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AB157705

Guinea Pig Complement C3 ELISA Kit

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(5 Publications)

Guinea Pig Complement C3 ELISA Kit is a Sandwich ELISA for the measurement of Guinea Pig Complement C3 in Guinea pig in Biofluids samples.

View Alternative Names

Complement C3, C3

1 Images
Sandwich ELISA - Guinea Pig Complement C3 ELISA Kit (AB157705)
  • sELISA

Supplier Data

Sandwich ELISA - Guinea Pig Complement C3 ELISA Kit (AB157705)

Representative standard curve using ab157705 Complement C3 GuineaPig ELISA Kit.

Key facts

Detection method

Colorimetric

Sample types

Serum

Reacts with

Guinea pig

Assay type

Sandwich

Results type

Quantitative

Sensitivity

= 1.3083 ng/mL

Range

3.13 - 3260 ng/mL

Assay Platform

Microplate

Reactivity data

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Product details

Abcam's Complement C3 Guinea Pig ELISA Kit is an in vitro enzyme-linked immunosorbent assay (ELISA) for the quantitative measurement of Complement C3 levels in serum and blood .

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.

Precision

[ { "reproducibilityType": "Intra", "sample": "Overall", "replicates": 0, "mean": null, "standardDeviation": null, "coefficientOfVariability": "< 10" }, { "reproducibilityType": "Inter", "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
Multi
Storage information
Please refer to protocols

Supplementary information

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

Complement component 3 (C3) commonly known as C3 complement is a central protein in the complement system which plays a significant role in immune response. C3b a fragment of C3 is produced when C3 undergoes cleavage. C3 is a large protein with a mass of approximately 185 kDa. The liver primarily secretes C3 into the bloodstream. It circulates in the plasma and is found in high concentration making it one of the most abundant components of the complement system.
Biological function summary

Complement component C3 forms part of the innate immune system by promoting opsonization which enhances phagocytosis of pathogens. C3b binds to pathogens' surfaces facilitating their recognition by phagocytes. C3 as part of a complex with C3 convertase also has a role in amplifying the activation of the complement cascade. The proteolytic cleavage of C3 into C3b and C3a leads to the activation of other components forming the membrane attack complex and orchestrating inflammation.

Pathways

The complement component C3 functions within both the classical and alternative complement pathways. It acts as a convergence point where the complement activation pathways meet. C3 is activated into C3b and C3a which are key to amplifying the cascade. Furthermore C3 interacts with proteins such as factor B and factor D in the alternative pathway and C4 and C2 in the classical pathway facilitating the formation of C3 convertase necessary for pathway progression.

Complement C3 shows associations with immune-related and inflammatory diseases. Deficiencies or malfunctions of complement C3 can lead to increased susceptibility to infections due to impaired opsonization and clearance of pathogens. Additionally overactivation of the complement system involving C3 can contribute to autoimmune disorders such as systemic lupus erythematosus. Other proteins linked to these diseases include C4 in lupus and factor H in age-related macular degeneration which controls complement pathway activation.

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 (5)

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

ACS nano 16:10566-10580 PubMed35822898

2022

PEGylated Polyester Nanoparticles Trigger Adverse Events in a Large Animal Model of Trauma and in Naı̈ve Animals: Understanding Cytokine and Cellular Correlations with These Events.

Applications

Unspecified application

Species

Unspecified reactive species

Nuzhat Maisha,Chhaya Kulkarni,Narendra Pandala,Rose Zilberberg,Leasha Schaub,Leslie Neidert,Jacob Glaser,Jeremy Cannon,Vandana Janeja,Erin B Lavik

ACS biomaterials science & engineering 6:4903-4915 PubMed33313396

2020

Development of a Sensitive Assay to Screen Nanoparticles for Complement Activation.

Applications

Unspecified application

Species

Unspecified reactive species

Nuzhat Maisha,Tobias Coombs,Erin Lavik

Arthritis research & therapy 21:145 PubMed31196172

2019

Calorie restriction with regular chow, but not a high-fat diet, delays onset of spontaneous osteoarthritis in the Hartley guinea pig model.

Applications

Unspecified application

Species

Unspecified reactive species

Lauren B Radakovich,Angela J Marolf,Lauren A Culver,Kelly S Santangelo

Bioconjugate chemistry 29:2436-2447 PubMed29965731

2018

Engineering Intravenously Administered Nanoparticles to Reduce Infusion Reaction and Stop Bleeding in a Large Animal Model of Trauma.

Applications

Unspecified application

Species

Unspecified reactive species

Chimdiya Onwukwe,Nuzhat Maisha,Mark Holland,Matt Varley,Rebecca Groynom,DaShawn Hickman,Nishant Uppal,Andrew Shoffstall,Jeffrey Ustin,Erin Lavik

Scientific reports 8:3118 PubMed29449604

2018

Intravenous synthetic platelet (SynthoPlate) nanoconstructs reduce bleeding and improve 'golden hour' survival in a porcine model of traumatic arterial hemorrhage.

Applications

Unspecified application

Species

Unspecified reactive species

DaShawn A Hickman,Christa L Pawlowski,Andrew Shevitz,Norman F Luc,Ann Kim,Aditya Girish,Joyann Marks,Simi Ganjoo,Stephanie Huang,Edward Niedoba,Ujjal D S Sekhon,Michael Sun,Mitchell Dyer,Matthew D Neal,Vikram S Kashyap,Anirban Sen Gupta
View all publications
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