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免疫球蛋白G(IgG)检测试剂盒

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  • ¥900 - 1890
  • 钰博生物
  • 见说明书
  • 德国/美国/中国
  • 2025年07月15日
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    • 详细信息
    • 询价记录
    • 文献和实验
    • 技术资料
    • 库存

      1000

    • 供应商

      上海钰博

    • 检测范围

      见说明书

    • 检测方法

      酶联免疫

    • 应用

      科研

    • 标记物

      见说明书

    • 样本

      血清/组织/尿液

    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
    规格 96T
    免疫球蛋白G(IgG)检测试剂盒
    ELISA Kit for Immunoglobulin G (IgG)
    FOR IN VITRO AND RESEARCH USE ONLY, NOT FOR USE IN CLINICAL DIAGNOSTIC PROCEDURES!
    Organism species Chicken (Gallus)
    Product No. CEA544Ga
    Sample type Serum, plasma and other biological fluids.
    Format 96T
    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
    免疫球蛋白G(IgG)检测试剂盒This assay has high sensitivity and excellent 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): 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
    免疫球蛋白G(IgG)检测试剂盒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
    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 immediately.
    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 immediately.
    Test principle
    This assay employs 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 (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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    • 免疫球蛋白G(immunoglobulin GIgG

         是血清中免疫球蛋白主成分,约占血清中免疫球蛋白总含量的75%。其中40~50%分布于血清中,其余分布在组织中。分子量约为150000道尔顿。人类血清中的IgG主要为单体,正常人的IgG包括四个亚型,其IgG1 占60~70%,IgG2 占15~20%,IgG3 占5~10%,IgG4 占1~7%。这些亚型在补体激活的经典途中结合能力各不相同。IgG主要由脾脏和淋巴结中的浆细胞合成,是唯一能通过胎盘的抗体,对防止新生儿出生数周内的感染起很大作用。婴儿初生后第3个月已能合成

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