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免疫球蛋白G(IgG)检测试剂盒
发布时间:2015-05-13   点击次数:447次

免疫球蛋白G(IgG)检测试剂盒

适用生物 Chicken (Gallus,鸡)
免疫球蛋白G(IgG)检测试剂盒检测范围 1.23-100ug/mL 灵敏度 0.48ug/mL
样本类型 Serum, plasma and other biological fluids.
实验时长 2.5h 实验方法 竞争抑制法 免疫球蛋白G(IgG)检测试剂盒规格 96T
ELISA Kit for Immunoglobulin G (IgG)
FOR IN VITRO AND RESEARCH USE ONLY, NOT FOR USE IN CLINICAL DIAGNOSTIC PROCEDURES!

Organism species Chicken (Gallus)
免疫球蛋白G(IgG)检测试剂盒Sample type Serum, plasma and other biological fluids.
Format 96-well strip plate
Assay length 2.5 hours
Detection range 1.23-100ug/mL The standard curve concentrations used for the ELISA’s were 100ug/mL, 33.33ug/mL, 11.11ug/mL, 3.7ug/mL, 1.23ug/mL
Sensitivity The minimum detectable dose of this kit is typically less than 0.48ug/mL.

Specificity
This assay has high sensitivity and excellent 免疫球蛋白G(IgG)检测试剂盒specificity for detection of Immunoglobulin G (IgG).
No significant cross-reactivity or interference between Immunoglobulin G (IgG) and analogues was observed.
Recovery
Matrices listed below were spiked with certain level of recombinant Immunoglobulin G (IgG) and the recovery rates were calculated by comparing the measured value to the expected amount of Immunoglobulin G (IgG) in samples.

Matrix Recovery range (%) Average(%)
serum(n=5) 97-105 101
EDTA plasma(n=5) 89-96 93
heparin plasma(n=5) 98-105 101

Precision
Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Immunoglobulin G (IgG) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 免疫球蛋白G(IgG)检测试剂盒3 samples with low, middle and high level Immunoglobulin G (IgG) 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 Immunoglobulin G (IgG) 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
serum(n=5) 85-94% 93-102% 88-104% 86-103%
EDTA plasma(n=5) 99-105% 97-105% 85-96% 81-98%
heparin plasma(n=5) 94-103% 81-98% 82-95% 91-99%

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免疫球蛋白G(IgG)检测试剂盒 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 50μL standard or sample to each well.
    And then add 50μL prepared Detection Reagent A immediay.
    Shake and mix. Incubate 1 hour at 37oC;
3. Aspirate and wash 3 times;
4. Add 100μL prepared Detection Reagent B. Incubate 30 minutes at 37oC;
5. Aspirate and wash 5 times;
6. Add 90μL Substrate Solution. Incubate 15-25 minutes at 37oC;
7. Add 50μL Stop Solution. Read at 450 nm immediay.
Test principle
This assay employs免疫球蛋白G(IgG)检测试剂盒 the competitive inhibition enzyme immunoassay technique. A monoclonal antibody specific to Immunoglobulin G (IgG) has been pre-coated onto a microplate. A competitive inhibition reaction is launched between biotin labeled Immunoglobulin G (IgG) and unlabeled Immunoglobulin G (IgG) (Standards or samples) with the pre-coated antibody specific to Immunoglobulin G (IgG). After incubation the unbound conjugate is washed off. Next, avidin conjugated to Horseradish Peroxidase免疫球蛋白G(IgG)检测试剂盒 (HRP) is added to each microplate well and incubated. The amount of bound HRP conjugate is reverse proportional to the concentration of Immunoglobulin G (IgG) in the sample. After addition of the substrate solution, the intensity of color developed is reverse proportional to the concentration of Immunoglobulin G (IgG) in the sample.

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