Target Selector TM ctdna EGFR Kit Catalog number: 2193

Transcription

1 USER GUIDE Target Selector TM ctdna EGFR Kit Catalog number: 2193 USG Page 1 of 28

2 For Research Use Only. Not for use in diagnostic procedures. Copyright 2018 by Biocept, Inc. All rights reserved. This document or any portion thereof may not be reproduced in any form or transmitted outside of the recipient s organization in any form by any means electronic, mechanical, photocopy, recording, or used in any manner whatsoever without the express written permission of the company. USG Page 2 of 28

3 TABLE OF CONTENTS Manufacturer... 4 Product Description... 4 Assay Principle... 4 EGFR Kit Components and storage conditions... 5 User-supplied reagents and consumables... 6 Sample Collection, Handling and Storage... 6 Notes for the Assay... 6 EGFR Kit Protocol... 7 IMPORTANT!... 7 Preparing Standards... 7 Preparing Master Mix... 8 Plate set up for EGFR mutant assay... 9 Plate set up for EGFR WT assay... 9 Setup run on QuantStudio Target Selector assay Data Analysis Quantitative Analysis Specificity Analysis Target selector assay -Troubleshooting Technical Support/Questions Sanger sequencing protocol PCR Purification PCR Template Quantitation Cycle Sequencing BigDye Xterminator Purification Sequencing run on 3500Dx Review Sequencing Results Export Sequencing Results Sanger sequencing -Troubleshooting USG Page 3 of 28

4 MANUFACTURER The Target Selector TM ctdna EGFR Kit (the EGFR kit ) is manufactured by Biocept, Inc. at 5810 Nancy Ridge Dr., San Diego, CA PRODUCT DESCRIPTION The EGFR kit is a research use only ( RUO ) kit. It allows selective amplification and identification of most common epidermal growth factor (EGFR) mutations such as exon 19 deletions (Del19), L858R and T790M from either genomic DNA or circulating tumor DNA (ctdna). It also includes EGFR wild type (EGFR WT) assay. The EGFR kit combines Real time-pcr as well as melt curve analysis of the mutant PCR product and is followed by Sanger sequencing to verify the presence of the mutation. ASSAY PRINCIPLE The Target Selector assay is a Real-Time PCR based mutation enrichment assay and is based on selective blocking of wild-type amplification with a blocker than contains a sensor (switch) and an anchor portion. In contrast to blocked wild-type amplification, EGFR mutant templates are readily amplified in the presence of same blocker allowing for selective enrichment. A mismatch in the mutant template leads to a significant reduction in the melting temperature of the sensor (switch) portion of the blocker allowing the forward primer to extend with the mutant template. Under the same conditions, the forward primer is blocked, due to the stability of the sensor (switch) region since it is fully complementary with wild-type. When the temperature is raised above the melting temperature of the forward primer, as shown in the left panel of figure 1, the non-extended forward primer on the wild-type template falls off before the blocker comes off. However, with the mutant template the extended forward primer has a high enough melting temperature that it remains bound to the template when the blockers fall off, thus extending further and supporting amplification as shown in right panel of figure 1. Detection of the amplification product is done by unquenching the fluorophore (F) signal when the blocker is bound to the template. The location of the quencher (Q) is at the 5 end as show in figure 1 below. For wild-type EGFR amplification primers and a blocker for a region on EGFR exon 20 are used. Since any mutation of the DNA template in the region covered by the sensor portion of the blocker can potentially lead to amplification of this template, Sanger sequencing is necessary to confirm identity of the EGFR mutants Del19, L858R and T790M.The amplification products are therefore purified after the EGFR target selector assay and used for templates in Sanger sequencing reactions to confirm the presence of mutations. USG Page 4 of 28

5 Figure 1: Mechanism of the Foot-print version of the selector assay EGFR KIT COMPONENTS AND STORAGE CONDITIONS The EGFR kit contains enough reagents to perform 24 test (RUO) samples for each target assay. This includes 12 reactions for standards, 1 NTC and 24 test samples for a total of 37 reactions. Table 1: EGFR Kit components with recommended storage conditions Reagent Part no Volume total (µl) Storage ( C) Premix Del19 Selector Assay PN Premix L858R Selector Assay PN Premix T790M Selector Assay PN Premix EGFR WT Selector Assay PN Selector DNA Polymerase 1U/ µl PN Del19 Sequencing Primer PN L858R Sequencing Primer PN T790M Sequencing Primer PN Del19 Standard A PN L858R Standard A PN T790M Standard A PN EGFR WT Standard A PN DNA Suspension buffer PN USG Page 5 of 28

6 USER-SUPPLIED REAGENTS AND CONSUMABLES MicroAmp Optical 96-well Reaction plate with barcode, Catalog number Eppendorf twin.tec PCR plate 96 LoBind, Semi-Skirted, Catalog number MicroAmp Optical Adhesive Film Kit, Catalog number MicroAmp Clear Adhesive Film, Catalog number Eppendorf DNA Lo-bind tubes, PCR clean, Catalog number Qiagen MinElute PCR Purification Kit (50), Catalog number BigDye Terminator v1.1 Cycle Sequencing Kit, Catalog number BigDye Xterminator Purification Kit SAMPLE COLLECTION, HANDLING AND STORAGE The EGFR kit can be used with DNA extracted the following sample types. Extract and purify DNA samples according to your laboratory practices. Genomic DNA from Formalin-fixed paraffin-embedded tumor tissue samples (FFPE slides & blocks) or Fresh-frozen tissue samples. Circulating tumor DNA (ctdna) from plasma or serum. Cell lines DNA. It is optional to quantitate the gdna or cfdna by measuring the UV absorbance (A260/A280) or by fluorescence-based quantitation. NOTES FOR THE ASSAY This assay has been optimized using the QuantStudio5 (QS5) Real-Time PCR system. It is recommended to use Low ROX normalization for QuantStudio5. A single sequencing primer is provided for each of the assays. The Selector DNA Polymerase is a high-fidelity polymerase and is recommended for use with this assay. Each EGFR target selector assay is run on an individual 96 well plate. Effective range of DNA template input for this assay is up to 250ng. It is recommended to run the standard curve the first time for each Assay. For future experiments repeat standard curve dilution series or run a standard C as the calibrator for each corresponding assay. The sensitivity and specificity of each assay is > 99 % For more information on Sensitivity, Specificity and Limit of Detection on each target selector assay, please refer to the analytical validation report published in AACR Annual Meeting 2018, Validation of Highly sensitive TargetSelector ctdna assays for EGFR, BRAF and KRAS mutations. USG Page 6 of 28

7 EGFR KIT PROTOCOL IMPORTANT! The following procedures are optional but highly recommended prior to PCR setup Use a dedicated room/hood for selector assay reaction set up to avoid contamination from post PCR products. Use clean lab coat and be aware of possible contamination of samples and change gloves. Wipe the hood/bench and pipettes with 0.5% bleach and let sit for 15 min. Wipe the hood/bench and pipettes with 70% ethanol, wipe dry. Wipe the inside of micro centrifuge lid, micro centrifuge rotor and vortex with 0.5% bleach soaked kimwipe. Wipe the inside of mirco centrifuge lid, micro centrifuge rotor and vortex with 70% ethanol and let dry. Racks used for holding Eppendorf tubes should be soaked in 0.5% bleach for 15 min, washed with dih 20, sprayed with ethanol and patted dry onto paper towel. PREPARING STANDARDS 1. Remove selector assay standards (Std A) and thaw on ice. 2. Once thawed, vortex all standards ~3-5 seconds to mix thoroughly and briefly centrifuge for 5 seconds to collect all liquid to bottom of the tube. 3. The following controls are required for each setup: No Template control (NTC) and a four-point standard curve diluted from Std A. 4. Use Table 2 as a guide for preparing three additional standards in a sequential 8-fold serial dilution for each target selector assay (EGFR Del19, EGFR L858R, EGFR T790M, EGFR WT) using Std A provided with the kit. Table 2: Example of a 40 µl Serial Dilution of EGFR selector assay standards Standard Standard Input DNA suspension buffer Fold Dilution Std A undiluted Std B 5µl Std A 35 µl 1:8 Std C 5µl Std B 35 µl 1:8 Std D 5µl Std C 35 µl 1:8 Note: The starting copy number of Std A for each target selector assay is 5000 copies. The standards (Std A, Std B, Std C and Std D) are run in triplicates. USG Page 7 of 28

8 PREPARING MASTER MIX 1. Thaw each assay premix on ice, vortex and centrifuge briefly before pipetting. 2. Please refer to the online calculator for assay setup on our website at for reaction volumes. Alternatively, you could follow the instructions below for preparing master mix. 3. Use Table 3 as a reference to calculate reagent volumes of master mix for each EGFR mutant selector assay (Del19, T790M, L858R). Determine the number of samples including standards and test for each target selector assay to calculate the reagent volumes. 4. Make each EGFR mutant selector assay master mix into a labeled 1.5 ml microfuge tube, mix well and centrifuge briefly. Table 3: Calculations for Master Mix preparation of EGFR mutant assay (Del19, L858R and T790M) Component Volume per reaction (1X reaction*) Mutant Assay Premix 9.2 µl Selector DNA polymerase 1U/ µl 0.8 µl Total volume (excluding template) 10 µl *Multiply volumes in this table by the number of samples being tested (including controls) 5. Use Table 4 as a reference to calculate reagent volumes of EGFR WT selector assay master mix. Determine the number of research samples including standards and test for each assay to calculate the reagent volumes 6. Make EGFR WT assay Master mix into a labeled 1.5 ml microfuge tube, mix well and centrifuge briefly. Table 4: Calculations for Master Mix preparation of EGFR WT assay Component Volume per reaction (1X reaction*) EGFR WT Premix 16.2 µl Selector DNA polymerase 1U/ µl 0.8 µl Total volume (excluding template) 17 µl *Multiply volumes in this table by the number of samples being tested (including standards). Note: Calculate extra 10% of reagent volumes for the final master mix to allow for losses during pipetting. USG Page 8 of 28

9 PLATE SET UP FOR EGFR MUTANT ASSAY 1. Label an individual 96 well plate for each of the EGFR Target Selector Assays (Del19, L858R, T790M) with appropriate sample and target information. 2. Pipette 10 µl of master mix (Table 3) into each well required. 3. Add 10 µl of the prepared Standards into the respective wells labeled as Std A, Std B, Std C and Std D as shown in Table 5. The Standards are run in triplicates. 4. Add up to 10 µl of DNA template for the test samples (make DNA volume to 10 µl using DNA suspension buffer) into each well labeled as Test for a total volume of 20 µl per well. PLATE SET UP FOR EGFR WT ASSAY 5. Label a 96 well plate for the EGFR WT Assay. 6. Pipette 17 µl of master mix (Table 4) into each well required. 7. Add 3 µl of the prepared Standards into the respective wells labeled as Std A, Std B, Std C and Std D as shown in Table 5. The Standards are run in triplicates 8. Add up to 3 µl of DNA template (make DNA volume to 3 µl using DNA suspension buffer) for the EGFR WT assay plate into each well labeled as Test for a total volume of 20 µl per well Note: Briefly vortex and spin the DNA template tubes before adding on the plate. Use separate tips for each sample and avoid cross contamination of the samples by splashing. 9. For wells marked NTC, add appropriate volume of the DNA suspension buffer to make up final volume to 20 µl. 10. Below is an example of plate layout with the standards, test sample and NTC Table 5: Example Plate layout with standards and test samples A Std A Std A Std A Test 1 Test 9 Test 17 B Std B Std B Std B Test 2 Test 10 Test 18 C Std C Std C Std C Test 3 Test 11 Test 19 D Std D Std D Std D Test 4 Test 12 Test 20 E NTC Test 5 Test 13 Test 21 F Test 6 Test 14 Test 22 G Test 7 Test 15 Test 23 H Test 8 Test 16 Test 24 Empty wells 11. Seal the 96 well plate with optical adhesive film and vortex the plate briefly using an Eppendorf MixMate or any other plate mixer. 12. Spin the plate at 2000rpms for 2 minutes. Note: It is optional to run replicates of NTC and test samples. USG Page 9 of 28

10 SETUP RUN ON QUANTSTUDIO 5 The QuantStudio design and analysis software template documents (. edt files) for each Target selector assay provided with the kit are available on our website at The template files include all the below mentioned settings. Please use the following passwords to unlock the template files. i.egfr WT Assay EGFRWT, ii. EGFR Del 19 Assay Del19, iii. EGFR L858R Assay L858R, iv- EGFR T790M assay T790M 1. Launch the QuantStudio Design and Analysis Software v1.4 from the icon on the desktop 2. In the home screen, select Create New Experiment if using first time or Open Existing Experiment if using the provided (. edt) template. 3. Select Enter run experiment information from the menu and click ok. 4. The workflow bar used for navigation through experiment design and analysis. 5. Under the Properties tab, name your experiment with the assay, plate id, data and initials with an underscore between each and select other properties as below from drop-down lists. a. Instrument type - QuantStudio 5 system b. Block type - 96-well 0.2 ml Block c. Experiment Type - Standard Curve d. Chemistry - SYBR Green Reagents e. Run Mode - Standard 6. Under the Method tab, adjust the reaction volume to 20 µl and the cycling conditions are as follows for each selector assay. Table 6: Cycling conditions for Del19 and L858R Assay Del 19 L858R Stage 1 95 C 2 min 1.6 C/s 95 C 2 min 1.6 C/s Stage 2 98 C 10 secs 1.1 C/s 98 C 10 secs 1.1 C/s (45 cycles) 72 C 10 secs 1.1 C/s 76 C 10 secs 1.1 C/s (data collection) 45 C 13 secs 1.1 C/s 60 C 13 secs 1.1 C/s 60 C 1 min 1.1 C/s 62 C 1 min 1.1 C/s C 10 secs 1.1 C/s Stage 3 95 C 15 secs 1.6 C/s 95 C 15 secs 1.6 C/s (continuous data collection 40 C 15 secs 1.6 C/s 40 C 15 secs 1.6 C/s for dissociation step) 95 C 1 sec 0.15 C/s to 95 C 95 C 1 sec 0.15 C/s to 95 C Infinite hold 4 C 1.6 C/s 4 C 1.6 C/s Duration 2 hr 30 min 2 hr 17 min USG Page 10 of 28

11 Table 7: Cycling conditions for T790M and EGFR WT Assay T790M EGFR WT Stage 1 95 C 2 min 1.6 C/s 95 C 2 min 1.6 C/s Stage 2 98 C 10 secs 1.6 C/s 98 C 10 secs 1.6 C/s (45 cycles) 71 C 10 secs 1.6 C/s 71 C 10 secs 1.6 C/s (data collection) 50 C 13 secs 1.6 C/s 50 C 13 secs 1.6 C/s 66 C 1 min 1.6 C/s 66 C 1 min 1.6 C/s Stage 3 95 C 15 secs 1.6 C/s 95 C 15 secs 1.6 C/s (continuous data collection 40 C 15 secs 1.6 C/s 40 C 15 secs 1.6 C/s for dissociation step) 95 C 1 sec 0.15 C/s to 95 C 95 C 1 sec 0.15 C/s to 95 C Infinite hold 4 C 1.6 C/s 4 C 1.6 C/s Duration 2 hr 5 min 2 hr 5 min Note: WT and T790M have the same cycling conditions. 7. Under the Plate tab: Set up standards as follows a. Select Action -> Define and Set up Standards b. Select Singleplex from the Model drop-down list c. Define the standard curve, enter the parameters for the dilution series i. Number of dilution points: 4 ii. Number of replicates: 3 iii. Starting Quantity 5000 iv. Serial dilution factor 1:8 d. Under Select and arrange wells for the standard, select the option Let me select wells then drag the cursor to select the appropriate block of wells e. Select apply and close the window. The standards should now be populated in the wells selected and displayed on the plate map. f. Define and assign well attributes in the Quick setup pane of the Plate tab. i. Assign the sample name as Std A, Std B, Std C and Std D for the wells with task Standard ii. Drag the cursor to select appropriate sample well. Enter new sample and target names in the selected wells. iii. In the plate attributes, select the passive reference to ROX Note: When entering a new sample or target name in the Quick Set up pane, the software automatically populates default values for Reporter (FAM) and Quencher (NGQ-MGB) assigns the task (Unknown) which can be viewed in advanced Setup tab. USG Page 11 of 28

12 g. For No-template control, select the target from drop down menu, then under the Action tab select the task Negative Control. 8. Under the Export tab, confirm the file name is the same as the experiment name and that Auto Export and Results are selected. Also make sure the file is saved as a.txt file and set your export location 9. Open the QS5 instrument drawer and load your plate, ensuring A1 is oriented towards the top left corner. 10. Under the Run section click START RUN and select a specific QS5 instrument to start 11. When the run is done, click STOP RUN either on QS5 screen or in QS Analysis software in the computer. 12. Click Done after file is transferred on QS5 instrument. Retrieve plate and save at -20 C for downstream analysis. TARGET SELECTOR ASSAY DATA ANALYSIS 1. Launch the QuantStudio Design & Analysis software v1.4, click Open in open Existing information tab. Select the plate run (. eds or. edt file) from the saved folder. 2. Select Edit option and enter the password if there is a password set up. Note: If you used the provided. edt templates, please use the following passwords to unlock the run files. i.egfr WT Assay EGFRWT, ii. EGFR Del 19 Assay Del19, iii. EGFR L858R Assay L858R, iv- EGFR T790M assay T790M. QUANTITATIVE ANALYSIS 3. In the Results tab, by default the amplification plot is displayed for the selected wells. Note: If no data are displayed, click Analyze. 4. Click the to configure the plot. 5. Confirm or correct baseline and threshold values. Identify any outliers 6. It is optional to use below Table 5 to manually preset threshold ( Rn) for threshold cycle (Ct) determination or to use provided (. edt) templates. Table 8:Threshold values for Ct determination Target name Rn Del L858R 0.04 T790M 0.44 EGFR WT 0.36 USG Page 12 of 28

13 7. Identify and examine abnormal amplification, including a. Increased fluorescence (amplification) in negative control wells b. Absence of detectable fluorescence at an expected cycle Note: If you notice abnormal amplification or a complete absence of fluorescence, refer to the QS5 user guide for troubleshooting information. 8. In the Results tab, select Standard curve from the drop-down list. It displays the standard curve for samples designated as standards. 9. Confirm that the slope, R 2 -value, amplification efficiency and error meet the expected criteria. Note: Please refer to Chapter 3 in QuantStudio Design and Analysis desktop software user guide (Pub.no. MAN ) to evaluate the results in the Standard Curve Plot. 10. Visually check if all the test sample Ct values fall within the standard curve range. a. Example standard curve for each EGFR target is shown below (Figures 2-5). b. Linear regression results of the below standard curve plots are shown in table 9 below: Table 9:Linear Regression Results of 4-point standard curve Target name y. intercept slope Efficiency (%) R 2 EGFR WT EGFR L858R EGFR T790M EGFR Del Note: Calibrator method It is highly recommended to run a 4-point standard curve (master curve) the first time for each Assay or each lot of reagents. For future experiments, it is optional to repeat 4-point standard curve or run Std C in triplicates as a calibrator (QC measure) for each target assay plate. Verify if the median value of calibrator is within 3 standard deviation of mean value of Std C from the master curve. USG Page 13 of 28

14 Figure 2: Standard curve of EGFR Del19 Figure 3: Standard curve of EGFR L858R USG Page 14 of 28

15 Figure 4: Standard curve of EGFR T790M Figure 5: Standard curve of EGFR WT USG Page 15 of 28

16 SPECIFICITY ANALYSIS 11. In the Results tab, select the Melt Curve plot from the drop-down list. The Melt curve plot is displayed for the selected wells of the selected stage. 12. Click Analysis -> Analysis settings and select the Melt curve settings tab. 13. Check the box for Enable Multi-peak calling. It is optional to set either the dominant peak percent or a peak calling threshold as below. a. EGFR WT: Peak level relative to dominant peak = 10.0 b. Del 19: Peak level relative to dominant peak = 10.0 c. L858R: Peak calling threshold = d. T790M: Peak calling threshold = Multiple peak melting temperature for the targets are as below a. L858R = 68.0 C < t < 70.0 C b. T790M = 68.4 C < t < 69.7 C or 72.8 C < t < 73.9 C Note: The above cut off values are only general guidelines based on our internal validation of the assay. These values should be verified and adjusted according to your results. Results may vary according to your sample type. 15. Examples of melt profiles of the four-point standards for each target assay are shown below. Notes: T790M and WT target assay show 2 melting peaks indicating the melting temperature of the sensor and anchor region of the blocker. No specific melting temperature profile for Del19 target assay. The specific L858R product peak is observed between 68.0 C and 70.0 C. The smaller peaks observed in L858R target assay melt profile is from low concentration samples which is an artifact of the target selector technology. There is a synonymous mutation at L858 position (CTG to TTG). Sanger sequencing is required to identify this mutation from L858R. Click File -> save to save the analysis. 16. Navigate to the Export tab of the QS5 software. Set the export location to the desired folder. Under File Type select.txt then click the Export button. USG Page 16 of 28

17 Figure 6: Melt curve plot of EGFR Del19 standards Figure 7: Melt curve plot of EGFR L858R standards USG Page 17 of 28

18 Figure 8: Melt curve plot of EGFR T790M standards Figure 9: Melt curve plot of EGFR WT Standards USG Page 18 of 28

19 TARGET SELECTOR ASSAY -TROUBLESHOOTING Issue Cause Possible resolution Amplification in No Template Control (NTC) wells Random contamination of wells by template when loading PCR plate Follow the procedures recommended prior to PCR set up in protocol Reagent contamination with No PCR product is evident either on the qpcr graph or on a gel PCR product is evident on a gel, but not in the qpcr graph Increased fluorescence (early Ct values) in one of the wells Technical replicates are not overlapping and have a difference in Ct values > 1 cycles template The protocol was not followed correctly DNA contained PCR inhibitors or was otherwise degraded qpcr instrument settings were incorrect There was an issue with your specific qpcr instrument Possible background signal from uneven distribution of ROX dye Pipetting error, insufficient mixing of solutions or low expression of target resulting in stochastic amplification Verify that all steps have been followed and the correct reagents, dilutions, volumes and cycling parameters have been used Re-purify the DNA sample or repeat the DNA extraction Confirm that you are using the correct instrument settings and refer to your instrument manual to tips and troubleshooting Mix the reagents thoroughly, Repeat the assay for the well with early Ct values Calibrate pipettes, use positivedisplacement pipettes, mix all solutions thoroughly during preparation and during use. TECHNICAL SUPPORT/QUESTIONS For any questions regarding the kit, please contact us at or CustomerService@biocept.com USG Page 19 of 28

20 SANGER SEQUENCING PROTOCOL This section of the protocol describes the steps necessary to sequence the target selector assay products. The first step is to purify the PCR products following which the purified PCR product is used in a Sanger cycle sequencing reaction with a sequencing primer for each target provided with the assay. After the Sanger cycle sequencing reaction, the product is purified using BigDye Xterminator purification kit and loaded for sequence analysis on the ThermoFisher 3500Dx Genetic Analyzer. PCR PURIFICATION MinElute PCR purification kit from Qiagen is the recommended kit for PCR purification. It is the user s option to use the Qiagen kit or any other preferred column-based purification method. Please refer to MinElute handbook from Qiagen for detailed purification instructions. 1. Spin PCR reaction plate down at 2000 rpm for 2 minutes, carefully remove adhesive seal. 2. From each test reaction well, pipette 18 µl of PCR product into 1.5 ml Eppendorf tubes. Note: If the sample volume is less than 18 µl, then make up the final volume to 18 µl using DNA suspension buffer. 3. Add 90 µl Buffer PB into the tube and mix well. 4. Optional If the ph indicator I has been added to buffer PB, check that color of the mixture is yellow, else add 10 µl 3M sodium acetate, ph 5.0 into the tube and mix well. The color of the mixture will turn yellow. 5. Load the sample mixture to a MinElute column and close the cap. 6. Centrifuge the column at 18,000 x g for 1 minute. 7. Discard flow-through and place the column back to the same collection tube. 8. Add 750 µl Buffer PE to the column and centrifuge at 18,000 x g for 1 minute. 9. Discard flow-through and place the column to a new 2 ml collection tube. 10. Centrifuge the column at 18,000 x g for 1 minute and discard the tubes containing flow-through. Note: This step removes any residual ethanol which can interfere with downstream applications. 11. Place the column to a new 1.5 ml Eppendorf tube. 12. Add 10 µl Buffer EB to the center of the membrane. 13. Let the column stand for 1 minute at room temperature. 14. Centrifuge the column at 1,000 x g for 1 minute. Discard the MinElute column. 15. Check the concentration of the eluted DNA. USG Page 20 of 28

21 PCR TEMPLATE QUANTITATION The purified product is quantified by using Nanodrop Check the instrument manual for instructions on how to quantify the DNA. CYCLE SEQUENCING 1. Thaw out BigDye Terminator mix v1.1 from the BigDye Terminator v1.1 Cycle Sequencing Kit, sequencing primers from assay and purified PCR templates for each target selector assay. Vortex the reagents and samples briefly. Spin down the tubes. 2. Make 30ng/ µl dilutions of purified PCR templates for each target selector assay. 3. Use Table 10 as a guide to prepare master mix for each target selector assay. Notes: Table 10: Sequencing reaction Master mix Master mix Volume per reaction 1X Big Dye Terminator mix v1.1 Ready 4 µl Reaction Mix Sequencing buffer 4 µl Nuclease-free H20 7 µl Total reaction volume 15 µl Multiply volumes in this table by the number of samples being tested plus the pgem control. Calculate extra 10% of reagent volumes for the final master mix to allow for losses during pipetting. 4. Use a Microamp 96-well plate (same plate to be loaded in 3500Dx) and prepare the sequencing reaction for each target selector assay samples as shown in table 11, starting with column 1 (A1 to H1), then continue to column 2 (A2 to H2) and so on respectively. Notes: Table 11: Cycle Sequencing Mix Components Volume per well Nuclease-free H20 3 µl PCR template (30ng/ µl) 1 µl Sequencing primer (3.2 µm) 1 µl Master mix (from table 3) 15 µl Total volume 20 µl If the concentration of PCR template from target selector assay is different that 30ng/ µl, make the final amount to 30ng and adjust the amount of H20 accordingly, so that final combined volume of PCR template and H20 are 4 µl. Add 20 µl water to the empty wells of a column containing samples. USG Page 21 of 28

22 5. In the same 96 well plate, prepare the sequencing reaction for pgem control as shown in table 12. Table 12: pgem Control Reaction Mix Components Volume per well pgem 3Zf (+) dsdna control 1 µl M13(-21) control primer 4 µl Master mix (from table 3) 15 µl Total volume 20 µl 6. Seal the 96 well plate with optical adhesive film and spin the plate at 2000rpms for 2 minutes. 7. Place the plate on Veriti thermocycler, place a microamp optical film compression pad on top and close lid. Start the run with cycling conditions as shown below: Stage 1 96 C 1 min Stage 2 96 C 10 secs (25 cycles) 50 C 5 secs 60 C 4 min Infinite hold 4 C 8. After the run finishes, take out the plate and spin down at 2000rpms for 2 minutes. BIGDYE XTERMINATOR PURIFICATION This step is done to clean-up the sequencing reaction products of salts, unincorporated dye terminators and dntp s which can interfere with base calling. 1. Take out the SAM solution provided with the BigDye Xterminator Purification kit from the refrigerator and equilibrate to room temperature. 2. Use Table 13 as a guide to determine the amount of SAM solution and Big Dye Xterminator beads to make the premix. 3. Briefly vortex the SAM solution and pipette the volume calculated in to a clean 5 ml Eppendorf tube. Vortex the bottle of Big Dye Xterminator beads for 20 seconds to mix well. Pipette the calculated volume of Xterminator solution using a wide-bore filter tip to mix with the SAM solution in 5mL tube. Table 13: SAM/BigDye Xterminator Premix Component Volume per reaction (1X) SAM Solution 85 µl Xterminator Solution 25 µl Total volume 110 µl Notes: Multiply volumes in this table by the number of reactions required. Calculate extra 10% of reagent volumes for the final working solution to allow for losses during pipetting. USG Page 22 of 28

23 4. Carefully remove the optical adhesive film from the sequencing plate. 5. Vortex the premix from table 11 for 20 seconds at high speed. Pipette 110 µl of Xterminator premix to each reaction well and mix gently up and down several times. Note: Fill empty wells in last column with 110 µl of nuclease-free H 20. IMPORTANT! The premix needs to be vortexed before adding to each well for optimal performance. 6. Seal the plate using optical adhesive film. Carefully seal each well to prevent crosscontamination. Invert the plate a few times, then vortex on Eppendorf MixMate at 2500 rpm for 40 minutes. 7. Centrifuge the plate at 2000 x g for 5 minutes. Remove the plate seal and place a septum for loading on 3500X. Note: Purification with Centri-Sep plates or purification with ethanol/edta precipitation are other alternate methods to purification by BigDye Xterminator. Please refer to BigDye Terminator v3.1 Cycle Sequencing kit user guide for more information on alternate methods of purification. SEQUENCING RUN ON 3500DX This user guide assumes that 3500 Dx instrument has been set up and 3500 Dx series software has been installed. For any questions on instrument and software set up please refer to Applied Biosystems 3500 Genetic Analyzer user guide or contact their technical support. 1. If the instrument is not already on, click the power ON/OFF button on the front of the instrument and wait for the green status light to turn on. 2. Click the TRAY button on the outside of the instrument to bring the autosampler to forward position. Wait until the autosampler stops at the forward position. 3. Check the instrument status, ensure the green light is on and not flashing before proceeding. 4. Click on the 3500 Dx software icon on desktop, enter user name and password in the 3500 Log in dialog box. Click Ok. In the Mode selection dialog box, click Research Use Only (RUO) Mode. This launches the 3500-series data collection software 2011 v1.0. USG Page 23 of 28

24 5. In Dashboard, check consumable status to ensure that consumables are not expired, and adequate buffer levels are at the fill lines. Note: For detailed instructions on maintenance tasks, consumable status please refer to chapter 2 in Applied Biosystems 3500 Genetic Analyzer user guide. 6. In the Dashboard, set the oven temperature to 60 C and click Start Pre-Heat. Pre-heat the oven for at least 30minutes before starting a run if the instrument is cold. 7. In the Dashboard, click Create New Plate, and in the Define plate properties screen, enter the plate name and select the number of wells, plate type, capillary length and polymer as shown below: 8. Click on the Assign Plate Contents, at the bottom of this page and proceed to the next screen. 9. A 96 well plate layout will pop up, enter the sample name for each reaction well on 96 well plate map. 10. At the bottom right of the assign plate contents screen, expand customize sample info pane. 11. Select the wells with sample names and assign Assays, File Name Conventions and Results Groups. 12. Enable the checkbox next to selected assay name, file name conventions and results group to assign it to selected wells. USG Page 24 of 28

25 13. Select Save Plate and select Save as to assign a plate name. 14. Prepare plate assembly as follows. Align the holes in the septa strip with the wells of the plate, then firmly press downward onto the plate. Place the sample plate into the plate base. Snap the plate retainer (cover) onto the plate, septa and plate base as shown in figure 10. Figure 10: Plate Assembly for sequencer 15. Verify that the holes of the plate retainer and the septa strip are aligned. If holes are not aligned, re-assemble and then assemble the plate assembly. 16. Load the assembled plate unit in the instrument: Place the plate unit in the autosampler with labels facing you (or instrument door) and the notched corner of the plate in the notched corner of the autosampler. 17. Close the instrument door to re-initialize the instrument. 18. In the Assign Plates for Run screen, click Link Plate for Run. A message will pop up Plate loaded successfully. Click ok. 19. In Load plates for Run screen, review the consumables information, the calibration information and ensure the status is acceptable for a run. 20. Enter a run name (MMDDYY_SequencingPrimer_Initial_specific info). 21. Access the Preview run screen from the navigation pane by selecting Preview Run. 22. The preview run screen contains an injection list and a plate view. The injection list is linked to the plate view. Click an injection to select the associated wells in the plate view. 23. To modify the injection list at any time before a run, select an injection, then click Move up, Move down and delete as needed. 24. Click Start Run. The Monitor run screen is now automatically displayed. Note: It takes, approximately, 10 seconds for the instrument to initialize after the instrument door is closed. Do not start a run until the instrument status light is green. 25. The current injection is highlighted in green in the plate view, the injection list is linked to the plate view. 26. When an injection is complete, it is flagged with in the injection and analysis columns. USG Page 25 of 28

26 REVIEW SEQUENCING RESULTS 1. Open Sequencing Analysis Software 6 and enter Username and Password. 2. Under File, select Add Samples and open the folder containing the sequencing results. Select all samples of interest, then click Add Selected Samples and Click OK. 3. Click green arrow to analyze the sequencing data. 4. Enable check box under show to display sequence. 5. Adjust sequence display using the toggle buttons 6. A snipping tool can be used to crop the mutation sequence region of interest. Then click the save icon to save the image. 7. Review sequence quality such as Metric Analysis results Sample basecalling and trimming results. Note: For detailed data review information and to understand the Quality Values please refer to chapter 4 in Applied Biosystems 3600/2500xL Genetic Analyzer User Guide. 8. Reference traces for each EGFR Target selector Assay is shown below in figure 10, 11 and 12. USG Page 26 of 28

27 EXPORT SEQUENCING RESULTS 1. Filter the table of interest. 2. Select an export option: Results, Reports or Traces. 3. Select the export options and location for the export file, click OK. Figure 11: Del19 Sequencing Region (Del ) Figure 12: T790M Sequencing Region USG Page 27 of 28

28 Figure 13: L858R Sequencing Region (CAG: A>C or AG>CT or CA>AC) Note: There is also a synonymous mutation that is sometimes observed at L858 position (CTG to TTG). SANGER SEQUENCING -TROUBLESHOOTING For troubleshooting information on both instrument and sequencing run, please refer to Appendix E in Applied Biosystems 3600/2500xL Genetic Analyzer User Guide. USG Page 28 of 28