Use your antibodies-online credentials, if available.
No Products on your Comparison List.
Your basket is empty.
Find out more
Show all species
Show all synonyms
Select your species and application
anti-Mouse (Murine) IL1B Antibodies:
anti-Rat (Rattus) IL1B Antibodies:
anti-Human IL1B Antibodies:
Go to our pre-filtered search.
Human Monoclonal IL1B Primary Antibody for CyTOF, FACS - ABIN4899223
Yates, Burgess, Kocsis-Angle, Antal, Dority, Embury, Piotrkowski, Brunden: Amyloid beta and amylin fibrils induce increases in proinflammatory cytokine and chemokine production by THP-1 cells and murine microglia. in Journal of neurochemistry 2000
Show all 15 Pubmed References
Human Monoclonal IL1B Primary Antibody for CyTOF, FACS - ABIN4899224
Oliver, Lovric, Yu, Christou, Aiken, Cooper, Walsh: Development of a Novel Model for the Assessment of Dead-Space Management in Soft Tissue. in PLoS ONE 2015
Show all 15 Pubmed References
Dog (Canine) Polyclonal IL1B Primary Antibody for IF (p), IHC (p) - ABIN728503
Zhong, Shu, Wang, Luo, Zhong, Ran, Zheng, Yin, Ling: Enhanced homing of mesenchymal stem cells to the ischemic myocardium by ultrasound-targeted microbubble destruction. in Ultrasonics 2011
Show all 11 Pubmed References
Bacteria Polyclonal IL1B Primary Antibody for ELISA, EM - ABIN269770
Petrovski, Ayna, Majai, Hodrea, Benko, Mádi, Fésüs: Phagocytosis of cells dying through autophagy induces inflammasome activation and IL-1β release in human macrophages. in Autophagy 2011
Show all 10 Pubmed References
Mouse (Murine) Polyclonal IL1B Primary Antibody for Neut, WB - ABIN223538
Scott, Ma, Viriyakosol, Terkeltaub, Liu-Bryan: Engagement of CD14 mediates the inflammatory potential of monosodium urate crystals. in Journal of immunology (Baltimore, Md. : 1950) 2006
Show all 6 Pubmed References
Dog (Canine) Polyclonal IL1B Primary Antibody for IHC, ELISA - ABIN1582289
Choi, Lim, Hwang, Lee, Cho, Kim: Anti-ischemic and anti-inflammatory activity of (S)-cis-verbenol. in Free radical research 2010
Show all 6 Pubmed References
Human Polyclonal IL1B Primary Antibody for IHC (p), IHC - ABIN446969
Omran, Peng, Zhang, Xiang, Xue, Gan, Kong, Yin: Interleukin-1β and microRNA-146a in an immature rat model and children with mesial temporal lobe epilepsy. in Epilepsia 2012
Show all 5 Pubmed References
Mouse (Murine) Monoclonal IL1B Primary Antibody for IP, Neut - ABIN1176987
Fei, Gott, Edwards, Schuyler: Experimental hypersensitivity pneumonitis: in vitro effects of interleukin-2 and interferon-gamma. in The Journal of laboratory and clinical medicine 1995
Show all 4 Pubmed References
Mouse (Murine) Polyclonal IL1B Primary Antibody for ELISA, FACS - ABIN4324365
Triantafilou, Kar, Vakakis, Kotecha, Triantafilou: Human respiratory syncytial virus viroporin SH: a viral recognition pathway used by the host to signal inflammasome activation. in Thorax 2012
Show all 4 Pubmed References
Human Monoclonal IL1B Primary Antibody for FACS - ABIN4895765
Hussain, Kong, Jordan, Conrad, Madden, Fokt, Priebe, Heimberger: A novel small molecule inhibitor of signal transducers and activators of transcription 3 reverses immune tolerance in malignant glioma patients. in Cancer research 2007
Show all 4 Pubmed References
Leukocyte expression of IL-1beta was detectable only following injury, which activated leukocytes throughout zebrafish embryos in a caspase (show CASP3 Antibodies) dependent manner.
Embryo and larva leukocytes upregulate IL-1beta expression proportional to the dose of ultraviolet radiation exposure in an immune response at the organismal level.
findings reveal that the Il-1beta-Myd88 (show MYD88 Antibodies) axis and NADPH oxidase (show NOX1 Antibodies)-mediated ROS (show ROS1 Antibodies) signaling are two independent pathways that differentially regulate neutrophil migration during sterile inflammation.
the expression levels of IL-1beta and TNF-alpha in high cholesterol diet (HCD)-fed zebrafish larvae
These results represent the first demonstration of processing and secretion of zebrafish IL-1beta in response to a pathogen.
The current study demonstrated that honey can stimulate or suppress the mRNA expression of some pro-inflammatory cytokines in mice brains. Furthermore, honey suppresses the TNF-alpha (show TNF Antibodies) mRNA expression in the presence of T. gondii infection but it stimulates the IL-1beta and IL-6 (show IL6 Antibodies) mRNA expression. Treatment of the mice with honey reduces parasite multiplication in the brain.
IL-1beta has a direct effect on NGAL (show LCN2 Antibodies) production by tubular epithelial cells.
Following vasectomy, IL1alpha (show IL1A Antibodies), IL1beta, IL1ra (show IL1RN Antibodies), IL10 (show IL10 Antibodies), and TNF-alpha (show TNF Antibodies) may mediate immune reaction in whole epididymis, whereas IL6 (show IL6 Antibodies) and TGF-beta1 (show TGFB1 Antibodies) may mediate regionally different immune response primarily in the lower part of epididymis.
Elevations of CO2 cause oligomerization of the inflammasome components ASC (show STS Antibodies), NLRP3 (show NLRP3 Antibodies), caspase 1 (show CASP1 Antibodies), thioredoxin interacting protein (show TXNIP Antibodies), and calreticulin (show CALR Antibodies) - a protein from endoplasmic reticulum, leading to IL-1beta synthesis. An increased production rate of MPs containing elevated amounts of IL-1beta persists for hours after short-term exposures to elevated CO2
dimerized or endogenous caspase-8 (show CASP8 Antibodies) can also directly cleave IL-1beta into its biologically active form, in the absence of canonical inflammasome components.
In this newborn mouse lung hypoxia-reoxygenation model, we found downregulation of genes of mediators of inflammation, an antiapoptotic gene expression pattern, and downregulation of DNA glycosylases. Sod1 (show SOD1 Antibodies) and Il1b were significantly differentially expressed when comparing reoxygenation using 60% O2 with air.
Report direct role of pleural cells in the pathogenesis of bleomycin-induced pulmonary fibrosis via caspase-1 (show CASP1 Antibodies)/IL-1beta pathway.
the senescence associated secretory phenotype was also increased significantly in the kidney of Sod1 (show SOD1 Antibodies)(-/)(-) mice compared to WT mice as measured by the expression of transcripts for IL-6 (show IL6 Antibodies) and IL-1b
These studies elucidate an important role for neutrophils and IL-1beta in lung carcinogenesis.
PLCd1 (show PLCD1 Antibodies) negatively regulates lipopolysaccharide-induced production of IL-1b and Fc gamma receptor (show FCGR1A Antibodies)-mediated phagocytosis in macrophages.
An association with IL-1beta-511 locus and IL-1beta-511-TLR4 (show TLR4 Antibodies)-896 diplotype (CC-AA) and Type 2 Diabetes Mellitus is discussed.
IL-1beta degrades the ventilatory hypoxic response by stimulating production of prostaglandin
The plasma levels of interleukin (IL)-1beta, tumor necrosis factor (TNF)-alpha (show TNF Antibodies), tissue inhibitor of metalloproteinases (TIMP)-1 (show TIMP1 Antibodies) are increased in myelofibrosis (MF) patients.
Absolute numbers of MIF (show AMH Antibodies) and IL-1beta mRNA molecules are both accurate and reliable predictors of antidepressant response.
results showed that Gypenoside dose-dependently inhibited IL-1beta-induced NO and PGE2 production in human osteoarthritis chondrocytes.
tuberculous lymphadenitis (TBL) is therefore, characterized by reduced systemic and antigen-specific concentrations of IL-1beta and IL-18 (show IL18 Antibodies), which are reversible following anti-TB treatment, indicating that these cytokines are potential correlates of protective immunity in TBL.
p27(kip1 (show CDKN1B Antibodies)) overexpression regulates IL-1beta in the microenvironment of stem cells and eutopic endometriosis
Among the polymorphisms studied, only IL1beta (-511C>T) was associated with dizziness, (p = 0.01), suggesting that IL1beta may be related to hypotensive episodes and increased vascular permeability in dengue patients.
Both rs16944 and rs1143643 single nucleotide polymorphisms (SNPs) within the IL1B gene show specific environmental stressor-dependent effects on mood disorder symptoms.
Increased levels of IL-17A (show IL17A Antibodies) and IL-1beta cytokines and decreased expression of MITF (show MITF Antibodies) suggested a possible role of these cytokines in dysregulation of melanocytic activity in the lesional skin and hence might be responsible for the progression of active vitiligo (show MITF Antibodies).
This study showed that classical swine fever virus and p7 protein induced IL-1beta secretion and that p7 protein was a short-lived protein degraded by the proteasome.
local expression of IL-1beta and IL-8 (show IL8 Antibodies) in non-bacterial thrombotic endocarditis, Staphylococcus aureus infective endocarditis, animals with S. aureus sepsis without endocarditis and controls
IL1B regulates expression of IL1R1 (show IL1RN Antibodies) and IL1RAP (show IL1RAP Antibodies) and stimulates expression of PTGS1 (show PTGS1 Antibodies) and PTGS2 (show PTGS2 Antibodies) that are considered to be the most rate-limiting enzymes for endometrial synthesis of prostaglandins during the peri (show PLIN1 Antibodies)-implantation period of pregnancy in pigs.
the results presented here strongly suggest IL-1beta as a key molecule guiding tissue remodelling events after myocardial infarction.
The presence of embryos increased endometrial IL1B protein locally, while no differences regarding IL1R1 (show IL1RN Antibodies) protein and IL1B and IL1R1 (show IL1RN Antibodies) mRNA were detected.
For the inflammasome-dependent IL-1beta release, bovine monocytes require ATP in addition to a primary stimulus. This IL-1beta release depends on potassium efflux, but, in contrast to human and murine monocytes, does not require calcium influx or generation of reaction oxygen and is independent of the P2X7 receptor (show P2RX7 Antibodies).
Role of TGF-beta1 (show TGFB1 Antibodies) and TNF-alpha (show TNF Antibodies) in IL-1beta mediated activation of proMMP-9 in pulmonary artery smooth muscle cells: involvement of an aprotinin sensitive protease.
Testicular IL-1 alpha (show IL1A Antibodies) and IL-1 beta concentrations were highest in the early post-natal period; however, IL-1 (show IL1A Antibodies) bioactivity and IL-6 (show IL6 Antibodies) concentrations were greatest in the immediate pre-pubertal period.
Data describe the expression of IL-8, IL-1beta and their respective receptors, CXCR1 and IL-1R1 in bovine theca cells, and suggest that VEGF is associated with the IL system in theca cells in ovary.
Genes for IL-1alpha and IL-1beta are expressed and a functional IL-1R is present in bovine corpora lutea throughout luteal phase. IL-1alpha and IL-1beta may have different roles as regulating PGF (show PGF Antibodies)(2alpha) and PGE (show LIPF Antibodies)(2) production during luteal phase.
non-metalloproteinase mechanisms participate in IL-1 (show IL1A Antibodies)-induced matrix degradation and loss of tissue material properties
dynamic compression stimulates cell proliferation and proteoglycan (show Vcan Antibodies) synthesis in the presence of IL-1beta and/or inhibitors of the MAPKs and NFkappaB and AP-1 (show JUN Antibodies) signalling pathways
These results indicate that activation of the intrinsic antistaphylococcal response in bovine endothelial cells (BEC), enhanced by TNF-alpha (show TNF Antibodies) and IL-1beta, is effective to eliminate S. aureus and S. epidermidis.
the low friction of articular cartilage can be modified by TGF-beta1 (show TGFB1 Antibodies) and IL-1beta treatment and that the friction coefficient depends on multiple factors, including superficial zone protein localization and surface roughness
Mild heat shock increased the production of inflammatory cytokines, IL-1beta and IL-6 (show IL6 Antibodies) in rabbit cornea cells.
IL-1beta and TNF-alpha (show TNF Antibodies) expression increases significantly during acute lung injury. Ambroxol combined with low-dose heparin inhibits teh release of IL-1beta and TNF-alpha (show TNF Antibodies).
IL-1beta induced a significant reduction in the relative intrinsic activity of GLUT5 (show SLC2A5 Antibodies) and in this decrease are involved NO signal pathways; blockage of D-fructose intestinal uptake by IL-1beta may play an essential role in the pathophysiology of septic shock.
The inhibitory effect of IL-1beta on D-galactose absorption across mucosal side of enterocyte could be mediated by the activation of several kinases and nuclear factor kappa B.
Glucosamine hydrochloride treatment can can partially decrease the expression levels of IL-1 beta and increase the expression levels of TGF-beta 1 (show TGFB1 Antibodies), which delays the development of osteoarthritis.
In this study evidence is provided that exogenous PGF2alpha differentially modulates luteal expression of IL1B transcripts depending on luteal stage.
results revealed that a transient episode of raised-intensity phonation causes a significant increase in vocal fold inflammatory mRNA expression - IL-1beta,COX-2 (show COX2 Antibodies), and TGFbeta1 (show TGFB1 Antibodies)
Increased PGE2 production led to reduction in 5-LO (show ALOX5 Antibodies) products in LPS (show IRF6 Antibodies)-treated equine whole blood via IL-1b.
Results suggested that chemokine (show CCL1 Antibodies) expression by cultured equine BECs following exposure to pulmonary hemorrhage conditions may contribute to the development of inflammatory airway disease in horses.
IL-1beta-induced up-regulation of matrix metalloproteinase 13 (show MMP13 Antibodies) mRNA was blocked by all concentrations of geldanamycin tested
This study examined effects of in vitro exposure to solutions of hay (show GTF2H5 Antibodies) dust, lipopolysaccharides, or beta-glucan on cytokine expression in pulmonary mononuclear cells isolated from healthy horses and horses with recurrent airway obstruction.
The protein encoded by this gene is a member of the interleukin 1 cytokine family. This cytokine is produced by activated macrophages as a proprotein, which is proteolytically processed to its active form by caspase 1 (CASP1/ICE). This cytokine is an important mediator of the inflammatory response, and is involved in a variety of cellular activities, including cell proliferation, differentiation, and apoptosis. The induction of cyclooxygenase-2 (PTGS2/COX2) by this cytokine in the central nervous system (CNS) is found to contribute to inflammatory pain hypersensitivity. This gene and eight other interleukin 1 family genes form a cytokine gene cluster on chromosome 2.
, IL-1 beta
, interleukin-1 beta
, preinterleukin 1 beta
, prointerleukin-1 beta
, Interleukin-1 beta
, precursor interleukin-1beta
, interleukin-1 beta proprotein
, interleukin 1 beta
, lymphocyte proliferation-potentiating factor