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anti-Human 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 - ABIN2191766
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 - ABIN2191765
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 authors show here, using scanning electron microscopy and confocal microscopy, that platelet-poor-plasma from subjects with type 2 diabetes had a much greater propensity for hypercoagulability and for fibrin amyloidogenesis, and that these could both be reversed by LBP.
rs2232618T allele of LBP significantly increased the risk of sepsis (Review)
circulating LBP plasma concentration and hs-CRP were significantly increased in subjects with homeostatic model assessment of insulin resistance (HOMA-IR) >/=2.6 when compared with those with HOMA-IR<2.6 (P<.0001); there was no difference in TNF-alpha or IL-6 concentrations between groups
This study shows a remarkable reversal of amyloid fibrin formation by LBP addition to the plasma of Parkinson's Disease patients .
Serum LBP 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-induced inflammation and insulin resistance in human obesity and metabolic syndrome
LBP, 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, IL-10, IL-6 and CRP show a different time course in patients with and without post-stroke infection.
Serum LBP level is significantly elevated in polycystic ovary syndrome women and is associated with insulin resistance.
LBP serves not only as an extracellular LPS shuttle but in addition facilitates intracellular transport of LPS.
LBP level was not significantly different in neutropenic systemic inflammatory response syndrome patients and sepsis patients.
Report increased secretion of Fetuin A, LBP and HMGB-1 from subcutaneous adipose tissue in metabolic syndrome.
Low levels of microbial translocation marker LBP are associated with sustained viral response after anti-HCV treatment in HIV-1/HCV co-infected patients
serum level elevated in late-onset neonatal sepsis in very low birth weight infants
Adjusting for body mass index and waist circumference, LBP levels remained significantly increased in metabolic syndrome and increased with increasing numbers of MetS risk factors.
study suggested that elevated plasma LBP was associated with an increased risk of developing MetS among middle-aged and older Chinese, especially in normal-weight individuals.
In preterm neonates born to asymptomatic women with PPROM, LBP in cord blood at delivery is an excellent diagnostic biomarker of Fetal inflammatory response syndrome/funisitis with prognostic potential.
report pre-ART IL-6 and LBP levels as well as IL-6, LBP and I-FABP levels during IRIS-event as potential biomarkers in TB-IRIS
In childnre, LBP was independently associated with BMI and with measures of obstructive sleep apnea severity as well as with metabolic dysfunction, particularly insulin resistance as indicated by the homeostasis model assessment of insulin resistance.
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 on adipocyte differentiation.
Differential expression of LBP and TGFB1, along with other genes, in different mesenchymal stromal cells preparations, produces the variable responses to external stimuli.
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-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
In the case of intraperitoneal infection of LBP-deficient mice with Salmonella typhimurium, no local inflammatory response is evident, neutrophil influx is delayed, and the mice succumb to the infection.
plays an essential role in the innate immune response to Gram-positive pneumococci
Locally produced LBP is an essential component of an effective innate immune response to E. coli peritonitis.
LBP is one of the critical molecules regulating the acute and chronic airway response to inhaled lipopolysaccharides (LPS).
LBP knockout mice are protected from toxicity with a decrease in hepatic necrosis following acetaminophen challenge. This suggests a novel role for LBP in modulating acetaminophen-induced liver injury.
LBP does not contribute to an effective host response in Mycobacterium tuberculosis infection in mice.
LBP per se possesses a protective effect on acute necrotizing pancreatitis
In conclusion, hemorrhagic shock and resuscitation to mice cause severe, LBP-mediated hepatocellular damage.
Oxidized phospholipid inhibition of toll-like receptor (TLR) signaling is restricted to TLR2 and TLR4: roles for CD14, LPS-binding protein, and MD2 as targets for specificity of inhibition.
LPS-binding protein mediates LPS-induced liver injury and mortality in the setting of biliary obstruction.
Marked concomitant increases in plasma LBP and endotoxin-like activity following murine trypanosome infection might play an important role in the pathogenesis of trypanosomosis
Our study provides an overview of the gene expression profile between wild LBP and mutant LBP on the LPS-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) was demonstrated in all seven adipose tissue depots. Expression of AGP 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 in suppressing TLR4/NF-kappaB activation mediated by LPS. These findings suggested that BRLBP may be a useful agent to treat LPS-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).
BPI fold containing family D, member 2
, LPS-binding protein
, lipopolysaccharide-binding protein
, lipopolysaccharide binding protein
, lipopolysaccharide-binding protein-like