細胞分離液分離后，核細胞中的血小板怎么去除？
更新時間：2010-12-14 點擊：1665
PBMC Separation from Whole Blood
HANK’S and LSM are stored in the 4°C glass door fridge.
1. Allow HANK’s and Lymphocyte Separation Media （LSM） to warm to
room temperature before using these solutions.
2. Take out one FCS （Fetal Calf Serum） tube for each sample from the -20°C
freezer and put on ice. Each tube contains 900μl of FCS. Perform the
following steps in the fume hood.
3. Invert Heparin blood tube gently to mix. Pour off blood into a 50ml
conical tube.
4. Add 15ml of HANK solution to blood and mix well together.
5. Mix LSM by inverting the bottle several times. Underlay blood with 8ml
of Lymphocyte separation solution, being careful not to disturb the layers.
6. Centrifuge at 2,100 RPM at room temperature for 20 minutes with the
brake off.
7. Transfer the PBMC’s （middle opaque layer） to a new 50 ml conical tube
that contains about 2ml of HANK’s solution （this prevents cell from
clumping）.
8. Add new HANK solution to the 50ml mark and mix well. Aliquot 10μl of
cells into a 0.5ml eppendorf tube for cell counting with Trypan Blue. Use a
dilution of 2:1 for cell counting, by adding 20μl of Trypan Blue to your
10μl of sample.
9. Centrifuge the tube at 1,200RPM for 10-12 minutes at room temperature
with brake on. Pour off supernatant and tap tube to resuspend cells.
10. Add 100μl of DMSO to each FCS aliquot and add this mixture to your
cells.
11. Aliquot your cells into a 1.8ml cryogenic vial.
12. Place into the cryogenic container and freeze in the -80°C freezer. You will
move these to the -140°C later.細胞分離液
HANK’S and LSM are stored in the 4°C glass door fridge.
1. Allow HANK’s and Lymphocyte Separation Media （LSM） to warm to
room temperature before using these solutions.
2. Take out one FCS （Fetal Calf Serum） tube for each sample from the -20°C
freezer and put on ice. Each tube contains 900μl of FCS. Perform the
following steps in the fume hood.
3. Invert Heparin blood tube gently to mix. Pour off blood into a 50ml
conical tube.
4. Add 15ml of HANK solution to blood and mix well together.
5. Mix LSM by inverting the bottle several times. Underlay blood with 8ml
of Lymphocyte separation solution, being careful not to disturb the layers.
6. Centrifuge at 2,100 RPM at room temperature for 20 minutes with the
brake off.
7. Transfer the PBMC’s （middle opaque layer） to a new 50 ml conical tube
that contains about 2ml of HANK’s solution （this prevents cell from
clumping）.
8. Add new HANK solution to the 50ml mark and mix well. Aliquot 10μl of
cells into a 0.5ml eppendorf tube for cell counting with Trypan Blue. Use a
dilution of 2:1 for cell counting, by adding 20μl of Trypan Blue to your
10μl of sample.
9. Centrifuge the tube at 1,200RPM for 10-12 minutes at room temperature
with brake on. Pour off supernatant and tap tube to resuspend cells.
10. Add 100μl of DMSO to each FCS aliquot and add this mixture to your
cells.
11. Aliquot your cells into a 1.8ml cryogenic vial.
12. Place into the cryogenic container and freeze in the -80°C freezer. You will
move these to the -140°C later.細胞分離液
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