脑源性神经营养因子(BDNF)检测试剂盒产品图

脑源性神经营养因子(BDNF)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
  • YBEA011Hu
  • 2026年05月29日
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    • 详细信息
    • 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 Homo sapiens (Human,人)
    脑源性神经营养因子(BDNF)检测试剂盒
    检测范围 0.156-10ng/mL 灵敏度 0.068ng/mL
    样本类型 Serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids
    实验时长 4.5h 实验方法 双抗夹心法
    规格 96T
    脑源性神经营养因子(BDNF)检测试剂盒
    ELISA Kit for Brain Derived Neurotrophic Factor (BDNF)
    FOR IN VITRO AND RESEARCH USE ONLY, NOT FOR USE IN CLINICAL DIAGNOSTIC PROCEDURES!
    Organism species Homo sapiens (Human)
    Product No. SEA011Hu
    Sample type Serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids
    Format 96T
    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 0.068ng/mL.
    Specificity
    脑源性神经营养因子(BDNF)检测试剂盒This assay has high sensitivity and excellent specificity for detection of Brain Derived Neurotrophic Factor (BDNF).
    No significant cross-reactivity or interference between Brain Derived Neurotrophic Factor (BDNF) and analogues was observed.
    Precision
    Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Brain Derived Neurotrophic Factor (BDNF) were tested 20 times on one plate, respectively.
    Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Brain Derived Neurotrophic Factor (BDNF) were tested on 3 different plates, 8 replicates in each plate.
    CV(%) = SD/meanX100
    Intra-Assay: CV<10%
    Inter-Assay: CV<12%
    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
    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
    脑源性神经营养因子(BDNF)检测试剂盒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 Brain Derived Neurotrophic Factor (BDNF). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Brain Derived Neurotrophic Factor (BDNF). 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 Brain Derived Neurotrophic Factor (BDNF), 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 Brain Derived Neurotrophic Factor (BDNF) in the samples is then determined by comparing the O.D. of the samples to the standard curve.

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