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GLP-2 ELISA 试剂盒

大鼠 GLP-2 ELISA Kit, Colorimetric is an assay for quantification of 大鼠 GLP-2.
产品编号 ABIN956056
发货至: 中国
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Quick Overview for GLP-2 ELISA 试剂盒 (ABIN956056)

抗原

See all GLP-2 ELISA试剂盒
GLP-2 (Glucagon-like peptide 2 (GLP-2))

适用

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大鼠

检测方法

Colorimetric

实验类型

Competition ELISA

应用范围

ELISA
  • 原理

    The Rat GLP-2 (Glucagon-Like Peptide-2) EIA is for the quantitative determination of GLP-2 in rat serum or plasma.

    Analytical Method

    Quantitative

    特异性

    Does not cross-react with rat Glucagon and rat GLP-1 within the range of 300 pmol/mL.

    产品特性

    The proglucagon gene is expressed in both pancreatic A cells and intestinal L cells. Tissue-specific post-translational processing of proglucagon by the prohormone convertase produces the different proglucagon derived peptides (PGDPs ) in both pancreas and intestine. The most notable pancreatic PGDP is glucagon, whereas the L cells produce several structurally related peptides, including glucagon-like peptide (GLP)-1 and GLP-2, as well as glicentin and oxyntomodulin, which contain glucagon sequence in their molecules. Among PGDPs, GLP-2 has recently been found to show intestinal epithelial proliferation. Advantages of this assay include sensitive quantification, high specificity and no interference from other body fluid factors or physiologically active substances. The Rat GLP-2 Calibrator is highly purified synthetic product.This EIA kit is based on a competitive enzyme immunoassay using a highly specific antibody to rat GLP-2 and a biotin/avidin-affinity system. The 96-well plate is coated with goat anti-rabbit IgG antibody. Rat GLP-2 Calibrator or samples, biotinylated rat GLP-2 and anti-rat GLP-2 polyclonal antibody antibody are added to the wells for a competitive immuno-reaction. After plate rinsing, HRP-labeled streptoavidins are added to bind to the antigen-antibody complex so that HRP-labeled streptoavidin-biotinylated rat GLP-2-antibody complexes are formed on the surface of the wells. Finally, excess HRP-labeled streptoavidins are rinsed, HRP-enzyme activity is determined, and the concentration of rat GLP-2 is calculated.

    组件

    1. Antibody-Coated Plate MTP: 1 plate (96-well) Goat Anti-rabbit IgG
    2. GLP-2 Calibrator Lyophilized: 1 vial (50 ng/vial) Synthetic rat GLP-2
    3. Labeled Antigen Lyophilized: 1 vial Biotinylated rat GLP-2
    4. GLP-2 Antibody Liquid: 1 bottle (6 mL) Rabbit anti-rat GLP-2
    5. SA-HRP Concentrate Liquid: 1 bottle (0.2 mL) HRP-labeled streptoavidin
    6. Diluent for SA-HRP Liquid: 1 bottle (12 mL) Phosphate buffer
    7. Substrate Buffer Liquid: 1 bottle (26 mL) 0.015% Hydrogen peroxide
    8. OPD Tablet: 2 tablets o-Phenylenediamine hydrochloride
    9. Stop Solution Liquid: 1 bottle (12 mL) 2 N H2SO4
    10. Buffer Solution Liquid: 1 bottle (35 mL) Phosphate buffer
    11. Wash Solution Liquid: 1 bottle (50 mL) Concentrated saline Concentrate 12. Plate Seal: 3 sheets

    试剂未包括

    Photometer for microtiter plate (plate reader), which can read absorbance up to 2.5 at 492 nm
    Rotator for microtiter plate
    Washing device for microtiter plate and dispenser for approximately 0.3 mL with aspiration system
    Micropipettes, multi-channel pipettes for 8 wells or 12 wells and their tips
    Test tubes for preparation of Calibrator Solution
    Graduated cylinder (1,000 mL)
    Distilled water or de-ionized water
  • 板类型

    Pre-coated

    试剂准备

    1. Preparation of Calibrator Solutions: Reconstitute the GLP-2 Calibrator (lyophilized rat GLP-2, 50 ng/vial) with 0.5 mL of Buffer Solution, giving a 100 ng/mL Calibrator Solution after reconstitution. 0.1 mL of the reconstituted Calibrator Solution is diluted with 0.2 mL of Buffer Solution to yield a 33.33 ng/mL Calibrator Solution. Repeat the serial dilution to make Calibrator Solutions at 11.11, 3.704, 1.235, 0.412 and 0.137 ng/mL. Buffer Solution is used as the zero calibrator (0 ng/mL). Note: Calibrator Solution must be prepared immediately before assay. Use clean test tubes or vessels.

      2. Preparation of Labeled Antigen: Reconstitute Labeled Antigen with 9 mL of Buffer Solution. Note: Labeled Antigen must be prepared immediately before assay. Use clean test tubes or vessels.

      3. Preparation of SA-HRP diluted solution: Add 0.12 mL of SA-HRP Concentrate to the bottle of SA-HRP Diluent (12 mL) and mix thoroughly. Note: SA-HRP solution must be prepared immediately before assay. Use clean test tubes or vessels.

      4. Preparation of Substrate Solution: Dissolve one OPD Tablet in 12 mL of Substrate Buffer. Note: Substrate Solution must be prepared immediately before assay. Use clean test tubes or vessels.

      5. Preparation of Wash Solution: Dilute 50 mL of Wash Solution Concentrate to 1,000 mL with distilled or de-ionized water. Diluted Wash Solution is stable for 6 months at 4°C. Note: During storage of the Wash Solution Concentrate at 4°C, precipitates may be observed, however, they will dissolve when diluted.
      6. Other reagents are ready for use.

    实验流程

    1. Warm the reagents and samples to room temperature (20-30°C) before beginning the test.
      2. Add 300 µL of Wash Solution into wells. Aspirate the Wash Solution in the wells. Repeat this washing procedure twice.
      3. Add 75 µL of Labeled Antigen solution into the wells. Then add 25 µL of the prepared Calibrator Solutions (0, 0.137, 0.412, 1.235, 3.704, 11.11, 33.33, 100 ng/mL) or samples. Next, add 50 µL of rat GLP-2 Antibody to the wells.
      4. Cover the plate with the Plate Seal and incubate at 4°C overnight (16 -18 hours).
      5. Remove the Plate Seal and aspirate the solution in the wells. Wash the wells three times with approximately 0.3 mL/well of Wash Solution.
      6. Pipette 100 µL of SA-HRP Solution into each of the wells.
      7. Cover the plate with a Plate Seal and incubate at room temperature for 1 hour. During the incubation, the plate should be rotated on a plate rotator.
      8. Remove the Plate Seal, aspirate and wash the wells five times with approximately 0.3 mL/well of Wash Solution.
      9. Add 100 µL of Substrate Solution into the wells, cover the plate with a Plate Seal and incubate for 30 minutes at room temperature.
      10. Add 100 µL of Stop Solution into the wells to stop the reaction.
      11. Read the optical absorbance of the wells at 490 nm. The optical absorbance of reaction solution in wells should be read as soon as possible after stopping the color reaction. Note: Perform all determinations in duplicate. During continuous rotation of test plate, the plate rotator may be heated. It is recommended to place polystyrene foam or plywood between the plate and the rotator.

    结果分析

    Calculate mean absorbance values of wells containing the Calibrators and plot a calibration curve on semilogarithmic graph paper (abscissa: concentration of Calibrators, ordinate: absorbance values of Calibrators). Use the calibration curve to read GLP-2 concentrations in samples from the corresponding absorbance values. When a sample value exceeds 100 ng/mL, it must be diluted with Buffer Solution and re-assayed until the sample value is within the assay range.

    限制

    仅限研究用
  • 储存条件

    4 °C
  • 抗原 See all GLP-2 ELISA试剂盒

    GLP-2 (Glucagon-like peptide 2 (GLP-2))

    别名

    GLP-2
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