ELISA Kit for Golgi Protein 73 (GP73)
GOLM1; GOLPH2; C9orf155; Golgi Membrane Protein 1; Golgi Phosphoprotein 2
- Product No.SEB668Ra
- Organism SpeciesRattus norvegicus (Rat)Same name, Different species.
- Test MethodDouble-antibody Sandwich
- Assay Length3h
- Detection Range0.78-50ng/mL
- SensitivityThe minimum detectable dose of this kit is typically less than 0.31ng/mL.
- Sample Typeserum, plasma, tissue homogenates and other biological fluids
- DownloadInstruction Manual
- FOBUS$ 505
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- Packages (Simulation)
- Packages (Simulation)
- Results demonstration
- Typical Standard Curve
- ISO9001: 2008, ISO13485: 2003 Registered
Specificity of the ELISA Kit for Golgi Protein 73 (GP73)
This assay has high sensitivity and excellent specificity for detection of Golgi Protein 73 (GP73).
No significant cross-reactivity or interference between Golgi Protein 73 (GP73) and analogues was observed.
Recovery of the ELISA Kit for Golgi Protein 73 (GP73)
Matrices listed below were spiked with certain level of recombinantGolgi Protein 73 (GP73) and the recovery rates were calculated by comparing the measured value to the expected amount of Golgi Protein 73 (GP73) in samples.
|Matrix||Recovery range (%)||Average(%)|
Precision of the ELISA Kit for Golgi Protein 73 (GP73)
Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Golgi Protein 73 (GP73) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Golgi Protein 73 (GP73) were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
Linearity of the ELISA Kit for Golgi Protein 73 (GP73)
The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Golgi Protein 73 (GP73) and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.
Stability of the ELISA Kit for Golgi Protein 73 (GP73)
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 of the ELISA Kit for Golgi Protein 73 (GP73)
|Pre-coated, ready to use 96-well strip plate||1||Plate sealer for 96 wells||4|
|Detection Reagent A||1×120µL||Assay Diluent A||1×12mL|
|Detection Reagent B||1×120µL||Assay Diluent B||1×12mL|
|TMB Substrate||1×9mL||Stop Solution||1×6mL|
|Wash Buffer (30 × concentrate)||1×20mL||Instruction manual||1|
Assay procedure summary of the ELISA Kit for Golgi Protein 73 (GP73)
1. Prepare all reagents, samples and standards;
2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;
3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;
4. Aspirate and wash 3 times;
5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;
6. Aspirate and wash 5 times;
7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;
8. Add 50µL Stop Solution. Read at 450nm immediately.
Test principle of the ELISA Kit for Golgi Protein 73 (GP73)
The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Golgi Protein 73 (GP73). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Golgi Protein 73 (GP73). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Golgi Protein 73 (GP73), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Golgi Protein 73 (GP73) in the samples is then determined by comparing the O.D. of the samples to the standard curve.
|Catalog No.||Organism species: Rattus norvegicus (Rat)||Applications (RESEARCH USE ONLY!)|
|SEB668Ra||ELISA Kit for Golgi Protein 73 (GP73)||Enzyme-linked immunosorbent assay for Antigen Detection.|