ࡱ> ~  !"#$%&'()*+,-./0123456789:;<=>?@ABCDENGHIJKLMOPQRSTUVWXYZ[\]^_`abcdefghijklmnopqrstuvwxyz{|}Root Entry FPkSummaryInformation(DocumentSummaryInformation8WordDocument Oh+'04 X d p|,gՋBRvS(uNyf[xvz N_(uN;Sf[ʋe0HOĖNormalAdministrator5@r,@)kpMicrosoft Office Word՜.+,D՜.+,l(     MC SYSTEM -3 (\dlKSOProductBuildVer2052-9.1.0.49930TableFData  P:KSKSC\\8L:kN$;hV"?|, FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC PROCEDURES. Goose Parvovirus virus antibody (GPV-Ab) ELISA Kit instruction Intended use This GPV-Ab ELISA kit is intended Laboratory for Research use only and is not for use in diagnostic or therapeutic procedures.The Stop Solution changes the color from blue to yellow and the intensity of the color is measured at 450 nm using a spectrophotometer. In order to measure the concentration of GPV-Ab in the sample, this GPV-Ab ELISA Kit includes a set of calibration standards. The calibration standards are assayed at the same time as the samples and allow the operator to produce a cutoff value. The existence or not of GPV-Ab in the samples is then determined by comparing the O.D. of the samples to the CUT OFF. Sample collection and storages Serum - Use a serum separator tube and allow samples to clot for 30 minutes before centrifugation for 10 minutes at approximately 3000g. Remove serum and assay immediately or aliquot and store samples at -20! or -80!.Avoid repeated freeze-thaw cycles Plasma - Collect plasma using EDTA or heparin as an anticoagulant. Centrifuge samples for 30 minutes at 3000g at 2-8! within 30 minutes of collection. Store samples at -20!or -80!. Avoid repeated freeze-thaw cycles. Cell culture supernates and other biological fluids - Remove particulates by centrifugation and assay immediately or aliquot and store samples at -20!or -80!. Avoid repeated freeze-thaw cycles. Note: The samples shoule be centrifugated dequately and no hemolysis or granule was allowed. Materials required but not supplied 1. Standard microplate reader(450nm) 2. Precision pipettes and Disposable pipette tips. 3. 37 ! incubator Precautions 1. Do not substitute reagents from one kit to another. Standard, conjugate and microplates are matched for optimal performance. Use only the reagents supplied by manufacturer. 2. Do not remove microplate from the storage bag until needed. Unused strips should be stored at 2-8C in their pouch with the desiccant provided. 3. Mix all reagents before using. Remove all kit reagents from refrigerator and allow them to reach room temperature ( 20-25C) Materials supplied Name96 determinations48 determinationsMicroelisa stripplate12*8strips12*4stripsNegative control0.5ml0.5mlPositive control0.5ml0.5mlHRP-Conjugate reagent10.0ml5.0ml20X Wash solution25ml15mlSample Diluent6.0ml3.0mlChromogen Solution A6.0ml3.0mlChromogen Solution B6.0ml3.0mlStop Solution6.0ml3.0mlClosure plate membrane22User manual11Sealed bags11Reagent preparation 20wash solution:Dilute with Distilled or deionized water 1:20. Assay procedure 1. Prepare all reagents before starting assay procedure. It is recommended that all Standards and Samples be added in duplicate to the Microelisa Stripplate. 2. Separately add Positive control and Negative control 50l to the Positive and Negative well; Add testing sample 10l then add Sample Diluent 40l to testing sample well. 3. Add 100l of HRP-conjugate reagent to each well, cover with an adhesive strip and incubate for 60 minutes at 37C. 4. Aspirate each well and wash, repeating the process four times for a total of five washes. Wash by filling each well with Wash Solution (400l) using a squirt bottle, manifold dispenser or autowasher. Complete removal of liquid at each step is essential to good performance. After the last wash, remove any remaining Wash Solution by aspirating or decanting. Invert the plate and blot it against clean paper towels. 5. Add chromogen solution A 50l and chromogen solution B 50l to each well. Gently mix and incubate for 15 minutes at 37C. Protect from light. 6. Add 50l Stop Solution to each well. The color in the wells should change from blue to yellow. If the color in the wells is green or the color change does not appear uniform, gently tap the plate to ensure thorough mixing. 7. Read the Optical Density (O.D.) at 450 nm using a microtiter plate reader within 15 minutes. Determine the result 1. Test validity: the average of Positive control welle"1.00; the average of Negative control well d"0.15. 2. Calculate Critical (CUT OFF): Critical= the average of Negative control well + 0.15. Negative Result: sample OD< Calculate Critical (CUT OFF) is Negative. Positive Result: sample ODe" Calculate Critical (CUT OFF) is Positive. Storage and validity Storage 2-8!. validity six months. FOR RESEARCH USE ONLY; NOT FOR THERAPEUTIC OR DIAGNOSTIC APPLICATIONS! PLEASE READ THROUGH ENTIRE PROCEDURE BEFORE BEGINNING! ,gՋBRvS(uNyf[xvz N_(uN;Sf[ʋe EGoose \EvukbSOGPV-Ab ELISAhKmՋBRv O(uffN hKmSt ՋBRvǑ(uSbNek9Y_lvTMQu8TDՋELISA 0_HQSEYNWpukbSvS_T[-N O!kReQh,g0HRPhvhKmbS ~Ǐ)nv^{_^mm0(u^irTMB>fr TMB(WǏ'lSirvvPS NlSb݄r v^(Wxv\O(u NlSbg~vĞr0(uvhN(W450nml NKm[8TIQ^OD

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