alpha 2 Macroglobulin Kit ELISA
Aperçu rapide pour alpha 2 Macroglobulin Kit ELISA (ABIN1672904)
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Méthode de détection
Type de méthode
Gamme de detection
Application
Type d'échantillon
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Seuil minimal de détection
- 625 pg/mL
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Fonction
- Sandwich Human A2M/Alpha 2-Macroglobulin ELISA Kit to quantitate Human A2M 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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Target protein isolated from human plasma
Capture antibody and Detection antibody: polyclonal antibody from goat, 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
- < 20 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%): 7.1%, 6.1%, 7.7%
Inter-Assay Precision (CV%): 7.9%, 6.1%, 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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: "Neutrophil serine proteases and their endogenous inhibitors in coronary artery ectasia patients." dans: Anatolian journal of cardiology, Vol. 16, Issue 1, pp. 23-8, (2016) (PubMed).
: "Disequilibrium of Blood Coagulation and Fibrinolytic System in Patients With Coronary Artery Ectasia." dans: Medicine, Vol. 95, Issue 8, pp. e2779, (2016) (PubMed).
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- alpha 2 Macroglobulin (A2M) (alpha-2-Macroglobulin (A2M))
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Autre désignation
- A2M
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Sujet
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Background: Alpha-2-macroglobulin, also known as A2M or CPAMD5 is a large plasma protein found in the blood. This gene is mapped to 12p13.31. Alpha-2-macroglobulin is a protease inhibitor and cytokine transporter. It inhibits many proteases, including trypsin, thrombin and collagenase. A2M is implicated in Alzheimer disease (AD) due to its ability to mediate the clearance and degradation of A-beta, the major component of beta-amyloid deposits. This gene is able to inhibit all four classes of proteinases by a unique 'trapping' mechanism. This protein has a peptide stretch, called the 'bait region' which contains specific cleavage sites for different proteinases. When a proteinase cleaves the bait region, a conformational change is induced in the protein which traps the proteinase. The entrapped enzyme remains active against low molecular weight substrates (activity against high molecular weight substrates is greatly reduced). Following cleavage in the bait region a thioester bond is hydrolyzed and mediates the covalent binding of the protein to the proteinase.
Gene Full Name: alpha-2-macroglobulin
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ID gène
- 2
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UniProt
- P01023
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Pathways
- Lipid Metabolism
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