精氨酸酶(ARG)檢測試劑盒

適用生物 Homo sapiens (Human，人)
精氨酸酶(ARG)檢測試劑盒檢測范圍 3.13-200ng/mL 靈敏度 1.34ng/mL
樣本類型 Serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids.
實驗時長 4.5h 實驗方法 雙抗夾心法 精氨酸酶(ARG)檢測試劑盒規格 96T

ELISA Kit for Arginase (ARG)

FOR IN VITRO AND RESEARCH USE ONLY, NOT FOR USE IN CLINICAL DIAGNOSTIC PROCEDURES!

精氨酸酶(ARG)檢測試劑盒Specificity

This assay has high sensitivity and excellent specificity for detection of Arginase (ARG).
No significant cross-reactivity or interference between Arginase (ARG) and analogues was observed.

Recovery

Matrices listed below were spiked with certain level of recombinant Arginase (ARG) and the recovery rates were calculated by comparing the measured value to the expected amount of Arginase (ARG) in samples.

精氨酸酶(ARG)檢測試劑盒Precision

Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Arginase (ARG) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Arginase (ARG) 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 by testing samples spiked with appropriate concentration of Arginase (ARG) and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.

精氨酸酶(ARG)檢測試劑盒Stability

The stability of kit is determined 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

精氨酸酶(ARG)檢測試劑盒Assay procedure summary

1. Prepare all reagents, samples and standards;
2. Add 100μL standard or sample to each well. Incubate 2 hours at 37^oC;
3. Aspirate and add 100μL prepared Detection Reagent A. Incubate 1 hour at 37^oC;
4. Aspirate and wash 3 times;
5. Add 100μL prepared Detection Reagent B. Incubate 30 minutes at 37^oC;
6. Aspirate and wash 5 times;
7. Add 90μL Substrate Solution. Incubate 15-25 minutes at 37^oC;
8. Add 50μL Stop Solution. Read at 450nm immediay.

精氨酸酶(ARG)檢測試劑盒Test principle

The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Arginase (ARG). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Arginase (ARG). 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 contain Arginase (ARG), 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 Arginase (ARG) in the samples is then determined by comparing the O.D. of the samples to the standard curve.