Anti-LBP antibody [EPR10865]
- RabMAb
- Recombinant
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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
- 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
false
- 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
false
- 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
Reactivity data
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
Purity
Storage buffer
Shipped at conditions
Appropriate short-term storage duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
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.
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Target data
Publications (2)
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Oncology letters 19:159-166 PubMed31897126
2020
Applications
Unspecified application
Species
Unspecified reactive species
Mediators of inflammation 2017:9734837 PubMed28634422
2017
Applications
WB, IP
Species
Rat, Rat
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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