Cytochrome C Oxidase Subunit II (COX2) Magnetic Fluorescence Assay Kit

Mouse

Double-antibody Sandwich

Tissue homogenates, cell lysates and other biological fluids

0.02-20ng/mL

The minimum detectable dose of this kit is typically less than 0.007 ng/mL

This assay has high sensitivity and excellent specificity for detection of Cytochrome C Oxidase Subunit II (COX2), etc.
No significant cross-reactivity or interference between Cytochrome C Oxidase Subunit II (COX2), etc. and analogues was observed.

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.

Manufactured in a lab with traceable raw materials. Bulk orders can typically be prepared to the customer’s specifications, please inquire.

Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Cytochrome C Oxidase Subunit II (COX2), etc. were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Cytochrome C Oxidase Subunit II (COX2), etc. were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%

Enzyme & Kinase

1. Preparation of standards, reagents and samples before the experiment
2. Add 100uL standard or sample to each well,
add 10uL magnetic beads, and incubate 90min at 37 degree C on shaker
3. Remove liquid on magnetic frame, add 100uL prepared Detection Reagent A. Incubate 60min at 37 degree C on shaker
4. Wash plate on magnetic frame for three times
5. Add 100uL prepared Detection Reagent B, and incubate 30 min at 37 degree C on shaker
6. Wash plate on magnetic frame for three times
7. Add 100uL sheath solution, swirl for 2 minutes, read on the machine.

Analyte-specific antibodies are pre-coated onto color-coded microparticles. Microparticles, standards, and samples are pipetted into wells and the immobilized antibodies bind the analytes of interest. After washing away any unbound substances, a biotinylated antibody cocktail specific to the analytes of interest is added to each well. Following a wash to remove any unbound biotinylated antibody, Streptavidin-Phycoerythrin conjugate (Streptavidin-PE), which binds to the biotinylated detection antibodies, is added to each well. A final wash removes unbound Streptavidin-PE and the microparticles are resuspended in buffer and read using fluorescent spectrum analyzer.The MFI developed isproportional to the concentration of analytes of interest in the sample.

Manufactured in an ISO 9001:2015 and ISO 13485:2016 Certified Laboratory.