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AB4212

FITC Anti-C3c antibody

4

(1 Review)

|

(16 Publications)

Rabbit Polyclonal C3 antibody - conjugated to FITC. Suitable for ICC/IF and reacts with Human samples. Cited in 16 publications. Immunogen corresponding to Native Full Length Protein corresponding to Human C3.

View Alternative Names

CPAMD1, C3, Complement C3, C3 and PZP-like alpha-2-macroglobulin domain-containing protein 1

1 Images
Immunocytochemistry/ Immunofluorescence - FITC Anti-C3c antibody (AB4212)
  • ICC/IF

Supplier Data

Immunocytochemistry/ Immunofluorescence - FITC Anti-C3c antibody (AB4212)

ICC/IF image of ab4212 stained HepG2 cells. The cells were 4% formaldehyde fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab4212, 1μg/ml) overnight at +4°C. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43μM.

Key facts

Host species

Rabbit

Clonality

Polyclonal

Isotype

IgG

Conjugation

FITC

Excitation/Emission

Ex: 495nm, Em: 519nm

Carrier free

No

Reacts with

Human

Applications

ICC/IF

applications

Immunogen

Native Full Length Protein corresponding to Human C3.

P01024

Specificity

<p>This antibody reacts with human C3c complement and with the C3c part of C3 and C3b.</p>

Reactivity data

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Properties and storage information

Form
Liquid
Purity
IgG fraction
Purification notes
Traces of contaminating antibodies have been removed by solid phase absorption with human plasma proteins.
Storage buffer
Preservative: 0.05% Sodium azide Constituents: 1% BSA
Shipped at conditions
Blue Ice
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
+4°C

Supplementary information

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

The C3c fragment is part of the complement system which plays an important role in the innate immune system. C3c also known as complement component 3c forms when C3 undergoes cleavage. The molecular mass of C3c ranges from approximately 135 to 186 kDa depending on the level of cleavage. It presents primarily in plasma and serum being part of the larger C3 molecule which is produced by the liver. Within tissues C3c can also appear in inflammatory sites where complement activation occurs.
Biological function summary

C3c functions as a by-product of complement activation and is associated with immune defense processes. It does not independently participate in the formation of the complement complex but results from the breakdown of C3 into C3b and other fragments. This fragment may play roles in modulating immune responses through its interaction with complement receptors. The presence of C3c marks the location and intensity of complement activation in tissue or circulation indirectly indicating the body's response to pathogens or damaged cells.

Pathways

The C3c fragment serves as an indirect marker within the complement cascade particularly signaling the involvement of the classical and alternative complement pathways. The generation of C3c follows the activation of these pathways highlighting the initial activation of C3 into active fragments such as C3b. Proteins related to these pathways include factors H and I which regulate C3b breakdown ensuring controlled progression of this immune response.

C3c levels offer insights into pathological conditions like systemic lupus erythematosus (SLE) and glomerulonephritis. Elevated levels of C3c in serum may indicate excessive complement activation and consumption often observed in these diseases. The association of C3c with disease is often mediated through its precursor C3 with abnormal C3 activation linked to tissue damage in autoimmune conditions. Proteins like C4 and complement receptor (CR1) may also connect to these disorders as they interact in pathways leading to inflammatory responses characterized by complement activity.

Product protocols

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

Target data

Precursor of non-enzymatic components of the classical, alternative, lectin and GZMK complement pathways, which consist in a cascade of proteins that leads to phagocytosis and breakdown of pathogens and signaling that strengthens the adaptive immune system.. Complement C3b. Non-enzymatic component of C5 convertase (PubMed : 28264884, PubMed : 31507604, PubMed : 3653927, PubMed : 3897448). Generated following cleavage by C3 convertase, it covalently attaches to the surface of pathogens, where it acts as an opsonin that marks the surface of antigens for removal (PubMed : 28264884, PubMed : 31507604, PubMed : 3653927, PubMed : 3897448, PubMed : 833545, PubMed : 8349625). Complement C3b binds covalently via its reactive thioester, to cell surface carbohydrates or immune aggregates (PubMed : 6903192). Together with complement C4b, it then recruits the serine protease complement C2b to form the C5 convertase, which cleaves and activate C5, the next component of the complement pathways (PubMed : 12878586, PubMed : 18204047, PubMed : 2387864). In the alternative complement pathway, recruits the serine protease CFB to form the C5 convertase that cleaves and activates C5 (PubMed : 624565, PubMed : 6554279).. C3a anaphylatoxin. Mediator of local inflammatory process released following cleavage by C3 convertase (PubMed : 6968751, PubMed : 37169960, PubMed : 37852260). Acts by binding to its receptor, C3AR1, activating G protein-coupled receptor signaling, promoting the phosphorylation, ARRB2-mediated internalization and endocytosis of C3AR1 (PubMed : 8702752, PubMed : 37169960, PubMed : 37852260). C3a anaphylatoxin stimulates the activation of immune cells such as mast cells and basophilic leukocytes to release inflammation agents, such as cytokines, chemokines and histamine, which promote inflammation development (PubMed : 23383423). Also acts as potent chemoattractant for the migration of macrophages and neutrophils to the inflamed tissues, resulting in neutralization of the inflammatory triggers by multiple ways, such as phagocytosis and generation of reactive oxidants (PubMed : 23383423, PubMed : 342601, PubMed : 5778786).. Acylation stimulating protein. Adipogenic hormone that stimulates triglyceride synthesis and glucose transport in adipocytes, regulating fat storage and playing a role in postprandial triglyceride clearance (PubMed : 10432298, PubMed : 15833747, PubMed : 16333141, PubMed : 19615750, PubMed : 2909530, PubMed : 8376604, PubMed : 9059512). Appears to stimulate triglyceride synthesis via activation of the PLC, MAPK and AKT signaling pathways (PubMed : 16333141). Acts by binding to its receptor, C5AR2, activating G protein-coupled receptor signaling, promoting the phosphorylation, ARRB2-mediated internalization and endocytosis of C5AR2 (PubMed : 11773063, PubMed : 12540846, PubMed : 19615750). In contrast to C3a anaphylatoxin peptide, does not show pro-inflammatory activity (PubMed : 37852260).. C3-beta-c. Acts as a chemoattractant for neutrophils in chronic inflammation.
See full target information C3

Publications (16)

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

Haematologica : PubMed40820810

2025

KLF4 overexpression protects against complement-mediated endothelial injury in transplant-associated thrombotic microangiopathy.

Applications

Unspecified application

Species

Unspecified reactive species

Shuhui Jiang,Jiaqian Qi,Tingting Pan,Zhenzhen Yao,Siyi Lu,Yifei Han,Depei Wu,Yue Han

Nature communications 16:2666 PubMed40102474

2025

Complement-mediated enhancement of SARS-CoV-2 antibody neutralisation potency in vaccinated individuals.

Applications

Unspecified application

Species

Unspecified reactive species

Jack Mellors,Raman Dhaliwal,Stephanie Longet,Tom Tipton,Eleanor Barnes,Susanna J Dunachie,Paul Klenerman,Julian Hiscox,Miles Carroll

Cell death & disease 15:592 PubMed39147758

2024

Astrocytes and the tumor microenvironment inflammatory state dictate the killing of glioblastoma cells by Smac mimetic compounds.

Applications

Unspecified application

Species

Unspecified reactive species

Kyle Malone,Melanie Dugas,Nathalie Earl,Tommy Alain,Eric C LaCasse,Shawn T Beug

Scientific reports 14:11020 PubMed38745067

2024

The STING inhibitor (ISD-017) reduces glomerulonephritis in 129.B6.Fcgr2b-deficient mice.

Applications

Unspecified application

Species

Unspecified reactive species

Isara Alee,Papasara Chantawichitwong,Asada Leelahavanichkul,Søren R Paludan,Trairak Pisitkun,Prapaporn Pisitkun

Journal of dental sciences 18:1008-1015 PubMed37404619

2023

Clinical, histological and direct immunofluorescence features in oral mucosal patches striae diseases with malignant potential.

Applications

Unspecified application

Species

Unspecified reactive species

Chun-Lei Li,Xiao-Meng Ren,Xin Fang,Hai-Yan Luo,Hong Hua

Frontiers in medicine 10:891513 PubMed36860338

2023

The loss of glycocalyx integrity impairs complement factor H binding and contributes to cyclosporine-induced endothelial cell injury.

Applications

Unspecified application

Species

Unspecified reactive species

Chia Wei Teoh,Magdalena Riedl Khursigara,Carolina G Ortiz-Sandoval,Jee Woo Park,Jun Li,Arlette Bohorquez-Hernandez,Valentina Bruno,Emily E Bowen,Spencer A Freeman,Lisa A Robinson,Christoph Licht

British journal of haematology 199:603-615 PubMed35864790

2022

Upregulation of HIF-1α contributes to complement activation in transplantation-associated thrombotic microangiopathy.

Applications

Unspecified application

Species

Unspecified reactive species

Jiaqian Qi,Tingting Pan,Tao You,Yaqiong Tang,Tiantian Chu,Jia Chen,Yi Fan,Shuhong Hu,Fei Yang,Changgeng Ruan,Depei Wu,Yue Han

Journal of cellular physiology 236:5012-5021 PubMed33400289

2021

Uromodulin aggravates renal tubulointerstitial injury through activation of the complement pathway in rats.

Applications

Unspecified application

Species

Unspecified reactive species

Li Yu,Fei Pei,Qiaoling Sun,Fei Shen,Xiangdong Yang,Zhao Hu,Maojing Liu

Nature medicine 27:279-288 PubMed33335322

2020

Phase 1/2 trial of SARS-CoV-2 vaccine ChAdOx1 nCoV-19 with a booster dose induces multifunctional antibody responses.

Applications

Unspecified application

Species

Unspecified reactive species

Jordan R Barrett,Sandra Belij-Rammerstorfer,Christina Dold,Katie J Ewer,Pedro M Folegatti,Ciaran Gilbride,Rachel Halkerston,Jennifer Hill,Daniel Jenkin,Lisa Stockdale,Marije K Verheul,Parvinder K Aley,Brian Angus,Duncan Bellamy,Eleanor Berrie,Sagida Bibi,Mustapha Bittaye,Miles W Carroll,Breeze Cavell,Elizabeth A Clutterbuck,Nick Edwards,Amy Flaxman,Michelle Fuskova,Andrew Gorringe,Bassam Hallis,Simon Kerridge,Alison M Lawrie,Aline Linder,Xinxue Liu,Meera Madhavan,Rebecca Makinson,Jack Mellors,Angela Minassian,Maria Moore,Yama Mujadidi,Emma Plested,Ian Poulton,Maheshi N Ramasamy,Hannah Robinson,Christine S Rollier,Rinn Song,Matthew D Snape,Richard Tarrant,Stephen Taylor,Kelly M Thomas,Merryn Voysey,Marion E E Watson,Daniel Wright,Alexander D Douglas,Catherine M Green,Adrian V S Hill,Teresa Lambe,Sarah Gilbert,Andrew J Pollard

Neuroscience bulletin 35:661-672 PubMed30900142

2019

Antidepressant-Like Action of Single Facial Injection of Botulinum Neurotoxin A is Associated with Augmented 5-HT Levels and BDNF/ERK/CREB Pathways in Mouse Brain.

Applications

Unspecified application

Species

Unspecified reactive species

Yang Li,Jing Liu,Xu Liu,Cun-Jin Su,Qi-Lin Zhang,Zhi-Hong Wang,Lei-Fang Cao,Xue-Yan Guo,Ya Huang,Weifeng Luo,Tong Liu
View all publications

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