HEPATITIS C – anti HCV
Contents
1. immunocomplex the colorless Chromogens are hydrolyzed by the bound HRP conjugate to a blue colored product The blue color turns yellow after stopping the reaction with sulfuric acid The amount of color intensity can be measured and is proportional to the amount of antibody captured in the wells and to the sample respectively Wells containing samples negative for anti HCV remain colorless COMPONENTS 96 Tests MICROWELL PLATE 1plate Blank microwell strips fixed on white strip holder The plate is sealed in aluminum pouch with desiccant 8x12 12x8 well strips per plate Each well contains recombinant HCV antigens The microwell strips can be broken to be used separately Place unused wells or strips in the plastic sealable storage bag together with the desiccant and return to 2 8 C NEGATIVE CONTROL 1 vial Blue colored liquid filled in a vial with green screw cap 0 2ml per vial Protein stabilized buffer tested non reactive for HCV antibodies Preservatives 0 1 ProClin 300 Ready to use as supplied Once open stable for one month at 2 8 C POSITIVE CONTROL SERUM 1vial Red colored liquid filled in a vial with red screw cap 0 2ml per vial anti HCV antibodies diluted in protein stabilized buffer Preservatives 0 1 ProClin 300 Ready to use as supplied Once open stable for one month at 2 8 C SPECIMEN DILUENT ivial Blue liquid filled in a white vial with blue screw cap 14 ml per vial Protein stabilized bu2. the negative control is lower than 0 02 take it as 0 02 If higher than 0 02 see the Quality control range Example 1 Calculation of NC Well No B1 C1 D1 Negative controls OD value 0 02 0 012 0 016 NC 0 016 The mean value is lower than 0 02 so take it as 0 02 2 Calculation of Cut off C O 0 02 0 12 0 140 If one of the Negative control values does not meet the Quality control range specifications it should be discarded and the mean value is calculated again using the remaining two values If more than one negative control OD value does not meet the Quality control range specifications the test is invalid and must be repeated 2 Quality control range The test results are valid if the Quality Control criteria are verified It is recommended that each laboratory must establish appropriate quality control system with quality control material similar to or identical with the patient sample being analyzed 1 The OD value of the Blank well which contains only Chromogens and Stop solution is less than 0 080 at 450 nm 2 The OD value of the Positive control must be equal to or greater than 0 800 at 450 630nm or at 450nm after blanking 3 The OD value of the Negative control must be less than 0 100 at 450 630nm or at 450nm after blanking 3 Interpretations of the results S the individual absorbance OD of each specimen Negative Results S C O lt 1 samples giving absorbance less than the Cut of
3. For Research Use Only Not for Diagnostic Use MpressBio HEPATITIS C anti HCV Catalog WC3196 ANTIBODIES TO HEPATITIS C VIRUS ELISA KIT Two Step Incubation Indirect Principle INSTRUCTIONS FOR USE This kit is an enzyme linked immunosorbent assay for qualitative detection of antibodies to hepatitis C virus in human serum or plasma For research use only SUMMARY Hepatitis C virus HCV is an envelope single stranded positive sense RNA 9 5 kb virus belonging to the family of Flaviviridae Six major genotypes and series of subtypes of HCV have been identified Isolated in 1989 HCV is now recognized as the major cause for transfusion associated non A non B hepatitis The disease is characterized with acute and chronic form although more than 50 of the infected individuals develop severe life threatening chronic hepatitis with liver cirrhosis and hepatocellular carcinomas Since the introduction in 1990 of anti HCV screening of blood donations the incidence of this infection in transfusion recipients has been significantly reduced The first generation of HCV ELISAs showed limited sensitivity and specificity and was produced using recombinant proteins complementary to the NS4 c100 3 region of the HCV genome as antigens Second generation tests which included recombinant synthetic antigens from the Core c22 and nonstructural regions NS3 c33c c100 3 and NS4 c100 3 c200 resulted in a remarked improvement in sensiti
4. ample Add 10ul of Positive control Negative control and Specimen into their respective wells Note Use a_ separate disposal pipette tip for each specimen Negative and Positive Control as to avoid cross contamination Mix by tapping the plate gently Incubating 1 Cover the plate with the plate cover and incubate for 30minutes at 37 C It is recommended to use thermostat controlled water tank to assure the temperature stability and humidity during the incubation If dry incubator is used do not open the door frequently Step 6 Washing 1 After the end of the incubation remove and discard the plate cover Wash each well 5 times with diluted Wash buffer Each time allow the microwells to soak for 30 60 seconds After the final washing cycle turn the strips plate onto blotting paper or clean towel and tap it to remove any remainders Step 7 Adding HRP Conjugate Add 100ul HRP Conjugate to each well except the Blank Step 8 HRP Conjugate Incubating 2 Cover the plate with the plate cover and incubate for 30 minutes at 37 C Step9 Washing 2 At the end of the incubation remove and discard the plate cover Wash each well 5times with diluted Wash buffer as in Step6 Step 10 Coloring Dispense 50ul of Chromogen A and 50ul Chromogen B solution into each well including the Blank and mix by tapping the plate gently Incubate the plate at 37 C for 15minutes avoiding light The enzymatic reaction between the Chromogen A B
5. conjugate might be affected from dust reactive chemical and substances like sodium hypochlorite acids alkalis etc Do not perform the assay in the presence of such substances Materials Safety Data Sheet MSDS available upon request If using fully automated microplate processing system during incubation do not cover the plates with the plate cover The tapping out of the remainders inside the plate after washing can also be omitted ASSAY PROCEDURE Step 1 Reagents preparation Allow the reagents and Step 2 Step 3 Step 4 Step 5 samples to reach room temperature 18 30 C for at least 15 30 minutes Check the Wash buffer concentrate for the presence of salt crystals If crystals have formed in the solution resolubilize by warming at 37 C until crystals dissolve Dilute the stock wash Buffer 1 to 20 with distilled or deionized water Use only clean vessels to dilute the Wash buffer Numbering Wells Set the strips needed in strip holder and number sufficient number of wells including three Negative control e g B1 C1 D1 two Positive control e g E1 F1 and one Blank A1 neither samples nor HRP Conjugate should be added into the Blank well If the results will be determined by using dual wavelength plate reader the requirement for use of Blank well could be omitted Use only number of strips required for the test Adding Diluent Add 100ul Specimen Diluent into each well except the blank Adding S
6. f value are negative for this assay which indicates that no antibodies to hepatitis C virus have been detected with this anti HCV ELISA kit Positive Results S C 0 21 samples giving an absorbance greater than or equal to the Cut off value are considered initially reactive which indicates that antibodies to hepatitis C virus have probably been detected using this anti HCV ELISA kit Retesting in duplicates of any initially reactive sample is recommended Repeatedly reactive samples could be considered positive for antibodies to HCV Borderline Samples with absorbance O D SCut off x2 are considered borderline and retesting of those samples in duplicates is recommended LIMITATIONS 1 Non repeatable positive result may occur due to the general biological characteristics of ELISA assays The assay is design to achieve very high performance characteristics of sensitivity and specificity and the indirect model minimizes the unspecific reactions which can occur due to interference between unknown meters in sample and the rabbit anti human IgG used as a conjugate Antibodies may be undetectable during the early stages of the disease and in some Reproducibility Within run Between run Sample No MeanOD CV MeanOD CV Weak positive 10 0 436 9 1 0 401 9 5 Moderate 10 0 946 7 0 0 916 7 5 positive Strong positive 1 10 1 917 44 1 895 4 2 Strong positive 2 10 2 372 3 8 2 309 4 0 immunosuppresed
7. ffer casein and sucrose solution Ready to use as supplied Once open stable for one month at 2 8 C HRP CONJUGATE REAGENT 1vial Red colored liquid filled in a white vial with red screw cap 14ml per vial Horseradish peroxidase conjugated rabbit anti human IgG antibodies Ready to use as supplied Once open stable for one month at 2 8 C STOCK WASH BUFFER 1bottle DILUTE BEFORE USE Colorless liquid filled in a clear bottle with white screw cap 50ml per bottle PH 7 4 20 x PBS Contains Tween 20 as a detergent The concentrate must be diluted 1 to 20 with distilled deionized water before use Once diluted stable for one week at room temperature or for two weeks at 2 8 C CHROMOGEN SOLUTION A 1 vial Colorless liquid filled in a white vial with green screw cap 8ml per vial Urea peroxide solution Ready to use as supplied Once open stable for one month at 2 8 C CY CHROMOGEN SOLUTION B 1 vial Colorless liquid filled in a black vial with black screw cap 8ml per vial TMB solution Tetramethyl benzidine dissolved in citric acid Ready to use as supplied Once open stable for one month at 2 8 C STOP SOLUTION 1 vial Colorless liquid filled in a white vial with yellow screw cap 8ml per vial Diluted sulfuric acid solution 2 0M H2S04 Ready to use as supplied PLASTIC SEALABLE BAG 1 unit For enclosing the strips not in use CARDBOARD PLATE COVER 2 sheets To cover the plates during incubation and prevent e
8. he absorbance at 450nm or at 450nm with reference at 630nm All specimens from human origin should be considered as potentially infectious Materials from human origin may have been used in the kit These materials have been tested with tests kits with accepted performance and found negative for antibodies to HIV HCV TP and HBsAg However there is no analytical method that can assure that infectious agents in the specimens or reagents are completely absent Therefore handle reagents and specimens with extreme caution as if capable of transmitting infectious diseases Strict adherence to GLP Good Laboratory Practice regulations can ensure the personal safety Never eat drink smoke or apply cosmetics in the assay 16 17 18 19 20 21 laboratory Bovine derived sera may have been used in this kit Bovine serum albumin BSA and fetal calf sera FCS are derived from animals from BSE TSE free geographical areas The pipette tips vials strips and sample containers should be collected and autoclaved for 1hour at 121 C or treated with 10 sodium hypochlorite for 30minutes to decontaminate before any further steps for disposal The Stop solution 2M H2SO is a strong acid Corrosive Use it with appropriate care Wipe up spills immediately or wash with water if come into contact with the skin or eyes ProClin 300 used as a preservative can cause sensation of the skin The enzymatic activity of the HRP
9. in the assay Do not heat inactivate samples This can cause sample deterioration 2 Transportation and Storage Store samples at 2 8 C Samples not required for assaying within 3 days should be stored frozen 20 C or lower Multiple freeze thaw cycles should be avoided For shipment samples should be packaged and labeled in accordance with the existing local and international regulations for transport of clinical samples and ethological agents SPECIAL INSTRUCTIONS FOR WASHING 1 A good washing procedure is essential to obtain correct and precise analytical data 2 It is therefore recommended to use a good quality ELISA microplate washer maintained at the best level of washing performances In general no less than 5 automatic washing cycles with dispensing of 350 400ul well are sufficient to avoid false positive reactions and high background all wells turn yellow 3 To avoid cross contaminations of the plate with sample or HRP conjugate after incubation do not discard the content of the wells but allow the plate washer to aspirate it automatically 4 Anyway we recommend calibrating the washing system on the kit itself in order to match the declared analytical performances Assure that the microplate washer s liquid dispensing channels are not blocked or contaminated and sufficient volume of Wash buffer is dispensed each time into the wells 5 In case of manual washing we suggest to perform at least 5cycles d
10. individuals 2 Common sources for mistakes kits beyond the expiry date bad washing procedures contaminated reagents incorrect assay procedure steps insufficient aspiration during washing failure to add samples or reagents equipment timing volumes sample nature and quality 3 If after retesting of the initially reactive samples the assay results are negative these samples should be considered as non repeatable false positive and interpreted as negative As with many very sensitive ELISA assays false positive results can occur due to the several reasons most of which are related but not limited to inadequate washing step The prevalence of the marker will affect the assay s predictive values VALIDITY Please do not use this kit beyond the expiration indicated on the kit box and reagent labels INDICATIONS OF INSTABILITY OR DETERIORATION OF THE REAGENTS 1 Values of the Positive or Negative controls which are out of the indicated Quality control range are indicator of possible deterioration of the reagents and or operator or equipment errors In such case the results should be considered as invalid and the samples must be retested In case of constant erroneous results classified as due to deterioration or instability of the reagents immediately substitute the reagents with new ones 2 If after mixing of the Chromogen A and B solutions into the wells the the color of the mixture turns blue within few minutes d
11. ispensing 350 400ul well and aspirating the liquid for 5times If poor results high background are observed increase the washing cycles or soaking time per well 6 In any case the liquid aspirated out the strips should be treated with a sodium hypochlorite solution final concentration of 2 5 for 24 hours before liquids are disposed in an appropriate way 7 The concentrated Washing solution should be diluted 1 to 20 before use For one plate mix 50 ml of the concentrate with 950ml of water for a final volume of 1000m diluted Wash Buffer If less than a whole plate is used prepare the proportional volume of solution STORAGE AND STABILITY The components of the kit will remain stable through the expiration date indicated on the label and package when stored between 2 8 C do not freeze To assure maximum performance of this anti HCV ELISA kit during storage protect the reagents from contamination with microorganism or chemicals PRECAUTIONS AND SAFETY This kit is intended FOR Research Use Only The ELISA assay is a time and temperature sensitive method To avoid incorrect result strictly follow the test procedure steps and do not modify them 1 10 11 12 13 14 15 Do not exchange reagents from different lots or use reagents from other commercially available kits The components of the kit are precisely matched as to achieve optimal performance during testing Make sure that all reagents are wi
12. o not continue carrying out the testing and replace the reagents with fresh ones REFERENCES 1 Alter HJ 1978 You will wonder where the yellow went A 15 year retrospective of post transfusion hepatitis In Moore SB ed Transfusion Transmitted Viral Diseases Arlington VA Am Assoc Blood Banks pp 53 38 2 Alter HJ Purcell RH Holland PV et al 1978 Transmissible agent in non A non B hepatitis Lancet 459 463 3 Choo Q L Weiner AJ Overby LR Kuo G Houghton M 1990 Hepatitis C Virus the major causative agent of viral non A non B hepatitis Br Med Bull 46 423 441 4 Engvall E Perlmann P 1971 Enzyme linked immunosorbent assay ELISA qualitative assay of IgG Immunochemistry 8 871 874 Express Biotech International 503 Gateway Drive West Thurmont MD 21788 USA Tel 301 228 2444 Fax 301 560 6570 Toll Free 888 562 8914 www xpressbio com info xpressbio com XKpressBio
13. solutions produces blue color in Positive control and anti HCV positive sample wells Step 11 Stopping Reaction Using a multichannel pipette or manually add 50ul Stop Solution into each well and mix by tapping the plate gently Intensive yellow color develops in Positive control and anti HCV positive sample wells Step 12 Measuring the Absorbance Calibrate the plate reader with the Blank well and read the absorbance at 450nm If a dual filter instrument is used set the reference wavelength at 630nm Calculate the Cut off value and evaluate the results Note read the absorbance within 5 minutes after stopping the reaction INTERPRETATION OF RESULTS AND QUALITY CONTROL Each microplate should be considered separately when calculating and interpreting results of the assay regardless of the number of plates concurrently processed The results are calculated by relating each sample s optical density OD value to the Cut off value C O of the plate If the Cut off reading is based on single filter plate reader the results should be calculated by subtracting the Blank well OD value from the print report values of samples and controls In case the reading is based on dual filter plate reader do not subtract the Blank well OD from the print report values of samples and controls 1 Calculation of Cut off value C O NC 0 12 NC the mean absorbance value for three negative controls Important If the mean OD value of
14. thin the validity indicated on the kit box and are of the same lot Never use reagents beyond the expiry date stated on reagents labels or on the kit box CAUTION CRITICAL STEP Allow the reagents and samples to stabilize at room temperature 18 30 C before use Shake reagent gently before and return to 2 8 C immediately after use Use only sufficient volume of sample as indicated in the procedure steps Failure to do so may cause in low sensitivity of the assay Do not touch the bottom exterior of the wells fingerprints or scratches may interfere with microwell reading When reading the results ensure that the plate bottom is dry and there are no air bubbles inside the wells Never allow the microplate wells to dry after the washing step Immediately proceed to the next step Avoid the formation of air bubbles when adding the reagents Avoid assay steps long time interruptions Assure same working conditions for all wells Calibrate the pipette frequently to assure the accuracy of samples reagents dispensing Always use different disposal pipette tips for each specimen and reagents as to avoid cross contaminations Never pipette solutions by mouth The use of automatic pipettes is recommended Assure that the incubation temperature is 37 C inside the incubator When adding samples avoid touching the wells bottom with the pipette tip When reading the results with a plate reader it is recommended to determine t
15. vaporation or contamination of the wells PACKAGE INSERTS 1 copy ADDITIONAL MATERIALS AND INSTRUMENTS REQUIRED BUT NOT PROVIDED e Freshly distilled or deionized water Disposable gloves and timer e Appropriate waste containers for potentially contaminated materials e Disposable V shaped troughs e Dispensing system and or pipette single or multichannel disposable pipette tips Absorbent tissue or clean towel Dry incubator or water bath 37 0 5 C e Microshaker for dissolving and mixing conjugate with samples e Microwell plate reader single wavelength 450nm or dual wavelength 450nm and 630nm e Microwell aspiration wash system SPECIMEN COLLECTION TRANSPORTATION AND STORAGE 1 Sample Collection Either fresh serum or plasma samples can be used for this assay Blood collected by venipuncture should be allowed to clot naturally and completely the serum plasma must be separated from the clot as early as possible as to avoid hemolysis of the RBC Care should be taken to ensure that the serum samples are clear and not contaminated by microorganisms Any visible particulate matters in the sample should be removed by centrifugation at 3000 RPM for at least 20 minutes at room temperature or by filtration on 0 22u filters Plasma samples collected into EDTA sodium citrate or heparin may be tested but highly lipaemic icteric or hemolized samples should not be used as they could give erroneous results
16. vity and specificity Clinical studies show that significant amount of HCV infected individuals develop antibodies to NS5 non structural protein of the virus For this the third generation tests include antigens from the NS5 region of the viral genome in addition to NS3 c200 NS4 c200 and the Core c22 Third generation tests have improved sensitivity and shorten the time between infection with HCV and the appearance of detectable antibodies window period to 60 days PRINCIPLE OF THE ASSAY This kit employs solid phase indirect ELISA method for detection of antibodies to HCV in two step incubation procedure Polystyrene microwell strips are pre coated with recombinant highly immunoreactive antigens corresponding to the core and the non structural regions of HCV third generation HCV ELISA During the first incubation step anti HCV specific antibodies if present will be bound to the solid phase pre coated HCV antigens The wells are washed to remove unbound serum proteins and rabbit anti human IgG antibodies anti IgG conjugated to horseradish peroxidase HRP Conjugate are added During the second incubation step these HRP conjugated antibodies will be bound to any antigen antibody IgG complexes previously formed and the unbound HRP conjugate is then removed by washing Chromogen solutions containing Tetramethylbenzidine TMB and urea peroxide are added to the wells and in presence of the antigen antibody anti lgG HRP
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