实验概要
1.目的 检测小分子蛋白抗体
2.适用范围 单克隆抗体和多克隆抗体
实验原理
将经电泳分离的抗原转印到膜上作为固相,利用酶标记的抗抗体以检测已与固相抗原结合的受检抗体
主要试剂
试剂配制
4.1.1 40% Bis-acrylamide with 2.6% C (Acrylamide:Bis, 38.95:1.05)
丙烯酰胺 77.9g
双甲叉丙烯酰胺 2.1g
Total 200ml
4.1.2 30%胶溶液:
0.8 双甲叉丙烯酰胺 0.8g
29.2% 丙烯酰胺 29.2g
total 100ml
4.1.3 3M TrisHCl , pH 8.45
36.3g Trisbase
Total 100ml
4.1.4 WG ( water Glycerol):
Water: 58ml
Glycerol: 36ml
Total: 94ml
4.1.5 10x Electrophoresis Buffer stock pH8.3 (to make the working buffer, just dilute 10 times. Do not adjust pH , pH should be 8.3.)
Trisbase 60.5g
Tricine 89.5g
SDS 5g
total 500ml
4.1.6 10% SDS
SDS 10g
Total 100ml
4.1.7 2x Laemmli Stacking Buffer pH6.8:
0.25M Tris 15.14g
0.2% SDS 1g or 5ml 20% SDS
total 500ml
4.1.8 5x Stop Solution (Sample buffer) pH6.7:
Stock: to use:
20% Glycerol 100ml take 9.5ml stock
10% SDS 50g or 250ml 20% SDS add BME 0.5ml
250mM Tris 15.14g bromphenol blue or
total 475.00ml pyronine 4 to taste
4.1.9 transfer buffer
48mM Tris base 5.81g
39mM Glycine 2.93g
0.037% SDS 0.375g or 1.875ml of 20% SDS
40% MeOH 400ml
total 1000ml
4.1.10 TBST
10mM Tris-HCl, pH7.4
100mM NaCl
0.2% Tween-20
Total 1000ml
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