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- 详细信息
- 文献和实验
- 技术资料
- 库存:
99
- 供应商:
北京义翘神州科技股份有限公司
- 检测范围:
3.11
- 检测方法:
Solid Phase Sandwich ELISA
- 应用:
ELISA
- 适应物种:
Mouse
- 标记物:
见说明书
- 样本:
血清,细胞上清液
- 规格:
1 Kit (96 Tests)
反应种属:小鼠
试剂盒靶点:IL1A
试剂盒应用:ELISA
试剂盒保存:Unopened Kit: Store at 2 - 8℃
Opened/Reconstituted Reagents: Please refer to CoA
试剂盒介绍:For the quantitative determination of Mouse IL1A / IL-1A / IL-1F1 concentration in serum and cell culture supernates.
试剂盒线性范围:6.56-420
试剂盒包被抗体类型:rabbit mAb
试剂盒检测抗体类型:rabbit pAbKIT50114
试剂盒检测灵敏度:3.11
试剂盒天然样本检测量:The average concentration of Mouse IL1A in 10 normal mouse serum is 77.89 +/- 55.74 pg/mL ranging from 17.41 to 165.15 pg/mL. Mouse splenocytes (10E6 cells/mL) were cultured for 3 days in RPMI supplemented with 5% fetal bovine serum and stimulated with 5 ug/mL LPS. Aliquots of the cell culture supernates were removed and assayed for levels of natural mouse IL1A, and measured 8.11 pg/mL.
试剂盒特异性:This assay recognizes both recombinant and natural Mouse IL1A. The factors listed below were prepared at 50 ng/mL in dilution buffer and assayed for cross-reactivity. No cross-reactivity was observed.
试剂盒检测原理:Solid Phase Sandwich ELISA
试剂盒组成:1. 96 well microplate coated with Capture Antibody
2. Detection Antibody conjugated to HRP
3. Standards
4. Wash Buffer Concentrate
5. Dilution Buffer Concentrate
6. Color Reagent A
7. Color Reagent B
8. Stop Solution
试剂盒检测样品:血清,细胞上清液
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文献和实验人转录因子E2F1 ( E2F1 )ELISA 试剂盒 原理 本实验采用双抗体夹心 ABC-ELISA 法。用抗人 E2F1 单抗包被于酶标板上,标准品和样品中的 E2F1与单抗结合,加入生物素化的抗人 E2F1 ,形成免疫复合物连接在板上,辣根过氧化物酶标记的 Streptavidin 与生物素结合,加入底物工作液显蓝色,最后加终止液硫酸,在 450nm 处测 OD 值,E2F1 浓度与 OD 值成正比
A simple workflow allows the purification of high-quality DNA and RNA from the same sample (see flowchart). The 96-well purification plates of the kit are rapidly and conveniently processed using either a centrifuge (Centrifuge 4-15C and Plate Rotor 2 x 96
Notes on Making Rat x Y3 Monoclonal Antibody Producing Hybridomas
Although Y3/Ag1.2.3 has its own myeloma light chain, their are numerous characteristics that make this a better parent line for making hybridomas than the 'Y0' chain loss variants or using NS0 to make rat x mouse hybrids. These are: a) Hybridomas
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