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anti-Rat (Rattus) LBP Antibodies:
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Human Monoclonal LBP Primary Antibody for Func, ELISA - ABIN343177
Berner, Fürll, Stelter, Dröse, Müller, Schütt: Elevated levels of lipopolysaccharide-binding protein and soluble CD14 in plasma in neonatal early-onset sepsis. in Clinical and diagnostic laboratory immunology 2002
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Mouse (Murine) Monoclonal LBP Primary Antibody for ELISA - ABIN343174
Gutsmann, Mueller, Carroll, MacKenzie, Wiese, Seydel: Dual role of lipopolysaccharide (LPS)-binding protein in neutralization of LPS and enhancement of LPS-induced activation of mononuclear cells. in Infection and immunity 2001
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Human Monoclonal LBP Primary Antibody for IHC (p) - ABIN343175
Ren, Jin, Leung: Local expression of lipopolysaccharide-binding protein in human gingival tissues. in Journal of periodontal research 2004
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Mouse (Murine) Monoclonal LBP Primary Antibody for ELISA - ABIN343173
Dziarski, Tapping, Tobias: Binding of bacterial peptidoglycan to CD14. in The Journal of biological chemistry 1998
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Mouse (Murine) Monoclonal LBP Primary Antibody for BR, Func - ABIN2191765
Le Roy, Di Padova, Tees, Lengacher, Landmann, Glauser, Calandra, Heumann et al.: Monoclonal antibodies to murine lipopolysaccharide (LPS)-binding protein (LBP) protect mice from lethal endotoxemia by blocking either the binding of LPS to LBP or the presentation of LPS/LBP ... in Journal of immunology (Baltimore, Md. : 1950) 1999
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Mouse (Murine) Monoclonal LBP Primary Antibody for BR, Func - ABIN2191766
Le Roy, Di Padova, Adachi, Glauser, Calandra, Heumann: Critical role of lipopolysaccharide-binding protein and CD14 in immune responses against gram-negative bacteria. in Journal of immunology (Baltimore, Md. : 1950) 2001
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Human Polyclonal LBP Primary Antibody for IHC, IHC (p) - ABIN4330429
Bachmann, Burté, Pramana, Conte, Brown, Orimadegun, Ajetunmobi, Afolabi, Akinkunmi, Omokhodion, Akinbami, Shokunbi, Kampf, Pawitan, Uhlén, Sodeinde, Schwenk, Wahlgren, Fernandez-Reyes, Nilsson: Affinity proteomics reveals elevated muscle proteins in plasma of children with cerebral malaria. in PLoS pathogens 2014
The LBP gene is a macrophage-specific LXR target that promotes foam cell survival and atherogenesis.
LBP is a critical factor in the development of non-alcoholic fatty liver disease.
LBP is a proinflammatory soluble adipokine that acts as a brake for adipogenesis, strengthening the negative effects of palmitate and LPS (show TLR4 Antibodies) on adipocyte differentiation.
Differential expression of LBP and TGFB1 (show TGFB1 Antibodies), along with other genes, in different mesenchymal stromal cells preparations, produces the variable responses to external stimuli.
The Ehhadh (show EHHADH Antibodies) is indispensable for the production of medium-chain dicarboxylic acids, providing an explanation for the coordinated induction of mitochondrial and peroxisomal oxidative pathways during fasting.
findings describe a novel role for LBP in normal hippocampal development and raise the possibility that some of the behavioral sequelae of early life stress are mediated by reduced expression of LBP during a critical period of neurodevelopment.
The amino acid sequence for two mimic epitopes of the inflammatory site of LBP were determined to be WKAQKRFMKKSG and LKTRKLFWKYKD.
LBP plays an important role in early alcohol-induced liver injury by enhancing LPS (show TLR4 Antibodies)-induced signal transduction, most likely in Kupffer cells.
LBP plays an important role in resistance to lethal Salmonella peritonitis (but not to oral or intravenous infection) by facilitating the role of neutrophils in mediating acute inflammation.
role LBP plays in local pulmonary immune defenses to bacterial challenge
Serum LBP (show RPSA Antibodies) levels are associated with arterial stiffness, independent of obesity and traditional cardiovascular risk factors, especially in men with type 2 diabetes.
novel observation that sCD14 compared with lipopolysaccharide binding protein, offers a preferred target to ameliorate TLR especially TLR4 (show TLR4 Antibodies)-induced inflammation and insulin (show INS Antibodies) resistance in human obesity and metabolic syndrome
LBP (show RPSA Antibodies), an endotoxemia associated protein might be used as an inflammatory biomarker of both infectious and non-infectious origins in HCV-infected subjects
Data show that after matching for gender, age, and body mass index (BMI), serum lipopolysaccharide-binding protein (LBP) does not improve prediction of the development of type 2 diabetes mellitus (T2DM) independently.
The main findings of this study are that, in acute stroke patients, levels of LBP (show RPSA Antibodies), IL-10 (show IL10 Antibodies), IL-6 (show IL6 Antibodies) and CRP (show CRP Antibodies) show a different time course in patients with and without post-stroke infection.
Serum LBP (show RPSA Antibodies) level is significantly elevated in polycystic ovary syndrome women and is associated with insulin (show INS Antibodies) resistance.
LBP (show RPSA Antibodies) serves not only as an extracellular LPS (show IRF6 Antibodies) shuttle but in addition facilitates intracellular transport of LPS (show IRF6 Antibodies).
LBP (show RPSA Antibodies) level was not significantly different in neutropenic systemic inflammatory response syndrome patients and sepsis patients.
Report increased secretion of Fetuin A (show AHSG Antibodies), LBP (show RPSA Antibodies) and HMGB-1 (show HMGB1 Antibodies) from subcutaneous adipose tissue in metabolic syndrome.
Low levels of microbial translocation marker LBP (show RPSA Antibodies) are associated with sustained viral response after anti-HCV treatment in HIV-1/HCV co-infected patients
Our study provides an overview of the gene expression profile between wild LBP and mutant LBP on the LPS (show IRF6 Antibodies)-induced inflammatory response of bovine mammary epithelial cells , which will lead to further understanding of the potential effects of LBP mutations on bovine mammary glands.
The presence of lipopolysaccharide binding protein (LBP) and alpha1-acid glycoprotein (AGP (show ORM1 Antibodies)) was demonstrated in all seven adipose tissue depots. Expression of AGP (show ORM1 Antibodies) and LBP suggests that they may have roles as local and systemic inflammatory adipokines.
One possible anti-inflammatory mechanism can be attributed to the negative role of BRLBP (show IGFBP2 Antibodies) in suppressing TLR4 (show TLR4 Antibodies)/NF-kappaB (show NFKB1 Antibodies) activation mediated by LPS (show IRF6 Antibodies). These findings suggested that BRLBP (show IGFBP2 Antibodies) may be a useful agent to treat LPS (show IRF6 Antibodies)-induced mastitis
Single nucleotide polymorphisms in the lipopolysaccharide-binding protein may hold the secret of susceptibility to clinical mastitis in Chinese Holstein.
The protein encoded by this gene is involved in the acute-phase immunologic response to gram-negative bacterial infections. Gram-negative bacteria contain a glycolipid, lipopolysaccharide (LPS), on their outer cell wall. Together with bactericidal permeability-increasing protein (BPI), the encoded protein binds LPS and interacts with the CD14 receptor, probably playing a role in regulating LPS-dependent monocyte responses. Studies in mice suggest that the encoded protein is necessary for the rapid acute-phase response to LPS but not for the clearance of LPS from circulation. This protein is part of a family of structurally and functionally related proteins, including BPI, plasma cholesteryl ester transfer protein (CETP), and phospholipid transfer protein (PLTP).
lipopolysaccharide binding protein
, C-type lectin 21
, lipopolysaccharide-binding protein-like
, L-specific bifunctional protein
, enoyl-Coenzyme A, hydratase/3-hydroxyacyl Coenzyme A dehydrogenase
, multifunctional enzyme type 1
, peroxisomal bifunctional enzyme
, peroxisomal bifunctional enzyme type 1
, L-bifunctional enzyme
, L-specific multifunctional beta-oxdiation protein
, BPI fold containing family D, member 2
, LPS-binding protein
, lipopolysaccharide-binding protein