Bitte beachten Sie auch
www.keul.de
www.
biogentechnologies.de
www.pipettenshop.de
www.basislabor.com
Fenster schließen
 
deutsch  deutsch
home ELISA-Tests CLIA-Tests Prices Contact Imprint
 
Measles-IgG
 

Measles-IgG

Catalog-No. : E-MVG –K10

INTENDED USE
The E-MVG-K10 Measles IgG Elisa test system is an Enzyme-Linked Immunosorbent Assay kit providing material for the detection of IgG-class antibodies to the antigen of Measles virus in human serum or plasma.This assay is intended for in vitro use only.

SUMMARY AND EXPLANATION
Measles has been largely eliminated in recent years as a major childhood disease due to immunization campaigns. However, because of vaccination failure or subjects who have not been vaccinated, there has been an increasing tendency for young adults to become infected.  Measles causes a very contagious respiratory infection that can have severe consequences, especially in adults.  The screening of pregnant women, young adults and other high risk patients for circulating antibodies is important in determining the immune status.

 

PRINCIPLE OF THE TEST
The E-MVG-K10 Measles IgG kit is based on the ELISA technique. In the assay, controls and unknowns are incubated in microtitration wells coated with purified and inactivated Measles Virus antigen. After incubation and washing, the wells are treated with the conjugate, composed of anti-human IgG antibodies labeled with peroxidase. After a second incubation and washing step, the wells are incubated with the substrate tetramethylbenzidine (TMB). An acidic stopping solution is then added and the degree of enzymatic turnover of the substrate is determined by wavelength absorbance measurement at 450 nm. The absorbance measured is directly proportional to the concentration of anti-Measles virus IgG antibodies present.

REAGENTS
The  Measles IgG ELISA kit contains sufficient reagent for 96 wells. Each kit contains the following reagents:

MATERIAL PROVIDED

QUANTITY

CATALOG NO.

Measles virus  Antigen-Coated Microtitration Strip
Wash Concentrate
Sample Diluent
TMB-Substrate
Negative control
Cut off control
Positive control
2nd Antibody Conjugate
Stopping Solution

One Plate
One Bottle
One Bottle
One Bottle
One Vial
One Vial
One Vial
One Bottle
One Bottle

E-MVG-10
E-WSL-30
E-DLB-40
E-TMB-08
E-MVG-01
E-MVG-02
E-MVG-03
E-MVG-20
E-STP-09


MATERIAL NOT PROVIDED

  • Microtitration plate reader capable of absorbance measurement at 450 nm
  • Deionized/Distilled water
  • Precision pipette to deliver 10 mL, 100 mL, and 1 mL
  • Semi-automatic pipette to deliver 100 mL
  • Automatic microtitration plate washer
  • Absorbent material for blotting the strips


Antigen-Coated Microtitration Strips:
One stripholder containing 12x8 (96) microtitration wells coated with Measles virus antigen. Store at 2-8°C until expiration date. Remove the support and strips to be used from the foil package, and place the unused strips in the polythene bag with the silica gel, expel the air and seal by pressing the closure. Once opened, the product is stable for 4 weeks at 2-8°C.


Wash Concentrate:
One bottle, 100 mL, containing a phosphate buffered saline, concentrated 10-fold containing 0.5% Brij weight by volume (w/v). Dilute with deionized/distilled water prior to use. Store at 2-8°C until expiration date.


Sample Diluent:
One bottle, 100 ml, containing a protein solution with 0.09% sodium azide as a preservative. Store at 2-8°C until expiration date.


MEASLES
 IgG Controls:
Three vials, negative, cut off and positive , each 2 mL of human serum in a 0.01 M phosphate buffer with 0.09% sodium azide as a preservative. Store at 2-8°C until expiration date.


2nd Antibody Conjugate:
One bottle, 12 mL, containing anti-human IgG monoclonal antibodies labeled with peroxidase, in a phosphate buffer solution with 0.02% Proclin. Store at 2-8°C until expiration date.


TMB-Substrate:
One bottle, 12 mL, containing tetramethylbenzidine (TMB) and hydrogen peroxide stabilized in citrate buffer, pH 3.8. Store at 2-8°C until expiration date.


Stopping Solution:
One bottle, 15 mL, containing 0.3 M H2SO4 in solution.  Store at 2-8°C until expiration date.


PRECAUTIONS
For in vitro use
The following universal Good Laboratory Practices should be observed:
Do not eat, drink, smoke or apply cosmetics where immunodiagnostic material is being handled. Do not pipet by mouth. Wear lab coats and disposable gloves when handling immunodiagnostic material. Wash hands thoroughly afterwards. Cover working area with disposable absorbent paper. Wipe up spills immediately and decontaminate affected surfaces. Avoid generation of aerosols. Provide adequate ventilation. Handle and dispose of all reagents and materials in compliance with applicable regulations.
WARNING: POTENTIAL BIOHAZARDOUS MATERIAL
This kit may contain some reagents made with human source material (e.g. serum or plasma) or used in conjunction with human source material. The material in this kit has been tested by CE recommended methods and found to be non-reactive for HIV-1/2 Antibodies, HCV and HBsAg. No available test method can offer complete assurance of eliminating potential biohazardous risk. Handle all reagents and patient samples at a Biosafety Level 2, as recommended for any potentially infectious human material in the Centers for Disease Control/National Institutes of Health manual "Biosafety in Microbiological and Biomedical Laboratories," 4th Edition, April 1999.
WARNING AND PRECAUTION:
Some of the reagents in this kit contain sodium azide as a preservative at concentrations below the regulatory limit of < 0.1%. Although significantly diluted, concentrated sodium azide is an irritant to skin and mucous membranes, and may react with lead and copper plumbing to form explosive metal azides, especially if accumulated. Additionally, TMB and Sulfuric Acid, in concentrated amounts are also irritants to skin and mucous membranes. These substances are in diluted form and therefore may minimize exposure risks significantly but not completely. Provide adequate ventilation. Avoid contact with skin, eyes and clothing. In case of contact with any of these reagents, wash thoroughly with water and seek medical advice. Dispose all nonhazardous reagents by flushing with large volumes of water to prevent buildup of chemical hazards in the plumbing system.
For further information regarding hazardous substances in the kit, please refer to the component specific MSDS by request.


SPECIMEN COLLECTION AND HANDLING
Serum should be used, and the usual precautions for venipuncture should be observed. Specimens may be stored at 2-8°C for 2 days. For longer periods, store at -20°C. Do not use hemolyzed or lipemic specimens. Avoid repeated freezing and thawing of samples.


PREPARATION FOR ASSAY
A thorough understanding of this package insert is necessary for successful use of the product. Reliable results will only be obtained by using precise laboratory techniques and accurately following the package insert.  Bring all kit reagents and specimens to room temperature (~25°C) before use. Thoroughly mix the reagents and samples before use by gentle inversion. Do not mix various lots of any kit component within an individual assay. Do not use any component beyond the expiration date shown on its label. Incomplete washing will adversely affected the outcome and assay precision. To minimize potential assay drift due to variation in the substrate incubation time, care should be taken to add the stopping solution into the wells in the same order and speed to add the TMB Chromogen Solution. Avoid microbial contamination of reagents, especially of the conjugate, wash buffer and diluent. Avoid contamination of the TMB Chromogen Solution with the Conjugate. Use a clean disposable pipette tip for each reagent.  Avoid pipettes with metal parts.  Containers and semi-automatic pipette tips used for the Conjugate and TMB can be reused provided they are thoroughly rinsed with deionized/distilled water and dried prior to and after each usage. The enzyme used as the label is inactivated by oxygen, and is highly sensitive to microbial contamination, sodium azide, hypochlorous acid and aromatic chlorohydrocarbons often found in laboratory water supplies. Use high quality water. Avoid exposure of the reagents to excessive heat or sunlight during storage and incubation.


PREPARATION OF REAGENTS:
Wash Solution:
Dilute 1:10 with deionized/distilled water prior to use.  If crystals are present, they should be dissolved at 37°C before dilution. Pour 100 mL of the Wash Concentrate into a clean container and dilute by adding 900 mL of deionized/distilled water.  Mix thoroughly by inversion. The wash solution is stable for 5 days at room temperature and 2 weeks at 2-8°C when stored in a tightly sealed bottle.
Microtitration Strips:
Select the number of coated strips required for the assay. The remaining unused wells should be placed in the resealable pouch with a desiccant pack. The pouch must be resealed to protect from moisture.


Assay Procedure:
All specimens and reagents to reach room temperature (~25°C) before use. Serum Samples and Controls should be assayed in duplicate.

  1. Mark the microtitration strips to be used.
  2. Dilute serum samples 1:101 distributing 10 mL of serum into 1 mL of Assay Buffer.
  3. Pipette 100 mL of each diluted serum sample and ready to use controls to the appropriate wells. Leave one well for the blank, performed using 100 mL of the substrate mixture.
  4. Cover the wells with protective film and incubate for 45 minutes at 37°C.
  5. Aspirate and wash each well four (4) times for 30 seconds with Washing Solution using an automatic microplate washer or manually using a dispenser. Blot and dry by inverting plate on absorbent material.
    NOTE: Use of an automatic microplate washer is strongly recommended. Incomplete washing will adversely affect assay precision. If a microplate washer is not available, (a) completely aspirate the liquid from each well, (b) dispense 0.35 mL of the Wash Solution into each well, and (c) repeat step (a) and (b) four times.
  6. Add 100 mL of Enzyme-Labeled 2nd Antibody into each well.
  7. Cover the wells with protective film and incubate for 45 minutes at 37°C.
  8. Aspirate and wash each well four times for 30 seconds with Washing Solution using an automatic microplate washer or manually using a dispenser. Blot and dry by inverting plate on absorbent material.
  9. Add 100 mL of TMB Chromogen Solution to each well using a dispenser.
  10. Incubate for 15 minutes at room temperature. Avoid exposure to direct sunlight.
  11. Add 100 mL of Stopping Solution to each well using a dispenser.
  12. Read the absorbance of the solution in the wells within 30 minutes, using a microplate reader set to 450 nm. If wavelength correction is available, set the instrument to dual wavelength measurement at 450 nm with background wavelength correction set at 600 or 620 nm.


RESULTS
Calculate the mean absorbance for each control and unknown.
Qualitative results:
If the absorbance of the sample is higher than that of the Cut-Off, the sample is positive for the presence of specific IgG.
Calculate the ratio between the average OD value of the sample and that of the Cut-Off.  The sample is considered:
Positive: if the ratio is > 1.1.
Doubtful: if +/- 10% of the Cut-Off.
Negative: if the ratio is < 0.9.
If the result is doubtful, repeat the test. If it remains doubtful, collect a new serum sample.


LIMITATIONS OF THE PROCEDURE

  • A serum sample obtained during the early phase of infection, when only IgM antibodies are present, may be negative by this procedure.
  • The test result should be used in conjunction with information available from the evaluation of other clinical and diagnostic procedures.
  • Avoid repeated freezing and thawing of reagents and specimens.
  • Grossly hemolyzed, icteric or lipemic specimens should be avoided.
  • Heat inactivated sera should be avoided.

QUALITY CONTROL
Subtract the value of the blank from all the other readings.  The OD values of Cut-Off control must be at least 0.2.
Positive control  must have an OD at least 1.5 times that of Cut-Off.

PERFORMANCE CHARACTERISTICS
1.
Sensitivity and Specificity
110 human sera were analyzed by this Measles IgG Elisa and an Elisa reference method. Out of
110 samples, 81 were positive for the presence of IgG antibodies to Measles IgG by BGT BioGenTechnologies (BGT) Elisa, and reference Elisa also showed 81 of them as positive. The results are summarized below.

 PositiveNegativeFN (false negative)FP (false positive)
E-MVG –K10812900
Reference812900


2. Precision

2. Inter-assay Study
No of
Replicates 16
Serum 1Serum 2Serum 3
Mean0.3151.920.013
SD0.0040.0740.001
CV% 1.33.88.15


2. Intra-assay Study
No. of
Replicates 16
Serum 1Serum 2Serum 3
Mean0,2610,550,036
SD0,0090,0150.019
CV%3,62,787,8


REFERENCE

  1. D. Erdman et. al. Evaluation of a monoclonal antibody based capture enzyme immunoassays for detection of specific antibodies to measles virus. J. Clin Microbiology 29, 1466 (1991).
  2. D. Erdman et. al. Immunoglobulin M antibody response to measles virus following primary and secondary vaccination and natural virus infection. J. Med. Virology 41,44 (1993).
  3. H. Wasmuth and W. Miller. J. Med. Virology 32:189 (1990)
ELISA-Test-PFD

Instruction Measles IgG ELISA



img/seite/Tabelle-unten1.jpg

img/seite/ce-zeichen.gif     Manufacturer:img/seite/bgt-logo-neu.gif
BGT BioGenTechnologies GmbH
Von-Langen-Weg 10
48565 Steinfurt
Germany
Tel.: 02551/4090 Fax.: 02551/1298
web: http://www.biogentechnologies.de/
e-mail: info@biogentechnologies.de

 
 
© 2008-2012 by Immunoassays - BGT BioGenTechnologies