Magnetic Luminex Assay Kit for 3-Hydroxybutyrate Dehydrogenase 1 (BDH1) ,etc.

DBH; SDR9C1; D-beta-Hydroxybutyrate Dehydrogenase,Mitochondrial; Short Chain Dehydrogenase/Reductase Family 9C,Member 1

(Note: Up to 8-plex in one testing reaction)

  • Magnetic Luminex Assay Kit for 3-Hydroxybutyrate Dehydrogenase 1 (BDH1) ,etc. Packages (Simulation)
  • Magnetic Luminex Assay Kit for 3-Hydroxybutyrate Dehydrogenase 1 (BDH1) ,etc. Packages (Simulation)
  • Certificate ISO9001: 2008, ISO13485: 2003 Registered

Specificity of the Magnetic Luminex Assay Kit for 3-Hydroxybutyrate Dehydrogenase 1 (BDH1) ,etc.

This assay has high sensitivity and excellent specificity for detection of 3-Hydroxybutyrate Dehydrogenase 1 (BDH1) ,etc..
No significant cross-reactivity or interference between 3-Hydroxybutyrate Dehydrogenase 1 (BDH1) ,etc. and analogues was observed.

Recovery of the Magnetic Luminex Assay Kit for 3-Hydroxybutyrate Dehydrogenase 1 (BDH1) ,etc.

Matrices listed below were spiked with certain level of recombinant 3-Hydroxybutyrate Dehydrogenase 1 (BDH1) ,etc. and the recovery rates were calculated by comparing the measured value to the expected amount of 3-Hydroxybutyrate Dehydrogenase 1 (BDH1) ,etc. in samples.

Matrix Recovery range (%) Average(%)
serum(n=5) 94-102 98
EDTA plasma(n=5) 86-97 91
heparin plasma(n=5) 80-105 101
sodium citrate plasma(n=5) 82-93 87

Precision of the Magnetic Luminex Assay Kit for 3-Hydroxybutyrate Dehydrogenase 1 (BDH1) ,etc.

Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level 3-Hydroxybutyrate Dehydrogenase 1 (BDH1) ,etc. were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level 3-Hydroxybutyrate Dehydrogenase 1 (BDH1) ,etc. were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%

Linearity of the Magnetic Luminex Assay Kit for 3-Hydroxybutyrate Dehydrogenase 1 (BDH1) ,etc.

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of 3-Hydroxybutyrate Dehydrogenase 1 (BDH1) ,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) 94-102% 89-96% 92-104% 78-91%
EDTA plasma(n=5) 78-89% 96-103% 83-101% 81-104%
heparin plasma(n=5) 87-98% 84-102% 84-92% 96-105%
sodium citrate plasma(n=5) 95-105% 79-89% 78-102% 86-101%

Stability of the Magnetic Luminex Assay Kit for 3-Hydroxybutyrate Dehydrogenase 1 (BDH1) ,etc.

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.

Assay procedure summary of the Magnetic Luminex Assay Kit for 3-Hydroxybutyrate Dehydrogenase 1 (BDH1) ,etc.

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.

Test principle of the Magnetic Luminex Assay Kit for 3-Hydroxybutyrate Dehydrogenase 1 (BDH1) ,etc.

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 the Luminex or Bio-Plex analyzer.The MFI developed is proportional to the concentration of analytes of interest in the sample.

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