蛋白C(PROC)檢測試劑盒

適用生物 Homo sapiens (Human，人)
蛋白C(PROC)檢測試劑盒檢測范圍 62.5-4000pg/mL 靈敏度 24.8pg/mL
樣本類型 Plasma.
實(shí)驗(yàn)時(shí)長 4.5h 實(shí)驗(yàn)方法 雙抗夾心法 蛋白C(PROC)檢測試劑盒規(guī)格 96T
ELISA Kit for Protein C (PROC)
FOR IN VITRO AND RESEARCH USE ONLY, NOT FOR USE IN CLINICAL DIAGNOSTIC PROCEDURES!

Organism species Homo sapiens (Human)
Product No. SEA734Hu
Sample type Plasma.
Format 96-well strip plate
Assay length 4.5 hours
Detection range 62.5-4000pg/mL The standard curve concentrations used for the ELISA’s were 4000pg/mL, 2000pg/mL, 1000pg/mL, 500pg/mL, 250pg/mL, 125pg/mL, 62.5pg/mL
Sensitivity The minimum detectable dose of this kit is typically less than 24.8pg/mL.

Specificity
This assay has high sensitivity 蛋白C(PROC)檢測試劑盒and excellent specificity for detection of Protein C (PROC).
No significant cross-reactivity or interference between Protein C (PROC) and analogues was observed.
Recovery
Matrices listed below were spiked with certain level of recombinant Protein C (PROC) and the recovery rates were calculated by comparing the measured value to the expected amount of Protein C (PROC) in samples.

Matrix Recovery range (%) Average(%)
sodium citrate plasma(n=5) 95-102 98

Precision
Intra-assay Precision (Precision 蛋白C(PROC)檢測試劑盒within an assay): 3 samples with low, middle and high level Protein C (PROC) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Protein C (PROC) were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%
Linearity
The linearity of the kit was assayed 蛋白C(PROC)檢測試劑盒by testing samples spiked with appropriate concentration of Protein C (PROC) and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.

Sample 1:2 1:4 1:8 1:16
sodium citrate plasma(n=5) 95-104% 83-93% 79-88% 96-105%

Stability
The stability of kit is determined蛋白C(PROC)檢測試劑盒 by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.
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 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
1. Prepare all reagents, samples and standards;
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 immediay.
Test principle
The test principle applied in this蛋白C(PROC)檢測試劑盒 kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Protein C (PROC). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Protein C (PROC). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that 蛋白C(PROC)檢測試劑盒contain Protein C (PROC), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Protein C (PROC) in the samples is then determined by comparing the O.D. of the samples to the standard curve.