Tumor Necrosis Factor Alpha (TNF-Alpha) BioAssay™ ELISA Kit (Rabbit)

Katalog-Nummer 530089-96T

Size : 96Tests

Marke : US Biological

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530089 Tumor Necrosis Factor Alpha (TNF-Alpha) BioAssay™ ELISA Kit (Rabbit) discontinued

Clone Type
Polyclonal
Shipping Temp
Blue Ice
Storage Temp
4°C/-20°C

This Tumor Necrosis Factor Alpha (TNF-Alpha) BioAssay™ ELISA Kit is a sandwich ELISA for the in vitro quantitative determination of TNF-Alpha concentrations in rabbit serum, plasma and other biological fluids.||Detection Range:|15.63-1000pg/ml||Sensitivity:|9.38pg/ml||Precision:|Intra-Assay %CV: <10%|Inter-Assay %CV: <10%||Specificity:|Recognizes rabbit TNF-Alpha. No significant cross-reactivity or interference between rabbit TNF-Alpha and analogues was observed.||Test Principle:|The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to rabbit TNF-Alpha. Standards or samples are added to the micro ELISA plate wells and combined with the specific antibody. Then a biotinylated detection antibody specific for rabbit TNF-Alpha and Avidin-Horseradish Peroxidase (HRP) conjugate are added successively to each micro plate well and incubated. Free components are washed away. The substrate solution is added to each well. Only those wells that contain rabbit TNF-Alpha, biotinylated detection antibody and Avidin-HRP conjugate will appear blue in color. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (O.D.) is measured spectrophotometrically at a wavelength of 450nm ± 2nm. The O.D. value is proportional to the concentration of rabbit TNF-Alpha. You can calculate the concentration of rabbit TNF-Alpha in the samples by comparing the O.D. of the samples to the standard curve.||Kit Components:|Microtiter Strips, 1x96 wells, Pre-coated; ready to use|Reference Standard, 2 vials|Concentrated Biotinylated Detection Ab (100×), 1x120ul|Concentrated HRP Conjugate (100×),1x120ul|Reference Standard & Sample Diluent, 1x20ml|Biotinylated Detection Ab Diluent, 1x14ml|HRP Conjugate Diluent, 1x14ml|Concentrated Wash Buffer (25×), 1x30ml|Substrate Reagent, 1x10ml|Stop Solution, 1x10ml||Storage and Stability:|Unused kit is stable for 6 months after receipt.  Store Microtiter Strips, Standard, and Antibody-Biotin at 4°C if kit will be used within 30 days; otherwise store at -20°C until expiration date. Store the rest of the components at 4°C. Protect HRP Conjugate and Substrate Reagent from light. For maximum recovery, centrifuge the original vials after thawing and prior to removing the cap.||Assay Procedure Summary:|1. Prepare all reagents, samples and standards.|2. Add 100ul standard or sample to each well. Incubate 90 minutes at 37°C.|3. Aspirate and add 100ul prepared Biotin Working Solution. Incubate 1 hour at 37°C.|4. Aspirate and wash 3 times.|5. Add 100ul prepared HRP Detection Working Solution. Incubate 30 minutes at 37°C.|6. Aspirate and wash 5 times.|7. Add 90ul Substrate. Incubate 15 minutes at 37°C.|8. Add 50ul Stop Solution. Read at 450nm immediately.

Applications
Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications without the expressed written authorization of United States Biological. Toxicity and Hazards: All products should be handled by qualified personnel only, trained in laboratory procedures.
References
1. Fu Z, Ye Q F, Zhang Y, et al. Hypothermic Machine Perfusion Reduced Inflammatory Reaction By Downregulating The Expression Of Matrix Metalloproteinase 9 In A Reperfusion Model Of Donation After Cardiac Death[J]. Artificial Organs, 2016.|2. Yang Z, Zhong Z, Li M, et al. Hypothermic Machine Perfusion Increases A20 Expression Which Protects Renal Cells Against Ischemia/Reperfusion Injury By Suppressing Inflammation, Apoptosis And Necroptosis[J]. International Journal of Molecular Medicine, 2016, 38(1): 161-171.|3. Wang Y L, Gao G P, Wang Y Q, et al. Inhibitory Effects Of S100A4 Gene Silencing On Alkali Burn-Induced Corneal Neovascularization: An In Vivo Study[J]. Molecular Vision, 2017, 23: 286.|4. Menchetti L, Barbato O, Filipescu I E, et al. Effects Of Local Lipopolysaccharide Administration On The Expression Of Toll-Like Receptor 4 And Pro-Inflammatory Cytokines In Uterus And Oviduct Of Rabbit Does[J]. Theriogenology, 2017.|5. Pan Y Y, Zhou F H, Song Z H, et al. Oleanolic acid protects against pathogenesis of atherosclerosis, possibly via FXR-mediated angiotensin (Ang)-(1-7) upregulation[J]. Biomedicine & Pharmacotherapy, 2018, 97: 1694-1700.|Sample Type: Serum and culture supernatant|6. Chaniotakis I, Antoniou E, Kostomitsopoulos N, et al. Stress response to ovariohysterectomy in rabbits: role of anaesthesia and surgery[J]. Journal of Obstetrics and Gynaecology, 2018: 1-5.|7. Zhang D, Liu W, Wen Z, et al. Establishment of a New Zealand White Rabbit Model for Lethal Toxin (LT) Challenge and Efficacy of Monoclonal Antibody 5E11 in the LT-Challenged Rabbit Model[J]. Toxins, 2018, 10(7):289.