PLAUR Kit ELISA
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- Antigène Voir toutes PLAUR Kits ELISA
- PLAUR (Plasminogen Activator, Urokinase Receptor (PLAUR))
- Épitope
- AA 24-297
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Reactivité
- Souris
- Méthode de détection
- Colorimetric
- Type de méthode
- Sandwich ELISA
- Gamme de detection
- 62.5-4000 pg/mL
- Seuil minimal de détection
- 62.5 pg/mL
- Application
- ELISA
- Fonction
- Sandwich High Sensitivity ELISA kit for Quantitative Detection of Mouse uPAR
- Marque
- PicoKine™
- Type d'échantillon
- Cell Culture Supernatant, Serum, Plasma (heparin), Plasma (EDTA)
- Analytical Method
- Quantitative
- Specificité
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Expression system for standard: NSO
Immunogen sequence: L24-T297 - Réactivité croisée (Details)
- There is no detectable cross-reactivity with other relevant proteins.
- Sensibilité
- <5pg/mL
- Matériel non inclus
- Microplate reader in standard size. Automated plate washer. Adjustable pipettes and pipette tips. Multichannel pipettes are recommended in the condition of large amount of samples in the detection. Clean tubes and Eppendorf tubes. Washing buffer (neutral PBS or TBS). Preparation of 0.01M TBS: Add 1.2g Tris, 8.5g Nacl
- Immunogène
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Expression system for standard: NSO
Immunogen sequence: L24-T297 - Featured
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- Indications d'application
- 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.
- Commentaires
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Tissue Specificity: Expressed in angiogenic endothelial cells (at protein level). .
- Plaque
- Pre-coated
- Protocole
- mouse uPAR ELISA Kit was based on standard sandwich enzyme-linked immune-sorbent assay technology. A monoclonal antibody from rat specific for uPAR has been precoated onto 96-well plates. Standards(NSO, L24-T297) and test samples are added to the wells, a biotinylated detection polyclonal antibody from goat specific for uPAR 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 mouse uPAR amount of sample captured in plate.
- Procédure de l'essai
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Aliquot 0.1 mL per well of the 4000pg/mL, 2000pg/mL,1000pg/mL, 500pg/mL, 250pg/mL, 125pg/mL, 62.5pg/mL mouse uPAR standard solutions into the precoated 96-well plate. Add 0.1 mL of the sample diluent buffer into the control well (Zero well). Add 0.1 mL of each properly diluted sample of mouse cell culture supernates, serum or plasma(heparin, EDTA) to each empty well. See "Sample Dilution Guideline" above for details. It is recommended that each mouse uPAR standard solution and each sample be measured in duplicate.
- Précision du teste
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- Sample 1: n=16, Mean(pg/ml): 256, Standard deviation: 13.06, CV(%): 5.1
- Sample 2: n=16, Mean(pg/ml): 1862, Standard deviation: 8.38, CV(%): 4.5
- Sample 3: n=16, Mean(pg/ml): 3015, Standard deviation: 114.6, CV(%): 3.8,
- Sample 1: n=24, Mean(pg/ml): 362, Standard deviation: 23.2, CV(%): 6.4
- Sample 2: n=24, Mean(pg/ml): 2165, Standard deviation: 114.7, CV(%): 5.3
- Sample 3: n=24, Mean(pg/ml): 3230, Standard deviation: 190.6, CV(%): 5.9
- Restrictions
- For Research Use only
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- Conseil sur la manipulation
- Avoid multiple freeze-thaw cycles.
- Stock
- -20 °C,4 °C
- Stockage commentaire
- Store at 4°C for 6 months, at -20°C for 12 months. Avoid multiple freeze-thaw cycles
- Date de péremption
- 12 months
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- Antigène Voir toutes PLAUR Kits ELISA
- PLAUR (Plasminogen Activator, Urokinase Receptor (PLAUR))
- Autre désignation
- PLAUR (PLAUR Produits)
- Synonymes
- Cd87 Kit ELISA, u-PAR Kit ELISA, uPAR Kit ELISA, CD87 Kit ELISA, U-PAR Kit ELISA, UPAR Kit ELISA, URKR Kit ELISA, Par Kit ELISA, Plaur3 Kit ELISA, uPAR-2 Kit ELISA, uPAR-3 Kit ELISA, PLAUR Kit ELISA, plasminogen activator, urokinase receptor Kit ELISA, Plaur Kit ELISA, PLAUR Kit ELISA
- Sujet
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Protein Function: Acts as a receptor for urokinase plasminogen activator. Plays a role in localizing and promoting plasmin formation. Mediates the proteolysis-independent signal transduction activation effects of U-PA.
Background: The urokinase-type plasminogen activator receptor(uPAR) is a key molecule in the regulation of cell-surface plasminogen activation and, as such, plays an important role in many normal as well as pathological processes.1 The cDNA for Mo3, an activation antigen expressed by human monocytes and myelomonocytic cell lines after stimulation by a variety of agents. Mo3 expression in vivo is associated predominantly with macrophages in inflammatory sites. It is a highly glycosylated protein of about 50 kD in monocytes where it is anchored to the plasma membrane by glycosyl-phosphatidylinositol linkage. The complete coding sequence of the cDNA has been found to encode 335 amino acids including a predicted signal peptide of 22 residues and a hydrophobic C-terminal portion. Mo3 is identical to the human receptor for the urokinase plasminogen activator.2 UPAR is a useful prognostic marker for biologically aggressive forms of endometrial cancer.3 PLAUR is located at chromosome 19q13.1-q13.2.1
Synonyms: Urokinase plasminogen activator surface receptor,U-PAR,uPAR,CD87,Plaur,
Full Gene Name: Urokinase plasminogen activator surface receptor
Cellular Localisation: Isoform 1: Cell membrane, Lipid-anchor, GPI- anchor. - ID gène
- 18793
- UniProt
- P35456
- Pathways
- Inositol Metabolic Process
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