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Human TL1A-DR3 inhibition Kit (TR-FRET)

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货号-规格
价格
Qty.
FRT-02-100tests
¥6300.00
FRT-02-500tests
¥22050.00
FRT-02-10000tests (500tests X 20)
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合计0件 产品金额¥ 0

产品详情

  • 优势与特点(FAB)

    1. Cost effective - Sufficient quantity at a lower price, accounting for dilution and pipetting losses.
    2. Comprehensive validation - Validated with various antibody subtypes and antibody drugs.
    3. Simple and fast operation - No complicated washing steps, significantly reducing time.
    4. High batch consistency - Strict control over raw materials and finished product quality, ensuring a stable supply.
    5. Accurate and reliable results - High sensitivity with minimal matrix effects.
    6. High throughput capability - Supports 500 tests, ideal for high-throughput screening.
    7. Fast completion - Results in just 1 hour.
  • 产品参数(Product Specifications)

    Assay Type
    Inhibition-TR-FRET
    Analyte
    Anti-TL1A Neutralizing Antibody
    Format
    100T/500T
    Reactivity
    Human
    Regulatory Status
    RUO
    Sensitivity
    IC50=2.816nM
    Standard Curve Range
    0.1302 nM-66.6667 nM
    Assay Time
    1 hr
    Suitable Sample Type
    For screening assay of neutralizing antibodies binding to the human TL1A
    Sample volume
    10 μL

  • 产品概述(Product Overview)

    The Human TL1A-DR3 inhibition Kit (TR-FRET) is based on a homogeneous (no wash) competition TR-FRET technology (Time-Resolved Fluorescence Resonance Energy Transfer) to screening for inhibitors of human TL1A binding to human DR3 within 0.5-1 hours. It can also be used as a universal detection tool to identify the ability of TL1A to bind to human DR3.

  • 存储(Storage)

    1. Unopened kit should be stored at 2℃-8℃ upon receiving.

    2. Find the expiration date on the outside packaging and do not use reagents past their expiration date.

    3. The opened kit should be stored per components table. The shelf life is 30 days from the date of opening.

  • 组分(Materials Provided)

    ID
    Components
    Size
    FRT02-C01
    Human TL1A Protein Europium-chelate
    100 tests/500 tests
    FRT02-C02
    FA Labeled Human DR3 Protein
    100 tests/500 tests
    FRT02-C03
    Monoclonal Anti-TL1A Antibody, Human IgG1
    20 μg/100 tests 100 μg/500 tests
    FRT02-C04
    Sample Dilution Buffer
    10 mL/100tests & 500tests
    FRT02-C05
    Detection Buffer
    10 mL/100tests & 500tests

  • 原理(Assay Principles)

    This Human TL1A-DR3 inhibition kit (TR-FRET) is based on TR-FRET technology (Time-Resolved Fluorescence Resonance Energy Transfer). Use a mixture of biotinylated human TL1A and Europium-chelate labeled streptavidin as the donor and FA labeled human DR3 protein as the acceptor.

    - In the absence of inhibitors for human TL1A binding to human DR3, the donor and acceptor are in close proximity due to the binding of human TL1A and FA-labeled human DR3. Upon excitation with a specific light source, the donor emits a 620 nm signal, which is absorbed by the acceptor, resulting in a 665 nm emission.

    - In the presence of inhibitors that block the binding of human TL1A to human DR3, the donor-acceptor interaction is disrupted, preventing FRET from occurring.

  • 质量管理控制体系(QMS)

    1. 质量管理体系(ISO, GMP)
    2. 质量优势
    3. 质控流程

数据展示

  • 活性(Bioactivity)-TR-FRET

    Please refer to DS document for the assay protocol.

     TL1A-DR3 TR-FRET

    Inhibition of Europium-chelate labeled human TL1A: FA labeled human DR3 binding by Human Anti-TL1A Neutralizing Antibody
    Premix serial dilutions of Human Anti-TL1A Neutralizing Antibody (1:2 serial dilution, from 10 μg/mL to 0.01953125 μg/mL (66.6667-0.1302 nM)) and Human TL1A Protein Europium-chelate and incubate at room temperature (20℃-25℃) for 0.5 hours. Then add FA Labeled Human DR3 Protein and incubate at room temperature (20℃-25℃) for 0.5 hours. Detection was performed with IC50 of 2.816nM. The assay was performed according to the above-described Datasheet (QC tested).

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背景介绍

The TL1A protein, belongs to the tumor necrosis factor (TNF) family and is a receptor for TNFRSF25 and TNFRSF6B. TL1A is involved in the activation of NF-κB and C-Jun pathways, which can be used as a regulator of mucosal immunity and participate in the immune pathway of inflammatory bowel disease (IBD) pathogenesis.

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