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PLAU ELISA Kit

Dieses Colorimetric ELISA kit dient der quantitativen Messung von Human PLAU. Es wurde in 6 Publikationen zitiert.
Produktnummer ABIN411365
642,40 €
Zzgl. Versandkosten 20,00 € und MwSt
96 tests
Lieferung nach: Deutschland
Lieferung in 8 bis 12 Werktagen

Kurzübersicht für PLAU ELISA Kit (ABIN411365)

Target

Alle PLAU ELISA Kits anzeigen
PLAU (Plasminogen Activator, Urokinase (PLAU))

Bindungsspezifität

AA 1-431

Reaktivität

  • 24
  • 11
  • 9
  • 8
  • 7
  • 4
  • 4
  • 4
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Human

Nachweismethode

Colorimetric

Methodentyp

Sandwich ELISA

Detektionsbereich

62.5 pg/mL - 4000 pg/mL

Applikation

ELISA

Proben

Cell Culture Supernatant, Cell Lysate, Plasma (EDTA), Plasma (heparin), Serum
  • Untere Nachweisgrenze

    62.5 pg/mL

    Verwendungszweck

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

    Analytische Methode

    Quantitative

    Spezifität

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

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

    Kreuzreaktivität (Details)

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

    Sensitivität

    < 5 pg/mL

    Bestandteile

    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

    Benötigtes Material

    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.
  • Applikationshinweise

    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.

    Probenmenge

    100 μL

    Plattentyp

    Pre-coated

    Protokoll

    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.

    Testpräzision

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

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Handhabung

    Avoid multiple freeze-thaw cycles.

    Lagerung

    -20 °C,4 °C

    Informationen zur Lagerung

    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.)

    Haltbarkeit

    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 Alle PLAU ELISA Kits anzeigen

    PLAU (Plasminogen Activator, Urokinase (PLAU))

    Andere Bezeichnung

    PLAU

    Hintergrund

    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

    Gen-ID

    5328

    UniProt

    P00749

    Pathways

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