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IL-1 beta ELISA 试剂盒

This Colorimetric ELISA kit is designed for the quantitative measurement of 人 IL-1 beta.
产品编号 ABIN8090669
发货至: 中国
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Quick Overview for IL-1 beta ELISA 试剂盒 (ABIN8090669)

抗原

See all IL-1 beta (IL1B) ELISA试剂盒
IL-1 beta (IL1B) (Interleukin 1, beta (IL1B))

适用

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人

检测方法

Colorimetric

实验类型

Sandwich ELISA

检测范围

3.906 pg/mL - 250 pg/mL

应用范围

ELISA

样品类型

Cell Culture Supernatant, Cell Samples, Fecal, Plasma, Serum, Tissue Lysate

质量等级

Quick
  • 最低检测浓度

    3.906 pg/mL

    原理

    Human IL-1β (Interleukin 1 Beta) QuickTest ELISA Kit

    Analytical Method

    Quantitative

    特异性

    Specifically binds with IL-1β , no obvious cross reaction with other analogues. Recommended Sample Dilution Ratio The following table shows the recommended dilution ratios for this kit for a limited number of samples for your reference only. (When the sample content is very low, the original solution can be added without dilution, but it is necessary to ensure that the pH is between 6.8 and 8.0, and it does not contain more than 10 % organic solvents or high-concentration protein denaturants.) 1. Common sample validation: Sample Type Recommended Dilution Ratio Content Healthy serum (n=18) undiluted 0-6.5pg/mL Healthy plasma (EDTA, Citrate , heparin) (n=16) 1/2 dilution ND-7.2pg/mL Human peripheral blood lymphocyte were cultured with 10 %FBS + 1640 + double antibody, and the cell culture supernatant was detected after 12 hours. undiluted ND Human peripheral blood lymphocyte were cultured with 10 %FBS + 1640 + double antibody+1 μg/mL PHA, and the cell culture supernatant was detected after 12 hours. 1/10-1/20 dilution 4011 pg/mL THP-1 cells were cultured with 5 %FBS + 1640 + double antibody+1 μg/mL LPS, and the cell culture supernatant was detected after 12 hours. 1/5 dilution 1235pg/mL 2. KO sample validation (Detect IL-1β KO THP-1 cells): Sample Type Dilution Ratio Content Wild THP-1 cells were treated with 80nM TPA and cultured overnight, and then stimulated with 100 ng/mL LPS for 6 hours. The cell culture supernatant was taken for detection. 1/10 dilution 1196 pg/mL KO THP-1 cells were treated with 80nM TPA and cultured overnight, and then stimulated with 100 ng/mL LPS for 6 hours. The cell culture supernatant was taken for detection. undiluted ND KO THP-1 cells were treated with 80nM TPA and cultured overnight, and then stimulated with 100 ng/mL LPS for 6 hours. After that, 300 ng/mL Brefeldin A (BFA) was added and cultured for 3 hours. Add cell lysis buffer(Catalogue No.:E050), collect the lysate solution (total protein concentration measured by BCA assay: 1.66 mg/mL) to detect. undiluted ND Note:ND is lower than the sensitivity of the kit and was not detected 3. Capture antibody and detection antibody by WB KO validation (Detect IL-1β KO THP-1 cells):

    灵敏度

    2.344 pg/mL

    组件

    • ELISA Microplate(Dismountable)
    • Lyophilized Standard
    • Cap/Det Ab (Ready to use
    • Red)
    • TMB Substrate
    • Sample Dilution Buffer (blue)
    • Sample Dilution Buffer
    • Stop Solution
    • Plate Sealer
    • Product Description

    试剂未包括

    • Microplate reader (wavelength: 450nm)
    • 37 °C incubator (CO2 incubator for cell culture is not recommenced.)
    • Automated plate washer or multi-channel pipette/5 mL pipettor
    • Precision single (0.5-10μL
    • 5-50μL
    • 20-200μL
    • 200-1000μL) and multi-channel pipette with disposable tips(Calibration is required before use.)
    • Sterile tubes and Eppendorf tubes with disposable tips
    • Absorbent paper and loading slot
    • Deionized or distilled water
  • 应用备注

    Optimal working dilution should be determined by the investigator.

    说明

    Sandwich ELISA, Double Antibody

    样本量

    50 μL

    实验时间

    1.5 h

    板类型

    Pre-coated

    实验流程

    Step 1: Take out the required plate wells, add 50 µL Cap/Det Ab into each well, then add 50 µL Standard or Sample into individual well. (When adding standard or sample, the disposable tip lightly touches the liquid level. Change the disposable tips for different samples and standards.) Gently tap the plate for 10s to ensure thorough mixing then static incubate for 60 minutes at 37 °C. Washing: Wash the plate five times without immersion. Step 2: Add 90 µL TMB substrate solution, seal the plate and static incubate for 10-20 minutes at 37 °C. (Accurate TMB visualization control is required.) Step 3: Add 50 µL stop solution. Read at 450nm immediately and calculate.

    限制

    仅限研究用
  • 注意事项

    Avoid direct light exposure to antibody solutions

    储存条件

    4 °C

    储存方法

    Store sealed Kit at 2-8° C. Do Not Cryopreserve. Store ELISA Microplate for 1 month at 2-8°C, Store for 12 month at -20°C. Put the leftover strips into a sealed foil bag with the desiccant

    有效期

    12 months
  • 抗原 See all IL-1 beta (IL1B) ELISA试剂盒

    IL-1 beta (IL1B) (Interleukin 1, beta (IL1B))

    别名

    IL-1beta

    背景

    Interleukin-1 beta, IL-1 beta, Catabolin, IL1B, IL1F2

    UniProt

    P01584

    途径

    NF-kappaB Signaling, Interferon-gamma Pathway, TLR signaling, Negative Regulation of Hormone Secretion, Cellular Response to Molecule of Bacterial Origin, Carbohydrate Homeostasis, Glycosaminoglycan Metabolic Process, Myometrial Relaxation and Contraction, Regulation of Leukocyte Mediated Immunity, Positive Regulation of Immune Effector Process, Autophagy, Cancer Immune Checkpoints, Inflammasome
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