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PD-1 [Biotinylated] : PD-L1 Inhibitor Screening ELISA Assay Pair Matched Antibody Pair

ScA, ELISA 适用: 人 ScA, ELISA unconjugated
产品编号 ABIN2762507
$660.00
加上运输费 $45.00
96 tests ABIN2762507
96 tests ABIN2762507
local_shipping 发货至: 美国
2至3个工作日
  • 抗原
    适用
    检测方法
    Colorimetric
    实验类型
    Sandwich ELISA
    检测范围
    0.01875-0.3 μg/mL
    最低检测浓度
    0.01875 μg/mL
    应用范围
    Screening Assay (ScA), ELISA
    原理
    This inhibitor screening ELISA pair is designed to facilitate the identification and characterization of new PD-1 pathway inhibitors.
    品牌
    MABSol®
    产品特性
    • This pair is useful for screening for inhibitors of human PD-1 binding to human PD-L1.
    • By employing the pre-labeled PD-1 protein, we eliminate the often time-consuming labeling process, and greatly simplify the experimental procedures.
    • Both biotinylated PD-1 and PD-L1 proteins are expressed in the HEK293 cells. The use of human cells as expression host confers authentic post-translational modifications essential for their binding activities.
    • We include anti-PD1 neutralizing mAb as a standard positive control. This would allow the users to validate their experiments.
    • Our biotin labeling platform produces biotinylated proteins with high detection sensitivity and minimal lot-to-lot variation. These features ensure that the assay kit has desired detection sensitivity and the results are reproducible.
    组件
    - Human PD-L1
    - Human PD-1-Biotin
    - Streptavidin-HRP
    - Anti-PD-1 Neutralizing Antibody
    试剂未包括
    - Coating Buffer: PBS (Phosphate Buffered Saline), pH 7.4, 12 mL is sufficient for 96 tests.
    - Wash Buffer: PBS with 0.05 % (v/v) Tween-20, 500 mL is sufficient for 96 tests.
    - Blocking Buffer: Wash Buffer with 2 % (w/v) bovine serum albumin, 35 mL is sufficient for 96 tests.
    - Dilution Buffer: Wash Buffer with 0.5 % (w/v) bovine serum albumin, 50 mL is sufficient for 96 tests.
    - Substrate Stock: Solution 10 mg/mL TMB in Dimethyl sulfoxide, 1 mL is sufficient for 96 tests. Protect from light.
    - Substrate Dilution Buffer: 50 mM disodium hydrogen phosphate (Na2HPO4) and 25 mM citric acid, adjust pH to 5.5 with 1 M Sodium hydroxide (NaOH), 25 mL is sufficient for 96 tests.
    - TMB Substrate Working Solution:
    For each plate dilute 250 μL substrate stock solution in 25 mL substrate dilution buffer and add 12 μL 5 % H2O2 (pipette 10 μL 30 % H2O2 into 50 μL distilled water), mix well.
    Notes:
    1) The TMB Substrate Working Solution should be freshly prepared and used within 15 minutes.
    2) If you choose to use other commercially available ready-to-use TMB substrate solutions, you should follow the manufacturer's instruction
    - Stop Solution: 1 M sulfuric acid (aqueous), 6 mL is sufficient for 96 tests.
    - High binding surface 96-well microplate, clear flat bottom
    - Microplate sealing film
    - Pipettes and pipette tips
    - UV/Vis microplate spectrophotometer (absorbance 450nm, correction wavelength set to 600 nm).
  • 抗原
    背景
    Immune checkpoint pathway is a focal point of today's cancer research. PD-1 is one of the best characterized checkpoint proteins. The binding between PD-1 and its ligand PD-L1 suppresses T-cell activation and allows cancer cells to escape from body's immune surveillance. Therefore, the pharmaceutical inhibition of PD-1 or its ligand has been considered a promising strategy by many oncologists.
  • 应用备注
    This pair is useful for screening for inhibitors of human PD-1 binding to human PD-L1.
    说明

    METHOD VERIFICATION
    PD-1 [BIOTINYLATED]:PD-L1 BINDING IN THE ABSENCE OF INHIBITORS:
    Immobilized human PD-L1 protein at 2 μg/mL (100 μL/well) can bind human PD-1-Biotin with a linear range of 0.01875-0.3 μg/mL when detected by Streptavidin-HRP. Background was subtracted from data points before curve fitting.

    INHIBITION OF PD-1 [BIOTINYLATED] : PD-L1 BINDING BY ANTI-PD-1 NEUTRALIZING ANTIBODY
    Serial dilutions of anti-PD-1 neutralizing antibody (1:2 serial dilutions, from 10 μg/mL to 0.078 μg/mL) was added into PD-L1 : PD-1-Biotin binding reactions. The assay was performed according to the above described protocol. Background was subtracted from data points prior to log transformation and curve fitting.
    Preparation of Standard Serial Dilutions
    1) Pipette 480 μL Dilution Buffer into tube Std-1 and 150 μL Dilution Buffer into the remaining tubes (tube Std.-2 to tube Std.-8).
    2) Add 20 μL anti-PD-1 neutralizing antibody stock solution (250 μg/mL) to tube Std.-1 to make the final concentration 10 μg/mL. Mix well.
    3) To make a 1:2 serial dilutions, pipette 150 μL solution to the next tube as illustrated in Fig.3.
    IMPORTANT: Mix thoroughly at each step during the dilution process.

    样本量
    50 μL
    实验流程
    This assay employs a simple colorimetric ELISA platform, which measures the binding between immobilized human PD-L1 and in-house developed biotinylated PD-1 protein. This product is uniquely suitable for rapid high-throughput screening of putative PD-1 and PD-L1 inhibitors. Briefly, we provide you with a human PD-1-Biotin protein, a human PD-L1 protein, an anti-PD-1 neutralizing antibody (as method verified Std.), and Streptavidin-HRP reagent. Your experiment will include 4 simple steps:
    • Coat the plate with human PD-L1.
    • Add your molecule of interest to the tests.
    • Add human PD-1-Biotin to bind the coated human PD-L1.
    • Add Streptavidin-HRP followed by TMB or other colorimetric HRP substrate.
    Finally, the ability of your compound to inhibit PD-1 : PD-L1 binding will be determined by comparing OD readings among different experimental groups
    实验流程

    Your experiment will include 4 simple steps: a) Coat the plate with human PD-L1, b) add your molecule of interest to the reactions, c) add biotinylated human PD-1 to bind with PD-L1, and d) add Streptavidin-HRP followed by TMB or other colorimetric HRP substrate to measure the binding activities. The ability of your compound to inhibit PD-1 : PD-L1 binding will be determined by comparing OD readings among different experimental groups.

    限制
    仅限研究用
  • 状态
    Lyophilized
    溶解方式
    Reconstitute the provided lyophilized materials to stock solutions with PBS as recommended. Solubilize for 15 to 30 minutes at room temperature with occasional gentle mixing. Avoid vigorous shaking or vortexing. The reconstituted stock solutions should be stored at -80°C Avoid freeze-thaw cycles.
    储存条件
    -20 °C
    储存方法
    Room temperature (RT) for 1 month in lyophilized state. -20°C for 1 year in lyophilized state. -80°C for 2 months under sterile conditions after reconstitution.
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