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SKU:LMA165Ra

Magnetic Luminex Assay Kit for Pepsinogen A (PGA) ,etc.

Magnetic Luminex Assay Kit for Pepsinogen A (PGA) ,etc.

Regular price $730.00 USD
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Detection range
Size
Sensitivity

Product No.

LMA165Ra

Organism Species

Rattus norvegicus (Rat).

Sample Type

Serum, plasma, tissue homogenates and other biological fluids

Test Method

Double-antibody Sandwich

Assay Length

3.5h

Detection Range

0.1-100ng/mL

Sensitivity

The minimum detectable dose of this kit is typically less than 0.033 ng/mL.

UOM

1Plex 2Plex 3Plex 4Plex 5Plex 6Plex 7Plex 8Plex

 

Specificity

This assay has high sensitivity and excellent specificity for detection of Pepsinogen A (PGA) ,etc..
No significant cross-reactivity or interference between Pepsinogen A (PGA) ,etc. and analogues was observed.

Recovery

Matrices listed below were spiked with certain level of recombinant Pepsinogen A (PGA) ,etc. and the recovery rates were calculated by comparing the measured value to the expected amount of Pepsinogen A (PGA) ,etc. in samples.

Matrix Recovery range (%) Average(%)
serum(n=5) 94-101 98
EDTA plasma(n=5) 95-103 99
heparin plasma(n=5) 85-101 97

Precision

Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Pepsinogen A (PGA) ,etc. were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Pepsinogen A (PGA) ,etc. 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 Pepsinogen A (PGA) ,etc. 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) 96-105% 79-104% 97-105% 94-101%
EDTA plasma(n=5) 80-97% 92-99% 96-103% 93-101%
heparin plasma(n=5) 80-103% 97-104% 91-98% 93-101%

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
96-well plate 1 Plate sealer for 96 wells 4
Pre-Mixed Standard 2 Standard Diluent 1×20mL
Pre-Mixed Magnetic beads (22#:PGA) 1 Analysis buffer 1×20mL
Pre-Mixed Detection Reagent A 1×120μL Assay Diluent A 1×12mL
Detection Reagent B (PE-SA) 1×120μL Assay Diluent B 1×12mL
Sheath Fluid 1×10mL Wash Buffer (30 × concentrate) 1×20mL
Instruction manual 1

Assay procedure summary

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

 

Magazine Citations
the journal of international advanced otology Role of Laryngopharyngeal Reflux in the Pathogenesis of Otitis Media with Effusion PubMed: 26223722
Sensors (Basel) Label-Free Detection of Salivary Pepsin Using Gold Nanoparticle/Polypyrrole Nanocoral Modified Screen-Printed Electrode Pubmed:29882917
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