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Human CD14 Protein expressed in CHO Cells - ABIN2666875
Baumann, Aspalter, Sharif, Pichlmair, Blüml, Grebien, Bruckner, Pasierbek, Aumayr, Planyavsky, Bennett, Colinge, Knapp, Superti-Furga: CD14 is a coreceptor of Toll-like receptors 7 and 9. in The Journal of experimental medicine 2010
Show all 9 references for ABIN2666875
Human CD14 Protein expressed in Human Cells - ABIN2002018
Simmons, Tan, Tenen, Nicholson-Weller, Seed: Monocyte antigen CD14 is a phospholipid anchored membrane protein. in Blood 1989
Show all 5 references for ABIN2002018
Cynomolgus CD14 Protein expressed in Human Cells - ABIN2009950
Goyert, Ferrero, Rettig, Yenamandra, Obata, Le Beau: The CD14 monocyte differentiation antigen maps to a region encoding growth factors and receptors. in Science (New York, N.Y.) 1988
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Rat (Rattus) CD14 Protein expressed in Human Cells - ABIN2009460
Heidenreich: Monocyte CD14: a multifunctional receptor engaged in apoptosis from both sides. in Journal of leukocyte biology 1999
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Human CD14 Protein expressed in HEK-293 Cells - ABIN2180686
Kirkland, Viriyakosol: Structure-function analysis of soluble and membrane-bound CD14. in Progress in clinical and biological research 1998
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Human CD14 Protein expressed in Wheat germ - ABIN1348531
Gu, Werner, Bergmann, Whitcomb, Büchler, Fortunato: Necro-inflammatory response of pancreatic acinar cells in the pathogenesis of acute alcoholic pancreatitis. in Cell death & disease 2013
these results indicate that CD14 is a co-receptor of TLR4 (show TLR4 Proteins) in the S100A9 (show S100A9 Proteins)-induced cytokine response.
this study shows that lipid rafts may serve as sites in which LPS (show TLR4 Proteins) receptors (CD14) are sorted for endocytosis, rather than being platforms for the assembly of TLR4 (show TLR4 Proteins)-centered signaling complexes
These findings suggested that the degree of lung injury was reduced during the acute inflammatory reaction when NFkappaB was inhibited, and that the expression of sphingomyelin synthase 2 (show SGMS2 Proteins) may affect the induction of the NFkappaB pathway by lipopolysaccharide through CD14.
Results demonstrate remarkable sophistication of microglial CD14 in enabling, facilitating and moderating innate immune responses to infectious and non-infectious CNS threats of diverse kinds
CD14-mediated lipid signaling induced epithelial apoptosis, whereas TLR4 (show TLR4 Proteins) antagonistically promoted cell survival and cancer development.
fucosyllactose directly inhibits lipopolysaccharide-mediated inflammation during E. coli infection of intestinal epithelial cells through attenuation of CD14 induction.
studies revealed a novel physical association between SP-R210S, CD14, and SR-A (show MSR1 Proteins) leading to an enhanced response to LPS (show TLR4 Proteins), and found that SP-R210L and SP-R210S regulate internalization of CD14 via distinct macropinocytosis-like mechanisms
Data indicate that Toll-like receptor 4 (TLR4 (show TLR4 Proteins)) endocytosis and the TIR-domain-containing adapter-inducing IFN-beta (show IFNB1 Proteins) (TRIF (show RNF138 Proteins))-signaling pathway in macrophages during endotoxin tolerance in the absence of cluster of differentiation 14 (CD14).
27OHChol can prime monocytes/macrophages by up-regulation of CD14 such that LPS (show TLR4 Proteins)-mediated inflammatory reaction is accelerated, thereby contributing to aggravated development of atherosclerotic lesions.
microglial HSPGs facilitate CD14-dependent TLR4 (show TLR4 Proteins) activation and that heparanase (show HPSE Proteins) can modulate this mechanism
these results indicate that CD14 (show NDUFA2 Proteins) is a co-receptor of TLR4 (show TLR4 Proteins) in the S100A9 (show S100A9 Proteins)-induced cytokine response.
our data showed the contribution on the TLR4 (show TLR4 Proteins)+896A/G and CD14 (show NDUFA2 Proteins)-159C/T polymorphism-related immune dysfunction including increased non-classical (inflammatory) monocyte proportion-related LPS (show IRF6 Proteins) hyper-inflammatory response and decreased classical (phagocytic) monocyte proportion-related impaired phagocytosis in febrile acute de-compensated cirrhotic patients complicated with severe sepsis.
Patients with CD14 C (-159) T gene polymorphism, a co-receptor of TLR4, have an increased risk of NAFLD development.
Single nucleotide polymorphism CD14 (show NDUFA2 Proteins)-159 C/T was linked to greater Atopic dermatitis risk at 2 to 3 years of age.
While there was no association with any respiratory phenotype (as determined by symptoms), the CD14 (show NDUFA2 Proteins) CT/TT genotype appeared to be protective to increased exposure to NO2 and NO
CD14 (show NDUFA2 Proteins) expression is significantly upregulated in human masticatory mucosa during wound healing
we report that exogenous CnB (show PPP3R1 Proteins) is taken up by cells in a time- and concentration-dependent manner via clathrin-dependent receptor-mediated internalization. Our findings further confirm that uptake is mediated by the TLR4 (show TLR4 Proteins)/MD2 (show LY96 Proteins) complex together with the co-receptor CD14 (show NDUFA2 Proteins)
We investigated the association of single-nucleotide polymorphisms in TLR4 (show TLR4 Proteins) and CD14 (show NDUFA2 Proteins) and carotid intima-media thickness, a surrogate measurement for CVD, in HIV-infected individuals on antiretroviral therapy and HIV-uninfected controls.
Anti-platelet drugs exert an immunomodulatory action by counteracting CD14 (show NDUFA2 Proteins)(high)CD16 (show CD16 Proteins)(+) monocyte increase under pro-inflammatory conditions, with this effect being dependent on the amplitude of P-selectin (show SELP Proteins) reduction.
These findings suggest the potential role of sCD14 in the pathogenesis of chronic HBV infection, especially the development of HCC (show FAM126A Proteins), and the potential usefulness of sCD14 as a biomarker for discriminating clinical diseases and predicting survival of HCC (show FAM126A Proteins) patients in chronic HBV infection.
Transcription levels of TLR2, TLR4 (show TLR4 Proteins), and CD14 in Holstein cows with retained placenta significantly decreased between the first and the seventh day postpartum.
Data from an in vitro co-culture model suggest that an early response of endometrium in uterine infection is up-regulation of expression of CD14 and TLR4 (toll-like receptor 4 (show TLR4 Proteins)).
This study study confirmed that expression of CD14 in blood polymorpnuclear cells (PMN (show TBCE Proteins)), resident PMN (show TBCE Proteins) and inflammatory PMN (show TBCE Proteins) from heifer mammary glands was accompanied by apoptosis and necrosis.
data are consistent with a role for lipopolysaccharide binding protein (show LBP Proteins) and soluble CD14 antigen molecules in mediating mammary gland responses to lipopolysaccharide(lipopolysaccharide binding protein- LBP (show LBP Proteins))
Toll-like receptor 4 (show TLR4 Proteins) mRNA and CD14 mRNA and protein were detected in bovine endometrial stromal and epithelial cells by RT-PCR and flow cytometry.
SNP and association analyses have provided baseline information that may be used at defining the role of CD14 in mediating bacterial infections
VB-201 may counter inflammation where TLR-2 and/or CD14 complicity is essential, and is therefore beneficial for the treatment of atherosclerosis.
Determine native soluble CD14 concentrations in serum from healthy and septic foals, in the colostrum of healthy mares and in plasma from adult horses with recurrent airway obstruction and control horses.
CD14 mRNA was demonstrated for the intestinal samples with no variation between the intestinal segments analysed.
The protein encoded by this gene is a surface antigen that is preferentially expressed on monocytes/macrophages. It cooperates with other proteins to mediate the innate immune response to bacterial lipopolysaccharide. Alternative splicing results in multiple transcript variants encoding the same protein.
monocyte differentiation antigen CD14
, myeloid cell-specific leucine-rich glycoprotein
, CD14 antigen
, lipopolysaccharide receptor