高遷移率族蛋白 1 (HMGB1) ELISA 試劑盒 | Cloud clone貨號SEA399Hu
ELISA Kit for High Mobility Group Protein 1 (HMGB1)
高遷移率族蛋白 1 (HMGB1) ELISA 試劑盒 (酶聯免疫吸附試驗法) | 貨號SEA399Hu,偵測的靈敏度62.5-4,000pg/mL、最低靈敏度28.3pg/mL。ELISA原理為利用抗體與抗原之間的高度專一性,做為定量標誌的方法;無論測量抗原或測量抗體都有很高的靈敏度跟專一性。Cloud-Clone corp提供高靈敏度之ELISA (酵素免疫分析套組/酶聯免疫吸附試驗法),專門生產研究用檢測試劑的生技公司,於美國研發和生產,產品線包括ELISA Kit、CLIA Kit、Antibody及recombinant protein;ELISA產品系列超過6000種以上,物種齊全包括rat、mouse、rabbit、cavia、human、porcine、bovine、simian等多物種商品。品質保證。ELISA商品的型式多元, 提供三明治ELISA、競爭型ELISA、高靈敏度設計ELISA。Uncoated ELISA型式;包括Capture Antibody, Detection Antibody、Standard、Streptavidin-HRP、TMB Substrate, 96-well Plate。
Specificity
This assay has high sensitivity and excellent specificity for detection of High Mobility Group Protein 1 (HMGB1).
No significant cross-reactivity or interference between High Mobility Group Protein 1 (HMGB1) and analogues was observed.
Recovery
Matrices listed below were spiked with certain level of recombinant High Mobility Group Protein 1 (HMGB1) and the recovery rates were calculated by comparing the measured value to the expected amount of High Mobility Group Protein 1 (HMGB1) in samples.
Matrix | Recovery range (%) | Average(%) |
serum(n=5) | 96-105 | 101 |
EDTA plasma(n=5) | 81-95 | 89 |
heparin plasma(n=5) | 79-90 | 84 |
Reagents and materials provided
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 |
Assay procedure summary
- Prepare all reagents, samples and standards;
2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;
3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;
4. Aspirate and wash 3 times;
5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;
6. Aspirate and wash 5 times;
7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;
8. Add 50µL Stop Solution. Read at 450nm immediately.
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