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Human Measles virus IgG antibody (MV-Ab-IgG) ELISA Kit

Citations(0)Uniprot : N/A
  • Cat.No.: AE62481HU

  • Reactivity: Human (Homo sapiens)

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48T 96T
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Product Details

Species Reactivity Human (Homo sapiens)
UniProt N/A
Abbreviation MV-Ab-IgG
Alternative Names N/A
Range Request Information
Sensitivity Request Information
Sample Type Serum, Plasma, Other biological fluids
Detection Method Indirect ELISA
Analysis Method Qualitative
Assay Duration 1-3h
Sample Volume 1-200 μL
Detection Wavelengt 450 nm

Test principle

The microtiter plate provided in this kit has been pre-coated with MV. Samples are then added to the appropriate microtiter plate wells with a Horseradish Peroxidase (HRP)-conjugated Anti-Human IgG and incubated. Then substrate solutions are added to each well. Only those wells that contain MV-Ab-IgG and enzyme-conjugated Anti-Human IgG will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. 

 

Product Overview

Measles virus (MV) is a single-stranded, negative-sense, enveloped RNA virus of the genus Morbillivirus within the family Paramyxoviridae. Humans are the natural hosts of the virus; no animal reservoirs are known to exist. The measles virus is the cause of measles, an infection of the respiratory system. Symptoms include fever, cough, runny nose, red eyes and a generalized, maculopapular, erythematous rash. The virus is highly contagious and is spread by coughing and sneezing via close personal contact or direct contact with secretions. The measles virus has two envelope glycoproteins on the viral surface- hemagglutinin (H) and membrane fusion protein (F). These proteins are responsible for host cell binding and invasion. Three receptors for the H protein have been identified to date: complement regulatory molecule CD46, the signaling lymphocyte activation molecule (SLAM) and the cell adhesion molecule Nectin-4.

 

Components


Reagents

Quantity

Reagents

Quantity

Assay plate (96 Wells)

1

Instruction manual

1

Positive Control

1 x 0.5 mL

Negative Control

1 x 0.5 mL

HRP-Conjugate

1 x 12 mL

Sample Diluent

2 x 50 mL

Wash Buffer (concentrate 20 x)

1 x 20 mL Stop Solution 1 x 6 mL
Substrate A 1 x 6 mL

Substrate B

1 x 6 mL

Adhesive Films 4    

 

 

Specificity

This assay has high sensitivity and excellent specificity for detection of Human MV-Ab-IgG. No significant cross-reactivity or interference between Human MV-Ab-IgG and analogues was observed.
 

Recovery

Matrices listed below were spiked with certain level of recombinant Human MV-Ab-IgG and the recovery rates were calculated by comparing the measured value to the expected amount of Human MV-Ab-IgG in samples.
 

Precision

Intra-assay Precision (Precision within an assay) Three samples of known concentration were tested twenty times on one plate to assess intra-assay precision. Inter-assay Precision (Precision between assays) Three samples of known concentration were tested in forty separate assays to assess inter-assay precision. CV (%) = SD/meanX100 Intra-Assay: CV<8% Inter-Assay: CV<12%
 

Linearity

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Human MV-Ab-IgG and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.
 

Stability

The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calculated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

 

Sample collection and storage

Serum: Use a serum separator tube (SST) and allow samples to clot for two hours at room temperature or overnight at 2 - 8°C before centrifugation for 15 minutes at 1000 × g. Remove serum and assay immediately or aliquot and store samples at ≤ -20°C. Avoid repeated freeze-thaw cycles.
Plasma: Collect plasma using EDTA, or heparin as an anticoagulant. Centrifuge for 15 minutes at 1000 × g at 2 - 8°C within 30 minutes of collection. Assay immediately or aliquot and store samples at ≤ -20°C. Avoid repeated freeze-thaw cycles.
Other biological fluids: Centrifuge samples for 20 minutes at 1000 × g. Remove particulates and assay immediately or store samples in aliquot at -20°C or -80°C. Avoid repeated freeze/thaw cycles.

 

Kits storage instructions

Store at 2-8°C. Please refer to Instruction Manual.