IL-1β (human), ELISA kit



ADI-900-130A	96 wells	696.00 USD
Do you need bulk/larger quantities?

Replaces Prod. #: ADI-900-130

Sensitive - quantify down to 1 pg/mL
Efficient - only 50 µl diluted sample required saving precious materials
Specific - no cross-reactivity with related cytokines
Results from up to 40 samples in duplicate in just 3 hours
Ready-to-use reagents and pre-coated plates reduce errors and save your time

The IL-1β (human), EIA kit is a colorimetric immunometric enzyme immunoassay kit with results in < 3 hours. Absorbance is read at 450 nm. Quantify 1 pg/mL IL-1β with lot sample volume needed saving you precious sample.

Product Details

Alternative Name:	Interleukin-1β

Sensitivity:	1 pg/mL

Assay Time:	< 3 hours

Applications:	ELISA, Colorimetric detection

Application Notes:	For the quantitative determination of IL-1β in culture supernatant, plasma, serum, and urine of human origin.

Wavelength:	450 nm

Species reactivity:	Human

Crossreactivity:	The following substances were tested and found to have no cross-reactivity: human IL-1α, IL-1ra, IL-2, IL-3, IL-4, IL-6, IL-7, IL-8, IL-10, IFN-α, TGF-β, GM-CSF, G-CSF, OSM, MIP-1α, MIP-1β, LIF, MCP-1, G-CSF, RANTES, PF-4, βTG, GRO, IP-10, SCF, TNF-α, and TNF-β.

Shipping:	Shipped on Blue Ice

Short Term Storage:	+4°C

Long Term Storage:	+4°C

Contents:	Standard, Standard Diluent Buffer, Coated 96-well plate, Conjugate, Streptavidin-HRP, Streptavidin-HRP Diluent, Wash Buffer Concentrate, TMB Solution, Stop Solution, Plate Sealers

Scientific Background:	The interleukin-1 (IL-1) cytokine family consists of IL-1α, IL-1β, and IL-1Rα (receptor antagonist) which are expressed primarily by endothelial cells and activated macrophages. IL-1α and IL-1β elicit pro-inflammatory cytokine production and cellular activation, and are the primary mediators of hypothalamic regulation that results in fever. IL-1α and IL-1βsignals are transmitted via a dual subunit IL-1 receptor composed of IL-1R1 and the IL-1 receptor accessory protein (IL-1RAcP). IL-1RAcP is vital to IL-1 signaling, as it recruits the IL-1 receptor-associated kinase (IRAK) to the receptor complex, initiating NF-κB pathway activation.

Technical Info/Product Notes:	Cited samples: Cytokine ELISAs Cited Samples

UniProt ID:	P01584

Regulatory Status:	RUO - Research Use Only

Compatibility:	This product is compatible with the Absorbance 96 Plate Reader.

Product Literature References

Effects of photobiomodulation and a physical exercise program on the expression of inflammatory and cartilage degradation biomarkers and functional capacity in women with knee osteoarthritis: a randomized blinded study: P.G. Vassão, et al.; Adv. Rheumatol. 61, 62 (2021), Abstract;

Involvement of the P2X7 receptor in the migration and metastasis of tamoxifen-resistant breast cancer: effects on small extracellular vesicles production: M. Park, et al.; Sci. Rep. 9, 11587 (2019), Abstract; Full Text

COMP-angiopoietin-1 ameliorates inflammation-induced lymphangiogenesis in dextran sulfate sodium (DSS)-induced colitis model: A. S. Lee, et al.; J. Mol. Med. (Berl.) 96, 459 (2018), Application(s): EIA w. mouse serum, Abstract; Full Text

Follow-Up of Peripheral IL-1β and IL-6 and Relation with Apoptotic Death in Drug-Resistant Temporal Lobe Epilepsy Patients Submitted to Surgery: L. Lorigados Pedre, et al.; Behav. Sci. (Basel) 8, 21 (2018), Abstract;

Gene therapy with RALA/iNOS composite nanoparticles significantly enhances survival in a model of metastatic prostate cancer: C.M. McCrudden, et al.; Cancer Nanotechnol. 9, 5 (2018), Abstract; Full Text

Cell phone use is associated with an inflammatory cytokine profile of parotid gland saliva: E.C. Siqueira, et al.; J. Oral Pathol. Med. 45, 682 (2016), Application(s): ELISA using human saliva, Abstract;

Vitamin D2 suppresses amyloid-β 25-35 induced microglial activation in BV2 cells by blocking the NF-κB inflammatory signaling pathway: S. Raha, et al.; Life Sci. 161, 37 (2016), Application(s): Assessment of the inhibitory effect of VD2 on the production of pro-inflammatory cytokines, Abstract;