LEGEND MAX™ Mouse IFN-β ELISA Kit

Pricing & Availability
Regulatory Status
RUO
Other Names
Fibroblast interferon (Fi-IFN, F-IFN), Type-1 interferon, acid-stable interferon, R1-GI factor, IFN-β Pre-coated ELISA Kit
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IFNb_Mouse_leg_070612
  • IFNb_Mouse_leg_070612
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439407 1 Pre-coated Plate 463€
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Description

Interferon-β is a member of the type I interferon class. Type I IFNs are involved in the innate immune system, being released non-specifically during the early stage of infection in response to stimuli such as viruses, dsRNA, LPS, and bacterial components. Once secreted by virus-infected or activated cells, they bind to the IFNα/β receptor (IFNAR), which is found on almost all cell types. Then, via the JAK-STAT pathway, they induce the expression of hundreds of IFN-stimulated genes (ISGs). While the function of many of these proteins remains to be elucidated, a hallmark of type I IFNs is their anti-viral activities, both general and specific against particular viruses. Type I IFNs also regulate cell growth and apoptosis, and exert various immunomodulatory and inflammatory effects. As such, they are clinically relevant, both as therapeutics and as targets of inhibition for the treatment of various autoimmune diseases and cancer.


Mouse IFN-β is a ~20 kD monomeric glycoprotein. It has 50% amino acid sequence homology with mouse IFN-α, its closest related protein, and 62% homology with human IFN-β. IFN-β is currently the therapeutic of choice for treating multiple sclerosis.

BioLegend’s LEGEND MAX™ Mouse IFN-β ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (ELISA), in which, a specific antibody is pre-coated on a 96-well strip-well plate.

BioLegend’s LEGEND MAX™ Mouse IFN-β ELISA Kit is specifically designed for the accurate quantitation of mouse IFN-β from cell culture supernatant, serum, plasma or other bodily fluids. It is ready-to-use, accurate, and sensitive.

Product Details
Technical Data Sheet (pdf)

Kit Contents

Kit Contents
  • Anti-Mouse IFN-β Pre-coated 96-well Strip Microplate
  • Mouse IFN-β Dectection Antibody
  • Mouse IFN-β Standard
  • Avidin-HRP D
  • Matrix C (for serum and plasma samples only)
  • Assay Buffer A
  • Wash Buffer (20X)
  • Substrate Solution F
  • Stop Solution
  • Plate Sealers

Product Details

Verified Reactivity
Mouse
Application

ELISA

Application References

(PubMed link indicates BioLegend citation)
  1. Shah S, et al. 2013. J. Immunol. 191:3514. PubMed
  2. Wang S, et al. 2013. J Virol. 87:11851. PubMed
Product Citations
  1. Oldenburg R, et al. 2018. Front Immunol. 9:2. PubMed
  2. Xie X, et al. 2021. BMC Med. 19:247. PubMed
  3. Zhou C, et al. 2020. Immunity. 52:767. PubMed
  4. Shah S, et al. 2013. J Immunol. 191:3514. PubMed
  5. Yan S, et al. 2018. J Immunol. 200:1016. PubMed
  6. Zhou P, et al. 2018. Nat Commun. 9:1243. PubMed
  7. Zhao M, et al. 2021. PLoS Pathog. 17:e1009901. PubMed
  8. Klopfenstein N, et al. 2021. PLoS Pathog. 17:e1009387. PubMed
  9. Cheng WY, et al. 2018. Front Immunol. 9:1297. PubMed
  10. Yoshida A, et al. 2018. J Virol. 92:e02094. PubMed
  11. Wu D, et al. 2022. Cell Death Dis. 13:731. PubMed
  12. Piersma SJ, et al. 2020. Elife. 9:00. PubMed
  13. Jiang H, et al. 2016. J Immunol. 197: 2880 - 2890. PubMed
  14. Kwon HK, et al. 2019. Exp Mol Med. 51:50. PubMed
  15. Ferri F, et al. 2015. Nat Commun. 6: 8900. PubMed
  16. Fritzlar S, et al. 2019. MBio. 10:e00960. PubMed
  17. Synn CB, et al. 2022. Yonsei Med J. 63:42. PubMed
  18. Stavrou S, et al. 2018. MBio. 9:e00923. PubMed
  19. Chen Y, et al. 2021. Front Immunol. 12:672165. PubMed
  20. Li K, et al. 2021. Sci Adv. 7: . PubMed
  21. Srikanth S, et al. 2019. Nat Immunol. 20:152. PubMed
  22. Kim KS, et al. 2021. J Leukoc Biol. 109:865. PubMed
  23. Reimer E, et al. 2020. J Cell Sci. 134:00:00. PubMed
  24. Nanda S, et al. 2016. J Immunol. 197(11):4266-4273. PubMed
  25. Sousa J, et al. 2020. Nat Commun. 11:1949. PubMed
  26. Shepardson K, et al. 2016. MBio. 7: e00506-16. PubMed
  27. Wu Y, Ren D, Chen G 2016. J Immunol. 197: 3336 - 3347. PubMed
  28. Zhu M, et al. 2015. J Immunol. 195: 289 - 297. PubMed
  29. Huang F, et al. 2021. Front Immunol. 12:707298. PubMed
  30. Raychowdhury R, et al. 2021. Immunohorizons. 5:818. PubMed
  31. Qiu W, et al. 2021. Nat Commun. 1582:12. PubMed
  32. Khan M, et al. 2020. PLoS Pathog. 16:e1009020. PubMed
  33. Chen X, et al. 2021. J Immunol. :. PubMed
  34. Lv M, et al. 2015. Sci Rep. 5: 12954. PubMed
  35. Wang L, et al. 2022. Nat Commun. 13:7107. PubMed
  36. Yang S, et al. 2019. Sci Adv. 5:eaav7999. PubMed
  37. Li X, et al. 2022. Sci Rep. 12:17058. PubMed
  38. Zhang Y, et al. 2022. Nat Commun. 13:4948. PubMed
  39. Saddawi-Konefka R, et al. 2022. Nat Commun. 13:4298. PubMed
  40. Karki R, et al. 2020. J Immunol. 204:2514. PubMed
  41. Wang S, et al. 2013. J Virol. 87:11851. PubMed
  42. Tong Y, et al. 2018. EBioMedicine. 39:132. PubMed
Sensitivity
1.9 pg/mL
Standard Range
7.8-500 pg/mL
Materials Not Included
  • Microplate reader able to measure absorbance at 450 nm
  • Adjustable pipettes to measure volumes ranging from 1 µL to 1,000 µL
  • Deionized water
  • Wash bottle or automated microplate washer
  • Log-Log graph paper or software for data analysis
  • Tubes to prepare standard dilutions
  • Timer
  • Plate Shaker
  • Polypropylene vials

Antigen Details

Cell Sources
Fibroblasts, epithelial cells
Biology Area
Apoptosis/Tumor Suppressors/Cell Death, Cell Biology, Signal Transduction
Molecular Family
Cytokines/Chemokines
Gene ID
15977 View all products for this Gene ID
UniProt
View information about IFN-beta on UniProt.org

Related FAQs

In your LEGEND MAX™ ELISA Kits, there is a step that calls for washing the plates before adding sample. What is the purpose of this step?

We typically use a stabilizer for pre-coated plates. The additional washing step is designed to remove these components before you start the assay. If you do not perform the washing, the effect on assay performance is negligible.

I have multiple LEGEND MAX™ ELISA kits that I want to run simultaneously. Can I use the same wash buffer for all the kits?

The wash buffer provided in all our LEGEND MAX™ kits is the same and the part numbers on the wash buffer bottles in these kits should be identical. For ELISA MAX™ Deluxe and ELISA MAX™ Standard Sets, we provide a recipe for the wash buffer on each kit’s technical data sheet. This recipe is the same for all ELISA MAX™ sets.

For some of your ELISA kits, why do my serum samples require dilution with assay buffer?

In some cases, dilution with assay buffer is required to minimize the matrix difference between the samples and the standards to achieve better accuracy.

Go To Top Version: 3    Revision Date: 01.16.2017

For Research Use Only. Not for diagnostic or therapeutic use.

 

This product is supplied subject to the terms and conditions, including the limited license, located at www.biolegend.com/terms) ("Terms") and may be used only as provided in the Terms. Without limiting the foregoing, BioLegend products may not be used for any Commercial Purpose as defined in the Terms, resold in any form, used in manufacturing, or reverse engineered, sequenced, or otherwise studied or used to learn its design or composition without express written approval of BioLegend. Regardless of the information given in this document, user is solely responsible for determining any license requirements necessary for user’s intended use and assumes all risk and liability arising from use of the product. BioLegend is not responsible for patent infringement or any other risks or liabilities whatsoever resulting from the use of its products.

 

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