Emfret-cDNA及合成纯化-试剂-生物在线
Emfret

Emfret

商家询价

产品名称: Emfret

英文名称: Emfret

产品编号: Emfret

产品价格: 0

产品产地: 德国

品牌商标: Emfret

更新时间: 2023-08-17T09:55:27

使用范围: null

上海信裕生物科技有限公司
  • 联系人 : 徐经理
  • 地址 : 上海市闵行莘庄工业区春东路508号A1-2F
  • 邮编 : 200612
  • 所在区域 : 上海
  • 电话 : 152****8802
  • 传真 : 021-37680378
  • 邮箱 : shxysw02@163.com

 

Emfret


德国Emfret公司专注心血管和血液系统研究用抗体研发和生产,供应的抗体包括清除血液中血小板、流式细胞术鉴定分析小鼠血小板表面糖蛋白,Emfret公司的抗体不仅适用于流失分析、WB检测,还可用于免疫组化/免疫荧光及免疫共沉淀检测。

 

Emfret  Technical Protocols

 Flow cytometric analysis of mouse platelet surface glycoproteins

           - Preparation of diluted or washed whole blood  

           - Preparation of washed mouse platelets  

           - Single-color analysis of platelet surface glycoprotein expression 

           - Two-color analysis of platelet activation

  Immunohistochemistry (with acetone-fixed frozen sections)

  Immunoprecipitation

  Immunoblot (Western Blot Analysis)

 


Emfret  Flow cytometric analysis of mouse platelet surface glycoproteins

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Buffers and reagents

Tris buffered saline/Heparin (TBS/Hep): 20 mM Tris/HCl; 137 mM NaCl; pH 7.3; containing 20 U/ml Heparin.

Phosphate buffered saline (PBS): 137 mM NaCl; 2.7 mM KCl; 1.5 mM KH2PO4; 8 mM Na2HPO4; pH 7.14.

Tyrode’s Buffer (modified): 134 mM NaCl; 0.34 mM Na2HPO4; 2.9 mM KCl; 12 mM NaHCO3; 20 mM Hepes; pH 7.0; 5 mM glucose; 0.35% (w/v) bovine serum albumin

Apyrase: 10 U/ml stock in H2Obidest (stored at -20°C)

Prostacyclin (Prostaglandin 2, PGI2): 1 mM stock in H2Obidest (stored at -20°C)

CaCl2: 1 M stock in H2Obidest

 

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Preparation of diluted or washed whole blood

  1. Take 50 µl blood with a heparinized glass capillary (e.g. ringcap) from the retro-orbital plexus into 1.5 ml tubes containing 200 µl of TBS/Heparin (20 U/ml).
  2. Dilute in 1 ml of Tyrode´s buffer and use for flow cytometric analysis. 
  3. To prepare washed blood, centrifuge the diluted blood at 900 x g for 5 min, remove the supernatant and resuspend the pellet in 1.25 ml Tyrode´s buffer.
  4. Add 1 mM CaCl2 directly before the start of the experiment.

Note: For thrombin-induced platelet activation, plasma has to be removed to prevent anti-thrombin activity

 

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Preparation of washed mouse platelets

The preparation of washed platelets is a more time consuming method, that requires a larger amount of blood, but yields a platelet preparation that can be used for several hours.

  1. Collect 0.5 - 1 ml blood with 1.5 cm glass capillaries from the retro-orbital plexus into a 1.5 ml tube containing 200 µl of TBS/Heparin (20 U/ml).
  2. Centrifuge the sample for 5 min at 500 x g and transfer the platelet rich plasma (PRP) into a new tube. For best recovery of platelets, take the complete white phase including some red blood cells.
  3. Centrifuge the platelet suspension for 8 min at 300 x g, and transfer the PRP without any red blood cells into a new tube.
  4. Add 0.5 µM prostacyclin (PGI2) and centrifuge at 1300 x g for 5 min.
  5. Resuspend the platelet pellet in 1 ml Tyrode’s buffer, add 0.02 U/ml apyrase and 0.5 µM prostacyclin, incubate for 5 min at 37°C, and centrifuge for 5 min at 1300 x g.
  6. Repeat step 5 and resuspend the platelet pellet in 0.5 ml Tyrode’s buffer, add 0.02 U/ml of apyrase and incubate for 30 min at 37°C.

 

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Single color analysis of platelet surface glycoproteins

  1. Combine 5 µl of specific or negative control antibodies and 25 µl diluted whole or washed blood in the assay tube and vortex mix for 1-2 seconds.
  2. Incubate for 15 min at room temperature.
  3. Stop reaction by addition of 400 µl PBS and analyze within 30 min.