SKU(재고 관리 코드):CEA619Ge
ELISA Kit for Leukotriene C4 (LTC4)
ELISA Kit for Leukotriene C4 (LTC4)
Enzyme-linked immunosorbent assay for Antigen Detection.
Product No.
CEA619Ge
Organism Species
Pan-species (General).
Sample Type
Serum, plasma, tissue homogenates, cell culture supernates and other biological fluids
Test Method
Competitive Inhibition
Assay Length
2h
Detection Range
370.4-30,000pg/mL
Sensitivity
The minimum detectable dose of this kit is typically less than 147.4pg/mL.
UOM
48T 96T 96T*5 96T*10 96T*100
Specificity
This assay has high sensitivity and excellent specificity for detection of Leukotriene C4 (LTC4).
No significant cross-reactivity or interference between Leukotriene C4 (LTC4) and analogues was observed.
Recovery
Matrices listed below were spiked with certain level of Leukotriene C4 (LTC4) and the recovery rates were calculated by comparing the measured value to the expected amount of Leukotriene C4 (LTC4) in samples.
Matrix | Recovery range (%) | Average(%) |
serum(n=5) | 85-101 | 89 |
EDTA plasma(n=5) | 85-99 | 96 |
heparin plasma(n=5) | 91-104 | 97 |
Precision
Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Leukotriene C4 (LTC4) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Leukotriene C4 (LTC4) were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%
Linearity
The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Leukotriene C4 (LTC4) 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) | 95-103% | 79-101% | 78-88% | 82-92% |
EDTA plasma(n=5) | 79-95% | 80-90% | 80-93% | 93-101% |
heparin plasma(n=5) | 80-96% | 98-105% | 95-102% | 94-102% |
Stability
The stability of 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 condition.
To minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.
Reagents and materials provided
Reagents | Quantity | Reagents | Quantity |
Pre-coated, ready to use 96-well strip plate | 1 | Plate sealer for 96 wells | 4 |
Standard | 2 | Standard Diluent | 1×20mL |
Detection Reagent A | 1 | Assay Diluent A | 1×12mL |
Detection Reagent B | 1×120µL | Assay Diluent B | 1×12mL |
Reagent Diluent | 1×300µL | Stop Solution | 1×6mL |
TMB Substrate | 1×9mL | Instruction manual | 1 |
Wash Buffer (30 × concentrate) | 1×20mL |
Assay procedure summary
1. Prepare all reagents, samples and standards;
2. Add 50µL standard or sample to each well.
And then add 50µL prepared Detection Reagent A immediately.
Shake and mix. Incubate 1 hour at 37°C;
3. Aspirate and wash 3 times;
4. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;
5. Aspirate and wash 5 times;
6. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;
7. Add 50µL Stop Solution. Read at 450 nm immediately.
Magazine | Citations |
Toxicology and aApplied Pharmacology_ | 5-lipoxygenase activation is involved in the mechanisms of chronic hepatic injury in a rat model of chronic aluminum overload exposure pubmed:27368151 |
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