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抗Human CFP 抗体:
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抗Rat (Rattus) CFP 抗体:
Human Monoclonal CFP Primary Antibody for Func, IHC (fro) - ABIN2473073
Shafa: Visually elicited response of the frog cerebellum. in Brain research 1977
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Human Monoclonal CFP Primary Antibody for IHC (fro), ELISA - ABIN2473074
Hourcade: The role of properdin in the assembly of the alternative pathway C3 convertases of complement. in The Journal of biological chemistry 2006
Show all 2 Pubmed References
All Species Polyclonal CFP Primary Antibody for WB - ABIN411450
Bhattacharya, Ansari, Hamatake, Walker, Kazmierski, Striker: Pharmacological disruption of hepatitis C NS5A protein intra- and intermolecular conformations. in The Journal of general virology 2014
In conclusion, we challenge the view of properdin as a pattern recognition molecule by providing evidence that it binds to different exogenous and endogenous molecular patterns in only a C3-dependent manner.
data indicate that properdin enhances platelet/granulocyte aggregates (PGAs) formation via increased production of C5a, and that inhibition of properdin function has therapeutic potential to limit thromboinflammation in diseases characterized by increased PGA formation
this study shows that RNA interference of properdin in dendritic cells decreased alloantigen-specific T-cell proliferation
studies demonstrate an essential role of properdin oligomerization in vivo while our monomers enable detailed structural insight paving the way for novel modulators of complement.
can directly interact with neutrophil myeloperoxidase (显示 MPO 抗体) resulting in activation of alternative pathway of complement
Our data show that physiological forms of human properdin bind directly to human platelets after activation by strong agonists in the absence of C3
Factor h (显示 CFH 抗体) and properdin recognize different epitopes on renal tubular epithelial heparan sulfate.
Properdin released from human polymorphonuclear cells does not bind to zymosan or E. coli, but when incubated in properdin-depleted serum this form of properdin binds efficiently to both substrates in a strictly complement C3 (显示 C3 抗体)-dependent manner.
Properdin and SC5b-9 may be novel biomarkers for future risk of type 2 diabetes in this high-risk population and warrant further investigation.
Immune human serum that contained bactericidal Abs directed against the 2C (显示 C4BPA 抗体)7 lipooligosaccharide epitope (显示 C4BPA 抗体)required functional properdin to kill C4BP-binding strains, but not C4BP-nonbinding strains.
Properdin (显示 CFB 抗体) deficiency protects from 5-fluorouracil-induced small intestinal mucositis in a complement activation-independent, interleukin-10 (显示 IL10 抗体)-dependent mechanism
We induced anti-myeloperoxidase vasculitis in mice and showed that neither MASP-2- nor properdin-deficient mice were protected, suggesting that alternative pathway activation does not require properdin or the lectin pathway.
The results show that Properdin (显示 CFB 抗体) plays a key role in allergen-induced airway inflammation and represents a potential therapeutic target for human asthma.
Authors conclude that properdin (显示 CFB 抗体) controls the strength of immune responses by affecting humoral as well as cellular phenotypes during acute bacterial infection and ensuing inflammation.
Properdin (显示 CFB 抗体) deficiency exacerbated renal injury in mice lacking complement factor H (显示 CFH 抗体).
deficiency of properdin (显示 CFB 抗体) in mice with factor H (显示 CFH 抗体) mutation exacerbates C3 glomerulonephritis
Murine antigonococcal antiserum required functional properdin (显示 CFB 抗体) to kill C4BP-binding strains, but not C4BP-nonbinding strains.
properdin (显示 CFB 抗体) may be added to the list of complement proteins which influence lipid metabolism, energy storage and insulin (显示 INS 抗体) resistance, and further support the hypothesis of a dual role of complement in adipose tissue
At the initial phase of local, zymosan-induced inflammation, properdin (显示 CFB 抗体)-deficient and wild-type mice showed bone erosion, proteoglycan (显示 Vcan 抗体) loss and cell infiltration.
Properdin (显示 CFB 抗体) localizes to mast cells, has the ability to directly associate with Escherichia coli DH5alpha, and plays a significant role in the outcome of polymicrobial sepsis.
This gene encodes a plasma glycoprotein that positively regulates the alternative complement pathway of the innate immune system. This protein binds to many microbial surfaces and apoptotic cells and stabilizes the C3- and C5-convertase enzyme complexes in a feedback loop that ultimately leads to formation of the membrane attack complex and lysis of the target cell. Mutations in this gene result in two forms of properdin deficiency, which results in high susceptibility to meningococcal infections. Multiple alternatively spliced variants, encoding the same protein, have been identified.
complement factor P
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, Properdin P factor, complement