仪器资讯
B-淋巴细胞激活抗原B7-2(LAB7-2)检测试剂盒
适用生物 Homo sapiens (Human，人)
检测范围 0.156-10ng/mL 灵敏度 0.062ng/mL
样本类型 Serum, plasma, tissue homogenates, cell lysates and other biological fluids.
实验时长 4.5h 实验方法 双抗夹心法 规格 96T
B-淋巴细胞激活抗原B7-2(LAB7-2)检测试剂盒
ELISA Kit for B-Lymphocyte Activation Antigen B7-2 (LAB7-2)
FOR IN VITRO AND RESEARCH USE ONLY, NOT FOR USE IN CLINICAL DIAGNOSTIC PROCEDURES!
Organism species Homo sapiens (Human)
Product No. SEA824Hu
Sample type Serum, plasma, tissue homogenates, cell lysates and other biological fluids.
Format 96-well strip plate
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 0.062ng/mL.
B-淋巴细胞激活抗原B7-2(LAB7-2)检测试剂盒 Specificity
This assay has high sensitivity and excellent specificity for detection of B-Lymphocyte Activation Antigen B7-2 (LAB7-2).
No significant cross-reactivity or interference between B-Lymphocyte Activation Antigen B7-2 (LAB7-2) and analogues was observed.
Recovery
Matrices listed below were spiked with certain level of recombinant B-Lymphocyte Activation Antigen B7-2 (LAB7-2) and the recovery rates were calculated by comparing the measured value to the expected amount of B-Lymphocyte Activation Antigen B7-2 (LAB7-2) in samples.
B-淋巴细胞激活抗原B7-2(LAB7-2)检测试剂盒
Matrix Recovery range (%) Average(%)
serum(n=5) 93-101 96
EDTA plasma(n=5) 78-90 82
heparin plasma(n=5) 90-104 98
Precision
Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level B-Lymphocyte Activation Antigen B7-2 (LAB7-2) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level B-Lymphocyte Activation Antigen B7-2 (LAB7-2) 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 B-Lymphocyte Activation Antigen B7-2 (LAB7-2) and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.
B-淋巴细胞激活抗原B7-2(LAB7-2)检测试剂盒
Sample 1:2 1:4 1:8 1:16
serum(n=5) 83-101% 97-105% 95-102% 80-94%
EDTA plasma(n=5) 87-94% 84-98% 99-105% 97-105%
heparin plasma(n=5) 93-101% 93-105% 92-101% 93-101%
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 首ld 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 immediately.
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 B-Lymphocyte Activation Antigen B7-2 (LAB7-2). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to B-Lymphocyte Activation Antigen B7-2 (LAB7-2). 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 B-Lymphocyte Activation Antigen B7-2 (LAB7-2), 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 B-Lymphocyte Activation Antigen B7-2 (LAB7-2) in the samples is then determined by comparing the O.D. of the samples to the standard curve.
