MicroVue™ C4a EIA

The MicroVue C4a Enzyme Immunoassay is for the measurement of C4a in human or primate serum, plasma, and other biological or experimental samples.


Product Specifications

Citations 19
Specimen

Serum/EDTA Plasma 10 μL

LLOQ 5.0 ng/mL
ULOQ 61 ng/mL
Assay Time 2.5 hours
Cross Reactivity

African Green Monkey, Cynomolgous monkey, Rhesus monkey

Ordering Information

For Research Use Only in the United States. Not for use in diagnostic procedures.
Catalog Number A035
Catalog Number (CE) A036
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 C4a Enzyme Immunoassay is for the measurement of C4a in human or primate serum, plasma, and other biological or experimental samples.

Size 96 wells/test
Form

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

Specimen Serum/EDTA Plasma 10 μL
Limit of Detection (LOD) 0.29 ng/mL
Lower Limit of Quantitation (LLOQ) 5.0 ng/mL
Upper Limit of Quantitation (ULOQ) 61 ng/mL
Intra Assay 3.7–4.3%
Inter Assay 4.0–4.4%
Standards 5
Controls 2
Sample Values

Serum 20.9–4437.2 ng/mL, EDTA Plasma 383.5–8168.2 ng/mL

Assay Time 2.5 hours
Cross Reactivity

African Green Monkey, Cynomolgous monkey, Rhesus monkey

Storage

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

Background

Under normal conditions, activation of the classical or lectin complement pathways results in the cleavage of the complement protein, C4 into C4a and C4b by the protease, C1s. C4a is rapidly cleaved to its more stable, less active form C4a-des Arg form by endogenous serum carboxypeptidase N enzyme. Thus, quantitation of C4a-des Arg should provide a reliable measurement of classical or lectin complement pathway activation that has occurred in test samples. The MicroVue C4a assay, a rapid, highly specific and quantitative procedure for measuring C4a levels, is designed for investigations into the role or status of complement pathway activation in numerous research settings, and for monitoring the generation of C4a in vivo or in vitro. C4a is the weakest of the anaphylatoxins, compared with C3a and C5a, however, it does play a role in bringing about vascular permeability changes, the induction of smooth muscle contraction and the release of histamine from mast cells and basophils. C4a is believed to play a role in several autoimmune diseases including rheumatoid arthritis, SLE and acute glomerulonephritis. It has recently been implicated as a marker for both acute and chronic Lyme disease.

Citations

Title Year Applications Sample Species Sample Sample Details

Complement activation in patients with neuromyelitis optica

2014

ELISA

Human

Plasma

Neuromyelitis optica

Optimized Treatment of Heparinized Blood Fractions to Make Them Suitable for Analysis

2015

ELISA

Human

Plasma

Complete kinetic follow-up of symptoms and complement parameters during a hereditary angioedema attack.

2017

ELISA

Human

Plasma

Hereditary Angioedema

Clinical Value of Complement Activation Biomarkers in Overt Diabetic Nephropathy

2019

ELISA

Human

Urine

Diabetic nephropathy

Subvisible Particles in IVIg Formulations Activate Complement in Human Serum.

2020

ELISA

Human

Serum

IVIg formulations

C1R Mutations Trigger Constitutive Complement 1 Activation in Periodontal Ehlers-Danlos Syndrome.

2019

ELISA

Human

Fibroblasts

Supernatent

Complement fragments are biomarkers of antibody-mediated endothelial injury.

2019

ELISA

Human

Plasma

Antibody-mediated endothelial injury

Cloaking Silica Nanoparticles with Functional Protein Coatings for Reduced Complement Activation and Cellular Uptake.

2020

ELISA

Human

Serum

SiNP coated proteins

Alternative complement pathway activation in thrombotic microangiopathy associated with lupus nephritis.

2020

ELISA

Human

Serum

Lupus Nephritis, Thrombotic Microangiopathy

Alternative complement pathway activation in thrombotic microangiopathy associated with lupus nephritis.

2020

ELISA

Human

Urine

Lupus Nephritis, Thrombotic Microangiopathy

Air Bubbles Activate Complement and Trigger Hemostasis and C3-Dependent Cytokine Release Ex Vivo in Human Whole Blood.

2021

ELISA

Human

Plasma

Comparison of Complement Pathway Activation in Autoimmune Glomerulonephritis.

2022

ELISA

Human

Urine

AAV, FSGS, IgAN, MN, and LN

Complement activation in pediatric patients with recurrent acute otitis media

2013

ELISA

Human

Ear Fluid (MEE)

Complement activation in pediatric patients with recurrent acute otitis media

2013

ELISA

Human

Serum

Binding of Soluble Yeast β-Glucan to Human Neutrophils and Monocytes is Complement-Dependent

2013

ELISA

Human

Serum

Associations between abnormal rod-mediated dark adaptation and health and functioning in older adults with normal macular health

2014

ELISA

Human

Plasma

Imprime PGG-Mediated Anti-Cancer Immune Activation Requires Immune Complex Formation

2016

ELISA

Human

Plasma

Imprime yeast treated

rIgG1 Fc Hexamer Inhibits Antibody-Mediated Autoimmune Disease via Effects on Complement and FcγRs

2018

ELISA

Human

Serum

Fc activation

Complement activation is responsible for acute toxicities in rhesus monkeys treated with a phosphorothioate oligodeoxynucleotide

2002

ELISA

Rhesus Monkey

Serum