Rat Interferon Gamma Induced Protein 10kDa (IP10) ELISA Kit
The Rat Interferon-Gamma Induced Protein 10kDa (IP-10) ELISA Kit is specifically designed for the precise measurement of IP-10 levels in rat serum, plasma, and tissue lysates. With its exceptional sensitivity and specificity, this kit ensures accurate and reproducible results, making it an indispensable tool for various research applications.IP-10 is a key chemokine involved in immune responses, attracting and activating immune cells such as T cells and macrophages.
Its dysregulation has been implicated in various inflammatory and autoimmune diseases, underscoring its significance as a biomarker for studying these conditions and potential therapeutic interventions.With the Rat Interferon-Gamma Induced Protein 10kDa (IP-10) ELISA Kit, researchers can explore the role of IP-10 in immune regulation and inflammation, advancing our understanding of these complex processes and paving the way for novel treatment strategies.
Product Name:
Rat Interferon Gamma Induced Protein 10kDa (IP10) ELISA Kit
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)
83-100
91
EDTA plasma (n=5)
90-103
96
Heparin plasma (n=5)
89-102
95
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.
