Determine the necessary mass, volume, or concentration for preparing a solution.
100 ml ベースライン干渉を最小限に抑える必要がある、感度の高いクロマトグラフィーおよび分析ワークフロー向け。
Room temperature Normal に出荷。正確な仕様については、ロット固有の COA をご確認ください。
SDS、COA、データシート、仕様書をダウンロードできます。ロット固有の COA はロット番号検索で入手可能です。
クロマトグラフィー、有機合成、クロスカップリング反応に関する 0 件の査読済み論文で引用されています。
This product uses the principle that the concentration difference of salt ions inside and outside cells can cause cell membrane swelling to lyse red blood cells. It is mainly used for the removal of red blood cells in experiments, such as the separation and purification of lymphocytes, the separation and purification of dispersed tissue cells through enzyme digestion, and the removal of red blood cells in experiments such as tissue cell egg white and nucleic acid extraction.
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Instructions for use:
1. Add 3 times the volume of red blood cell lysate to 1 volume of fresh whole blood (such as 1 ml of fresh whole blood and 3 ml of red blood cell lysate), gently vortex or invert and mix well.
Attention: If fresh tissue cells are processed, they need to be digested into a single cell suspension by trypsin or other enzymes, and then centrifuged to collect the cells before proceeding with subsequent operations.
2. Incubate on ice for 15 minutes, gently vortex and mix twice during this time. Note: After red blood cell lysis, the solution should be clear and transparent.
Collect white blood cells by centrifugation at 3.4 ℃ and 450 × g for 10 minutes, and carefully discard the supernatant.
4. Add twice the volume of red blood cell lysate to the above precipitate, gently vortex and resuspend white blood cells (if the initial blood volume is 1 ml, add 2 ml of red blood cell lysate).
Collect white blood cells by centrifugation at 5.4 ℃ and 450 × g for 10 minutes, carefully and thoroughly aspirate the supernatant.
6. Resuspend cells for subsequent experiments. Note: If extracting RNA, it is best to start using a solution without RNase from this step.
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