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Human Monoclonal Interleukin 8 Primary Antibody for CyTOF, ELISA (Capture) - ABIN4900105
Phillips: Rapid analysis of inflammatory cytokines in cerebrospinal fluid using chip-based immunoaffinity electrophoresis. in Electrophoresis 2004
Show all 62 Pubmed References
Human Polyclonal Interleukin 8 Primary Antibody for IHC (p), WB - ABIN3042619
Liu, Shan, Dong, Liu, Ma, Liu: Combined early fluid resuscitation and hydrogen inhalation attenuates lung and intestine injury. in World journal of gastroenterology 2013
Show all 37 Pubmed References
Human Polyclonal Interleukin 8 Primary Antibody for ELISA, WB - ABIN3043250
Li, Li, Li, Deng, Tian, Jiang, Wang, Wang: A rat model for stable chronic obstructive pulmonary disease induced by cigarette smoke inhalation and repetitive bacterial infection. in Biological & pharmaceutical bulletin 2012
Show all 35 Pubmed References
Human Polyclonal Interleukin 8 Primary Antibody for IF (p), IHC (p) - ABIN728053
Lu, Wei, Shao, Tang, Huang, Zhang, Yang, Jing: Assessment of atherosclerotic plaques in the rabbit abdominal aorta with interleukin-8 monoclonal antibody-targeted ultrasound microbubbles. in Molecular biology reports 2013
Show all 4 Pubmed References
Human Monoclonal Interleukin 8 Primary Antibody for FACS - ABIN4897188
Thiel, Kesselring, Pries, Puzik, Wittkopf, Wollenberg: Expression of the T cell receptor αβ on a CD123+ BDCA2+ HLA-DR+ subpopulation in head and neck squamous cell carcinoma. in PLoS ONE 2011
Show all 3 Pubmed References
Human Polyclonal Interleukin 8 Primary Antibody for IHC, IHC (p) - ABIN4301105
Arafa, Abdel Haie, El-Azab, Abdel-Rahman, Sira: Significant hepatic expression of IL-2 and IL-8 in biliary atresia compared with other neonatal cholestatic disorders. in Cytokine 2016
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Human Monoclonal Interleukin 8 Primary Antibody for ICC - ABIN2689785
Matsushima, Oppenheim: Interleukin 8 and MCAF: novel inflammatory cytokines inducible by IL 1 and TNF. in Cytokine 1991
Show all 2 Pubmed References
Human Monoclonal Interleukin 8 Primary Antibody for Inhibition, FACS - ABIN2689787
Prussin, Metcalfe: Detection of intracytoplasmic cytokine using flow cytometry and directly conjugated anti-cytokine antibodies. in Journal of immunological methods 1996
Show all 2 Pubmed References
Human Monoclonal Interleukin 8 Primary Antibody for FACS - ABIN4897189
Epelman, Stack, Bell, Wong, Neely, Krutzik, Miyake, Kubes, Zbytnuik, Ma, Xie, Woods, Mody: Different domains of Pseudomonas aeruginosa exoenzyme S activate distinct TLRs. in Journal of immunology (Baltimore, Md. : 1950) 2004
Show all 2 Pubmed References
Cat (Feline) Monoclonal Interleukin 8 Primary Antibody for Func, FACS - ABIN2475055
Kadota, Yamada, Kawasaki, Takehara, Takemoto, Yoshimura: [Clinical studies of isosorbide dinitrate spray in postoperative patients]. in Masui. The Japanese journal of anesthesiology 1991
Show all 4 Pubmed References
hese findings suggest that variations in IL6 (show IL6 Antibodies), CXCL8, and TNF (show TNF Antibodies) are associated with the development and maintenance of mild persistent breast pain.
Results show that IL8 expression level is regulated by APE1 (show APEX1 Antibodies) which activates NF-KB.
aberrant miR (show MLXIP Antibodies)-520c-3p expression may lead to reduced IL-8 expression and promote the mesenchymal phenotype in breast cancer cells, thereby increasing invasive growth.
increased levels of IL-8 are associated with factors of worse prognosis in ovarian cancer
Significantly elevated blood levels of IL-8 in myelodysplastic syndrome patients.
IL-36-mediated IL-6 (show IL6 Antibodies) and CXCL8 production in human lung fibroblasts and bronchial epithelial cells may be involved in pulmonary inflammation especially caused by bacterial or viral infections.
Data suggest that semen exhibits substantial individual variation over time in pro-inflammatory seminal fluid cytokines IFNG (show IFNG Antibodies) and CXCL8. (IFNG (show IFNG Antibodies) = interferon gamma (show IFNG Antibodies); CXCL8 = C-X-C motif chemokine ligand 8 (show CCL8 Antibodies))
the elevated concentrations of CXCL13 (show CXCL13 Antibodies), CXCL8, and CXCL10 (show CXCL10 Antibodies) or their increasing CSF (show CSF2 Antibodies)/serum ratios may be potential biomarkers of neurosyphilis
Results implicated the important role of PRL-3 in glycolysis metabolism through improving IL-8 secretion in colorectal cancer cells, and PRL-3 mediated glycolysis contributed to the promotion of cancer metastasis.
IL-4 (show IL4 Antibodies) and IL-8 genetic polymorphisms determine susceptibility to chronic Aggregatibacter actinomycetemcomitans periodontitis.
inflammation triggered property of Microcystin-LR via IL-8/CXCR2 (show CXCR2 Antibodies) signaling
Topical application of glycolic acid suppresses the UVB induced IL-6 (show IL6 Antibodies), IL-8, MCP-1 (show CPT1B Antibodies) and COX-2 (show COX2 Antibodies) inflammation by modulating NF-kappaB (show NFKB1 Antibodies) signaling pathway in mouse skin.
Parenchymal polymorphonuclear myeloid-derived suppressor cell (PMN (show TBCE Antibodies)-MDSC), have a positive correlation with IL1a (show IL1A Antibodies), IL8, CXCL5 (show CXCL5 Antibodies), and Mip-1a (show CCL3 Antibodies), suggesting they may attract PMN (show TBCE Antibodies)-MDSC into the tumor
this study shows that ponciretin may attenuate ethanol-induced gastritis via the regulation of IL-8 secretion
Adh (show AVP Antibodies) binds to OR5M11 (show OR5M11 Antibodies), which enhances Actinobacillus pleuropneumoniae pathogenicity by activating p38 (show CRK Antibodies) which induces apoptosis of PAMs and IL-8 release
Findings suggest that IL8-dependent osteoclast activation may constitute an early event in the initiation of the joint specific inflammation in anti-citrullinated protein-positive rheumatoid arthritis.
Data suggest that CXCL1 (show CXCL1 Antibodies)/IL-8, released from osteoclasts in an autoantibody-dependent manner, produces pain by activating sensory neurons.
IL-8 signaling is up-regulated in alcoholic hepatitis.
expressions of IL-1beta (show IL1B Antibodies) and IL-8 in the brain increased after ApoE (show APOE Antibodies) knockout in mice
CYLD (show CYLD Antibodies) negatively regulates nontypeable Haemophilus influenzae-induced IL-8 expression via MKP-1 (show DUSP1 Antibodies)-dependent inhibition of ERK (show EPHB2 Antibodies).
Molecular characterization of the bovine IER3 (show IER3 Antibodies) gene: Down-regulation of IL-8 by blocking NF-kappaB (show NFKB1 Antibodies) activity mediated by IER3 (show IER3 Antibodies) overexpression in MDBK cells infected with bovine viral diarrhea virus-1.
STA3 (show ARHGEF3 Antibodies) facilitates TLR4 (show TLR4 Antibodies)-dependent IL-6 (show IL6 Antibodies) and IL-8 production via IL-6 (show IL6 Antibodies) receptor-positive feedback in endometrial cells.
As a pilot study, the present results revealed that identified SNPs in IL8 and TLR4 (show TLR4 Antibodies) genes can be used as a genetic marker and predisposing factor for resistance/susceptibility to digital dermatitis in dairy cows. However, TLR4 (show TLR4 Antibodies) gene may be a potential candidate for such disease.
Blood levels of cortisol, immunoglobulin G, and IL-8 in relationship to genetics and the incidence of bovine respiratory complex disease are reported.
Genetic variation at the IL8 locus explains a proportion of the inter-breed and inter-individual variation in immunity between neonatal calves which is likely to influence their resistance to infection.
In response to C. abortus infection, both ovine and bovine turbinate cells produce CXCL8 mRNA and protein late in the bacterial developmental cycle.
Studied association of IL8 -105G/A with mastitis somatic cell score in Chinese Holstein dairy cows. Results suggest genotype GG may be a useful genetic marker for mastitis resistance selection and breeding in Chinese Holstein dairy cows.
Data implicate a complex cascade of events during luteolysis, involving Il8 signaling, neutrophil recruitment, and immune cell action within the corpus luteum.
Cadmium exposure induced pulmonary inflammation and increased lung interleukin 8 secretion.
Exposure to follicular fluid transiently increased the transcript levels of IL8 and PTGS2 (show PTGS2 Antibodies), and decreased the expression of SOD2 (show SOD2 Antibodies), GPX3 (show GPX3 Antibodies), DAB2 (show DAB2 Antibodies), and NR3C1 (show NR3C1 Antibodies). TNF (show TNF Antibodies) and IL6 (show IL6 Antibodies) levels were also decreased while those of NAMPT (show NAMPT Antibodies) were unaffected.
This study evaluated the subcellular localization and other functions of TGEV nsp7 protein through analysis of its effects on cell growth, cell cycle progression, interleukin 8 (IL-8) expression, and NF-kappaB (show NFKB1 Antibodies) activation.
The JNK (show MAPK8 Antibodies)-activated AP-1 (show JUN Antibodies) subunit c-Jun (show JUN Antibodies) was critical for the up-regulation of IL-8 expression by PRRSV
These results suggest that porcine circovirus 2 induces IL-8 secretion via the TLR2/MyD88 (show MYD88 Antibodies)/NF-kappaB (show NFKB1 Antibodies) signalling pathway.
Facilitated degradation of the RGS16 (show RGS16 Antibodies) by porcine circovirus type 2 ORF3 (show ASZ1 Antibodies) further enhances NFkappaB translocation into the nucleus through the ERK1/2 signalling pathway and increased IL-6 (show IL6 Antibodies) and IL-8 mRNA transcripts.
Suggest that the interplay between TGFbeta (show TGFB1 Antibodies)-2 and LPS (show IRF6 Antibodies) regulates the levels of IL-8 in the immature newborn intestine.
Data suggest that MSK1 (show RPS6KA5 Antibodies) and MSK2 are the major CREB (show CREB1 Antibodies) kinases in fibroblast-like synoviocytes from rheumatoid arthritis patients stimulated with lysophosphatidic acid and that phosphorylation of CREB1 (show CREB1 Antibodies) at Ser (show SIGLEC1 Antibodies)-133 plays a significant role in IL-8 production.
Study presents evidence demonstrating a single species of exotoxin ApxI, derived from A. pleuropneumoniae serotype 10, induces the expression and production of proinflammatory cytokines IL-1beta (show IL1B Antibodies), IL-8 and TNF-alpha (show TNF Antibodies) in porcine alveolar macrophages.
local expression of IL-1beta (show IL1B Antibodies) and IL-8 in non-bacterial thrombotic endocarditis, Staphylococcus aureus infective endocarditis, animals with S. aureus sepsis without endocarditis and controls
In swine, IL-8, TNF-ALPHA (show TNF Antibodies), INOS (show NOS2 Antibodies) AND MIP-1BETA (show CCL4 Antibodies) were increased during mechanical ventilation in a time-related fashion.
Classical swine fever virus NS2 protein promotes interleukin-8 expression.
Stress decreased IL-8 gene expression in both CeA (show CEACAM3 Antibodies) lesioned and non-lesioned animals. But, CeA (show CEACAM3 Antibodies) lesions increased the tissue expression of IL-8 mRNA prior to and after stress exposure.
gene expression and epistasis analysis indicated that CXCL8(IL-8) was a functional target of vitamin D3-mediated HSPC (show PSMA7 Antibodies) regulation. Together, these findings highlight the relevance of developmental 1,25(OH)D3 availability for definitive hematopoiesis and suggest potential therapeutic utility in HSPC (show PSMA7 Antibodies) expansion
Targeted expression of the human oncogene (show RAB1A Antibodies) KRASG12V in zebrafish gills induces inflammation and cxcl8-l1 expression.
Data show that both Cxcl8-l1 and Cxcl8-l2 are required for larva survival upon Salmonella Typhimurium infection.
results explain how early H2O2 signal regulates neutrophil recruitment at all phases, directly via Lyn (show LYN Antibodies) oxidation or indirectly by modulating cxcl8 gene expression
The data identify HOXC9 (show HOXC9 Antibodies) as an endothelial cell active transcriptional repressor promoting the resting, antiangiogenic endothelial cell phenotype in an interleukin 8-dependent manner
Here, we report the characterisation of genes encoding the zebrafish Cxcl8, Cxcr1 (show CXCR1 Antibodies) and Cxcr2 (show CXCR2 Antibodies)
At the 2-wk time point, interleukin 8 gene expression was comparable in intervertebral discs injected with chondrocytes in controls, whereas its expression in IVDs injected with saline increased 50-fold
Data show that the serum levels of mast cell tryptase, monocyte chemoattractant protein-1 (MCP-1 (show CCL2 Antibodies)) and interleukin-8 (IL-8) decreased significantly in Dachengqi decoction treatment group.
The JNK (show MAPK8 Antibodies) pathway plays an important role in mechanical ventilation-stimulated TNF-alpha (show TNF Antibodies) expression in alveolar macrophages, but the injury-stimulated IL-8 expression may be regulated by other signaling pathways.
IL-8 and IL-1ra (show IL1RN Antibodies) showed correlation with the severity of colitis. These observations should significantly further understandings on the role of neutrophils and monocytes in the immunopathogenesis of ulcerative colitis
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.
Mapped six genes (EIF4G3 (show EIF4G3 Antibodies), HSP90 (show HSP90AB1 Antibodies), RBBP6 (show RBBP6 Antibodies), IL8, TERT (show TERT Antibodies), and TERC) on the chromosomes of Equus caballus, Equus asinus, Equus grevyi, and Equus burchelli by fluorescence in situ hybridization.
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.
These results suggest that MMP-1 (show MMP1 Antibodies) and IL-8 are both involved in the exercise-induced stress response, and this represents a starting point from which to understand the adaptive responses to this phenomenon.
Duck IL-8 is good immunostimulant to enhance the immune efficiency of avian influenza vaccine in ducks.
IL-8 homologue has been cloned and identified; the chemokine (show CCL1 Antibodies) CXC domain, which contained Glu (show DCTN1 Antibodies)-Leu-Arg motif and four cysteine residues, was well conserved
The protein encoded by this gene is a member of the CXC chemokine family. This chemokine is one of the major mediators of the inflammatory response. This chemokine is secreted by several cell types. It functions as a chemoattractant, and is also a potent angiogenic factor. This gene is believed to play a role in the pathogenesis of bronchiolitis, a common respiratory tract disease caused by viral infection. This gene and other ten members of the CXC chemokine gene family form a chemokine gene cluster in a region mapped to chromosome 4q.
T-cell chemotactic factor
, alveolar macrophage chemotactic factor I
, beta endothelial cell-derived neutrophil activating peptide
, beta-thromboglobulin-like protein
, chemokine (C-X-C motif) ligand 8
, granulocyte chemotactic protein 1
, lung giant cell carcinoma-derived chemotactic protein
, lymphocyte derived neutrophil activating peptide
, monocyte-derived neutrophil chemotactic factor
, monocyte-derived neutrophil-activating peptide
, neutrophil-activating peptide 1
, small inducible cytokine subfamily B, member 8
, tumor necrosis factor-induced gene 1
, C-X-C motif chemokine 15
, interleukin 8
, small inducible cytokine subfamily B, member 15
, small-inducible cytokine B15
, C-X-C motif chemokine 8
, neutrophil activating peptide 1
, alveolar macrophage-derived chemotactic factor-I
, neutrophil attractant/activation protein 1
, neutrophil attractant/activation protein-1
, permeability factor 1
, Interleukin-8-like protein
, Neutrophil attractant protein 1
, neutrophil attractant protein-1
, uncharacterized protein LOC100036815