EpiQuik™ DNMT3B Assay Kit
Contents
1. EpiQuik DNMT3B Assay Kit Base Catalog P 3013 PLEASE READ THIS ENTIRE USER GUIDE BEFORE USE Uses The EpiQuik DNMT3B Assay Kits are very suitable for measuring Dnmt3B amounts quantitatively from fresh tissue and cultured cells of human and mouse 110 Bi County Blvd Ste 122 Farmingdale NY 11735 Page 1 Tel 1 877 374 4368 m Fax 1 718 484 3956 m E mail info epigentek com Web www epigentek com Epigentek Group Inc All rights reserved Products are for research use only pamed ets Ta KIT CONTENTS Component 48 Assays 96 Assays Storage Cat P 3013 2 Cat P 3013 3 Upon Receipt DB1 10X Wash Buffer 12 ml 25 ml 4 C DB2 Assay Buffer 5ml 10 ml 4 C DB3 DNMT3B Standard 20 ug ml 16 ul 30 ul 20 C DB4 Capture Antibody 100 g ml 8 ul 16 ul 4 C DB5 Detection Antibody 200 ug ml 10 ul 20 ul 20 C DB6 Developing Solution 6 ml 12 ml 4 C DB7 Stop Solution 6ml 11 ml RT BB Blocking Buffer 10 ml 20 ml 4 C 8 Well Assay Strips With Frame 6 12 4 C User Guide 1 1 RT For maximum recovery of the products centrifuge the original vial prior to opening the cap SHIPPING amp STORAGE The kit is shipped in two parts one part at ambient room temperature and the second part on frozen ice packs at 4 C Upon receipt 1 Store DB3 and DB5 at 20 C away from light 2 Store DB1 DB2 DB4 DB6 Blocking buffer and the 8 Well Assay Strips at 4 C away2. a sufficient amount of standard is signal in only the insufficiently added to the wellin added 110 Bi County Blvd Ste 122 Farmingdale NY 11735 Page 8 Tel 1 877 374 4368 m Fax 1 718 484 3956 m E mail info epigentek com Web www epigentek com Printed 2014 10 13 Epigentek Group Inc All rights reserved Products are for research use only P 3013 standard curve wells Step 2c The standard is degraded due to improper storage conditions Follow the Shipping amp Storage guidance in this User Guide for storage of DB3 DNMT3B Standard High background present in the blank wells Insufficient washing of wells Check if washing recommendations at each step is performed according to the protocol Contaminated by sample or standard Ensure the well is not contaminated from adding sample or standard accidentally or from using contaminated tips Incubation time with Diluted DB5 is too long The incubation time at Step 3d should not exceed 90 min Over development of color Decrease the development time in Step 4a before adding DB6 Stop Solution in Step 4b No signal or weak signal only in sample wells Protein sample is not properly extracted or purified Ensure your protocol is suitable for histone protein extraction For the best results it is advised to use Epigentek s Nuclear extraction Kit Cat No OP 0002 Sample amount added into the wells is insufficient E
3. from light 3 Store all other components at room temperature The kit is stable for up to 6 months from the shipment date when stored properly Note 1 Check if wash buffer DB1 contains salt precipitates before using If so warm at room temperature or 37 C and shake the buffer until the salts are re dissolved 2 check if a blue color is present in DB6 Developing Solution which would indicate contamination of the solution and should not be used To avoid contamination transfer the amount of DB6 required into a secondary container tube or vial before adding DB6 into the assay wells MATERIALS REQUIRED BUT NOT SUPPLIED O Adjustable pipette or multiple channel pipette Multiple channel pipette reservoirs Aerosol resistant pipette tips Microplate reader capable of reading absorbance at 450 nm 1 5 ml microcentrifuge tubes Oo oO 00 o Incubator for 37 C incubation 110 Bi County Blvd Ste 122 Farmingdale NY 11735 Tel 1 877 374 4368 m Fax 1 718 484 3956 m E mail info epigentek com Web www epigentek com Epigentek Group Inc All rights reserved Products are for research use only Page 2 Printed 2014 10 13 P 3013 O Distilled water O Nuclear extracts O Parafilm M or aluminum foil GENERAL PRODUCT INFORMATION Quality Control Each lot of the EpiQuik DNMT3B Assay Kit is tested against predetermined specifications to ensure consistent product quality Epigentek guarantees the performance of al
4. in mammals DNMT1 DNMT2 and DNMT3 The DNMTS3 family comprises of three different proteins DNMT 3A DNMT3B and DNMT83L DNMT3A and DNMT3B have been demonstrated to methylate both unmethylated and hemimethylated DNA equally and is supposed to mediate de novo methylation together with DNMT1 Increased activation or amounts of DNMTS3 is believed to be involved in carcinogenesis and other genetic and epigenetic diseases Several methods such as Western blot are used for measuring levels of Dnmt3B However these methods available so far are inconvenient considerably time consuming labor intensive or have low throughput The EpiQuik Dnmt3B Assay Kit addresses these problems by using a unique procedure to measure the amount of Dnmt3B The kit has the following features e Very rapid procedure which can be finished within 3 5 hours e Innovative colorimetric assay to quantitatively measure the amount of DNMTS3B without the need for electrophoresis 110 Bi County Blvd Ste 122 Farmingdale NY 11735 Page 3 Tel 1 877 374 4368 m Fax 1 718 484 3956 m E mail info epigentek com Web www epigentek com Printed 2014 10 13 Epigentek Group Inc All rights reserved Products are for research use only P 3013 j b co s g see A e Strip microplate format makes the assay flexible manual or high throughput analysis e Simple reliable and consistent assay conditions PRINCIPLE amp PROCEDURE The EpiQuik DNMTS3B Assay Kit is design
5. 0 50 0 9 0 1 For Detailed Quantification 1 Generate a standard curve and plot OD value versus amount of DB3 Standard at each concentration point 2 Determine the slope as OD ng you can use Microsoft Excel statistical functions for slope calculation then calculate the amount of DNMTS3B using the following formulas Sample OD Blank OD DNMT3B ng mg protein 5 x 1000 Slope x Protein Amount ug Nuclear extract added into sample wells at Step 2d SUGGESTED BUFFER AND SOLUTION SETUP Table 1 Approximate amount of required buffers and solutions for defined assay wells based on the protocol 110 Bi County Blvd Ste 122 Farmingdale NY 11735 Page 7 Tel 1 877 374 4368 m Fax 1 718 484 3956 m E mail info epigentek com Web www epigentek com Printed 2014 10 13 Epigentek Group Inc All rights reserved Products are for research use only P 3013 Reagents 1 well 1 strip 2 strips 6 strips 12 strips 8 wells 16 wells 48 wells 96 wells Diluted DB1 2 5 ml 20 ml 40 ml 120 ml 240 ml DB2 100 ul 800 ul 1600 ul 4900 ul 9600 ul Blocking Buffer 0 15 ml 1 2 ml 2 5 ml 7 5 ml 14 5 ml DB3 Standard control N A N A 4 uL optional 8 ul 8 ul Diluted DB4 50 ul 400 ul 800 ul 2400 ul 4800 ul Diluted DB5 50 ul 400 ul 800 ul 2400 ul 4800 ul DB6 0 1 ml 0 8 ml 1 6 ml 4 8 ml 9 6 ml DB7 0 1 ml 0 8 ml 1 6 ml 4 8 ml 9 6 ml SUGGESTED STRIP WELL SETUP Tabl
6. 2 It is recommended to use 5 ug to 10 ug of nuclear extract per well Cover strip well microplate with Parafilm M or aluminum foil to avoid evaporation and incubate at 37 C for 90 to 120 min Remove the reaction solution from each well Add 150 ul of Blocking Buffer to each well then cover with Parafilm M or aluminum foil and incubate at 37 C for 30 min Remove the reaction solution from each well Wash each well three times with 150 ul of the Diluted DB1 1X Wash Buffer each time 3 Antibody Binding amp Signal Enhancing a Add 50 ul of the Diluted DB4 to each well then cover with Parafilm M or aluminum foil and incubate at room temperature for 60 min Remove the Diluted DB4 solution from each well Wash each well three times with 150 ul of the Diluted DB1 each time Add 50 ul of the Diluted DB5 to each well then cover with Parafilm M or aluminum foil and incubate at room temperature for 30 min Remove the Diluted DB5 solution from each well Wash each well four times with 150 ul of the Diluted DB1 each time Note Ensure any residual wash buffer in the wells is removed as much as possible at each wash step 4 Signal Detection a Add 100 ul of DB6 to each well and incubate at room temperature for 1 to 10 min away from light Begin monitoring color change in the sample wells and control wells The DB6 solution will turn blue in the presence of sufficient demethylated products Add 100 ul of DB7 to each well to stop e
7. ach assay can be between 1 ug and 20 ug with an optimal range of 5 to 10 ug Nuclear Extraction You can use your method of choice for preparing nuclear extracts from the treated and untreated samples Epigentek also offers a nuclear extraction kit Cat OP 0002 optimized for use with this kit Nuclear extracts should be stored at 80 C in aliquots until use 1 Working Buffer amp Solution Preparation a Prepare Diluted DB1 1X Wash Buffer 48 Assay Kit Add 13 ml of DB1 10X Wash Buffer to 117 ml of distilled water and adjust pH to 7 2 7 5 96 Assay Kit Add 26 ml of DB1 10X Wash Buffer to 234 ml of distilled water and adjust pH to 7 2 7 5 This Diluted DB1 1X Wash Buffer can now be stored at 4 C for up to six months b Prepare Diluted DB4 Capture Antibody Solution Dilute DB4 Capture Antibody with Diluted DB1 1X Wash Buffer at a ratio of 1 500 i e add 1 ul of DB4 to 500 ul of Diluted DB1 50 ul of Diluted DB4 will be required for each assay well c Prepare Diluted DB5 Detection Antibody Solution Dilute DB5 Detection Antibody with Diluted DB1 1X Wash Buffer at a ratio of 1 2000 i e add 1 ul of DB5 to 2000 ul of Diluted DB1 50 ul of Diluted DB5 will be required for each assay well d Prepare Diluted DNMT3B Standard Suggested Standard Curve Preparation Dilute DB3 DNMT3B Standard with DB2 to the concentrations of 1 2 5 10 and 20 ng ul according to the following dilution chart Resulting DB3 Tube DB3 20 ng l DB2 Conce
8. ay Ultra Kit Colorimetric P 3010 EpiQuik DNMT Activity Inhibition Assay Ultra Kit Fluorometric P 3011 EpiQuik DNMT1 Assay Kit P 3012 EpiQuik DNMTS3A Assay Kit 110 Bi County Blvd Ste 122 Farmingdale NY 11735 Page 10 Tel 1 877 374 4368 m Fax 1 718 484 3956 E mail info epigentek com Web www epigentek com Printed 2014 10 13 Epigentek Group Inc All rights reserved Products are for research use only P 3013
9. e 2 The suggested strip well plate setup for Dnmt1 quantification in a 48 assay format in a 96 assay format Strips 7 to 12 can be configured as Sample The controls and samples can be measured in duplicate Well Strip 1 Strip 2 Strip 3 Strip 4 Strip 5 Strip 6 A Blank Blank Sample Sample Sample Sample B DB3 2 ng DB3 2 ng Sample Sample Sample Sample c DB3 4ng DB3 4ng Sample Sample Sample Sample D DB3 10 ng DB3 10 ng Sample Sample Sample Sample E DB3 20 ng DB3 20 ng Sample Sample Sample Sample F DB3 40 ng DB3 40 ng Sample Sample Sample Sample G Sample Sample Sample Sample Sample Sample H Sample Sample Sample Sample Sample Sample TROUBLESHOOTING Problem Possible Cause Suggestion No signal or weak Reagents are added incorrectly Check if reagents are added in the proper signal in both the order with the right amount and if any positive control and steps in the protocol may have been sample wells omitted by mistake Incubation time and temperature Ensure the incubation time and are incorrect temperature described in the protocol are followed correctly Incorrect absorbance reading Check if appropriate absorbance wavelength 450 nm is used Kit was not stored or handled Ensure all components of the kit were properly stored at the appropriate temperature and the cap is tightly capped after each opening or use No signal or weak The standard amount is Ensure
10. ed for measuring total DNMT3B amount from tissues or cells In an assay with this kit the unique Dnmt affinity substrate is stably coated on the strip well The sample is added into the well and DNMTS3B contained in the sample binds to the substrate The bound DNMTS3B can be recognized with a specific DNMT3B antibody and colorimetrically quantified through an ELISA like reaction The amount of DNMT3B is proportional to the intensity of color development Prepare nuclear extract Incubate with capture reagent and assay buffer Add affinity antibody after washing wells l Add detection antibody after washing wells Add color developing solution for color develop ment then measure absorbance Schematic procedure of the EpiQuik DNMT3B Assay Kit PROTOCOL 0 6 05 ED nmti BOnntia DD nrt3b 0 4 0 3 0 2 0 1 1 5 10 20 Nuclear Extracts ug Nuclear extracts were prepared from MCF 7 cells using the EpiQuik Nuclear Extraction Kit and total amount of DNMT was measured For the best results please read the protocol in its entirety prior to starting your experiment Starting Materials 110 Bi County Blvd Ste 122 Farmingdale NY 11735 Tel 1 877 374 4368 m Fax 1 718 484 3956 m E mail info epigentek com Web www epigentek com Epigentek Group Inc All rights reserved Products are for research use only Page 4 Printed 2014 10 13 P 3013 Input Amount The amount of nuclear extracts for e
11. l products in the manner described in our product instructions Product Warranty If this product does not meet your expectations simply contact our technical support unit or your regional distributor We also encourage you to contact us if you have any suggestions about product performance or new applications and techniques Safety Suitable lab coat disposable gloves and proper eye protection are required when working with this product Product Updates Epigentek reserves the right to change or modify any product to enhance its performance and design The information in this User Guide is subject to change at any time without notice Thus only use the User Guide that was supplied with the kit when using that kit Usage Limitation The EpiQuik DNMT3B Assay Kit is for research use only and is not intended for diagnostic or therapeutic applications Intellectual Property The EpiQuik DNMT3B Assay Kit and methods of use contain proprietary technologies by Epigentek A BRIEF OVERVIEW Epigenetic inactivation of genes plays a critical role in many important human diseases especially in cancer A core mechanism for epigenetic inactivation of the genes is methylation of CpG islands in genome DNA Methylation of CpG islands involves the course in which DNA methyltransferases Dnmts transfer a methyl group from S adenosyl L methionine to the fifth carbon position of the cytosines At least three families of DNMTs have been so far identified
12. nsure a sufficient amount of nuclear extracts is used as indicated in Step 2 The sample can be titrated to determine the optimal amount to use in the assay Sample was not stored properly or has been stored for too long Ensure sample is stored in aliquots at 80 C with no more than 6 months for nuclear extracts Little or no DNMTS3B in the sample This problem may be a result of many factors If the affecting factors cannot be determined use new or re prepared nuclear extracts Uneven color development Insufficient washing of the wells Ensure the wells are washed according to the guidance of washing and residue washing buffer is removed as much as possible Delayed color development or delayed stopping of color development in the wells Ensure color development solution or stop solution is added sequentially and is consistent with the order you added the other reagents e g from well A to well G or from well 1 to well 12 RELATED PRODUCTS Nuclear Extract Preparation OP 0002 EpiQuik Nuclear Extraction Kit 110 Bi County Blvd Ste 122 Farmingdale NY 11735 Tel 1 877 374 4368 m Fax 1 718 484 3956 m E mail info epigentek com Web www epigentek com Epigentek Group Inc All rights reserved Products are for research use only Page 9 Printed 2014 10 13 P 3013 DNA Methyltransferase Activity Inhibition Assay P 3009 EpiQuik DNMT Activity Inhibition Ass
13. ntration 1 0 5 ul 9 5 ul 1 ng ul 2 0 5 ul 4 5 ul 2 ng ul 3 1 0 pl 3 0 ul 5 ng ul 4 2 0 ul 2 0 ul 10 ng l 5 4 0 ul 0 0 ul 20 ng ul Note Keep each of the diluted solutions except DB1 1X Wash Buffer on ice until use Any remaining diluted solutions other than Diluted DB1 should be discarded if not used within the same day 2 DNMT3B Binding a Predetermine the number of strip wells required for your experiment It is advised to run replicate samples include blank and positive controls to ensure that the signal generated is validated Carefully 110 Bi County Blvd Ste 122 Farmingdale NY 11735 Page 5 Tel 1 877 374 4368 m Fax 1 718 484 3956 m E mail info epigentek com Web www epigentek com Printed 2014 10 13 Epigentek Group Inc All rights reserved Products are for research use only P 3013 remove un needed strip wells from the plate frame and place them back in the bag seal the bag tightly and store at 4 C Blank Wells Add 100 ul of DB2 to each blank well Standard Wells Add 98 ul of DB2 and 2 ul of Diluted DNMT3B Standard to each standard well with a minimum of five wells each at a different concentration between 2 and 40 ng ul based on the dilution chart in Step 1e see Table 2 as an example Sample Wells Add 94 to 98 ul of DB2 and 2 to 6 ul of your nuclear extracts to each sample well Total volume should be 100 ul per well Note 1 Follow the suggested well setup diagrams
14. nzyme reaction when color in the positive control wells turns medium blue The color will change to yellow after adding DB7 and the absorbance should be read on a microplate reader within 2 to 10 min at 450 nm with an optional reference wavelength of 655 nm 110 Bi County Blvd Ste 122 Farmingdale NY 11735 Page 6 Tel 1 877 374 4368 m Fax 1 718 484 3956 m E mail info epigentek com Web www epigentek com Epigentek Group Inc All rights reserved Products are for research use only Printed 2014 10 13 P 3013 Note 1 Most microplate readers have the capability to carry out dual wavelength analysis and will automatically subtract reference wavelength absorbance from the test wavelength absorbance If your plate reader does not have this capability the plate can be read twice once at 450 nm and once at 655 nm Then manually subtract the 655 nm ODs from 450 nm ODs 2 If the strip well microplate frame does not fit in the microplate reader transfer the solution to a standard 96 well microplate 5 DNMT3B Calculation Calculate the average duplicate readings for the sample wells and blank wells Calculate DNMT3B change using the following formula Treated Tested Sample OD Blank OD pruts henge ee Se eh OP fone Untreated Control Sample OD Blank OD Example calculation Average OD450 of treated sample is 0 5 Average OD450 of untreated control is 0 9 Average OD450 of blank is 0 1 DNMT3B change en Ter X 10
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