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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
组织金属蛋白酶抑制因子1(TIMP1)检测试剂盒
检测范围 0.156-10ng/mL 灵敏度 0.056ng/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
组织金属蛋白酶抑制因子1(TIMP1)检测试剂盒
| Organism species | Homo sapiens (Human) |
| Product No. | SEA552Hu |
| Sample type | Serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids |
| Format | 96T |
| Assay length | 4.5 hours |
| Detection range | 0.156-10ng/mL The standard curve concentrations used for the ELISA’s were 10ng/mL, 5ng/mL, 2.5ng/mL, 1.25ng/mL, 0.625ng/mL, 0.313ng/mL, 0.156ng/mL |
| Sensitivity | The minimum detectable dose of this kit is typically less than 0.056ng/mL. |
No significant cross-reactivity or interference between Tissue Inhibitors Of Metalloproteinase 1 (TIMP1) and analogues was observed.
| Matrix | Recovery range (%) | Average(%) |
| serum(n=5) | 80-91 | 88 |
| EDTA plasma(n=5) | 88-96 | 91 |
| heparin plasma(n=5) | 90-97 | 94 |
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Tissue Inhibitors Of Metalloproteinase 1 (TIMP1) 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) | 89-96% | 81-99% | 91-105% | 80-101% |
| EDTA plasma(n=5) | 98-105% | 90-101% | 97-105% | 80-94% |
| heparin plasma(n=5) | 85-97% | 83-99% | 78-95% | 87-94% |
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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文献和实验颜色,有可能几十秒种就能显色。 5. PBS 的充分清洗。在 TUNEL 反应后和酶标反应后的清洗请严格遵守清洗条件,次数可增加到 5 次,以降低切片的非特异性着色。 6. 内源性 POD 的封闭。对于肝脏、肾脏等血细胞含量多的组织,可适当延长封闭时间和升高过氧化氢的浓度,可以达到较好的封闭效果,且不影响最终的特异性染色。 三、细胞通透的时间选择 1. 蛋白酶 k 的目的是通透细胞膜和核膜,从而使反应试剂能充分进入细胞核进行反应,提高阳性率。但浓度过高或孵育时间过长容易造成脱片,其作用类似
一、检测原理 Caspase (Cysteine-requiring Aspartate Protease)是在细胞凋亡过程中起重要作用的蛋白酶家族。Caspase在正常状态下以酶原的形式存在于胞浆中,没有活性;在细胞发生凋亡阶段,Caspase被激活,活化的Caspase可裂解相应的胞浆胞核底物,最终导致细胞凋亡。 Caspase分光光度法检测试剂盒的原理是将Caspase序列特异性的多肽偶联至黄色发光基团pNA (p-nitroaniline)。当该底物被活化的Caspase剪切后,黄色
类:· Serine proteases· Cysteine proteases· Aspartic acid proteases· Zinc metalloproteases图示:比色蛋白酶试验响应曲线。采用 Thermo Scientific Pierce 比色法蛋白酶检测试剂盒,通过与提供的胰蛋白酶标准品进行比较,测定 V-8 蛋白酶和颌下腺蛋白酶消化酪蛋白底物的活性。以上即为PTMs的概述(资料来自Thermo Fisher官网),欢迎留言评论
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