Lysophosphatidylcholine (LPC) Magnetic Fluorescence Assay Kit

General

Competitive Inhibition

Serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids

19.53-20000ng/mL

The minimum detectable dose of this kit is typically less than 6.51 ng/mL

This assay has high sensitivity and excellent specificity for detection of Lysophosphatidylcholine (LPC), etc.
No significant cross-reactivity or interference between Lysophosphatidylcholine (LPC), 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 Lysophosphatidylcholine (LPC), etc. were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Lysophosphatidylcholine (LPC), etc. were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%

1. Preparation of standards, reagents and samples before the experiment
2. Add 50uL standard or sample to each well,
add 10uL magnetic beads,and 50uL Detection Reagent A,incubate 90min at 37 degree C on shaker
3. Wash plate on magnetic frame for three times
4. Add 100uL prepared Detection Reagent B, and incubate 30 min at 37 degree C on shaker
5. Wash plate on magnetic frame for three times
6. Add 100uL sheath solution, swirl for 2 minutes, read on the machine.

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 launched between biotin labeled analytes of interest and unlabeled analytes of interest (Standards or samples) with the pre-coated antibody specific to analytes of interest. Following a wash to remove any unbound substances, Streptavidin-Phycoerythrin conjugate (Streptavidin-PE) 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 is reverseproportional to the concentration of analytes of interest in the sample.

The manual is for reference only and may differ from the manual shipped with the product. Please refer to the hard copy of the manual shipped with the product.

Custom multiplex assays, with combinations of targets, are also available. Please inquire for additional information.

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