Stabillity at RT
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
Applications
FLIA Kit for Antigen Detection.
Detection Range
0.1-100ng/mL
Sensitivity
The minimum detectable dose of this kit is typically less than 0.033 ng/mL
Specificity
No significant cross-reactivity or interference between Abscisic Acid (ABA) ,etc. by FLIA (Flow Luminescence Immunoassay) and analogues was observed.
This assay has high sensitivity and excellent specificity for detection of Abscisic Acid (ABA) ,etc. by FLIA (Flow Luminescence Immunoassay).
Research Area
FLIA Kit for Antigen Detection.
Organism species
Pan-species (General)
Alternative Names
AB-A
Dormin
abscisin II
Item Name
Abscisic Acid
Assay Length
3h
Method
Competitive Inhibition
Sample Type
serum, plasma, tissue homogenates, cell lysates, cell culture
supernates and other biological fluids
Format
48T, 96T, 96T×5, 96T×10, 96T×100
Assay Procedure
Competitive Inhibition
Test Principle
Analyte-specific antibodies are pre-coated onto color-coded microparticles. Microparticles, standards,Labeled antigen and samples are pipetted into wells and the immobilized antibodies bind the analytes of interest.A competitive inhibition reaction is lau
proportional to the concentration of analytes of interest in the sample.
Precision
CV(%) = SD/meanX100
Inter-Assay: CV<12%
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Abscisic Acid (ABA) ,etc. by FLIA (Flow Luminescence Immunoassay) were tested on 3 different plates, 8 replicates in each plate.
Intra-Assay: CV<10%
Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Abscisic Acid (ABA) ,etc. by FLIA (Flow Luminescence Immunoassay) were tested 20 times on one plate, respectively.
Assay procedure summary
 
 
 
 
1. Preparation of standards, reagents and samples before the experiment
2. Add 50μL standard or sample to each well,
3. Wash plate on magnetic frame for three times
4. Add 100μL prepared Detection Reagent B, and incubate 30 min at 37°
5. Wash plate on magnetic frame for three times
6. Add 100μL sheath solution, swirl for 2 minutes, read on the machine.
C on shaker
C on shaker
add 10μL magnetic beads,and 50μL Detection Reagent A,incubate 90min at 37°
UniProt ID
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