AssayMaxTM Human IL-10 ELISA Kit
Contents
1. incubate for 30 minutes Turn on the microplate reader and set up the program in advance e Wash the microplate as described above e Add 50 ul of Chromogen Substrate per well and incubate for 30 minutes or till the optimal blue color density develops Gently tap the plate to ensure thorough mixing and break the bubbles in the well with pipette tip e Add 50 ul of Stop Solution to each well The color will change from blue to yellow e Read the absorbance on a microplate reader at a wavelength of 450 nm immediately If wavelength correction is available subtract readings at 570 nm from those at 450 nm to correct optical imperfections Otherwise read the plate at 450 nm only Please note that some unstable black particles may be generated at high concentration points after stopping the reaction for about 10 minutes which will reduce the readings Data Analysis e Calculate the mean value of the duplicate triplicate readings for each standard and sample e To generate a standard curve plot the graph using the standard concentrations on the x axis and the corresponding mean 450 nm absorbance on the y axis The best fit line can be determined by regression analysis using log log or four parameter logistic curve fit e Determine the unknown sample concentration from the Standard Curve and multiply the value by the dilution factor Typical Data e The typical data is provided for reference only Individual laboratory means may vary from2. mixing of eis oe 5 reconstitution reagent dilutions e Thoroughly mix dilutions References 1 OpdalSH 2004 FEMS Immunol Med Microbiol 42 1 48 52 2 Weiss E et al 2004 J Am Acad Dermatol 50 5 657 75 quiz 676 8 3 Al Rasheed A et al 2004 J Periodontal Res 39 3 194 8 Version 3 2R Related products EMI3010 1 AssayMax Mouse IL 10 ELISA Kit Plasma Serum Cell Culture Supernatant and Tissue samples e ERI3010 1 AssayMax Rat IL 10 ELISA Kit Cell Culture samples www assaypro com e e mail Support assaypro com
3. the values listed Variations between laboratories may be caused by technique differences Average OD Standard Point Standard Curve The curve is provided for illustration only A standard curve should be generated each time the assay is performed H IL 10 Standard Curve OD 450 nm 0 1 1 0 10 0 h IL 10 ng ml Performance Characteristics This assay recognizes both natural and recombinant human IL 10 The minimum detectable dose of IL 10 as calculated by 2SD from the mean of a zero standard was established to be 0 09 ng ml e Intra assay precision was determined by testing replicates of three plasma samples in one assay e _ Inter assay precision was determined by testing three plasma samples in twenty assays Intra Assay Precision Inter Assay Precision Sample 1 2 3 1 2 3 n 20 20 20 20 20 20 CV Average CV Recovery Standard Added Value 0 2 2 ng ml Recovery 86 109 Average Recovery 97 Linearity e Plasma and serum samples were serially diluted to test for linearity Average Percentage of Expected Value Sample Dilution Plasma Serum No Dilution 100 99 1 2 101 102 1 4 98 98 Cross Reactivity Species Cross Reactivity Beagle None Bovine None Monkey None Mouse None Rat None Swine None Rabbit None Human 100 Troubleshooting Ca
4. ate onset condition and indicates that the lack of IL 10 may have an effect on bone homeostasis 3 Principle of the Assay The AssayMax Human Interleukin 10 ELISA Enzyme Linked Immunosorbent Assay kit is designed for detection of IL 10 in human plasma serum tissue extracts and cell culture samples This assay employs a quantitative sandwich enzyme immunoassay technique that measures IL 10 in less than 5 hours A murine monoclonal antibody specific for human IL 10 has been pre coated onto a 96 well microplate with removable strips IL 10 in standards and samples is sandwiched by the immobilized antibody and a biotinylated polyclonal antibody specific for human IL 10 which is recognized by a streptavidin peroxidase conjugate All unbound material is washed away and a peroxidase enzyme substrate is added The color development is stopped and the intensity of the color is measured Caution and Warning e This product is for Research Use Only and is Not For Use In Diagnostic Procedures Prepare all reagents working diluent buffer wash buffer standard biotinylated antibody and SP conjugate as instructed prior to running the assay e Prepare all samples prior to running the assay The dilution factors for the samples are suggested in this insert However the user should determine the optimal dilution factor e Spin down the SP conjugate vial and the biotinylated antibody vial before opening and using contents e The Stop Solutio
5. e stored for up to 30 days in a vacuum desiccator e Diluent 1x may be stored for up to 30 days at 2 8 C e Store Standard at 2 8 C before reconstituting with Diluent and at 20 C after reconstituting with Diluent Other Supplies Required e Microplate reader capable of measuring absorbance at 450 nm e Pipettes 1 20 ul 20 200 ul 200 1000 ul and multiple channel e Deionized or distilled reagent grade water Sample Collection Preparation and Storage e Plasma Collect plasma using one tenth volume of 0 1 M sodium citrate as an anticoagulant Centrifuge samples at 3000 x g for 10 minutes and assay Samples can be stored at 20 C or below for up to 3 months Avoid repeated freeze thaw cycles EDTA or Heparin can also be used as an anticoagulant e Serum Samples should be collected into a serum separator tube After clot formation centrifuge samples at 3000 x g for 10 minutes Remove serum and assay Samples can be stored at 20 C or below for up to 3 months Avoid repeated freeze thaw cycles e Cell Culture Supernatants Centrifuge cell culture media at 3000 x g for 10 minutes to remove debris Collect supernatants and assay Samples can be stored at 20 C or below Avoid repeated freeze thaw cycles e Tissue Extract tissue samples with 0 1 M Tris buffered saline pH7 4 containing 0 5 Triton X 100 and centrifuge at 14000 x g for 30 minutes Collect the supernatant measure the protein concentration and assay Freeze the
6. f crystals have formed in the concentrate mix gently until the crystals have completely dissolved Dilute the Wash Buffer Concentrate 1 20 with reagent grade water e SP Conjugate 100x Spin down the SP Conjugate briefly and dilute the desired amount of the conjugate 1 100 with MIX Diluent Any remaining solution should be frozen at 20 C Assay Procedure e Prepare all reagents standard solutions and samples as instructed Bring all reagents to room temperature before use The assay is performed at room temperature 20 25 C e Remove excess microplate strips from the plate frame and return them immediately to the foil pouch with desiccants inside Reseal the pouch securely to minimize exposure to water vapor and store in a vacuum desiccator e Add 50 ul of Human IL 10 Standard or sample per well Cover wells with a sealing tape and incubate for 2 hours Start the timer after the last addition e Wash five times with 200 ul of Wash Buffer manually Invert the plate each time and decant the contents hit 4 5 times on absorbent material to completely remove the liquid If using a machine wash six times with 300 ul of Wash Buffer and then invert the plate decanting the contents hit 4 5 times on absorbent material to completely remove the liquid e Add 50 ul of Biotinylated Human IL 10 Antibody to each well and incubate for 2 hours e Wash the microplate as described above e Add 50 ul of Streptavidin Peroxidase Conjugate per well and
7. n is an acidic solution e The kit should not be used beyond the expiration date Reagents e Human IL 10 Microplate A 96 well polystyrene microplate 12 strips of 8 wells coated with a murine monoclonal antibody against IL 10 e Sealing Tapes Each kit contains 3 precut pressure sensitive sealing tapes that can be cut to fit the format of the individual assay e Human IL 10 Standard Human IL 10 in a buffered protein base 16 ng lyophilized e Biotinylated Human IL 10 Antibody 50x A 50 fold concentrated biotinylated polyclonal antibody against IL 10 120 ul e _ MIX Diluent Concentrate 10x A 10 fold concentrated buffered protein base 30 ml e Wash Buffer Concentrate 20x A 20 fold concentrated buffered surfactant 30 ml 2 bottles e Streptavidin Peroxidase Conjugate SP Conjugate A 100 fold concentrate 80 ul e Chromogen Substrate A ready to use stabilized peroxidase chromogen substrate tetramethylbenzidine 8 ml e Stop Solution A 0 5 N hydrochloric acid to stop the chromogen substrate reaction 12 ml Storage Condition e Upon arrival immediately store components of the kit at recommended temperatures up to the expiration date e Store SP Conjugate and Biotinylated Antibody at 20 C e _ Store Microplate Diluent Concentrate 10x Wash Buffer Stop Solution and Chromogen Substrate at 2 8 C e Unused microplate wells may be returned to the foil pouch with the desiccant packs and resealed May b
8. order Insufficient amount of reagents added to wells e Check pipette calibration e Check pipette for proper performance Wash step was skipped e Consult the provided procedure for all wash steps Improper wash buffer e Check that the correct wash buffer is being used Improper reagent preparation e Consult reagent preparation section for the correct dilutions of all reagents Insufficient or prolonged incubation periods e Consult the provided procedure for correct incubation time Deficient Standard Curve Fit Non optimal sample dilution e Sandwich ELISA If samples generate OD values higher than the highest standard point P1 dilute samples further and repeat the assay e Competitive ELISA If samples generate OD values lower than the highest standard point P1 dilute samples further and repeat the assay e User should determine the optimal dilution factor for samples Contamination of reagents e A new tip must be used for each addition of different samples or reagents during the assay procedure Contents of wells evaporate e Verify that the sealing film is firmly in place before placing the assay in the incubator or at room temperature Improper pipetting e Pipette properly in a controlled and careful manner e Check pipette calibration e Check pipette for proper performance e Thoroughly agitate the lyophilized components after Insufficient
9. remaining extract at 20 C or below Avoid repeated freeze thaw cycles Reagent Preparation e Freshly dilute all reagents and bring all reagents to room temperature before use e _ MIX Diluent Concentrate 10x If crystals have formed in the concentrate mix gently until the crystals have completely dissolved Dilute the MIX Diluent Concentrate 1 10 with reagent grade water Store for up to 30 days at 2 8 C e Standard Curve Reconstitute the 16 ng of Human IL 10 Standard with 2 ml of MIX Diluent to generate an 8 ng ml standard stock solution Allow the standard to sit for 10 minutes with gentle agitation prior to making dilutions Prepare duplicate or triplicate standard points by serially diluting the standard stock solution 1 2 with equal volume of MIX Diluent to produce 4 2 1 0 5 0 25 and 0 125 ng ml solutions MIX Diluent serves as the zero standard 0 ng ml Any remaining solution should be frozen at 20 C and used within 30 days Standard Point Dilution IL 10 ng ml P1 1 part Standard 8 ng ml 8 000 1 part P1 1 part MIX Diluent 4 000 1 part P2 1 part MIX Diluent 2 000 P4 A part P3 1 part MIX Diluent 1 000 Pe 1partP5 1 part MIX Diluent 2 0250 lr NMkxDilene 000 e Biotinylated Human IL 10 Antibody 50x Spin down the antibody briefly and dilute the desired amount of the antibody 1 50 with MIX Diluent Any remaining solution should be frozen at 20 C e Wash Buffer Concentrate 20x I
10. uses Course of Action Low Precision Use of expired components e Check the expiration date listed before use e Do not interchange components from different lots Improper wash step e Check that the correct wash buffer is being used e Check that all wells are dry after aspiration e Check that the microplate washer is dispensing properly e If washing by pipette check for proper pipetting technique Splashing of reagents while loading wells e Pipette properly in a controlled and careful manner Inconsistent volumes loaded into wells e Pipette properly in a controlled and careful manner e Check pipette calibration e Check pipette for proper performance Insufficient mixing of reagent dilutions e Thoroughly agitate the lyophilized components after reconstitution e Thoroughly mix dilutions Improperly sealed microplate e Check the microplate pouch for proper sealing e Check that the microplate pouch has no punctures e Check that three desiccants are inside the microplate pouch prior to sealing T c oo N lt AJ u 52 77 gt so 3 zs uv 3 18 uv o x uv E gt Microplate was left unattended between steps e Each step of the procedure should be performed uninterrupted Omission of step e Consult the provided procedure for complete list of steps Steps performed in incorrect order e Consult the provided procedure for the correct
11. yssaypro AssayMax Human IL 10 ELISA Kit Assaypro LLC 3400 Harry S Truman Blvd St Charles MO 63301 T 636 447 9175 F 636 395 7419 WWW assaypro com For any questions regarding troubleshooting or performing the assay please contact our support team at support assaypro com Thank you for choosing Assaypro Assay Summary Step 1 Add 50 ul of Standard or Sample per well Incubate 2 hours Step 2 Wash then add 50 ul of Biotinylated Antibody per well Incubate 2 hours Step 3 Wash then add 50 ul of SP Conjugate per well Incubate 30 minutes Step 4 Wash then add 50 ul of Chromogen Substrate per well Incubate 30 minutes Step 5 Add 50 ul of Stop Solution per well Read at 450 nm immediately Symbol Key 3 Consult instructions for use Assay Template 12 11 10 Human Interleukin 10 IL 10 ELISA Kit Catalog No EI3010 1 Sample insert for reference use only Introduction Interleukin 10 IL 10 is a regulatory cytokine and its principal role in vivo is to limit inflammatory response IL 10 has been shown to influence both the susceptibility and course of various diseases 1 Interleukin 10 IL 10 is a key cytokine produced by a multitude of immune effector cells and possesses distinct regulatory effects on immune functioning in the skin 2 The accelerated alveolar bone loss observed in IL 10 mice is a l
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