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ELISA
病毒生产和病毒疫苗制备
天然疫苗和人工疫苗
Dynamic Flow A
Analysis of Ol
Detection of G
Measurement of 
DGK Assay
Carbohydrate-Specific&nb
Immunostaining Thin
分离人单核细胞和中性粒细胞-Purification of human mononuclear cells and neutrophi
[ 文章来源: | 文章作者: | 发布时间:2007-01-02|  字体: [ ]  

Purpose

Materials

  • 10ml 6% dextran + 7ml citrate/citric acid
    • Dextran: T500 --> 6g+100ml PBS
    • Citrate solution: 25g Na Citrate + 8g citric acid + 500 ml PBS
  • 43 ml blood
  • 12 ml RT Histopaque 1077
  • 18 ml cold H2O
  • 2 ml 10x PBS
  • M199 for HUVECs: 1L powder pocket M199 + 35g NaHCO3 + 25mM Hepes + 5 mM glutamine + 50 ug/ml Gentamycin.
  • 1M Hepes: 119.1 g Hepes + 500 ml dH2O.
  • Media A: 1X HBSS (10X:50ml) + 10 mM Hepes (1M: 5 ml) + 5 mM EDTA (0.5M: 5ml) + 2.5 % FBS (12.5 ml) in 500 ml.
  • Media B: RPMI1640 470 ml + Gent (1000X) 0.5 ml + Glutamine (100X) 5 ml + 5% FBS (25 ml)

Procedure

  1. Draw venous blood into 60 ml syringe with 10ml 6% dextran + 7 ml citrate/citric acid. Fill to 60 ml total (blood 43 ml).
  2. Mix and sediment 30 min at RT (white blood cells now with serum).
  3. Transfer serum/white blood cells to 50 ml tube, underlay 12 ml RT Histopaque 1077.
  4. Spin 2500 rpm/30min at RT.
To take mononuclear cells:
  1. Take off serum above band. (See attached figure, in preparation)
  2. Take mononuclear band + some Ficoll into two 15ml tubes.
  3. Add cold media A up to 15ml.
  4. Spin at 1800 rpm 4oC for 5min.
  5. Pool pellet into one 15ml tube and add cold media A.
  6. Wash cells three times (1400 rpm, 4oC, for 5 min) to remove platelets.
  7. Add media B and count cells.
To take neutrophils:
  1. Remove mononuclear band and serum with suction. (See attached figure, in preparation)
  2. Wash in PBS (or media A) to remove Histopaque (spin 1800 rpm/5 min at 4oC)
  3. Remove PBS (or media A) , add 18 ml cold H2O to lyse RBC, and add 2 ml 10x PBS.
  4. Spin 1400 rpm/5min at 4oC.
  5. Wash as needed, resuspend, and count cells.


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