The Bovine Hepcidin (HEPC) ELISA Kit is specifically designed for the quantitative detection of Hepcidin levels in bovine serum, plasma, and tissue homogenates. This kit offers exceptional sensitivity and accuracy, providing consistent and reliable results for a variety of research applications.Hepcidin is a key regulator of iron metabolism, controlling the absorption and distribution of iron in the body. Imbalances in Hepcidin levels have been linked to conditions such as anemia, iron overload disorders, and inflammatory diseases.
By accurately measuring Hepcidin levels, researchers can gain valuable insights into the role of iron metabolism in these conditions and potentially develop new therapeutic interventions.With its high performance and ease of use, the Bovine Hepcidin ELISA Kit is an indispensable tool for studying iron metabolism and related disorders in bovine models. It allows for precise and efficient analysis of Hepcidin levels, contributing to a deeper understanding of the complex mechanisms underlying iron regulation.
Matrices listed below were spiked with certain level of recombinant the index and the recovery rates were calculated by comparing the measured value to the expected amount of the index in samples.
Matrix
Recovery range (%)
Average(%)
Serum (n=5)
84-100
92
EDTA plasma (n=5)
83-98
90
Heparin plasma (n=5)
85-101
93
Linearity:
The linearity of the kit was assayed by testing samples spiked with appropriate concentration of the index and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.
Sample
1:2
1:4
1:8
1:16
Serum (n=5)
82-96%
83-98%
81-99%
93-101%
EDTA plasma (n=5)
88-101%
86-95%
90-102%
80-93%
Heparin plasma (n=5)
80-91%
82-90%
95-104%
79-95%
Intra-assay Precision:
Intra-Assay: CV <10%. 3 samples with low, middle and high level the index were tested 20 times on one plate, respectively.
Inter-assay Precision:
Inter-Assay: CV <12%. 3 samples with low, middle and high level the index were tested on 3 different plates, 8 replicates in each plate.
Stability:
The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage conditions. Note: To minimize unnecessary influences on the performance, operation procedures and lab conditions, especially room temperature, air humidity and incubator temperatures should be strictly regulated. It is also strongly suggested that the whole assay is performed by the same experimenter from the beginning to the end.
Step
Protocol
1.
Prepare all reagents, samples and standards
2.
Add 100µL standard or sample to each well. Incubate 2 hours at 37°C
3.
Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C
4.
Aspirate and wash 3 times
5.
Add 100µL prepared Detection Reagent B. Incubate 1 hour at 37°C
6.
Aspirate and wash 5 times
7.
Add 90µL Substrate Solution. Incubate 15-25 minutes at 37°C
8.
Add 50µL Stop Solution. Read at 450nm immediately.
