MicroVue™ iC3b EIA

The MicroVue iC3b Assay is enzyme immunoassay for the quantitation of iC3b fragment of C3 protein.


Product Specifications

Citations 12
Specimen

Serum/EDTA or Heparin Plasma 100 μL

LLOQ N/A
ULOQ N/A
Assay Time 1.5 hours
Cross Reactivity

None

Ordering Information

For Research Use Only in the United States. Not for use in diagnostic procedures.
Catalog Number A006
Catalog Number (CE)  
Size 96 wells/test
Price (USD) $725.00
Price (EURO) 640,00 €

Contact us

US Phone+1 (858) 552 1100
EU Phone+353 (91) 412 474
US Emailcontact-us@quidelortho.com
EU Emailcontact-emea@quidelortho.com

Specifications

Description

The MicroVue iC3b Assay is enzyme immunoassay for the quantitation of iC3b fragment of C3 protein.

Size 96 wells/test
Form

96 well plate with 12 eight-well strips in a resealable foil pouch

Specimen Serum/EDTA or Heparin Plasma 100 μL
Limit of Detection (LOD) N/A
Lower Limit of Quantitation (LLOQ) N/A
Upper Limit of Quantitation (ULOQ) N/A
Intra Assay N/A
Inter Assay N/A
Standards 3
Controls 2
Sample Values

None

Assay Time 1.5 hours
Cross Reactivity

None

Storage

Store the unopened kit at 2°C to 8°C. Refer to Product Insert for additional storage details.

Background

The Quidel iC3b Enzyme Immunoassay measures the amount of the iC3b present in samples. Activation of either complement pathway results in the assembly of C3 convertases that cleave C3 into two fragments – C3a and C3b. The C3a fragment is one of the complement anaphylatoxins. The C3b fragment has many important biological activities, including the promotion of phagocytosis by opsonization and participation as a structural component in C3 and C5 convertases. These biological activities of C3b are under stringent control in vivo. One mechanism limiting the in vivo lifetime of C3b involves the two-site cleavage of C3b by Factor I5 with the cooperation of Factor H6 or CR17 as cofactors. Factor H is a complement control protein. CR1 is the C3b/C4b receptor found on many cell types, including red blood cells, granulocytes, monocytes, and macrophages. Factor I two-site cleavage of C3b yields inactivated C3b, called iC3b. The biological activities of C3b are lost when it is cleaved by Factor I. iC3b fragments, either in fluid phase or bound to biological surfaces, express new biological activities due to their ability to interact with CR2 and CR3 receptors on a variety of cell types. The levels of iC3b can be significantly elevated in the serum and plasma of some patients with immune complex-associated diseases such as rheumatoid arthritis and systemic lupus erythematosus. iC3b levels may also be elevated in body fluids from other patients in which complement activation is known to occur, e.g., from patients with infections, burns, myocardial infarctions, glomerulonephritis, and acute respiratory distress syndrome. The correlation between iC3b levels and the clinical status or prognosis for patients with these and other diseases remains to be determined and is a question of potential significance to the biomedical community. The Quidel iC3b Enzyme Immunoassay provides a rapid, non-radioactive, highly specific and quantitative procedure for measuring this product of C3 activation. It may also be used as a research tool to monitor the generation of iC3b in vitro.

Citations

Title Year Applications Sample Species Sample Sample Details

Differentiated pattern of complement system activation between MOG-IgG-associated disease and AQP4-IgG-positive neuromyelitis optica spectrum disorder

2024

ELISA

Human

Serum

MOGAD, AQP4-NMOSD

Effect of Aerobic and Anaerobic Exercise on the Complement System of Proteins in Healthy Young Males.

2020

ELISA

Human

Plasma

Complement receptor 3 mediates Aspergillus fumigatus internalization into alveolar epithelial cells with the increase of intracellular phosphatidic acid by activating FAK.

2021

ELISA

Human

Serum

Aspergillus incubated

Complement activation by bisretinoid constituents of RPE lipofuscin.

2009

ELISA

Human

Serum

Macrophage scavenger receptor A mediates the uptake of gold colloids by macrophages in vitro

2011

ELISA

Human

Plasma

Genetic variation and cerebrospinal fluid levels of mannose binding lectin in pneumococcal meningitis patients

2013

ELISA

Human

CSF

C4d deposits on the surface of RBCs in trauma patients and interferes with their function

2014

ELISA

Human

Serum

Trauma

Inhibition of C3 Convertase Activity by Hepatitis C Virus as an Additional Lesion in the Regulation of Complement Components

2014

ELISA

Human

Serum

HCV

quantitative lateral flow assay to detect complement activation in blood.

2015

ELISA

Human

Plasma

Cerebrospinal fluid inflammatory markers in patients with Listeria monocytogenes meningitis

2014

ELISA

Human

CSF

Listeria meningitis

Complement Receptor 3 Has Negative Impact on Tumor Surveillance through Suppression of Natural Killer Cell Function

2017

ELISA

Human

Serum

A monoclonal antibody targeting amyloid β (Aβ) restores complement factor I bioactivity: Potential implications in age-related macular degeneration and Alzheimer's disease

2018

ELISA

Human

Plasma

Age-Related Macular Degeneration

A monoclonal antibody targeting amyloid β (Aβ) restores complement factor I bioactivity: Potential implications in age-related macular degeneration and Alzheimer's disease

2018

ELISA

Human

Plasma

Alzheimer's Disease