Human IL-5/Interleukin-5 ELISA Kit PicoKine(r)

Name: Human IL-5/Interleukin-5 ELISA Kit PicoKine(r)
SKU: EK0407_1x96wellplate_B70
Availability: BackOrder

EK0407

Product group Assays

Overview

Supplier
Boster Bio
Product Name
Human IL-5 PicoKine ELISA Kit
Delivery Days Customer
9
Applications
ELISA
Applications Supplier
ELI
Assay Detection Range
7.8 pg/ml - 500 pg/ml
Assay Sensitivity
<2 pg/ml
Assay Time
15-20
Certification
Research Use Only
Scientific Description
Human IL-5/Interleukin-5 ELISA Kit PicoKine® (96 Tests). Quantitate Human IL5 in cell culture supernatants, serum, plasma (heparin, EDTA) and urine. Sensitivity: 2pg/ml. The brand Picokine indicates this is a premium quality ELISA kit. Each Picokine kit delivers precise quantification, high sensitivity, and excellent reproducibility. Only our most reliable and effective kits qualify as Picokine, guaranteeing top-tier results for your assays.
Reactivity Supplier
Human IL-5
Storage Instruction
-20°C,2°C to 8°C
UNSPSC
41116158

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Li Q, Zhang J, Ma L, et al. ILC2s induce adaptive Th2-type immunity in different stages of tuberculosis through the Notch-GATA3 pathway. Int Immunopharmacol. 2021,101(Pt B):108330. doi: 10.1016/j.intimp.2021.108330
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Wei Q, Liao J, Jiang M, et al. Relationship between Th17-mediated immunity and airway inflammation in childhood neutrophilic asthma. Allergy Asthma Clin Immunol. 2021,17(1):4. doi: 10.1186/s13223-020-00504-3
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Cuiju W, Shibiao S, Ying T, et al. IL-2 and IL-2R gene polymorphisms and immune function in people residing in areas with high background radiation, Yangjiang, China. Int J Radiat Biol. 2020,96(11):1466-1472. doi: 10.1080/09553002.2020.1820607
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Tsai YG, Liou JH, Hung SI, et al. Increased Type 2 Innate Lymphoid Cells in Patients with Drug Reaction with Eosinophilia and Systemic Symptoms Syndrome. J Invest Dermatol. 2019,139(8):1722-1731. doi: 10.1016/j.jid.2018.10.048
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Tang Z, Ye G, Chen X, et al. Peripheral proinflammatory cytokines in Chinese patients with generalised anxiety disorder. J Affect Disord. 2018,225:593-598. doi: 10.1016/j.jad.2017.08.082
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