Mouse Cardiovascular ELISA Kits
Mouse PLAU/uPA(Urokinase-Type Plasminogen Activator) CLIA Kit (MOES00588)
- SKU:
- MOES00588
- Product Type:
- ELISA Kit
- ELISA Type:
- CLIA Kit
- Size:
- 96 Assays
- Sensitivity:
- 4.69pg/mL
- Range:
- 7.81-500pg/mL
- ELISA Type:
- Sandwich
- Synonyms:
- UPA, u-PA, ATF, URK, UP-A, Urokinase, Abbokinase
- Reactivity:
- Mouse
- Sample Type:
- Serum, plasma and other biological fluids
- Research Area:
- Cardiovascular
Description
| Assay type: | Sandwich |
| Format: | 96T |
| Assay time: | 4.5h |
| Reactivity: | Mouse |
| Detection method: | Chemiluminescence |
| Detection range: | 7.81-500 pg/mL |
| Sensitivity: | 4.69 pg/mL |
| Sample volume: | 100µL |
| Sample type: | Serum, plasma and other biological fluids |
| Repeatability: | CV < 15% |
| Specificity: | This kit recognizes Mouse PLAU/uPA in samples. No significant cross-reactivity or interference between Mouse PLAU/uPA and analogues was observed. |
This kit uses Sandwich-CLIA as the method. The micro CLIA plate provided in this kit has been pre-coated with an antibody specific to Mouse PLAU/uPA. Standards or samples are added to the appropriate micro CLIA plate wells and combined with the specific antibody. Then a biotinylated detection antibody specific for Mouse PLAU/uPA and Avidin-Horseradish Peroxidase (HRP) conjugate are added to each micro plate well successively and incubated. Free components are washed away. The substrate solution is added to each well. Only those wells that contain Mouse PLAU/uPA, biotinylated detection antibody and Avidin-HRP conjugate will appear fluorescence. The Relative light unit (RLU) value is measured spectrophotometrically by the Chemiluminescence immunoassay analyzer. The RLU value is positively associated with the concentration of Mouse PLAU/uPA. The concentration of Mouse PLAU/uPA in the samples can be calculated by comparing the RLU of the samples to the standard curve.
| UniProt Protein Function: | uPA: Specifically cleave the zymogen plasminogen to form the active enzyme plasmin. Defects in PLAU are the cause of Quebec platelet disorder (QPD). QPD is an autosomal dominant bleeding disorder due to a gain-of-function defect in fibrinolysis. Although affected individuals do not exhibit systemic fibrinolysis, they show delayed onset bleeding after challenge, such as surgery. The hallmark of the disorder is markedly increased PLAU levels within platelets, which causes intraplatelet plasmin generation and secondary degradation of alpha-granule proteins. Belongs to the peptidase S1 family. 2 isoforms of the human protein are produced by alternative splicing. |
| UniProt Protein Details: | Protein type:Motility/polarity/chemotaxis; EC 3. 4. 21. 73; Protease; Secreted; Secreted, signal peptide Cellular Component: cell surface; extracellular space; focal adhesion; membrane Molecular Function:peptidase activity; protein binding; serine-type endopeptidase activity Biological Process: angiogenesis; fibrinolysis; positive regulation of cell migration; positive regulation of cell proliferation; positive regulation of smooth muscle cell migration; proteolysis; regulation of cell adhesion mediated by integrin; regulation of cell proliferation; regulation of receptor activity; regulation of smooth muscle cell migration; response to hypoxia; skeletal muscle regeneration; smooth muscle cell migration; wound healing |
| UniProt Code: | P06869 |
| NCBI GenInfo Identifier: | 137113 |
| NCBI Gene ID: | 18792 |
| NCBI Accession: | P06869. 1 |
| UniProt Related Accession: | P06869 |
| Molecular Weight: | 48,268 Da |
| NCBI Full Name: | Urokinase-type plasminogen activator |
| NCBI Synonym Full Names: | plasminogen activator, urokinase |
| NCBI Official Symbol: | Plau |
| NCBI Official Synonym Symbols: | uPA; u-PA |
| NCBI Protein Information: | urokinase-type plasminogen activator |
| UniProt Protein Name: | Urokinase-type plasminogen activator |
| Protein Family: | Urokinase-type plasminogen activator |
| UniProt Gene Name: | Plau |
| UniProt Entry Name: | UROK_MOUSE |
As the RLU values of the standard curve may vary according to the conditions of the actual assay performance (e. g. operator, pipetting technique, washing technique or temperature effects), the operator should establish a standard curve for each test. Typical standard curve and data is provided below for reference only.
| Concentration (pg/mL) | RLU | Average | Corrected |
| 500 | 47026 56048 | 51537 | 51508 |
| 250 | 20789 21207 | 20998 | 20969 |
| 125 | 9585 9207 | 9396 | 9367 |
| 62.5 | 4215 4809 | 4512 | 4483 |
| 31.25 | 2378 2220 | 2299 | 2270 |
| 15.63 | 1255 1245 | 1250 | 1221 |
| 7.81 | 720 760 | 740 | 711 |
| 0 | 28 30 | 29 | -- |
Precision
Intra-assay Precision (Precision within an assay): 3 samples with low, mid range and high level Mouse PLAU/uPA were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, mid range and high level Mouse PLAU/uPA were tested on 3 different plates, 20 replicates in each plate.
| Intra-assay Precision | Inter-assay Precision | |||||
| Sample | 1 | 2 | 3 | 1 | 2 | 3 |
| n | 20 | 20 | 20 | 20 | 20 | 20 |
| Mean (pg/mL) | 25.39 | 60.18 | 243.31 | 25.56 | 62.03 | 229.45 |
| Standard deviation | 3.04 | 5.19 | 17.03 | 2.84 | 6.18 | 17.85 |
| C V (%) | 11.97 | 8.62 | 7.00 | 11.11 | 9.96 | 7.78 |
Recovery
The recovery of Mouse PLAU/uPA spiked at three different levels in samples throughout the range of the assay was evaluated in various matrices.
| Sample Type | Range (%) | Average Recovery (%) |
| Serum (n=5) | 88-102 | 95 |
| EDTA plasma (n=5) | 87-102 | 93 |
| Cell culture media (n=5) | 96-111 | 104 |
Linearity
Samples were spiked with high concentrations of Mouse PLAU/uPA and diluted with Reference Standard & Sample Diluent to produce samples with values within the range of the assay.
| Serum (n=5) | EDTA plasma (n=5) | Cell culture media (n=5) | ||
| 1:2 | Range (%) | 87-100 | 89-105 | 85-98 |
| Average (%) | 93 | 96 | 90 | |
| 1:4 | Range (%) | 92-105 | 97-111 | 102-116 |
| Average (%) | 99 | 104 | 109 | |
| 1:8 | Range (%) | 95-111 | 85-99 | 89-102 |
| Average (%) | 101 | 91 | 96 | |
| 1:16 | Range (%) | 85-96 | 95-109 | 87-100 |
| Average (%) | 91 | 100 | 94 |
An unopened kit can be stored at 4°C for 1 month. If the kit is not used within 1 month, store the items separately according to the following conditions once the kit is received.
| Item | Specifications | Storage |
| Micro CLIA Plate(Dismountable) | 8 wells ×12 strips | -20°C, 6 months |
| Reference Standard | 2 vials | |
| Concentrated Biotinylated Detection Ab (100×) | 1 vial, 120 µL | |
| Concentrated HRP Conjugate (100×) | 1 vial, 120 µL | -20°C(shading light), 6 months |
| Reference Standard & Sample Diluent | 1 vial, 20 mL | 4°C, 6 months |
| Biotinylated Detection Ab Diluent | 1 vial, 14 mL | |
| HRP Conjugate Diluent | 1 vial, 14 mL | |
| Concentrated Wash Buffer (25×) | 1 vial, 30 mL | |
| Substrate Reagent A | 1 vial, 5 mL | 4°C (shading light) |
| Substrate Reagent B | 1 vial, 5 mL | 4°C (shading light) |
| Plate Sealer | 5 pieces | |
| Product Description | 1 copy | |
| Certificate of Analysis | 1 copy |
- Set standard, test sample and control (zero) wells on the pre-coated plate and record theirpositions. It is recommended to measure each standard and sample in duplicate. Note: addall solutions to the bottom of the plate wells while avoiding contact with the well walls. Ensuresolutions do not foam when adding to the wells.
- Aliquot 100µl of standard solutions into the standard wells.
- Add 100µl of Sample / Standard dilution buffer into the control (zero) well.
- Add 100µl of properly diluted sample (serum, plasma, tissue homogenates and otherbiological fluids. ) into test sample wells.
- Cover the plate with the sealer provided in the kit and incubate for 90 min at 37°C.
- Aspirate the liquid from each well, do not wash. Immediately add 100µL of BiotinylatedDetection Ab working solution to each well. Cover the plate with a plate seal and gently mix. Incubate for 1 hour at 37°C.
- Aspirate or decant the solution from the plate and add 350µL of wash buffer to each welland incubate for 1-2 minutes at room temperature. Aspirate the solution from each well andclap the plate on absorbent filter paper to dry. Repeat this process 3 times. Note: a microplatewasher can be used in this step and other wash steps.
- Add 100µL of HRP Conjugate working solution to each well. Cover with a plate seal andincubate for 30 min at 37°C.
- Aspirate or decant the solution from each well. Repeat the wash process for five times asconducted in step 7.
- Add 100µL of Substrate mixture solution to each well. Cover with a new plate seal andincubate for no more than 5 min at 37°C. Protect the plate from light.
- Determine the RLU value of each well immediately.
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