CXCL2 Kit ELISA
Aperçu rapide pour CXCL2 Kit ELISA (ABIN2859287)
Antigène
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Reactivité
Méthode de détection
Type de méthode
Gamme de detection
Application
Type d'échantillon
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Seuil minimal de détection
- 15.6 pg/mL
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Fonction
- Sandwich Rat MIP-2 ELISA Kit to quantitate Rat Cxcl2 in cell culture supernatants, cell lysates, serum and plasma (heparin, EDTA).
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Analytical Method
- Quantitative
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Specificité
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Expression system for standard: E.coli
Immunogen sequence: S32-N100Capture antibody and Detection antibody: monoclonal antibody from mouse, polyclonal antibody from goat
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Réactivité croisée (Details)
- There is no detectable cross-reactivity with other relevant proteins.
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Sensibilité
- < 10 pg/mL
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Ingrédients
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- Pre-coated 96-well strip microplate
- Standard
- Biotinylated antibody (100x)
- Avidin-Biotin-Peroxidase Complex (100x)
- Sample Diluent
- Antibody Diluent
- Avidin-Biotin-Peroxidase Diluent
- Color Developing Reagent (TMB)
- Stop Solution
- Wash Buffer (25x)
- Adhesive plate sealers
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Matériel non inclus
- 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.
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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.
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Volume d'échantillon
- 100 μL
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Plaque
- Pre-coated
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Protocole
- 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.
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Précision du teste
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Intra-Assay Precision (CV%): 7.7%, 4.6%, 4%
Inter-Assay Precision (CV%): 9.3%, 4.7%, 4.8% -
Restrictions
- For Research Use only
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Conseil sur la manipulation
- Avoid multiple freeze-thaw cycles.
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Stock
- -20 °C,4 °C
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Stockage commentaire
- 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.)
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Date de péremption
- 12 months
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: "Alpha 1-antitrypsin ameliorates ventilator-induced lung injury in rats by inhibiting inflammatory responses and apoptosis." dans: Experimental biology and medicine (Maywood, N.J.), Vol. 243, Issue 1, pp. 87-95, (2018) (PubMed).
: "Dusuqing granules (DSQ) suppress inflammation in Klebsiella pneumonia rat via NF-κB/MAPK signaling." dans: BMC complementary and alternative medicine, Vol. 17, Issue 1, pp. 216, (2017) (PubMed).
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- CXCL2 (Chemokine (C-X-C Motif) Ligand 2 (CXCL2))
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Autre désignation
- CXCL2
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Sujet
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Background: Macrophage Inflammatory Protein 2 (MIP2), also known as C-X-C motif chemokine 2 (CXCL2), is a small cytokine belonging to the CXC chemokine family. MIP2 forms homotetramers. MIP2 is produced by activated monocytes and neutrophils and expressed at sites of inflammation. MIP2 is chemotactic for polymorphonuclear leukocytes.
Gene Full Name: C-X-C motif chemokine ligand 2
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ID gène
- 114105
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UniProt
- P30348
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Pathways
- Cellular Response to Molecule of Bacterial Origin
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