Determine the necessary mass, volume, or concentration for preparing a solution.
100 ml 최소한의 기준선 간섭이 필요한 민감한 크로마토그래피 및 분석 워크플로우용.
Room temperature Normal 출고. 정확한 사양은 로트별 COA를 확인하세요.
SDS, COA, 데이터시트, 사양서를 다운로드할 수 있습니다. 로트별 COA는 로트 번호 조회를 통해 확인할 수 있습니다.
크로마토그래피, 유기 합성 및 교차 커플링 반응 분야의 동료 심사 논문 0편에서 인용되었습니다.
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.
위험성, 취급, 보관 및 규제 준수를 포괄하는 종합 문서.
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