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PLAU ELISA Kit

This Colorimetric ELISA kit is designed for the quantitative measurement of Human PLAU. There are 6 publications available.
Catalog No. ABIN411365
$519.00
Plus shipping costs $50.00
96 tests
Shipping to: United States
Delivery in 4 to 7 Business Days

Quick Overview for PLAU ELISA Kit (ABIN411365)

Target

See all PLAU ELISA Kits
PLAU (Plasminogen Activator, Urokinase (PLAU))

Binding Specificity

AA 1-431

Reactivity

  • 27
  • 12
  • 10
  • 8
  • 8
  • 5
  • 5
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Human

Detection Method

Colorimetric

Method Type

Sandwich ELISA

Detection Range

62.5 pg/mL - 4000 pg/mL

Application

ELISA

Sample Type

Cell Culture Supernatant, Cell Lysate, Plasma (EDTA), Plasma (heparin), Serum
  • Minimum Detection Limit

    62.5 pg/mL

    Purpose

    Sandwich Human uPA / PLAU / URK ELISA Kit to quantitate Human PLAU in cell culture supernatants, cell lysates, serum and plasma (heparin, EDTA).

    Analytical Method

    Quantitative

    Specificity

    Expression system for standard: NS0
    Immunogen sequence: M1-L431

    Capture antibody and Detection antibody: monoclonal antibody from mouse, polyclonal antibody from goat

    Cross-Reactivity (Details)

    There is no detectable cross-reactivity with other relevant proteins.

    Sensitivity

    < 5 pg/mL

    Components

    1. Pre-coated 96-well strip microplate
    2. Standard
    3. Biotinylated antibody (100x)
    4. Avidin-Biotin-Peroxidase Complex (100x)
    5. Sample Diluent
    6. Antibody Diluent
    7. Avidin-Biotin-Peroxidase Diluent
    8. Color Developing Reagent (TMB)
    9. Stop Solution
    10. Wash Buffer (25x)
    11. Adhesive plate sealers

    Material not included

    Microplate Reader capable of reading absorbance at 450nm. Incubator. Automated plate washer (optional). Pipettes and pipette tips capable of precisely dispensing 0.5 μL through 1 mL volumes of aqueous solutions. Multichannel pipettes are recommended for large amount of samples. Deionized or distilled water. 500 mL graduated cylinders. Test tubes for dilution.
  • Application Notes

    Before using Kit, spin tubes and bring down all components to bottom of tube. Duplicate well assay was recommended for both standard and sample testing.

    Sample Volume

    100 μL

    Plate

    Pre-coated

    Protocol

    ELISA Kit is based on standard sandwich enzyme-linked immune-sorbent assay technology. An antibody has been precoated onto 96-well plates. Standards and test samples are added to the wells, a biotinylated detection antibody specific for target is added subsequently and then followed by washing with PBS or TBS buffer. Avidin-Biotin-Peroxidase Complex was added and unbound conjugates were washed away with PBS or TBS buffer. HRP substrate TMB was used to visualize HRP enzymatic reaction. TMB was catalyzed by HRP to produce a blue color product that changed into yellow after adding acidic stop solution. The density of yellow is proportional to the target amount in sample captured in plate.

    Assay Precision

    Intra-Assay Precision (CV%): 4.5%, 6.7%, 5.4%
    Inter-Assay Precision (CV%): 6.1%, 8.3%, 6.9%

    Restrictions

    For Research Use only
  • Handling Advice

    Avoid multiple freeze-thaw cycles.

    Storage

    -20 °C,4 °C

    Storage Comment

    Store at 4°C for 6 months, at -20°C for 12 months. Avoid multiple freeze-thaw cycles (Ships with gel ice, can store for up to 3 days in room temperature. Freeze upon receiving.)

    Expiry Date

    12 months
  • Bi, Zeng, Zhao, Wei, Yu, Wang, Yu, Cao, Shan, Wei: "miR-181a Induces Macrophage Polarized to M2 Phenotype and Promotes M2 Macrophage-mediated Tumor Cell Metastasis by Targeting KLF6 and C/EBPα." in: Molecular therapy. Nucleic acids, Vol. 5, Issue 9, pp. e368, (2016) (PubMed).

    Bronckaers, Hilkens, Fanton, Struys, Gervois, Politis, Martens, Lambrichts: "Angiogenic properties of human dental pulp stem cells." in: PLoS ONE, Vol. 8, Issue 8, pp. e71104, (2013) (PubMed).

    Kim, Lee, Choi, Yoo, Yang: "Implication of MMP-9 and urokinase plasminogen activator (uPA) in the activation of pro-matrix metalloproteinase (MMP)-13." in: Rheumatology international, Vol. 32, Issue 10, pp. 3069-75, (2012) (PubMed).

    Jiang, Zhang, Zhou, Zhang, Li, Zhang, Zhang, Qiao, Kong, Ma, Chen: "Relationships of uPA and VEGF expression in esophageal cancer and microvascular density with tumorous invasion and metastasis." in: Asian Pacific journal of cancer prevention : APJCP, Vol. 13, Issue 7, pp. 3379-83, (2012) (PubMed).

    Wang, Li, Han, Li, Mi, Sun, Song, Han, Zhao, Wang: "Integrin ?3 and its ligand regulate the expression of uPA through p38 MAPK in breast cancer." in: APMIS : acta pathologica, microbiologica, et immunologica Scandinavica, Vol. 118, Issue 12, pp. 909-17, (2010) (PubMed).

    Yang, Shi, Li, Yi: "Effects of shRNA targeting maspin on invasion of gastric carcinoma SGC7901 cell line." in: Oncology reports, Vol. 25, Issue 1, pp. 259-65, (2010) (PubMed).

  • Target See all PLAU ELISA Kits

    PLAU (Plasminogen Activator, Urokinase (PLAU))

    Alternative Name

    PLAU

    Background

    Background: Plasminogen activator,urokinase (PLAU, uPA) converts plasminogen to plasmin. Plasmin is involved in processing of amyloid precursor protein and degrades secreted and aggregated amyloid-beta, a hallmark of Alzheimer disease (AD). Urokinase has a molecular mass of about 54 kD and is composed of 2 disulfide-linked chains, A and B, of molecular masses 18 kD and 33 kD, respectively. It localized on 10q24. uPA facilitates cell migration by localizing proteolisys on the cell surface and by inducing intracellular signalling pathways. In human vascular smooth muscle cell (VSMC), uPA stimulates migration via the uPA receptor (uPAR) signalling complex containing TYK2 and phosphatidylinositol 3-kinase (PI3-K).

    Gene Full Name: plasminogen activator, urokinase

    Gene ID

    5328

    UniProt

    P00749

    Pathways

    Cellular Response to Molecule of Bacterial Origin, Carbohydrate Homeostasis, Autophagy, Smooth Muscle Cell Migration
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