Product Name:
Bovine Urokinase (uPA) ELISA Kit
Cat.#:
JL16560
Regulatory Status:
Alternative:
PLAU; ATF; URK; UK; UP-A; Abbokinase; Urokinase-Type Plasminogen Activator;Plasminogen Activator, Urokinase
Detection Method:
ELISA
Assay Type:
Sandwich
Detection Range:
0.156-10ng/mL
Sensitivity:
0.07ng/mL
Specificity:
This kit recognizes Bovine uPA in samples. No significant cross-reactivity or interference between Bovine uPA and analogues was observed.
Sample Type:
Serum, plasma and other biological fluids.
Assay Procedure:

Research Area:
Neuroscience
Product Datasheets
| uPA
Urokinase, also known as urokinase-type plasminogen activator (uPA), is a serine protease present in humans and other animals. The human urokinase protein was discovered, but not named, by McFarlane and Pilling in 1947.[5] Urokinase was originally isolated from human urine, and it is also present in the blood and in the extracellular matrix of many tissues. The primary physiological substrate of this enzyme is plasminogen, which is an inactive form (zymogen) of the serine protease plasmin. Activation of plasmin triggers a proteolytic cascade that, depending on the physiological environment, participates in thrombolysis or extracellular matrix degradation. This cascade had been involved in vascular diseases and cancer progression.| Typical data
As the OD values of the standard curve may vary according to the conditions of the actual assay performance (e.g. operator, pipetting technique, wash technique or temperature effects), the operator should establish a standard curve for each test. Typical standard curve and data are provided below for reference only.Concentration (ng/mL) | 10 | 5 | 2.5 | 1.25 | 0.625 | 0.312 | 0.156 | 0 |
OD | 2.15 | 1.63 | 1.13 | 0.71 | 0.5 | 0.33 | 0.23 | 0.07 |
Corrected OD | 2.08 | 1.56 | 1.06 | 0.64 | 0.43 | 0.26 | 0.16 | - |
| Repeatability
Intra-assay Precision (Precision within an assay):CV% < 10%; Inter-assay Precision (Precision between assays):CV% < 10%| Recovery
The recovery of Bovine 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=8) | 86-101 | 96 |
Plasma(n=8) | 92-105 | 103 |
| Linearity
Samples were spiked with high concentrations of Bovine uPA and diluted with Universal Diluent to produce samples with values within the range of the assay.Serum(n=4) | Plasma(n=4) | ||
1 : 2 | Range (%) | 85-95 | 88-96 |
Average (%) | 91 | 93 | |
1 : 4 | Range (%) | 89-103 | 87-108 |
Average (%) | 94 | 99 |






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