MIF Kit ELISA
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- Antigène Voir toutes MIF Kits ELISA
- MIF (Macrophage Migration Inhibitory Factor (Glycosylation-Inhibiting Factor) (MIF))
- Épitope
- AA 2-115
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Reactivité
- Humain
- Méthode de détection
- Colorimetric
- Type de méthode
- Sandwich ELISA
- Gamme de detection
- 156-10000 pg/mL
- Seuil minimal de détection
- 156 pg/mL
- Application
- ELISA
- Fonction
- Sandwich High Sensitivity ELISA kit for Quantitative Detection of Human MIF
- Marque
- PicoKine™
- Type d'échantillon
- Cell Culture Supernatant, Serum, Plasma (heparin), Plasma (EDTA), Milk
- Analytical Method
- Quantitative
- Specificité
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Expression system for standard: E.coli
Immunogen sequence: P2-A115 - Réactivité croisée (Details)
- There is no detectable cross-reactivity with other relevant proteins.
- Sensibilité
- <20pg/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: E.coli
Immunogen sequence: P2-A115 - Featured
- Discover our best selling MIF Kit ELISA
- Top Product
- Discover our top product MIF Kit ELISA
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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.
- Plaque
- Pre-coated
- Protocole
- human MIF ELISA Kit was based on standard sandwich enzyme-linked immune-sorbent assay technology. A monoclonal antibody from mouse specific for MIF has been precoated onto 96-well plates. Standards(E.coli, P2-A115) and test samples are added to the wells, a biotinylated detection polyclonal antibody from goat specific for MIF 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 human MIF amount of sample captured in plate.
- Procédure de l'essai
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Aliquot 0.1 mL per well of the 10000pg/mL, 5000pg/mL, 2500pg/mL, 1250pg/mL, 625pg/mL, 312pg/mL, 156pg/mL human MIF 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 human cell culture supernates, serum, plasma( heparin, EDTA) or human milk to each empty well. See "Sample Dilution Guideline" above for details. It is recommended that each human MIF standard solution and each sample be measured in duplicate.
- Précision du teste
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- Sample 1: n=16, Mean(pg/ml): 1442, Standard deviation: 90.85, CV(%): 6.3
- Sample 2: n=16, Mean(pg/ml): 3826, Standard deviation: 206.6, CV(%): 5.4
- Sample 3: n=16, Mean(pg/ml): 6427, Standard deviation: 315, CV(%): 4.9,
- Sample 1: n=24, Mean(pg/ml): 1625, Standard deviation: 121.9, CV(%): 7.5
- Sample 2: n=24, Mean(pg/ml): 4177, Standard deviation: 254.8, CV(%): 6.1
- Sample 3: n=24, Mean(pg/ml): 6782, Standard deviation: 393.4, CV(%): 5.8
- 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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-
Macrophage migration inhibitory factor as an incriminating agent in vitiligo." dans: Anais brasileiros de dermatologia, Vol. 93, Issue 2, pp. 191-196, (2018) (PubMed).
: "
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Macrophage migration inhibitory factor as an incriminating agent in vitiligo." dans: Anais brasileiros de dermatologia, Vol. 93, Issue 2, pp. 191-196, (2018) (PubMed).
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- Antigène Voir toutes MIF Kits ELISA
- MIF (Macrophage Migration Inhibitory Factor (Glycosylation-Inhibiting Factor) (MIF))
- Autre désignation
- MIF (MIF Produits)
- Synonymes
- mif Kit ELISA, Mif Kit ELISA, gif Kit ELISA, glif Kit ELISA, mmif Kit ELISA, LOC100136498 Kit ELISA, LOC100284350 Kit ELISA, LOC100284546 Kit ELISA, GIF Kit ELISA, Glif Kit ELISA, GLIF Kit ELISA, MMIF Kit ELISA, macrophage migration inhibitory factor L homeolog Kit ELISA, macrophage migration inhibitory factor Kit ELISA, macrophage migration inhibitory factor (glycosylation-inhibiting factor) Kit ELISA, mif.L Kit ELISA, mif Kit ELISA, MIF Kit ELISA, Mif Kit ELISA, PHATRDRAFT_49660 Kit ELISA, LOC100136498 Kit ELISA, cl405_1 Kit ELISA, LOC100284546 Kit ELISA
- Sujet
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Background: Macrophage migration inhibitory factor(MIF) is a protein which in humans is encoded by the MIF gene.1, 2 This gene is located to human chromosome 22q11.2.3 It is remarkably small, it has 3 exons separated by introns of only 189 and 95 bp, and covers less than 1 kb.4 This gene encodes a lymphokine that may be involved in cell-mediated immunity, immunoregulation, and inflammation.5 MIF plays a role in the regulation of macrophage function in host defense through the suppression of anti-inflammatory effects of glucocorticoids. This lymphokine and the JAB1 protein might form a complex in the cytosol near the peripheral plasma membrane, which may possibly indicate a role in integrin signaling pathways. MIF also plays a central role in the toxic response to endotoxemia and possibly septic shock.Macrophage migration inhibitory factor has been reported to interact with COP9 constitutive photomorphogenic homolog subunit 5, CD74, BNIPL, and CXCR4.
Synonyms: Macrophage migration inhibitory factor ,MIF ,
Full Gene Name: macrophage migration inhibitory factor (glycosylation-inhibiting factor)
- ID gène
- 4282
- UniProt
- I4AY87
- Pathways
- Regulation of Systemic Arterial Blood Pressure by Hormones, Positive Regulation of Immune Effector Process, Production of Molecular Mediator of Immune Response, Regulation of Carbohydrate Metabolic Process, Feeding Behaviour, Smooth Muscle Cell Migration, Negative Regulation of intrinsic apoptotic Signaling
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