- A micro ELISA plate --- The 96-well plate has been pre-coated with an anti-human zonulin antibody. This dismountable microplate can be divided into 12 x 8 strip plates.
- Two vials lyophilized standard --- Dilute a bottle of the standard at dilution series, read the OD values, and then draw a standard curve.
- Biotin-labeled zonulin antibody (100 x concentrate) 1 x 120 μl ---Act as the detection antibody.
- HRP-avidin (100 x concentrate) 1 x 120 μl --- Bind to the detection antibody and react with the TMB substrate to make the solution chromogenic.
- Biotin-antibody Diluent 1 x 15 ml ---Dilute the high concentration Biotin-antibody to an appropriate working solution.
- HRP-avidin Diluent 1 x 15 ml ---Dilute the high concentration HRP-avidin solution to an appropriate solution.
Human zonulin ELISA kit
Referência CSB-EQ027649HU-96T
Tamanho : 96T
Marca : Cusabio
| Size | 96T,5×96T,10×96T |
Product Details
Target Name
zonulin
Abbreviation
zonulin
Species
Homo sapiens (Human)
Sample Types
serum, plasma, tissue homogenates
Detection Range
0.625 ng/mL-40 ng/mL
Sensitivity
0.156 ng/mL
Assay Time
1-5h
Sample Loading Volume
50-100ul
Detection Wavelength
450 nm
Research Area
Others
Assay Principle
quantitative
Measurement
Sandwich
Precision
| Intra-assay Precision (Precision within an assay): CV%<8% | ||||||
| Three samples of known concentration were tested twenty times on one plate to assess. | ||||||
| Inter-assay Precision (Precision between assays): CV%<10% | ||||||
| Three samples of known concentration were tested in twenty assays to assess. | ||||||
Linearity
| To assess the linearity of the assay, samples were spiked with high concentrations of human zonulin in various matrices and diluted with the Sample Diluent to produce samples with values within the dynamic range of the assay. | ||||||
| Sample | Serum(n=4) | |||||
| 1:1 | Average % | 93 | ||||
| Range % | 86-97 | |||||
| 1:2 | Average % | 94 | ||||
| Range % | 89-98 | |||||
| 1:4 | Average % | 96 | ||||
| Range % | 93-105 | |||||
| 1:8 | Average % | 94 | ||||
| Range % | 86-98 | |||||
Recovery
| The recovery of human zonulin spiked to levels throughout the range of the assay in various matrices was evaluated. Samples were diluted prior to assay as directed in the Sample Preparation section. | ||||||
| Sample Type | Average % Recovery | Range | ||||
| Serum (n=5) | 95 | 90-101 | ||||
| EDTA plasma (n=4) | 97 | 90-104 | ||||
Typical Data
| These standard curves are provided for demonstration only. A standard curve should be generated for each set of samples assayed. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Materials provided
Materials not provided
- A microplate reader capable of measuring absorbance at 450 nm, with the correction wavelength set at 540 nm or 570 nm.
- An incubator can provide stable incubation conditions up to 37°C±5°C.
- Centrifuge
- Vortex
- Squirt bottle, manifold dispenser, or automated microplate washer
- Absorbent paper for blotting the microtiter plate
ELISA Data Analysis
Troubleshooting
and FAQs
and FAQs
Storage
Store at 2-8°C. Please refer to protocol.
Shelf Life
6 months
Description
The human zonulin ELISA kit is a valuable tool for detecting zonulin levels in human samples, such as serum, plasma, and tissue homogenates. With a detection range of 0.625 ng/mL to 40 ng/mL and a sensitivity of 0.156 ng/mL, it offers a precise measurement of zonulin concentrations. The assay principle is quantitative, utilizing a sandwich measurement technique that ensures accurate and reliable results. Researchers can perform the assay within a reasonable timeframe, as the assay time ranges from 1 to 5 hours. The sample volume required for analysis falls between 50-100 µl, making it suita...
Citations
- A Moratiel Pellitero, MD Isla Casado,Thesis & Dissertation,2025
- EM Gálvez Buerba,Universidad de Zaragoza,2025
- CM Ilie, CA Boromiz, IAM Stoian, LE Gaman,Current Issues in Molecular Biology,2025
- S Yang, S Feng, H Wu, C Zhong, S Zhan,Clinical Interventions in Aging,2025
- TH Lee, HI Lee, HT Roh, SY Cho,Life,2025
- Association between intestinal permeability, systemic inflammation, and re
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