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AB157711

Mouse Complement C3 ELISA Kit

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(39 Publications)

Mouse Complement C3 ELISA Kit ab157711 is a sandwich ELISA used to quantify Mouse Complement Factor 3 (C3) with a sensitivity of 1.65 ng/mL.

- Wide dynamic range – quantifies 3–200 ng/mL
- Validated in plasma and serum
- Colorimetric assay -450nm readout -works on any plate reader
- Cited in over 30 publications

View Alternative Names

Complement C3, HSE-MSF, C3

2 Images
Sandwich ELISA - Mouse Complement C3 ELISA Kit (AB157711)
  • sELISA

Supplier Data

Sandwich ELISA - Mouse Complement C3 ELISA Kit (AB157711)

Representative standard curve using ab157711 Complement C3 Mouse ELISA kit.

Sandwich ELISA - Mouse Complement C3 ELISA Kit (AB157711)
  • sELISA

Lab

Sandwich ELISA - Mouse Complement C3 ELISA Kit (AB157711)

Sample results.

Complement C3 measured in biological fluids of healthy species showing quantity (ng) per mL of tested sample. Samples were diluted 8000-128000 fold.

Key facts

Detection method

Colorimetric

Sample types

Plasma, Serum

Reacts with

Mouse

Assay type

Sandwich

Results type

Quantitative

Sensitivity

= 1.6578 ng/well

Range

3.13 - 200 ng/mL

Assay Platform

Microplate

Reactivity data

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Product details

Mouse Complement C3 ELISA Kit ab157711 is a sanwich ELISA to measure Mouse Complement factor 3 (C3) in Plasma and Serum with a sensitivity of 1.65 ng/mL.

How the assay works

In this assay the Complement C3 present in samples reacts with the anti- Complement C3 antibodies which have been adsorbed to the surface of polystyrene microtitre wells. After the removal of unbound proteins by washing, anti- Complement C3 antibodies conjugated with horseradish peroxidase (HRP), are added. These enzyme-labeled antibodies form complexes with the previously bound Complement C3. Following another washing step, the enzyme bound to the immunosorbent is assayed by the addition of a chromogenic substrate, 3,3',5,5'-tetramethylbenzidine (TMB). The quantity of bound enzyme varies directly with the concentration of Complement C3 in the sample tested; thus, the absorbance, at 450 nm, is a measure of the concentration of Complement C3 in the test sample. The quantity of Complement C3 in the test sample can be interpolated from the standard curve constructed from the standards, and corrected for sample dilution.

Assay specificity

Interferences:

These chemicals or biologicals will cause interferences in this assay causing compromised results or complete failure.

- Azide and thimerosal at concentrations higher than 0.1% inhibits the enzyme reaction.

Mouse Complement C3 ELISA Kit ab157711 protocol summary

1. Add standards or samples to the wells. Incubate for 20 min
2. Wash, then add 100µl of !x Enzyne-Antibody conjugate per well. Incubate for 20 min
3. Wash, then add 100 µl of TMB solution per well. Incubate 10 min in the dark
4. Add stop solution and read at 450 nm

How other researchers are using Mouse Complement C3 ELISA Kit ab157711

Mouse Complement C3 ELISA Kit ab157711 has been used in publications to evaluate C3 pathways as a therapeutic approach to membranous nephropathy (1), to evaluate synthetic RNA viruses as a treatment for cancer (2), and to asses CR3 modulation of Asperigillus fumigatus (3).

References:

(1)Nicola M Tomas et al. 2023 PMID: 36709213,
(2)Lorena Lerner et al. 2022 PMID: 36207308,
(3)Li Han et al. 2021 PMID: 34338598

Related and recommended products

Mouse Complement C3 ELISA Kit ab157711 is commonly used to study immune responses against infections as part of the complement system.

Other kits for measuring the complement system include:

- Mouse Complement C5a ELISA kit ab193718
- Mouse Complement C5 ELISA kit ab264609

These ELISA kits are also available for human:

- Human Complement C3 ELISA kit ab108823
- Human Complement C5a ELISA Kit ab193695
- Human Complement C5 ELISA Kit ab125963

Precision

[ { "reproducibilityType": "Inter", "sample": "Overall", "replicates": 0, "mean": null, "standardDeviation": null, "coefficientOfVariability": "< 10" }, { "reproducibilityType": "Intra", "sample": "Overall", "replicates": 0, "mean": null, "standardDeviation": null, "coefficientOfVariability": "< 10" } ]

Recovery

[ { "sample": "Serum", "range": null, "average": "> 85" } ]

What's included?

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Properties and storage information

Shipped at conditions
Blue Ice
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
+4°C
Storage information
+4°C

Supplementary information

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

Complement component C3 commonly referred to as C3 or complement 3 is a central protein in the complement system. C3 weighs approximately 185 kDa and is mainly synthesized in the liver. It circulates in the blood plasma in an inactive form. Upon activation C3 is cleaved into two fragments C3a and C3b. C3b plays an important role in opsonization and targeting pathogens for phagocytosis while C3a functions as an anaphylatoxin contributing to the inflammatory response.
Biological function summary

Complement C3 is integral to the immune response by initiating several key processes. It forms part of the C3 convertase complex which is a step within the complement cascade essential for pathogen clearance. Activation of complement C3 leads to the formation of C3b which tags pathogens for destruction by immune cells. It also influences the adaptive immune system providing a bridge to more specific immune responses.

Pathways

Complement C3 plays a part in both the classical and alternative complement pathways. In the classical pathway it interacts with proteins like C4 and C2 to form the C3 convertase complex. In the alternative pathway it is influenced by factor B and factor D allowing C3b to rapidly amplify the response against pathogens. In both pathways C3 is an important focal point to amplify immune response through the generation of C3 convertase enzymes.

Complement C3 dysfunction or dysregulation associates with conditions like age-related macular degeneration and systemic lupus erythematosus. In these diseases improper activation or deficiency of complement C3 exacerbates inflammation and tissue damage. C3b's interaction with protein factors like factor H and I is important to avoid excessive complement activation and imbalances can lead to pathological conditions.

Product protocols

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. 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. Complement C3b binds covalently via its reactive thioester, to cell surface carbohydrates or immune aggregates. 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. In the alternative complement pathway, recruits the serine protease CFB to form the C5 convertase that cleaves and activates C5.. C3a anaphylatoxin. Mediator of local inflammatory process released following cleavage by C3 convertase. Acts by binding to its receptor, C3AR1, activating G protein-coupled receptor signaling, promoting the phosphorylation, ARRB2-mediated internalization and endocytosis of C3AR1. 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. 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.. 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. Appears to stimulate triglyceride synthesis via activation of the PLC, MAPK and AKT signaling pathways. Acts by binding to its receptor, C5AR2, activating G protein-coupled receptor signaling, promoting the phosphorylation, ARRB2-mediated internalization and endocytosis of C5AR2. In contrast to C3a anaphylatoxin peptide, does not show pro-inflammatory activity.. C3-beta-c. Acts as a chemoattractant for neutrophils in chronic inflammation.
See full target information C3

Publications (39)

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

The Journal of clinical investigation 135: PubMed40338657

2025

Thrombospondin-1 inhibits alternative complement pathway activation in antineutrophil cytoplasmic antibody-associated vasculitis.

Applications

Unspecified application

Species

Unspecified reactive species

Swagata Konwar,Sophie Schroda,Manuel Rogg,Jessika Kleindienst,Eva L Decker,Martin Pohl,Barbara Zieger,Jens Panse,Hong Wang,Robert Grosse,Christoph Schell,Sabine Vidal,Xiaobo Liu,Christian Gorzelanny,Todor Tschongov,Karsten Häffner

Frontiers in immunology 15:1512470 PubMed39759517

2025

Complement activation drives the phagocytosis of necrotic cell debris and resolution of liver injury.

Applications

Unspecified application

Species

Unspecified reactive species

Sofie Vandendriessche,Matheus Silvério Mattos,Emilia Laura Bialek,Sara Schuermans,Paul Proost,Pedro Elias Marques

iScience 27:111064 PubMed39635125

2024

Complement C3 promotes islet β-cell dedifferentiation by activating Wnt/β-catenin pathway.

Applications

Unspecified application

Species

Unspecified reactive species

Lei Zhuang,Qi Li,Wenjun You,Shengke Wen,Tianxing Chen,Jianbin Su,Wei Zhao,Ji Hu

International journal of molecular sciences 25: PubMed39000309

2024

Mannan-Binding Lectin Is Associated with Inflammation and Kidney Damage in a Mouse Model of Type 2 Diabetes.

Applications

Unspecified application

Species

Unspecified reactive species

Gry H Dørflinger,Charlotte B Holt,Steffen Thiel,Jesper N Bech,Jakob A Østergaard,Mette Bjerre

Frontiers in immunology 15:1383123 PubMed38799460

2024

Moss-produced human complement factor H with modified glycans has an extended half-life and improved biological activity.

Applications

Unspecified application

Species

Unspecified reactive species

Todor Tschongov,Swagata Konwar,Andreas Busch,Christian Sievert,Andrea Hartmann,Marina Noris,Sara Gastoldi,Sistiana Aiello,Andreas Schaaf,Jens Panse,Peter F Zipfel,Paulina Dabrowska-Schlepp,Karsten Häffner

Cell 187:897-913.e18 PubMed38280374

2024

Gut complement induced by the microbiota combats pathogens and spares commensals.

Applications

Unspecified application

Species

Unspecified reactive species

Meng Wu,Wen Zheng,Xinyang Song,Bin Bao,Yuanyou Wang,Deepshika Ramanan,Daping Yang,Rui Liu,John C Macbeth,Elyza A Do,Warrison A Andrade,Tiandi Yang,Hyoung-Soo Cho,Francesca S Gazzaniga,Marit Ilves,Daniela Coronado,Charlotte Thompson,Saiyu Hang,Isaac M Chiu,Jeffrey R Moffitt,Ansel Hsiao,John J Mekalanos,Christophe Benoist,Dennis L Kasper

The EMBO journal 42:e113975 PubMed37718683

2023

Infection and inflammation stimulate expansion of a CD74 Paneth cell subset to regulate disease progression.

Applications

Unspecified application

Species

Unspecified reactive species

Iyshwarya Balasubramanian,Sheila Bandyopadhyay,Juan Flores,Jared Bianchi-Smak,Xiang Lin,Haoran Liu,Shengxiang Sun,Natasha B Golovchenko,Yue Liu,Dahui Wang,Radha Patel,Ivor Joseph,Panan Suntornsaratoon,Justin Vargas,Peter Hr Green,Govind Bhagat,Stephen M Lagana,Wang Ying,Yi Zhang,Zhihan Wang,Wei Vivian Li,Sukhwinder Singh,Zhongren Zhou,George Kollias,Laura A Farr,Shannon N Moonah,Shiyan Yu,Zhi Wei,Edward M Bonder,Lanjing Zhang,Pawel R Kiela,Karen L Edelblum,Ronaldo Ferraris,Ta-Chiang Liu,Nan Gao

Molecular therapy. Methods & clinical development 30:90-102 PubMed37746243

2023

Innate and adaptive AAV-mediated immune responses in a mouse model of Duchenne muscular dystrophy.

Applications

Unspecified application

Species

Unspecified reactive species

Michael R Emami,Alejandro Espinoza,Courtney S Young,Feiyang Ma,Philip K Farahat,Philip L Felgner,Jeffrey S Chamberlain,Xiangmin Xu,April D Pyle,Matteo Pellegrini,S Armando Villalta,Melissa J Spencer

Nature communications 14:473 PubMed36709213

2023

The classical pathway triggers pathogenic complement activation in membranous nephropathy.

Applications

Unspecified application

Species

Unspecified reactive species

Larissa Seifert,Gunther Zahner,Catherine Meyer-Schwesinger,Naemi Hickstein,Silke Dehde,Sonia Wulf,Sarah M S Köllner,Renke Lucas,Dominik Kylies,Sarah Froembling,Stephanie Zielinski,Oliver Kretz,Anna Borodovsky,Sergey Biniaminov,Yanyan Wang,Hong Cheng,Friedrich Koch-Nolte,Peter F Zipfel,Helmut Hopfer,Victor G Puelles,Ulf Panzer,Tobias B Huber,Thorsten Wiech,Nicola M Tomas

iScience 26:105750 PubMed36590177

2023

Neonatal intake of Omega-3 fatty acids enhances lipid oxidation in adipocyte precursors.

Applications

Unspecified application

Species

Unspecified reactive species

Rohan Varshney,Snehasis Das,G Devon Trahan,Jacob W Farriester,Gregory P Mullen,Gertrude Kyere-Davies,David M Presby,Julie A Houck,Patricia G Webb,Monika Dzieciatkowska,Kenneth L Jones,Matthew S Rodeheffer,Jacob E Friedman,Paul S MacLean,Michael C Rudolph
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