The anaerobic bacterium Finegoldia magna is part of the human commensal microbiota, but is also an important opportunistic pathogen. This bacterium expresses a subtilisin-like serine proteinase, SufA, which partially degrade the antibacterial chemokine MIG/CXCL9. Here, we show that MIG/CXCL9 is produced by human keratinocytes in response to inflammatory stimuli. In contrast to the virulent human pathogen Streptococcus pyogenes, the presence of F. magna had no enhancing effect on the MIG/CXCL9 expression by keratinocytes, suggesting poor detection of the latter by pathogen-recognition receptors. When MIG/CXCL9 was exposed to SufA-expressing F. magna, the molecule was processed into several smaller fragments. Analysis by mass spectrometry showed that SufA cleaves MIG/CXCL9 at several sites in the COOH-terminal region of the molecule. At equimolar concentrations, SufA-generated MIG/CXCL9 fragments were not bactericidal against F. magna, but retained their ability to kill S. pyogenes. Moreover, the ...

Weighed against tumor cells, the LP EpCAM+ cells indicated very high degrees of the chemokines CXCL3 and CXCL5, as well as the BAL fluid included raised CXCL1, CXCL2, CXCL5, and CXCL7. have already been utilized and described to build up approaches for targeted treatments, the genomic surroundings of lung SCC is emerging now. There arent yet any authorized targeted therapies for lung SCC. Sadly, therapeutic focuses on in lung ADC, such as for example and (also called serine-threonine kinase 11 [mutations have become rarely within human being squamous lung tumors. Lately, it had been reported that kinase-dead was within reduction is probable a significant determinant of lung squamous tumorigenesis. Despite signs that reduction may be central towards the era of squamous cell malignancies, deletion of only struggles to travel tumor development (Ji et al., 2007). (phosphatase and tensin homolog) can be another frequently mutated, erased, or epigenetically silenced tumor suppressor in human being ...

Human CXCL10 (IP-10) ELISA MAX™ Deluxe - CXCL10, also known as IP-10, is a glutamic acid-leucine-arginine motif negative chemokine structurally and functionally related to MIG (CXCL9) and ITAC (CXCL11).

MIG (CXCL9) Bovine Recombinant is a non-glycosylated polypeptide chain containing 104 amino acids and having a molecular mass of about 18.0kDa.

Recombinant Human MIG/CXCL9 produced in E. coli is a single, non-glycosylated polypeptide chain containing 103 amino acids and having a molecular mass of 11.7 kDa.

Human C-X-C Motif Chemokine 9 / Monokine Induced by Gamma Interferon (CXCL9 / MIG) standard, for use in running standard curves in AlphaLISA no-wash detection assay

MIG Human Recombinant produced in E.Coli is a single, non-glycosylated polypeptide chain containing 126 aa (23-125 a.a.) and having a molecular mass of 14kDa.

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Background Ulcerative colitis is characterized by relapsing mucosal inflammation where the lesions include tissue-damaging granulocytes. In addition, T cells and natural killer (NK) cells play important pathophysiologic roles. Chemokines are a large family of peptides that play key roles in the regulation of inflammation. The CXC-chemokines, growth-related oncogene (GRO)-α/CXCL1 and interleukin (IL)-8/CXCL8, both recruit neutrophils and possess mitogenic properties, whereas the interferon-dependent CXC-chemokines monokine induced by gamma-interferon (MIG)/CXCL9, interferon-γ inducible protein of 10 kD/CXCL10, and IFN-inducible T cell alpha chemoattractant/CXCL11 recruit and activate T cells and NK cells. Materials and methods The expression of CXC-chemokines was studied in eight controls and in 11 patients suffering from ulcerative colitis in the distal part of the colon, before and during topical treatment with corticosteroids. Perfusates (obtained before, after 7 days, and after 28 days of ...

This study examined the association of interferon-gamma-inducible protein-10 concentrations in serum and IL28B genotype associated with responses to pegylated

LEGEND MAX™ Human CXCL10 (IP-10) ELISA Kit with Pre-coated Plates - CXCL10, also known as IP-10, is a glutamic acid-leucine-arginine motif negative chemokine structurally and functionally related to MIG (CXCL9) and ITAC (CXCL11).

Aortic and plasma expression levels of IL-18 and CXCL16.(A) Reduced aortic mRNA expression of IL-18 and CXCL16, but no change in the expression of IFN-γ is obs

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CXCL12 izaziva potentnu hemotaksu limfocita.[4][5][6][7] Tokom embriogeneze on usmerava migraciju hematopoetskih ćelija i formiranje velikih krvnih sudova. Miševi bez CXCL12 gena su letalni pre rođenja, ili u toku prvog sata života. Kod odraslih CXCL12 igra važnu ulogu u angiogenezi putem regrutovanja endotelnih progenitorskih ćelija (EPC) iz koštane srži kroz CXCR4 zavistan mehanizam.[8] Ova funkcija čini CXCL12 veoma važnim faktorom u karcinogenezi i neovaskularizaciji vezanoj za progresiju tumora.[9] CXCL12 takođe ima ulogu u metastazi tumora gde su ćelije raka koje izražavaju CXCR4 receptor privučene ka metastaznim ciljnim tkivima koja oslobađaju ligand, CXCL12.[10] Kod raka dojke, međutim, povećano CXCL12 izražavanje određuje umanjeni rizik od metastaze.[11][12] ...

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Human CXCL9 standard, lyophilized, for use in running standard curves in LANCE Ultra TR-FRET assays. This standard is already provided in the LANCE Ultra human CXCL9/MIG Detection Kit, but can be ordered separately.

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References for Abcams Recombinant human CXCL5 protein (ab50039). Please let us know if you have used this product in your publication

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C-X-C motif chemokine 11 (CXCL11) is a protein that in humans is encoded by the CXCL11 gene.[3] C-X-C motif chemokine 11 is a small cytokine belonging to the CXC chemokine family that is also called Interferon-inducible T-cell alpha chemoattractant (I-TAC) and Interferon-gamma-inducible protein 9 (IP-9). It is highly expressed in peripheral blood leukocytes, pancreas and liver, with moderate levels in thymus, spleen and lung and low expression levels were in small intestine, placenta and prostate.[4] Gene expression of CXCL11 is strongly induced by IFN-γ and IFN-β, and weakly induced by IFN-α.[5] This chemokine elicits its effects on its target cells by interacting with the cell surface chemokine receptor CXCR3, with a higher affinity than do the other ligands for this receptor, CXCL9 and CXCL10.[4][6] CXCL11 is chemotactic for activated T cells. Its gene is located on human chromosome 4 along with many other members of the CXC chemokine family.[7][8] ...

Chemokines mediate diverse fundamental biological processes, including combating infection. Multiple chemokines are expressed at the site of infection; thus chemokine synergy by heterodimer formation may play a role in determining function. Chemokine function involves interactions with G-protein-coupled receptors and sulfated glycosaminoglycans (GAG). However, very little is known regarding heterodimer structural features and receptor and GAG interactions. Solution nuclear magnetic resonance (NMR) and molecular dynamics characterization of platelet-derived chemokine CXCL7 heterodimerization with chemokines CXCL1, CXCL4, and CXCL8 indicated that packing interactions promote CXCL7-CXCL1 and CXCL7-CXCL4 heterodimers, and electrostatic repulsive interactions disfavor the CXCL7-CXCL8 heterodimer. As characterizing the native heterodimer is challenging due to interference from monomers and homodimers, we engineered a

Chemokine (C-X-C motif) ligand 9 (CXCL9) is a small cytokine belonging to the CXC chemokine family that is also known as Monokine induced by gamma interferon (MIG). CXCL9 is a T-cell chemoattractant, which is induced by IFN-γ. It is closely related to two other CXC chemokines called CXCL10 and CXCL11, whose genes are located near the gene for CXCL9 on human chromosome 4. CXCL9, CXCL10 and CXCL11 all elicit their chemotactic functions by interacting with the chemokine receptor CXCR3. Neutrophil collagenase/matrix metalloproteinase 8 (MMP-8) degrades CXCL9 and cleaves CXCL10 at two positions. Gelatinase B/matrix metalloproteinase 9 (MMP-9) degrades CXCL10 and cleaves CXCL9 at three different sites in its extended carboxy-terminal region ...

CXCL16, hemokin (C-X-C motiv) ligand 16, je mali citokin iz CXC hemokin familije. On je veći od drugih hemokina (sadrži 254 aminokiselina). CXCL16 se sastoji od CXC hemokin domaina, mucinu-slične stabljike, transmembranskog domaina i citoplazmatičnog repa koji sadrži potentno mesto tirozin fosforilacije koje može da veže SH2.[1] Ovo su neuobičajene osobine za hemokin, i omobućavaju CXCL16 da bude izražen kao molekul na ćelijskoj površini, kao i rastvorni hemokin.[2] CXCL16 proizvode dendritiske ćelije koje se mogu naći u T ćelijskim zonama limfoidnih organa, i ćelije iz crvene pulpe slezine.[1] Među ćelijama koje se vezuju i migriraju u responsu na CXCL16 su nekoliko podgrupa T ćelija, i NKT ćelije.[1] CXCL16 interaguje sa hemokin receptorom CXCR6, takođe poznatim kao Bonzo.[3][1] Ekspresiju CXCL16 indukuju inflamatorni citokini IFN-gama i TNF-alfa.[2] Gen za ljudski CXCL16 je lociran na hromozomu 17.[1][4] ...

CXCL12 izaziva potentnu hemotaksu limfocita.[4][5][6][7] Tokom embriogeneze on usmerava migraciju hematopoetskih ćelija i formiranje velikih krvnih sudova. Miševi bez CXCL12 gena su letalni pre rođenja, ili u toku prvog sata života. Kod odraslih CXCL12 igra važnu ulogu u angiogenezi putem regrutovanja endotelnih progenitorskih ćelija (EPC) iz koštane srži kroz CXCR4 zavistan mehanizam.[8] Ova funkcija čini CXCL12 veoma važnim faktorom u karcinogenezi i neovaskularizaciji vezanoj za progresiju tumora.[9] CXCL12 takođe ima ulogu u metastazi tumora gde su ćelije raka koje izražavaju CXCR4 receptor privučene ka metastaznim ciljnim tkivima koja oslobađaju ligand, CXCL12.[10] Kod raka dojke, međutim, povećano CXCL12 izražavanje određuje umanjeni rizik od metastaze.[11][12] ...

CXCL10, hemokin (C-X-C motiv) ligand 10, ili IP-10[1] je mali citokin iz CXC hemokin familije koji je takođe poznat kao 10 kDa interferon-gama-inducirani protein (γ-IP10 ili IP-10). CXCL10 luči nekoliko ćelijski tipova u responsu na IFN-γ. U te ćelijske tipove spadaju monociti, endotelijalne ćelije i fibroblasti.[2] CXCL10 hemokinu je bilo pripisano nekoliko uloga, kao što su hemoatrakcija monocita/makrofaga, T ćelija, NK ćelija, i dendritskih ćelija, promocija adhezije T ćelija na endotelijalne ćelije, antitumorska aktivnost, i inhibicija formiranja kolonija kičmene moždine i angiogeneze.[3][4] CXCL10 gen je lociran na ljudskom hromozomu 4 u klasteru sa nekoliko drugih CXC hemokina.[5] Ovaj hemokin dejstvuje putem vezivanja na CXCR3 hemokin receptore na ćelijskoj površini.[6]. Tri-dimenzionalna kristalna struktura ovog hemokina je bila utvrđena u 3 različite grupe uslova u rezoluciji do 1.92 A.[7] PDB pristupni kodovi za CXCL10 strukture su: 1lv9, 1o7y, 1o7z i 1o80.[8] ...

Complete information for CXCL9 gene (Protein Coding), C-X-C Motif Chemokine Ligand 9, including: function, proteins, disorders, pathways, orthologs, and expression. GeneCards - The Human Gene Compendium

Cxcl12 - Cxcl12 (untagged ORF) - Rat chemokine (C-X-C motif) ligand 12 (stromal cell-derived factor 1) (Cxcl12), transcript variant 3, (10 ug) available for purchase from OriGene - Your Gene Company.

Cxcl11 - Cxcl11 (Myc-DDK-tagged) - Mouse chemokine (C-X-C motif) ligand 11 (Cxcl11), transcript variant 1 available for purchase from OriGene - Your Gene Company.

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Recombinant Human IP-10/CXCL10 produced inE. coliis a single, non-glycosylated polypeptide chain containing 77 amino acids and having a molecular mass of 8.5 kDa.

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BABY I Kender i det? Jeg synes godt nok at min aften har været alt for lang! Jeg har kedet mig, og kedet mig og KEDET MIG. Hvad gør man så? Det man elsker aller mest i sit liv ( my blog) Jeg elsker forresten også mit NIKON 3200 som er et fantastisk spejlfalsekamera! #feelingmyselfff ♥ Har fået taget mig en masse billeder af mig selv (i know selvglad) men…. ...

Human IL-8/CXCL8 HEK293 Cells Overexpression Lysate 10098-HNCH1L is validated in western blot (WB) as positive control. Sino Biological offers bulk order for high quality cell lysates which are produced in house.

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Tumor escape from immune-mediated destruction has been associated with immunosuppressive mechanisms that inhibit T cell activation. Although evidence for an active immune response, including infiltration with CD8+ T cells, can be found in a subset of patients, those tumors are nonetheless not immunologically rejected. In the current report, we show that it is the subset of T cell-inflamed tumors that showed high expression of three defined immunosuppressive mechanisms: indoleamine-2,3-dioxygenase (IDO), PD-L1/B7-H1, and FoxP3+ regulatory T cells (Tregs), suggesting that these inhibitory pathways might serve as negative feedback mechanisms that followed, rather than preceded, CD8+ T cell infiltration. Mechanistic studies in mice revealed that up-regulated expression of IDO and PD-L1, as well as recruitment of Tregs, in the tumor microenvironment depended on the presence of CD8+ T cells. The former was driven by interferon-γ and the latter by a production of CCR4-binding chemokines along with a ...

In the present study, it was demonstrated that IL-17A could stimulate the secretion of angiogenic CXC chemokines from liver cancer cells, which may recruit endothelial cells to the tumor cells in a CXCR2-dependent manner. Tumor angiogenesis was also promoted by IL-17A expression in vivo. The CXC chemokines can be classified as angiogenic or angiostatic predominantly based on the presence or absence of an ELR motif. The angiogenic CXC chemokines include CXCL1, CXCL2, CXCL3, CXCL5, CXCL6, CXCL8 and CXCL12, and the angiostatic chemokines include CXCL4, CXCL9, CXCL10, CXCL11 and CXCL14 (21). IL-17A was shown to increase the expression of CXCL1, CXCL2, CXCL3, CXCL5, CXCL6 and CXCL8 in Huh7.5 cells and upregulated CXCL2 in HepG2 cells. Additionally, angiostatic CXC chemokines were not affected by IL-17A in both cell lines. IL-17A has been reported to stimulate VEGFA production and promote angiogenesis in several cancer cell lines (16-18) and it has been shown previously that IL-17A does not affect ...

CXCL2_HUMAN (P19875 ), CXCL2_MOUSE (P10889 ), CXCL2_RAT (P30348 ), CXCL3_HUMAN (P19876 ), CXCL3_MOUSE (Q6W5C0 ), CXCL3_RAT (Q10746 ), CXCL5_HUMAN (P42830 ), CXCL5_MOUSE (P50228 ), CXCL5_RAT (P97885 ), CXCL6_BOVIN (P80221 ), CXCL6_HORSE (Q8MIN2 ), CXCL6_HUMAN (P80162 ), CXCL7_HUMAN (P02775 ), CXCL7_PIG (P43030 ), CXCL9_BOVIN (A9QWP9 ), CXCL9_HUMAN (Q07325 ), CXCL9_MOUSE (P18340 ), CXL10_BOVIN (Q2KIQ8 ), CXL10_CANLF (Q5KSV9 ), CXL10_HUMAN (P02778 ), CXL10_MACMU (Q8MIZ1 ), CXL10_MACNE (Q865F5 ), CXL10_MOUSE (P17515 ), CXL10_RAT (P48973 ), CXL11_BOVIN (A9QWQ1 ), CXL11_HUMAN (O14625 ), CXL11_MOUSE (Q9JHH5 ), CXL13_HUMAN (O43927 ), CXL13_MOUSE (O55038 ), CXL15_MOUSE (Q9WVL7 ), GRO2_RABIT (P47854 ), GROA_BOVIN (O46676 ), GROA_CAVPO (O55235 ), GROA_CRIGR (P09340 ), GROA_HUMAN (P09341 ), GROA_MOUSE (P12850 ), GROA_RAT (P14095 ), GROA_SHEEP (O46678 ), GROB_BOVIN (O46677 ), GROG_BOVIN (O46675 ), IL8_BOVIN (P79255 ), IL8_CANLF (P41324 ), IL8_CAVPO (P49113 ), IL8_CERAT (P46653 ), IL8_CHICK (P08317 ), ...

|p|Recombinant Human I-TAC is a single non-glycosylated polypeptide chain containing 73 amino acids.|/p| |p|Background: I-TAC/CXCL11 cDNA encodes a 94 amino acid (aa) residue precursor protein with a 21 aa residue putative signal sequence, which is cleav

The LANCE® Ultra Human CXCL9/MIG Detection Kit is designed for detection and quantitation of human CXCL9/MIG in cell culture media using a homogeneous TR-FRET (no-wash steps, no separation steps) assay.

CXCL10 / IP10 antibody [15J7] (chemokine (C-X-C motif) ligand 10) for Neut, WB. Anti-CXCL10 / IP10 mAb (GTX53293) is tested in Mouse samples. 100% Ab-Assurance.

CXCL11 antibody [22F1] (chemokine (C-X-C motif) ligand 11) for ELISA, WB. Anti-CXCL11 mAb (GTX54751) is tested in Human samples. 100% Ab-Assurance.

CXCL16 is a member of the CXC chemokine family and signals through the CXCR6 receptor. CXCL16 may play a role in attracting lymphocyte subsets

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IL-8/CXCL8 Immunoprecipitation (IP) Kit are used for Immunoprecipitation of IL-8/CXCL8 protein which expressed in vitro expression systems.

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Rutar, M, Natoli, R, Chia, R et al 2015, Chemokine-mediated inflammation in the degenerating retina is coordinated by Müller cells, activated microglia, and retinal pigment epithelium, Journal of Neuroinflammation, vol. 12, no. 8, pp. 1-15. ...

CXCL10 improves outcome by decreasing bacteremia in IFNAR−/− mice. (A) SEV129 wild-type mice (n = 10), IFNAR−/− mice (n = 11), or IFNAR−/− mice with

References for Abcams Recombinant Mouse CXCL5 protein (ab57029). Please let us know if you have used this product in your publication

Many in vitro applications for chemical induced dimerization (CID) have progressed into transgenic animals - for example, the MaFIA mouse. The B/B Homodimerizer (AP20187) has been the widely used in vivo.

Many in vitro applications for chemical induced dimerization (CID) have progressed into transgenic animals - for example, the MaFIA mouse. The B/B Homodimerizer (AP20187) has been the widely used in vivo.

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