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- 详细信息
- 文献和实验
- 技术资料
- 库存:
1000
- 供应商:
上海钰博
- 检测范围:
见说明书
- 检测方法:
酶联免疫
- 应用:
科研
- 标记物:
见说明书
- 样本:
血清/组织/尿液
细胞间粘附分子1(ICAM1)检测试剂盒
检测范围 78.13-5000pg/mL 灵敏度 37pg/mL
样本类型 Serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids.
实验时长 4.5h 实验方法 双抗夹心法
规格 96T
细胞间粘附分子1(ICAM1)检测试剂盒
| Organism species | Homo sapiens (Human) |
| Product No. | SEA548Hu |
| Sample type | Serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids. |
| Format | 96T |
| Assay length | 4.5 hours |
| Detection range | 78.13-5000pg/mL The standard curve concentrations used for the ELISA’s were 5000pg/mL, 2500pg/mL, 1250pg/mL, 625pg/mL, 312.5pg/mL, 156.25pg/mL, 78.13pg/mL |
| Sensitivity | The minimum detectable dose of this kit is typically less than 37pg/mL. |
No significant cross-reactivity or interference between Intercellular Adhesion Molecule 1 (ICAM1) and analogues was observed.
| Matrix | Recovery range (%) | Average(%) |
| serum(n=5) | 90-104 | 96 |
| EDTA plasma(n=5) | 79-91 | 78 |
| heparin plasma(n=5) | 78-101 | 87 |
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Intercellular Adhesion Molecule 1 (ICAM1) were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%
| Sample | 1:2 | 1:4 | 1:8 | 1:16 |
| serum(n=5) | 94-105% | 98-105% | 94-102% | 84-95% |
| EDTA plasma(n=5) | 85-102% | 89-96% | 97-104% | 91-101% |
| heparin plasma(n=5) | 83-101% | 86-103% | 94-102% | 79-104% |
To minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.
| Reagents | Quantity | Reagents | Quantity |
| Pre-coated, ready to use 96-well strip plate | 1 | Plate sealer for 96 wells | 4 |
| Standard | 2 | Standard Diluent | 1×20mL |
| Detection Reagent A | 1×120µL | Assay Diluent A | 1×12mL |
| Detection Reagent B | 1×120µL | Assay Diluent B | 1×12mL |
| TMB Substrate | 1×9mL | Stop Solution | 1×6mL |
| Wash Buffer (30 × concentrate) | 1×20mL | Instruction manual | 1 |
2. Add 100µL standard or sample to each well. Incubate 2 hours at 37oC;
3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37oC;
4. Aspirate and wash 3 times;
5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37oC;
6. Aspirate and wash 5 times;
7. Add 90µL Substrate Solution. Incubate 15-25 minutes at 37oC;
8. Add 50µL Stop Solution. Read at 450nm immediately.
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文献和实验多样的,但它与在大脑小血管中隔离受感染的红细胞(iRBCs)有关。这导致微血管阻塞和到达组织的氧气不足。细胞粘附一些寄生虫起源的分子已经被证实与细胞粘附有关。它们被输出到iRBCs表面,聚集在称为结节的突起中,并与内皮细胞表面表达的粘附分子结合。这种结合被发现通过Rho激酶激活Rho激酶信号通路,Rho激酶是一个小的gtpase家族,充当分子开关。这种激活可以触发内皮细胞的变化,影响血脑屏障。一些研究表明,逆转细胞粘附的治疗可以挽救生命,包括使用单克隆抗体治疗阻断配体-受体相互作用。新方法来自大肠杆菌的蛋白毒素
上包含的基因可编码上述信号通路中的粘附分子、受体、配体、接头蛋白、调控因子、转录因子、激酶及下游效应蛋白。信号转导在免疫细胞激活、增殖、分化和凋亡中扮演了重要的角色,而这些生物学过程也与许多重要的病理及生理免疫反应有关,如:抗病毒反应、自身免疫、过敏症、炎症,及免疫缺陷。 基因列表(Functional Gene Grouping): AKT and PI3K Family Members and Their Regulators: AKT1, AKT2, AKT3, APPL, BTK
突起;(2)细胞表面具有丰富的有助于抗原提呈的分子,如持续、高水平的表达MHCⅠ类、Ⅱ类分子,共刺激分子CD80(B71)和CD86(B72),细胞粘附分子CD11a(LFA1),CD11c,CD50(ICAM2),CD54(ICAM1),CD58(LFA3)和CD102(ICAM2),以及淋巴细胞功能相关抗原LFA1、LFA3等。人血中的DC前体开始表达CD2,4,13,16,32,33,但随着成熟渐渐失去表达,而粘附分子、共刺激分子、MHC抗原随着成熟而表达增加[2]。活化后,特别是CD
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