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AB169776

Anti-LBP antibody [EPR10865]

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(2 Publications)

Rabbit Recombinant Monoclonal LBP antibody. Suitable for IP, WB and reacts with Human samples. Cited in 2 publications.

View Alternative Names

Lipopolysaccharide-binding protein, LBP

3 Images
Immunoprecipitation - Anti-LBP antibody [EPR10865] (AB169776)
  • IP

Unknown

Immunoprecipitation - Anti-LBP antibody [EPR10865] (AB169776)

All lanes:

Immunoprecipitation - Anti-LBP antibody [EPR10865] (ab169776) at 1/1000 dilution

Lane 1:

Immunoprecipitation of LBP from Human plasma lysate using ab169776 at 1/10 dilution

Lane 2:

1 X PBS Negative control

Secondary

All lanes:

HRP-conjugated anti-rabbit IgG

Predicted band size: 53 kDa

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Western blot - Anti-LBP antibody [EPR10865] (AB169776)
  • WB

Unknown

Western blot - Anti-LBP antibody [EPR10865] (AB169776)

All lanes:

Western blot - Anti-LBP antibody [EPR10865] (ab169776) at 1/1000 dilution

Lane 1:

Human serum lysate at 10 µg

Lane 2:

Human plasma lysate at 10 µg

Secondary

All lanes:

Goat anti-rabbit HRP at 1/2000 dilution

Predicted band size: 53 kDa

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Western blot - Anti-LBP antibody [EPR10865] (AB169776)
  • WB

CiteAb

Western blot - Anti-LBP antibody [EPR10865] (AB169776)

LBP western blot using anti-LBP antibody [EPR10865] ab169776. Publication image and figure legend from Huang, X., Zeng, Y., et al., 2017, Mediators Inflamm, PubMed 28634422.

ab169776 was used in this publication in western blot. This may not be the same as the application(s) guaranteed by Abcam. For a full list of applications guaranteed by Abcam for ab169776 please see the product overview.

LBP gene overexpression further decreased LPS-induced downregulation of FKN mRNA and protein expression; LBP gene silencing, SB203580, and SC-514 suppressed LPS-induced downregulation of FKN mRNA and protein expression, respectively, in A549 cells. RT-PCR and ELISA were used to analyze the LBP and FKN mRNA and protein expression, respectively, in A549 cells. The LBP mRNA expression is shown in (a). The relative LBP mRNA levels (normalized to GAPDH mRNA) in LPS-stimulated cells are significantly higher than those in control cells (p < 0.05). The LBP mRNA levels of the LBP(+) group and LBP(-) group are upregulated and downregulated, respectively, when compared with the control group (p < 0.05 in all cases). The LBP mRNA levels of the LPS+LBP(+) group of cells are upregulated compared with those of the control group and LPS group (p < 0.05 in all cases). The LBP mRNA levels of the LPS+LBP(-) group of cells are upregulated compared with those of the control group and downregulated compared with those of the LPS group (p < 0.05 in all cases). The LBP mRNA level of the empty vector group is not different from that of the control group (p > 0.05). The FKN mRNA expression is shown in (e). The relative FKN mRNA levels (normalized to GAPDH mRNA) in LPS-stimulated cells are significantly lower than those in control cells (p < 0.05). The FKN mRNA levels of the LPS+LBP(+) group of cells are downregulated compared with those of the control group and the LPS group (p < 0.05 in all cases). The FKN mRNA levels of the LPS+LBP(-), LPS+SB, and LPS+SC groups of cells are downregulated compared with those of the control group and upregulated compared with those of the LPS group (p < 0.05 in all cases). The FKN mRNA levels of the TNF-α group are upregulated compared with those of the control group (p < 0.05). The results of ELISA and western blot in (b), (c), and (d) demonstrate that the LPS treatment significantly increases the levels of LBP protein expression (p < 0.05). The LBP protein levels of the LBP(+) group and LBP(-) group are upregulated and downregulated, respectively, compared with those of the control group (p < 0.05 in all cases). The LBP protein levels of the LPS+LBP group of cells are upregulated compared with those of the control group and the LPS group (p < 0.05 in all cases). The LBP protein levels of the LPS+LBP(-) group of cells are upregulated compared with those of the control group and downregulated compared with those of the LPS group (p < 0.05 in all cases). ELISA and western blot assay in (f), (g), and (h) demonstrate that the LPS treatment significantly reduces the levels of FKN protein expression (p < 0.05). The FKN protein levels of the LPS+LBP group of cells are downregulated compared with those of the control group and the LPS group (p < 0.05 in all cases). The FKN protein levels of the LPS+LBP(-), LPS+SB, and LPS+SC groups of cells are downregulated compared with those of the control group and upregulated compared with those of the LPS group (p < 0.05 in all cases). The FKN protein levels of the TNF-α group are higher than those of the control group (p < 0.05). Immunofluorescence staining results in (i) and (j) confirmed that TNF-α induced a high FKN-positive cell ratio in A549 cells. LPS decreased FKN-positive cell ratio in A549 cells; LBP gene overexpression further decreased FKN-positive cell ratio which was inhibited by LPS, LBP gene silencing, and SB203580. Also, SC-514 reduced the inhibition of LPS (p < 0.05 in all cases). The photomicrographs are 200x magnification. Data are presented as means ± SD of six independent experiments (n = 6). * represents p < 0.05 when compared with that in the CTL; # represents p < 0.05 when compared with that in the LPS; △ represents p < 0.05 when compared with that in the LPS+LBP(+). *p < 0.05 when compared with that in the control group; ◇ represents p < 0.05 when compared with that in the LPS+LBP(-) group; △ represents p < 0.05 when compared with that in the LPS+LBP(+).

false

Key facts

Host species

Rabbit

Clonality

Monoclonal

Clone number

EPR10865

Isotype

IgG

Carrier free

No

Reacts with

Human

Applications

WB, IP

applications

Immunogen

The exact immunogen used to generate this antibody is proprietary information.

Reactivity data

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Product details

Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.

What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:

  • - High batch-to-batch consistency and reproducibility
  • - Improved sensitivity and specificity
  • - Long-term security of supply
  • - Animal-free batch production

For more information, read more on recombinant antibodies.

Properties and storage information

Form
Liquid
Purity
Tissue culture supernatant
Storage buffer
pH: 7.2 - 7.4 Preservative: 0.01% Sodium azide Constituents: PBS, 50% Tissue culture supernatant, 40% Glycerol (glycerin, glycerine), 0.05% BSA
Shipped at conditions
Blue Ice
Appropriate short-term storage duration
1-2 weeks
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
-20°C
Aliquoting information
Upon delivery aliquot
Storage information
Avoid freeze / thaw cycle

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

Lipopolysaccharide-binding protein (LBP) also known as LPS-binding protein is an acute-phase protein that plays a critical role in the immune response to Gram-negative bacterial infections. This protein weighing approximately 60kDa is primarily expressed in the liver and found in the serum. LBP binds to lipopolysaccharides (LPS) which are components of the outer membrane of Gram-negative bacteria facilitating the transfer of LPS to CD14 receptors on immune cells. This transfer enhances the recognition of bacterial endotoxins triggering an immune response.
Biological function summary

LBP serves a significant role in enhancing the sensitivity of the immune system to bacterial endotoxins. It does not form a permanent part of a larger complex but works closely with other molecules like CD14 and MD-2 an accessory protein of the TLR4 receptor to mediate the innate immune response. By efficiently binding LPS LBP aids in transporting these molecules to cell surface receptors accelerating the detection and subsequent response to infections.

Pathways

LBP is heavily involved in the TLR4 signaling pathway which is important for the detection and response to Gram-negative bacterial infections. Through this pathway LBP and associated proteins such as CD14 and MD-2 help activate TLR4 triggering downstream NF-κB signaling. This activation leads to the production of pro-inflammatory cytokines and an upsurge in antimicrobial activities fortifying the body's defenses against bacterial invasion.

Enhanced LBP levels have been associated with sepsis a severe systemic response to bacterial infections which can often lead to septic shock. Given its pivotal role in recognizing bacterial endotoxins LBP is important in identifying infections making it a potential prospect for therapeutic targeting. Additionally its interaction with CD14 means that alterations in LBP function or expression levels might contribute to immune dysregulation seen in inflammatory diseases such as Crohn's disease where immune responses to gut microbiota play a central role.

Product protocols

For this product, it's our understanding that no specific protocols are required. You can visit:

Target data

Plays a role in the innate immune response. Binds to the lipid A moiety of bacterial lipopolysaccharides (LPS), a glycolipid present in the outer membrane of all Gram-negative bacteria (PubMed : 24120359, PubMed : 7517398). Acts as an affinity enhancer for CD14, facilitating its association with LPS. Promotes the release of cytokines in response to bacterial lipopolysaccharide (PubMed : 24120359, PubMed : 7517398).
See full target information Lipopolysaccharide-binding protein

Publications (2)

Recent publications for all applications. Explore the full list and refine your search

Oncology letters 19:159-166 PubMed31897126

2020

The clinical significance of lipopolysaccharide binding protein in hepatocellular carcinoma.

Applications

Unspecified application

Species

Unspecified reactive species

Quan-Yu Cai,Jing-Hua Jiang,Ri-Ming Jin,Guang-Zhi Jin,Ning-Yang Jia

Mediators of inflammation 2017:9734837 PubMed28634422

2017

Lipopolysaccharide-Binding Protein Downregulates Fractalkine through Activation of p38 MAPK and NF-B.

Applications

WB, IP

Species

Rat, Rat

Xia Huang,Yi Zeng,Yujie Jiang,Yueqiu Qin,Weigui Luo,Shulin Xiang,Suren R Sooranna,Liao Pinhu
View all publications

Product promise

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