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- 详细信息
- 文献和实验
- 技术资料
- 库存:
100
- 供应商:
远慕生物
- 检测范围:
科研实验
- 检测方法:
双抗体夹心酶联免疫法(ELISA)
- 样本:
血液、尿,粪便,脑脊液,胸腹水,前列腺液,精液,阴道分泌物等
- 规格:
96T/48T
人纤维介素蛋白(fgl2)ELISA试剂盒说明书
上海远慕生物做实验试剂,专业供应Elisa试剂盒、生物试剂、生化试剂、抗体、培养基、标准品|对照品等科研试剂!欢迎来电咨询订购:Elisa试剂盒现货低价!特价促销!
Human Fibrinogen like peptide 2,fgl2 ELISA Kit
产品货号:YM-KJ1121
规格:96T/48T
欢迎来电咨询订购:Elisa试剂盒,人纤维介素蛋白(fgl2)ELISA检测试剂盒
Kit composition:
Closure plate membrane: 2 (48) /2 (96)
Instruction: 1
Sealed bag: 1
Standard product: 0.5ml 2700ng/L * 1 0.5ml * 1 2-8
Enzyme labeled plate: 1 * 481 * 96 * 2-8
Sample dilution: 3ml * 1 ml * 1 2-8
Color reagent A solution: 3ml * 6 ml * 1 2-8
Color reagent B solution: 3ml * 6 ml * 1 2-8
Termination liquid: 3ml * 1 6ml * 1 2-8
Concentrated washing liquid: (20ml * 20) x 1 (20ml * 30) x 1 2-8
Objective: this kit is used to determine the content of serum, plasma and related liquid samples.
Operation steps:
Dilution and addition of 1 standard products:
2 samples: respectively, the blank hole (blank control hole without the sample and the enzyme label, and the remaining steps are the same), the sample hole.
3 temperature Education: 37 minutes after the closure of the sealing plate with a sealing plate.
4 with liquid: 30 (48T 20 times) the concentrated detergent liquid with distilled water 20 (48T 30 times) after dilution.
5. Washing: be careful torn off the seal plate membrane, discard liquid, drying, washing liquid to fill each hole, standing for 30 seconds after the discard, repeat 5 times, pat dry.
6 enzyme: 50 L per hole, except for the blank. 7 Wen Yu: operation with 3.
8 washing: operation with 5.
9 Color: first add color agent A50 L, and then add color B50 L, gently shake the mixture, 37 to 15 minutes.
10 termination: 50 L per hole with the end of the end of the reaction (at this time, blue).
11: Determination of the blank absorbance wavelength of 450nm zero air conditioning, in order to measure the hole (OD). Determination should be carried out within 15 minutes after the termination of the liquid.
人纤维介素蛋白(fgl2)ELISA试剂盒 试剂盒性能:
1.样品线性回归与预期浓度相关系数R值为0.95以上。
2.批内与批见应分别小于9%和11%
检测范围:
0.2IU/L - 6IU/L
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文献和实验膜淋巴结。脾和淋巴结通过血液尼龙过滤网挤压除去组织碎片并产生单个细胞悬浮。低渗休克法除去脾红细胞。细胞悬浮于RPMI-1640(加了FCS、HEPES、L-谷氨酰胺、丙酮酸钠……)。细胞接在96孔的平板中,每孔50万细胞和200uL培养基,或加5ug TAg 或加10ug的伴刀豆素蛋白A作为增殖的阳性对照。37度,5%CO2 孵育3天,最后18h时加入1uCi [3 H] thymidine。玻璃纤维过滤器收获细胞,合并入增殖细胞DNA的[3 H] thymidine用LSC检测。增殖指数用刺激
. 膜用丽春红染色,胶用考马斯亮蓝染色 14. Westernblot 试剂 盒显色 15. 分析比较记录 western blot的实验步骤及注意事项的资料 1. 把聚丙烯酰胺凝胶中的蛋白质电泳转移到硝酸纤维膜上。 1)转移缓冲液洗涤凝胶和硝酸纤维素膜,将硝酸纤维素膜铺在凝胶上,用5ml移液管在凝胶上来回滚动去除所有的气泡。 2)在凝胶/滤膜
6. 上清液为细胞裂解液可分装-20 ℃保存 7. 进行Bradford比色法测定蛋白质浓度 8. 取相同质量的细胞裂解液(体积*蛋白质浓度),并加等体积的2×电泳加样缓冲液 9. 沸水浴中3分钟 10. 上样 11. 电泳(浓缩胶20 mA,分离胶35 mA) 12. 电转膜仪转膜(100 mA 40分钟) 13. 膜用丽春红染色,胶用考马斯亮蓝染色 14. Westernblot 试剂盒显色
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