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anti-Human IL5 Antibodies:
anti-Mouse (Murine) IL5 Antibodies:
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Human Monoclonal IL5 Primary Antibody for CyTOF, ELISA (Capture) - ABIN4900785
Xavier-Elsas, Santos-Maximiano, Queto, Mendonça-Sales, Joseph, Gaspar-Elsas, Vargaftig: Ectopic lung transplantation induces the accumulation of eosinophil progenitors in the recipients' lungs through an allergen- and interleukin-5-dependent mechanism. in Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology 2007
Show all 13 Pubmed References
Mouse (Murine) Monoclonal IL5 Primary Antibody for ICS, Neut - ABIN1176999
Abrams: Immunoenzymetric assay of mouse and human cytokines using NIP-labeled anti-cytokine antibodies. in Current protocols in immunology / edited by John E. Coligan ... [et al.] 2008
Show all 9 Pubmed References
Human Monoclonal IL5 Primary Antibody for Inhibition, ELISA - ABIN2689772
Abrams, Roncarolo, Yssel, Andersson, Gleich, Silver: Strategies of anti-cytokine monoclonal antibody development: immunoassay of IL-10 and IL-5 in clinical samples. in Immunological reviews 1992
Show all 8 Pubmed References
Human Monoclonal IL5 Primary Antibody for Inhibition, ELISA - ABIN2689771
Butterfield, Leiferman, Abrams, Silver, Bower, Gonchoroff, Gleich: Elevated serum levels of interleukin-5 in patients with the syndrome of episodic angioedema and eosinophilia. in Blood 1992
Show all 5 Pubmed References
Human Monoclonal IL5 Primary Antibody for ELISA - ABIN2689775
Denburg, Silver, Abrams: Interleukin-5 is a human basophilopoietin: induction of histamine content and basophilic differentiation of HL-60 cells and of peripheral blood basophil-eosinophil progenitors. in Blood 1991
Show all 4 Pubmed References
Mouse (Murine) Monoclonal IL5 Primary Antibody for ELISA - ABIN2689774
Sander, Andersson, Andersson: Assessment of cytokines by immunofluorescence and the paraformaldehyde-saponin procedure. in Immunological reviews 1991
Show all 4 Pubmed References
Human Monoclonal IL5 Primary Antibody for FACS - ABIN4898071
Alisa, Boswell, Pathan, Ayaru, Williams, Behboudi: Human CD4(+) T cells recognize an epitope within alpha-fetoprotein sequence and develop into TGF-beta-producing CD4(+) T cells. in Journal of immunology (Baltimore, Md. : 1950) 2008
Show all 2 Pubmed References
Human Monoclonal IL5 Primary Antibody for CyTOF, FACS - ABIN4900611
Sen, Chunsong, Baojun, Linjie, Qun, San, Qiuping, Junyan, Zhang, Jinquan: Aberration of CCR7 CD8 memory T cells from patients with systemic lupus erythematosus: an inducer of T helper type 2 bias of CD4 T cells. in Immunology 2004
Show all 2 Pubmed References
Guinea Pig Polyclonal IL5 Primary Antibody for WB - ABIN610960
Beckhelling, Chang, Chevalier, Ford, Houliston: Pre-M phase-promoting factor associates with annulate lamellae in Xenopus oocytes and egg extracts. in Molecular biology of the cell 2003
eosinophilia in FE is secondary to dysregulation of IL-5 production in PBMC (and their component subsets).
Data indicate that interleukin-5 (IL-5) was that only serum cytokines show statistical significance between severe chronic obstructive pulmonary disease (COPD (show ARCN1 Antibodies)) and controls.
Serum IL-5 and IL-13 (show IL13 Antibodies) are reliable biomarkers for the blood eosinophilia asthma phenotype.
Obesity alters the lung neutrophil infiltration to enhance breast cancer metastasis through IL5 and GM-CSF (show CSF2 Antibodies).
simvastatin was demonstrated to inhibit IL-5-induced CCR3 (show CCR3 Antibodies) expression and chemotaxis of eosinophils mediated via the mevalonate pathway.
Interleukin-5/-targeted treatments offer promises to patients with eosinophilic respiratory disorders; review
Data indicate that interleukin 5 (IL-5)-associated single nucleotide polymorphisms (SNPs) were not associated with carotid intima-media thickness.
Post-liver transplant patients with food allergy showed a unique cytokine profile in response to various stimuli, with extremely elevated IL-5, low IL-10 (show IL10 Antibodies) secretion.
high levels of IL-33 (show IL33 Antibodies) and a high IL-33 (show IL33 Antibodies)/soluble ST2 (show SULT2A1 Antibodies) ratio correlates with elevated levels of IFN-gamma (show IFNG Antibodies), TNF-alpha (show TNF Antibodies) and IL-17alpha as well as IL-5, demonstrating that IL-33 (show IL33 Antibodies) has pleiotropic effects.
Production of IL-5 in response to both extract and the Bet v1-derived peptide mix strongly suggested that T cells were a major source of IL-5.
IL-33 (show IL33 Antibodies) acts directly on bone marrow ILC2s, making them an early source of IL-5 and part of a process that is central in IL-33 (show IL33 Antibodies)-driven eosinophilia.
these studies establish a basal defect in eosinophilopoiesis in IL-33 (show IL33 Antibodies)- and ST2 (show SULT2A1 Antibodies)-deficient mice and a mechanism whereby IL-33 (show IL33 Antibodies) supports eosinophils by driving both systemic IL-5 production and the expansion of IL-5Ralpha-expressing precursor cells
Increased production of IL-5 from Peyer's patch cells and the restored Th1 (show HAND1 Antibodies)-type immune response might cause the production of abnormal IgA (show IgA Antibodies) and might induce the glomerular deposition of IgA (show IgA Antibodies) in IGA (show IgA Antibodies) nephropathy.
E. granulosus infection remarkably reduces the severity of OVA-induced airway inflammation likely through enhancing IL-10 (show IL10 Antibodies) and down-regulation of IL-5 and IL-17A (show IL17A Antibodies).
selective proliferation of IgM (show CD40LG Antibodies) rheumatoid factor-secreting B-1a cells is induced by co-stimulation by the specific pathogen antigen and IL-5 in the development of MC in Capillaria hepatica-infected mice
IL5, a cytokine involved in allergic and infectious diseases, facilitates metastatic colonization through recruitment of sentinel eosinophils and regulation of other inflammatory/immune cells in the microenvironment of the distal lung.
In mice, low-dose IL-2 (show IL2 Antibodies)-anti-IL-2 (show IL2 Antibodies) antibody complexes drove group 2 innate lymphoid cells (ILC2) to produce IL-5 and proliferate.
Data (including data from knockout mice) suggest that up-regulation of IL5 production in lungs during influenza virus infection is due to infiltration of natural killer cells and alveolar macrophages into infected lung tissue.
A decrease in the levels of IL-5, IL-9 (show IL9 Antibodies), and IL-6R in the BALF.
This study showed that pronounced lung eosinophilia in horses can be transient, abate without specific treatment, and in this instance, lack correlation to upregulation of expression of either IL-4 (show IL4 Antibodies) or IL-5.
The protein encoded by this gene is a cytokine that acts as a growth and differentiation factor for both B cells and eosinophils. This cytokine is a main regulator of eosinopoiesis, eosinophil maturation and activation. The elevated production of this cytokine is reported to be related to asthma or hypereosinophilic syndromes. The receptor of this cytokine is a heterodimer, whose beta subunit is shared with the receptors for interleukine 3 (IL3) and colony stimulating factor 2 (CSF2/GM-CSF). This gene, together with those for interleukin 4 (IL4), interleukin 13 (IL13), and CSF2, form a cytokine gene cluster on chromosome 5. This cytokine, IL4, and IL13 are found to be regulated coordinately by long-range regulatory elements spread over 120 kilobases on chromosome 5q31.
B-cell differentiation factor I
, T-cell replacing factor
, eosinophil differentiation factor
, B-cell growth factor II
, cytotoxic T-lymphocyte inducer
, Interleukin 5 (colony-stimulating factor eosinophil)
, Interleukin 5 (colony-stimulating factor, eosinophil)
, colony-stimulating factor, eosinophil
, interleukin 5
, interleukin 5 (colony-stimulating factor, eosinophil)