Application of AAT protein expressed by pulmonary alveolar lavage fluid of lung cancer patient
A technology for alveolar lavage fluid and patients, which is applied in the direction of material inspection products, measuring devices, instruments, etc., and can solve problems such as correlations to be evaluated
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Embodiment 1
[0010] Example 1 Alveolar lavage fluid collection
[0011] Patients were first under local anesthesia with 2% lidocaine, followed by bronchoscopy using a fiberoptic bronchoscope (OlympusExera BF 240). To prevent any possibility of blood contamination, flushing of biopsy or brush specimen collection is required. The diseased side bronchi were rinsed twice by 50 ml of sterile saline, then this solution was slowly placed in glass tubes and placed in ice water for rinsing. Recover 40ml of alveolar lavage fluid. Immediately after separation, the lavage fluid was spun at 1500g for 10 minutes, and then the supernatant was frozen at -80°C.
Embodiment 2
[0012] Example 2 Detection of AAT protein
[0013] The concentration of AAT in alveolar lavage fluid was detected by enzyme-linked immunosorbent assay kit. BALF samples were diluted 500-fold and incubated in ELISA plates. Optical density was measured at 450 nm with a model 680 microplate analyzer (BIO-RAD). Using the concentrations of standard samples and the corresponding optical density values, draw a standard curve for each plate. At the same time, positive and negative controls were used in the test to improve the validity of the method.
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