp fragment.
Precautions：
For your own safety, please take protective measures such as wearing lab coats and gloves before using the reagents.
Instructions for Use：
1. Melt 6 x DNA loading buffer (SDS) at 37°C;
2. Gently swirl to ensure even mixing of the solution;
3. Add 1 portion of 6 × DNA loading buffer (SDS) to 5 portions of DNA samples;
4. Mix thoroughly;
5. Perform electrophoresis after sample loading.