anti-Integrin, alpha X (Complement Component 3 Receptor 4 Subunit) (ITGAX) Antikörper

Bezeichnung:: anti-Integrin, alpha X (Complement Component 3 Receptor 4 Subunit) Antikörper (ITGAX)

Auf www.antikoerper-online.de finden Sie aktuell 636 Integrin, alpha X (Complement Component 3 Receptor 4 Subunit) (ITGAX) Antikörper von 32 unterschiedlichen Herstellern. Zusätzlich bieten wir Ihnen Integrin, alpha X (Complement Component 3 Receptor 4 Subunit) Proteine (7) und und viele weitere Produktgruppen zu diesem Protein an. Insgesamt sind aktuell 647 Integrin, alpha X (Complement Component 3 Receptor 4 Subunit) Produkte verfügbar.

Synonyme:: AI449405, Cd11c, Cr4, N418, RGD1561123, SLEB6

Alle Antikörper anzeigen	Gen	GeneID	UniProt
	ITGAX	3687	P20702
	ITGAX	499271
	ITGAX	16411	Q9QXH4
Alle Spezies anzeigen Weitere Synonyme anzeigen

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Am meisten referenzierte anti-Integrin, alpha X (Complement Component 3 Receptor 4 Subunit) Antikörper

Mouse (Murine) Monoclonal ITGAX Primary Antibody für IHC (f), IHC (fro) - ABIN2688918 : Gao, Liu, Wen, Zhang, Durbin, Liu, Zheng: Differentiation of monocytic cell clones into CD8 alpha+ dendritic cells (DC) suggests that monocytes can be direct precursors for both CD8 alpha+ and CD8 alpha- DC in the mouse. in Journal of immunology (Baltimore, Md. : 1950) 2003 (PubMed)
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Human Monoclonal ITGAX Primary Antibody für CyTOF, FACS - ABIN4900698 : Zhang, Wang, Liu, Sun, Ding, Fu, Min, Zhu, Cao: Effective induction of immune tolerance by portal venous infusion with IL-10 gene-modified immature dendritic cells leading to prolongation of allograft survival. in Journal of molecular medicine (Berlin, Germany) 2004 (PubMed)
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Human Monoclonal ITGAX Primary Antibody für FACS, IHC (f) - ABIN302060 : Bullard, Hu, Adams, Schoeb, Barnum: p150/95 (CD11c/CD18) expression is required for the development of experimental autoimmune encephalomyelitis. in The American journal of pathology 2007 (PubMed)
Show all 9 Pubmed References
Mouse (Murine) Monoclonal ITGAX Primary Antibody für FACS - ABIN2688921 : Huleatt, Lefrançois: Antigen-driven induction of CD11c on intestinal intraepithelial lymphocytes and CD8+ T cells in vivo. in Journal of immunology (Baltimore, Md. : 1950) 1995 (PubMed)
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Human Monoclonal ITGAX Primary Antibody für FACS, IHC (f) - ABIN302018 : Sadhu, Ting, Lipsky, Hensley, Garcia-Martinez, Simon, Staunton: CD11c/CD18: novel ligands and a role in delayed-type hypersensitivity. in Journal of leukocyte biology 2007 (PubMed)
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Human Monoclonal ITGAX Primary Antibody für FACS, IHC (f) - ABIN302039 : Gang, Choi, Lee, Nham: Identification of critical residues for plasminogen binding by the alphaX I-domain of the beta2 integrin, alphaXbeta2. in Molecules and cells 2007 (PubMed)
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Mouse (Murine) Monoclonal ITGAX Primary Antibody für CyTOF, FACS - ABIN4289490 : Gheryani, Coffelt, Gartland, Rumney, Kiss-Toth, Lewis, Tozer, Greaves, Dear, Miller: Generation of a novel mouse model for the inducible depletion of macrophages in vivo. in Genesis (New York, N.Y. : 2000) 2013 (PubMed)
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Mouse (Murine) Monoclonal ITGAX Primary Antibody für CyTOF, FACS - ABIN4900697 : Yin, Zhao, Zhang, Zhang: Impact of CD200-Fc on dendritic cells in lupus-prone NZB/WF1 mice. in Scientific reports 2016 (PubMed)
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Human Monoclonal ITGAX Primary Antibody für FACS, IHC (f) - ABIN301988 : Vorup-Jensen, Chi, Gjelstrup, Jensen, Jewett, Xie, Shimaoka, Linhardt, Springer: Binding between the integrin alphaXbeta2 (CD11c/CD18) and heparin. in The Journal of biological chemistry 2007 (PubMed)
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Human Monoclonal ITGAX Primary Antibody für FACS, IHC (f) - ABIN302095 : Angel, Lala, Chen, Edgar, Ostrovsky, Dunbar: CD14+ antigen-presenting cells in human dermis are less mature than their CD1a+ counterparts. in International immunology 2007 (PubMed)
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Weitere Antikörper gegen Integrin, alpha X (Complement Component 3 Receptor 4 Subunit) Interaktionspartner

Human Integrin, alpha X (Complement Component 3 Receptor 4 Subunit) (ITGAX) Interaktionspartner

This study provides evidence that CD11c is involved in the susceptibility to Behcet's disease in a Chinese Han population.
The main mechanism of Integrin alphaXbeta2 I-domain binding to RAGE is a charge interaction, in which the acidic moieties of Integrin alphaXbeta2 I-domains, including E244, and D249, recognize the basic residues on the RAGE V-domain encompassing K39, K43, K44, R104, and K107.
Studies indicate that CD11c+ T-bet+ memory B cells exhibit a distinct transcriptome.
Studies indicate enriched expression of TBX21 (T-bet), which is important for B cell survival and response to antigen, was observed in CD11c+ B cells.
CD11c, expressed not only in Hairy cell leukemia but also in dendritic cells, macrophages and monocytes is a differentiation marker for inflammation. Prolonged inflammation in the microenvironment of CLL cells may cause a susceptibility to autoimmune disorders and secondary tumors in CLL, in this way, an increase in mortality.
We can achieve possible clinical significance of lymphoma tumor microenvironments through CD11c and FOXP3 immunohistochemistry stains in extranodal diffuse large B-cell lymphoma patients receiving R-CHOP therapy.
Circulating CD11c+ T cells were associated with the expression of multiple adhesion molecules in women, suggesting that these cells have high tissue homing potential. These data suggest that CD11c expression distinguishes a population of circulating T cells during bacterial infection with innate capacity and mucosal homing potential.
CD8+ T cells of Behcet's disease patients exhibited increased CD11c expression levels, which may contribute to disease pathogenesis.
High expression of CD11c decreased the risk of death and relapse, and may be regarded as an alternative indicator of favorable prognosis in patients with gastric cancer.
the CD11c molecule possesses four different cellular patterns in the periprosthetic tissues.
Data show that secreted aspartic protease 2 (Sap2) of Candida albicans inactivates human macrophage complement factor H (factor H), factor H-receptors CD11b/CD18 and CD11c/CD18.
Data show that the percentage of CD11c positive antigen presenting cells (CD11c(+) APCs) in the peripheral blood of active pulmonary tuberculosis (APT) patients was much higher than that in the controls.
Data suggest that blood neutrophils expressing CD11c antigen and EMR2 protein be considered as potential biomarkers for sepsis and systemic inflammatory response syndrome (SIRS), respectively.
Modification of Levels of Adhesion Molecule Expression of Human Innate Immune Cells by Glycopolymers of Marine Bacteria
beta2 integrins-mediated chemosensory adhesion and migration of polymorphonuclear leukocytes on the vascular graft surface, bacterial cellulose.
three of these five genes (CXCL14, ITGAX, and LPCAT2) harbored polymorphisms associated with aggressive disease development in a human GWAS cohort consisting of 1,172 prostate cancer patients.
infiltration of MBP(+) and CD11c(+) innate immune cells show a significant association with phenotype and disease extent of non-asthmatic chronic rhinosinusitis
CD11a, CD11c, and CD18 gene polymorphisms and susceptibility to Behcet's disease in Koreans.
LFA-1 and CR4 alpha chain phosphorylation is needed for chemokine-induced cross-talk to VLA-4
the phosphorylation site of CD11c as Ser-1158 is pivotal for adherence and phagocytosis.

Mouse (Murine) Integrin, alpha X (Complement Component 3 Receptor 4 Subunit) (ITGAX) Interaktionspartner

CD11c and its partner Itgb2 were required for DC capture of CD47-deficient cells. CD11b was not necessary for this process but could partially compensate in the absence of CD11c. Mice with DCs lacking Talin1, Itgb2, or CD11c were defective in supporting T-cell proliferation and differentiation induced by CD47-deficient cell associated antigen.
alphaXbeta2 uses the alphaX alphaI domain to bind iC3b on its C3c moiety at one of two sites.
Deleting IL-2 in CD11c(high)MHCII(+) cells induces spontaneous colitis resembling human inflammatory bowel disease.
Accumulation of lung CD11c+ DCs is significantly higher in both inflammatory and fibrotic phases of the disease but that percentages got reduced in the absence of TGF-beta.
The findings of this study indicate that radio-resistant cells, expressing CD11c-GFP+ and located in the CNS, irrespective of their origin, which might be the yolk sac or the periphery, show a phenotype capable of antigen presentation under neuroinflammatory conditions following induction of EAE.
These data demonstrated that the CD11c+ lamina propria mononuclear phagocytes from this postinfectious irritable bowel syndrome mouse model were not only able to transfer enteric inflammation to the normal mice but also caused abnormal intestinal function, characterized by epithelial barrier disruption and visceral hyperalgesia.
the CD11c promoter was unexpectedly active and triggered Mgat2 deletion within multiple hematopoietic lineages, showed remarkably poor penetrance within native DC populations, and produced almost undetectable levels of green fluorescent protein signal. These findings show that the CD11c promoter is not DC-specific, and extreme care should be taken in the interpretation of data using any mouse created using the CD11c-CRE
Studies indicate that the autoimmune phenotype in DEF6 and SWAP-70 knock-out (DKO) mice is characterized by the accumulation of B cell subset that expresses high levels of CD11c and T-bet (ABCs).
MyD88 signaling in lysozyme M and CD11c-expressing myeloid cells, as well as in pulmonary epithelial cells, is critical to restore inflammatory cytokine and antimicrobial peptide production, leading to efficient neutrophil recruitment and enhanced bacterial clearance.
Results implicate a monocytic origin of CD11c(+) cells in inflamed islets and suggest that therapeutic regulatory T cells directly or indirectly regulate their influx by altering the chemotactic milieu in the islets.
this study shows that PU.1 functions as a positive regulator of CD11c gene expression by directly binding to the Itgax promoter and through transactivation of the Irf4 gene
Murine CD11c+ T cells analyzed by flow cytometry display markers associated with non-conventional T cell subsets, including gammadelta T cells and invariant natural killer T (iNKT) cells.
Data concluded that the ablation of CD11c(hi) dendritic cells provided a subsidiary impact on blood-brain barrier (BBB) integrity and the expression of tight junction/adhesion molecules, thereby leading to exacerbated Japanese encephalitis (JE) progression.
CD11c(+) monocyte/macrophages promote chronic Helicobacter hepaticus-induced intestinal inflammation through the production of IL-23.
data demonstrate that CD11c(hi) DCs provide a critical and unexpected role to preserve the immune-privileged CNS in lethal neuroinflammation via regulating the differentiation, function, and trafficking of CD11b(+)Ly-6C(hi) monocytes.
The generation of mouse line with Flip deficiency in cells that express cre under the CD11c promoter is reported.
Probucol effectively retarded atherosclerosis at least partly through lipid-lowering and inhibiting immune maturation of CD11c dendritic cells in STZ-induced diabetic LDLR mice.
Dual function of PPARgamma in CD11c+ cells ensures immune tolerance in the airways.
CD11c-expressing B cells are located at the T cell/B cell border in spleen and are potent antigen-presenting cells.
Our findings suggest that increased numbers of CD11c(+) macrophages and elevated levels of TNF-alpha and MMP-3 in AT and ST may explain the relationship between hyperlipidaemia and OA.

Integrin, alpha X (Complement Component 3 Receptor 4 Subunit) (ITGAX) Antigen-Profil

Beschreibung des Gens

This gene encodes the integrin alpha X chain protein. Integrins are heterodimeric integral membrane proteins composed of an alpha chain and a beta chain. This protein combines with the beta 2 chain (ITGB2) to form a leukocyte-specific integrin referred to as inactivated-C3b (iC3b) receptor 4 (CR4). The alpha X beta 2 complex seems to overlap the properties of the alpha M beta 2 integrin in the adherence of neutrophils and monocytes to stimulated endothelium cells, and in the phagocytosis of complement coated particles.

Alternative names and synonyms associated with Integrin, alpha X (Complement Component 3 Receptor 4 Subunit) (ITGAX)

integrin subunit alpha X (ITGAX) Antikörper
integrin subunit alpha X (Itgax) Antikörper
integrin alpha X (Itgax) Antikörper

AI449405 Antikörper
Cd11c Antikörper
Cr4 Antikörper
N418 Antikörper
RGD1561123 Antikörper
SLEB6 Antikörper

Bezeichner auf Proteinebene für ITGAX

CD11 antigen-like family member C , integrin alpha-X , integrin, alpha X (antigen CD11C (p150), alpha polypeptide) , leu M5, alpha subunit , leukocyte adhesion glycoprotein p150,95 alpha chain , leukocyte adhesion receptor p150,95 , leukocyte surface antigen p150,95, alpha subunit , myeloid membrane antigen, alpha subunit , p150 95 integrin alpha chain , CD11C (p150) alpha polypeptide , complement receptor 4 , integrin aX

GENE ID	SPEZIES
3687	Homo sapiens
499271	Rattus norvegicus
16411	Mus musculus

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Show all anti-Integrin, alpha X (Complement Component 3 Receptor 4 Subunit) (ITGAX) Antikörper with Pubmed References

Human Integrin, alpha X (Complement Component 3 Receptor 4 Subunit) (ITGAX) Interaktionspartner

Mouse (Murine) Integrin, alpha X (Complement Component 3 Receptor 4 Subunit) (ITGAX) Interaktionspartner

Beschreibung des Gens

Alternative names and synonyms associated with Integrin, alpha X (Complement Component 3 Receptor 4 Subunit) (ITGAX)

Bezeichner auf Proteinebene für ITGAX