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anti-Human C3 Antibodies:
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Human Monoclonal C3 Primary Antibody for IA, WB - ABIN269584
Li, Chen, Tu, Zhao, Zhou, Li, Dai, Li, Nie, Li, Jia, Zeng, Wu: Localized-statistical quantification of human serum proteome associated with type 2 diabetes. in PLoS ONE 2008
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Human Monoclonal C3 Primary Antibody for WB - ABIN2838577
Ma, Li, Carreño, Patenia, Tsai, Xydes-Smith, Alousi, Champlin, Sale, Afshar-Kharghan: Complement component C3 mediates Th1/Th17 polarization in human T-cell activation and cutaneous GVHD. in Bone marrow transplantation 2014
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Rat (Rattus) Monoclonal C3 Primary Antibody for IHC (p), IHC - ABIN316449
Wang, Xiong, Zeng, Sun, Gong, Zhang: Mechanistic studies of a novel mycophenolic acid-glucosamine conjugate that attenuates renal ischemia/reperfusion injury in rat. in Molecular pharmaceutics 2014
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Human Monoclonal C3 Primary Antibody for IA, IP - ABIN2192052
Lachmann, Oldroyd, Milstein, Wright: Three rat monoclonal antibodies to human C3. in Immunology 1981
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Human Monoclonal C3 Primary Antibody for IA, FACS - ABIN2191942
Klos, Ihrig, Messner, Grabbe, Bitter-Suermann: Detection of native human complement components C3 and C5 and their primary activation peptides C3a and C5a (anaphylatoxic peptides) by ELISAs with monoclonal antibodies. in Journal of immunological methods 1988
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Cow (Bovine) Polyclonal C3 Primary Antibody for IHC (fro), IF (p) - ABIN681913
Trang, Hirai, Nabeta, Fuke, Yamaguchi: Membranoproliferative glomerulonephritis in a calf with nephrotic syndrome. in Journal of comparative pathology 2014
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Pig (Porcine) Polyclonal C3 Primary Antibody for FACS - ABIN2192159
Pérez de la Lastra, Harris, Hinchliffe, Holt, Rushmere, Morgan: Pigs express multiple forms of decay-accelerating factor (CD55), all of which contain only three short consensus repeats. in Journal of immunology (Baltimore, Md. : 1950) 2000
Mouse (Murine) Monoclonal C3 Primary Antibody for IA, FACS - ABIN2191788
Zhou, Fonseca, Pisalyaput, Tenner: Complement C3 and C4 expression in C1q sufficient and deficient mouse models of Alzheimer's disease. in Journal of neurochemistry 2008
Human Monoclonal C3 Primary Antibody for IHC (fro), FACS - ABIN2477803
Bergmann-Leitner, Leitner, Tsokos: Complement 3d: from molecular adjuvant to target of immune escape mechanisms. in Clinical immunology (Orlando, Fla.) 2006
Human Monoclonal C3 Primary Antibody for IHC (fro), FACS - ABIN2477804
Nishizawa, Nagata: Regulatory elements responsible for inducible expression of the granulocyte colony-stimulating factor gene in macrophages. in Molecular and cellular biology 1990
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The pooled ORs for rs551397, rs2274700, rs4151667, rs641153, rs1047286, rs9332739, and rs547154 in the heterozygote model were 0.53, 0.53 , 0.54, 0.48, 1.42, 0.50, and 0.52, respectively. We confirmed the protective role of C2/CFB/CFH polymorphisms in the development of Age-Related Macular Degeneration (AMD), and showed single nucleotide polymorphism in C3 was a high-risk factor for AMD
Evasion of C3b deposition at division septa and lateral amplification underneath the capsule requires localization of the FH-binding protein PspC at division sites.
Clinical Manifestation of Patients With Atypical Hemolytic Uremic Syndrome With the C3 p.I1157T Variation in the Kinki Region of Japan.
In our meta-analysis, C3 genetic polymorphisms unveiled a positive effect on the risk of advanced age-related macular degeneration, especially in Caucasians
Case Report: recurrent proliferative glomerulonephritis with persistent isolated C3 deposition.
A phage Ab against C3b that inhibited the alternative complement pathway, but not the classical pathway, was described in 2009. Studies using this Ab in a variety of assays have now demonstrated that it acts primarily by inhibiting tickover, thereby confirming that tickover really exists.
Anti-HLA class I and class II C3d-binding donor-specific antibodies carried a twofold and 1.5-fold increased risk of kidney graft loss, respectively.
Study shows no significant association of the C3 gene with uveitis, suggesting C3 confers either no or limited risk for uveitis susceptibility.
Here we have shown for the first time, that ligand- or insulin-mediated activation of PPARgamma in human hepatoma cell line HepG2 causes the downregulation of C3 gene expression and protein secretion
Single Nucleotide Polymorphism rs11569514 in C3 and haplotypes of C3 variants were associated with schizophrenia in a Han Chinese population.
alphaXbeta2 uses the alphaX alphaI domain to bind iC3b on its C3c moiety at one of two sites.
findings revealed a significant association between variant p.R102G in complement component C3 gene with exudative age-related macular degeneration in the Tunisian population
SNPs within the complement genes may contribute to IA, the first step to type 1 diabetes, with at least one SNP in C3 significantly associated with clinically diagnosed type 1 diabetes.
An increase in serum C4, as well as a decrease in C3, was an important outcome determinant for patients with immunoglobulin A nephropathy.
rituximab was not effective in few cases of complement-mediated C3 glomerulonephritis and dense deposit disease . Despite promising results in immunoglobulin-associated and idiopathic Membranoproliferative glomerulonephritis, current evidence on this treatment remains weak, and controlled and prospective data are urgently needed.
C3F polymorphism is associated with viral infections and protection from rejection after liver transplantation.
Pra1 targets C3 by cleaving C3 at a unique site. This inhibited effector function of the activation fragments. The newly formed C3a-like peptide lacked the C-terminal arginine residue needed for C3a-receptor binding and activation. Pra1 also bound to C3a and C3b generated by human convertases and blocked their effector functions, C3a binding to human C3a receptor, C3 antifungal activity, and C3b deposition.
data provide the first evidence that T17M rhodopsin mutant disrupts C3 secretion via the induction of ROS and the suppression of TWIST1.
The complement activation factors Bb, C3a, C5a, and MAC were increased significantly in early-onset severe pre-eclampsia (EOSPE) (all P<.01) and late-onset severe pre-eclampsia (LOSPE). (P value: .027, <.001, .001, and <.001, respectively) compared with E/L-control. C1q and C4d were increased significantly in LOSPE (P value: .003 and .014, respectively) compared with L-control.
High C3 was significantly associated with incidence of diabetes after risk factor adjustments
IgG3-antigen complexes are deposited on follicular dendritic cells in the presence of C1q and C3.
It has been shown that key proteins in the lectin arm of this pathway, MASP1, MASP2 and C3, are expressed in the developing cortex and that neuronal migration is impaired in knockout and knockdown mice.
Complement C3 role in the lung cancer progression.
Data report C3 as a novel myogenic factor secreted by undifferentiated preadipocyte that enhances myogenic differentiation of fetal progenitor cells and adult cells. The results show that complement C3 molecule internalizes myogenic and adipogenic precursor cells and then promotes their differentiation.
C3 deficiency can prolong MHC-II molecule mismatched skin allograft survival.
C3 role in the retinal epithelium and photoreceptor degeneration
These findings shed light on mechanisms of age-related retinal alterations by identifying C3 as a potential therapeutic target for retinal aging.
These findings suggest that C3 protects from early glaucomatous damage, a process that may involve EGFR signaling and other immune responses in the optic nerve head.
complement C3 or downstream complement activation fragments may play an important role in Abeta plaque pathology.
C5 and C5aR have critical roles in the development of C3 glomerulopathy.
Data show that months after irradiation (IR) complement component 3 (C3-/-) mice made fewer errors than WT mice in a reversal learning test indicating better learning capacity in C3-/- mice after IR.
Study show s the regulation of C3 Activation by the Alternative Complement Pathway in the Mouse Retina
Time-lapse video microscopy established the localization of the complement anaphylatoxin C3a and its receptor on enteric neural crest cells during their migration in the embryonic gut. C3a plays a role in regulating collective and directional cell migration, and in ganglia network organization during enteric nervous system ontogenesis. It regulates cell migration in a N-cadherin-dependent process.
nutrient sensing in the liver is coupled to release of C3 and potentially its metabolic and inflammatory functions.
Retinal C3 was expressed by microglia/macrophages located in the outer retina in AMD eyes. In rodent photo-oxidative damage, C3-expressing microglia/macrophages and complement activation were located in regions of lesion expansion in the outer retina over 2 months
Demonstrate local synthesis of complement proteins by both PDGFRbeta-positive pericytes and CD45-positive cells in kidney fibrosis.
Wild-type C57BL/6 mice with pristane-induced lupus developed a strong IFN signature, which was absent in immunoglobulin-deficient (muMT), C3(-/-) , and CD18(-/-) mice. In vivo phagocytosis of dead cells was impaired in C3-deficient mice.
Study found that cancer-cell-derived C3 activates the C3a receptor in the choroid plexus epithelium to disrupt the blood-cerebrospinal fluid (CSF) barrier. This effect allows plasma components, including amphiregulin, and other mitogens to enter the CSF and promote cancer cell growth.
We induced anti-myeloperoxidase vasculitis in mice and confirmed a role for complement activation by demonstrating protection in C3-deficient mice.
These data indicated that alpha7-nAChR caused the inhibition of ASPinduced activation of p38 kinase and NFkappa B to inhibit the production of MCP1 and keratinocytederived chemokine.
The structure of bovine C3 clearly demonstrates that the main chain around the thioester undergoes a helical transition upon activation, a rearrangement that is proposed to be the basis for the high level of reactivity of the thioester group.
Neural crest cells are coattracted via the complement fragment C3a and its receptor C3aR, revealing an unexpected role of complement proteins in early vertebrate development.
Complement component C3 plays a central role in the activation of complement system. Its activation is required for both classical and alternative complement activation pathways. People with C3 deficiency are susceptible to bacterial infection.
C3 and PZP-like alpha-2-macroglobulin domain-containing protein 1
, C3a anaphylatoxin
, acylation-stimulating protein cleavage product
, complement C3
, complement component C3
, complement component C3a
, complement component C3b
, acylation stimulating protein
, complement component 3d
, complement factor 3
, complement component 3
, complement C3 alpha chain
, complement component C3d