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Cleaver Scientific omniDOC Instruction Manual

Gel documentation system
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OmniDOC Gel Documentation System
Instruction Manual
Catalog No.
OMNIDOCi (PC Version)

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Summary of Contents for Cleaver Scientific omniDOC

  • Page 1 OmniDOC Gel Documentation System Instruction Manual Catalog No. OMNIDOCi (PC Version)

  • Page 2: Packing List

    White Light Table Module -1 x White light table -2 x M7 nuts Cleaver Scientific is liable for all missing or damaged parts / accessories within 7 days after customer received this instrument package. Please contact Cleaver Scientific immediately regarding this issue.

  • Page 3: Table Of Contents

    3.1 Installing Blue Light Module (Optional) ............13 3.2 Installing White Light Table Module (Optional) .......... 17 3.3 Installing USB wireless adapter ..............21 3.4 Installing the OmniDOC Gel Documentation System Software ....21 Section 4 Operation Instructions ..............26 4.1 Capture/Analysis Control Interface ............26 4.1.1 Capture Screen Interface ...............
  • Page 4 4.3 Image Analysis: Using “Gel Positive/Gel Negative” to analyze the sample 42 4.3.1 Load the image ................42 4.3.2 Processing the Image File .............. 43 4.3.3 Selecting the Image Lane ............... 53 4.3.4 Lane Analysis ................. 54 4.3.5 Image Summarization ..............60 4.4 Image Analysis: Using “Dot blot positive/ Dot blot negative”...

  • Page 5: Warning

    -- Consult the dealer or an experienced radio/TV technician for help. Notice: (1) Changes or modifications not expressly approved by the party responsible for could void the use is authority to operate the equipment. Cleaver Scientific OmniDOC Gel Documentation System has been tested...
  • Page 6 CE regulation. Also, OmniDOC Gel Documentation System is RoHS compliant to deliver confident product which meets the environmental directive. These limits are designed to provide reasonable protection against harmful interference when the instrument is operated in a commercial environment.
  • Page 7 Avoiding Electrical Shock Follow the guidelines below to ensure safe operation of the unit. OmniDOC Pro Gel Documentation System has been designed to use with shielded wires thus minimizing any potential shock hazard to the user. Cleaver Scientific recommends against the use of unshielded wires.
  • Page 8 1. Do not attempt to operate the device if damage is suspected. 2. Protect this unit from physical damage, corrosive agents and extreme temperatures (direct sunlight, etc.). 3. For proper ventilation and safety concerns, keep at least 10 cm of space behind the instrument, and at least 5 cm of space on each side.
  • Page 9 The symbols used on OmniDOC Gel Documentation System are explained below. Indicates an area where a potential shock hazard may exist. Consult the manual to avoid possible personal injury or instrument damage. Indicate a warning of UV radiation. While using the UV Transilluminator, be sure the operating personnel is properly protected.
  • Page 10 Potential Risk Preventive measures Do not put the machine near the table edge. Bruise Move the machine by cart. Do not put your hands on the open door. Pinch Prevent hard impact on the acrylic panel. Slash Do not open the darkroom door while you turn on UV radiation the UV light.

  • Page 11: Introduction

    Section 1 Section 1 Introduction 1.1 Overview OmniDOC Pro Gel Documentation System is the next generation of gel documentation instrument. It is specifically designed for ease of use for any lab experiment with gel imaging. OmniDOC Pro Gel Documentation System is packed with 5.0 megapixels high sensitivity and resolution scientific grade...

  • Page 12: Components Guide

    Section 1 1.3 Components guide USB wireless adapter Scientific grade camera and lens Front View Viewing window Darkroom door with UV safety switch 3.5” TFT display A-type USB port (For service use only) Internet port (For service use only) Main power Power socket &...

  • Page 13: Technical Specification

    Section 2 Section 2 Technical Specification CMOS scientific grade camera Camera Type CMOS scientific grade camera Sensor 5.0M Pixels Monochrome sensor Max. CMOS Resolution 2592 x 1944 pixels Pixel Density RAW 8 bit/10bit/12bit Power DC5V / 250mA Lens Focal Length Aperture F1.2 –...

  • Page 14: Installation Instructions

    3.1 Installing Blue Light Module (Optional) Section 3 Installation Instructions OmniDOC Pro Gel Documentation System comes with epi white light and trans-UV as standard. Optional blue light module or white light table is offered for expansion to offer higher flexibility. There are few procedures to install the optional devices: place the unit on a sturdy, level safe and dry place, then follow the instruction below for installation.
  • Page 15 Section 3 3.1 Installing Blue Light Module (Optional) Step2 Open the darkroom door and hold the left blue light on left inner wall. Step3 Connect the blue light quick connector with darkroom inner socket.
  • Page 16 Section 3 3.1 Installing Blue Light Module (Optional) Step4 Insert the blue light into the inner lining of darkroom. Step5 Put the other side of blue light into the stud of darkroom inner wall.
  • Page 17 Section 3 3.1 Installing Blue Light Module (Optional) Step6 Take a nut from parts kit. Use 7M/M socket wrench to tighten the nut on the stud. Step7 The blue light is fixed as shown below. Please repeat steps 2~6 for right side blue light to install it in the darkroom.

  • Page 18: Installing White Light Table Module (Optional)

    Section 3 3.2 Installing White Light Table Module (Optional) 3.2 Installing White Light Table Module (Optional) Step1 Get the white light table module ready. There are one white light table and 2 pieces of M7 nuts in the package. Before assembling, please check to make sure the screw studs on both sides of the white light table are in the upright position.
  • Page 19 Section 3 3.2 Installing White Light Table Module (Optional) Step3 Connect the white light table quick connector with darkroom inner socket Step4 Make sure the stud holders on the white light table align with the studs of darkroom.
  • Page 20 Section 3 3.2 Installing White Light Table Module (Optional) Step5 To take nuts from parts kit. Use 7M/M socket wrench to tighten nuts on the studs. Right Left Step6 The white light table is fixed as shown below. Left Right...
  • Page 21 Section 3 3.2 Installing White Light Table Module (Optional) Step7 All accessories are installed as shown below. Note: If necessary, please manually adjust the aperture to have the best performance while working with White Light Table. Aperture ring F1.2 - Close For more details, please refer to the operation instructions on 4.2.6.

  • Page 22: Installing Usb Wireless Adapter

    Section 3 3.4 Installing the OmniDOC Gel Documentation System Software 3.3 Installing USB wireless adapter Install USB wireless adapter into OmniDOC Gel Documentation System 3.4 Installing the OmniDOC Gel Documentation System Software *To install the program, please log in as an administrator on the computer.
  • Page 23 1. Turn on the OmniDOC Gel Documentation System 2. Search for Wi-Fi network “UVCI-1200-********” from your computer, select and key in as following information: SSID: uvci-1200-******** Password: Put OmniDOC Gel Documentation System Software CD into your Step2 computer and select omniDOC setup program. SSID...
  • Page 24 Section 3 3.4 Installing the OmniDOC Gel Documentation System Software Step3 Install OmniDOC setup program. Step4 Check the license agreement then press the “Next” button.
  • Page 25 Section 3 3.4 Installing the OmniDOC Gel Documentation System Software Step5 Save the program in destination folder. Step6 Click install to begin the installation.
  • Page 26 Section 3 3.4 Installing the OmniDOC Gel Documentation System Software Step7 Complete the installation program. Step8 The short paths will be shown on desktop. Double click on OmniDOC Gel Documentation System icon to open the software. Note: Please restart the computer when you finish installing the software.

  • Page 27: Operation Instructions

    4.1 Capture/Analysis Control Interface 4.1.1 Capture Screen Interface 2~ 17 Function 18 ~ 21 Time Set Display screen: This area shows the real-time or captured image. Function: Connect UVCI: Through the Wi-Fi to connect OmniDOC System with the PC / laptop/ iPad.
  • Page 28 Section 4 4.1 Capture/Analysis Control Interface Capture: This button allows you to acquire the current image and save it Print: Print out the image using the printer. Negative: To reverse the image between black and white (not applicable to colored images). Freeze Image: This button freezes your image.
  • Page 29 Section 4 4.1 Capture/Analysis Control Interface UV: ON/OFF switch for the UV transilluminator UV Intensity: Change the UV light intensity between 70% and 100% illumination. Time Set: Reduce: Decrease the exposure time of scientific grade camera. Exposure Time: Manually input the exposure time (range: 0.01- 30 sec) to adjust.

  • Page 30: Analysis: Image Process Interface

    Section 4 4.1 Capture/Analysis Control Interface 4.1.2 Analysis: Image Process Interface In the capture screen interface, press Analysis to enter the gel analysis interface. 2~13 a. Open the data file. b. Save the file. c. Exit the program. Step: Next Step: Go to next step to select analysis mode: gel positive/ gel negative/ dot positive/ dot negative.
  • Page 31 Section 4 4.1 Capture/Analysis Control Interface Flip: Flip the image according to the orientation you desired. Brightness: Adjust the brightness of the image. Contrast: Adjust the contrast level of image. Negative: To reverse the image between black and white (not applicable to colored images).

  • Page 32: Analysis: Image Editor Interface

    Section 4 4.1 Capture/Analysis Control Interface 4.1.3 Analysis: Image Editor Interface Step: Previous Step: Return to previous step, current setting will be deleted. Next Step: Go to next step. Editor: Add Lane: Add the lane to analysis. Delete Lane: To cancel the lane. Note: Be sure to add all lanes you wish to analyze before you proceed to the next step...

  • Page 33: Analysis: Image Analyze Interface

    Section 4 4.1 Capture/Analysis Control Interface 4.1.4 Analysis: Image Analyze Interface 1~ 9 Step: Previous Step: Return to previous step, current setting will be deleted. Next Step: Go to next step. Home: Return to Image Process Interface. Analyze: Auto Find: Find the peaks automatically. Add Peak: Add the peak manually.
  • Page 34 Section 4 4.1 Capture/Analysis Control Interface Delete Peak: Delete the peak manually. Base Line: Set the base line manually for selecting peaks. Previous Lane: Go back to last lane. Next Lane: Go to next lane.

  • Page 35: Analysis: Image Summary Interface

    Section 4 4.1 Capture/Analysis Control Interface 4.1.5 Analysis: Image summary Interface 1~ 2 Step: Previous Step: Return to previous step, current setting will be deleted. Home: Return to Image Process Interface.

  • Page 36: Start The Operation

    Place the gel onto the center of the UV Transilluminator. 4.2.2 Select the appropriate filter Make sure you use the appropriate filter, the default type is optical EtBr filter. For different applications, please contact Cleaver Scientific or your regional distributor for suitable filters.

  • Page 37: Turn On The Power And Connect The System With Pc

    4.2 Start the Operation 4.2.3 Turn on the power and connect the system with Connect your computer to the OmniDOC Gel Documentation System network via Wi-Fi, please refer to section 3.4 Installing the OmniDOC Gel Documentation System Software for detail instruction...

  • Page 38: Adjust The Setting For Best Imaging

    Section 4 4.2 Start the Operation License Key Note: The license key must match the camera serial number 4.2.4 Adjust the setting for best imaging For adjusting exposure time, refer to section 4.1.1: Time set. For other screen interface description, refer to section 4.1.1: Function.

  • Page 39: Adjust The Lens Iris

    Section 4 4.2 Start the Operation With environmental safe dye (such as Novel Juice and Midori Green Direct), you may use optional blue light module for less invasion to your DNA sample Protein samples imaging (Protein gels such as Coomassie blue or silver stain;...

  • Page 40: Default Setting

    Section 4 4.2 Start the Operation 4.2.7 Default setting The system allows the user to change the default settings by pressing the button (as box1). After setting up the parameters, "Start up settings" (as box 2) will come into effect once you restart the system and act as default permanently until you change it next time.

  • Page 41: Freeze Image

    Section 4 4.2 Start the Operation Advanced features: The display will show the Saturation The display will show the date stamp if you warning if you enable the “saturation enable the “Date stamp” from Advanced detection” from Advanced features. features. The image will adjust to saturation detect level you set.

  • Page 42: Acquire And Save The Image

    Section 4 4.2 Start the Operation 4.2.9 Acquire and save the image To capture the image, click on the “Capture” button then a dialog will pop up to save the image. Select the image file format you desire and choose the data location and give a file name. Image format: bmp / jpeg / png / tiff Note: Default format of saved images can be changed according to your preference in the "Default setting".

  • Page 43: Load The Image

    Section 4 4.3 Image Analysis: Using “Gel Positive/Gel Negative” to analyze the sample 4.3 Image Analysis: Using “Gel Positive/Gel Negative” to analyze the sample 4.3.1 Load the image To start the image analysis, first you will have to choose your image from the data file.

  • Page 44: Processing The Image File

    Section 4 4.3 Image Analysis: Using “Gel Positive/Gel Negative” to analyze the sample Step2 The image will be shown on the center of a new window. 4.3.2 Processing the Image File You will be directed to the image processing tool box as shown below. Step1 Crop: Crop the image by press the “Crop”...
  • Page 45 Section 4 4.3 Image Analysis: Using “Gel Positive/Gel Negative” to analyze the sample Step1-1 The image will be shown below as you selected. * Remember: Always rotate the image before you crop!”...
  • Page 46 Section 4 4.3 Image Analysis: Using “Gel Positive/Gel Negative” to analyze the sample Step2 Rotate: To rotate the image, first select the “Rotate” button (as box 1) then the toolbar (as box 2) will pop up. Toolbar: : Rotate counter-clock wise : Rotate clock wise : Confirm action : Cancel...
  • Page 47 Section 4 4.3 Image Analysis: Using “Gel Positive/Gel Negative” to analyze the sample Step2-1 You may rotate the image counter-clock wise or clock wise in two ways: a. Using the toolbar labelled as box 1, press "!" to confirm action. b.
  • Page 48 Section 4 4.3 Image Analysis: Using “Gel Positive/Gel Negative” to analyze the sample : Invert the image from left to right. : Confirm action : Cancel Step4 Brightness: Adjusting the brightness of the image by pressing on the “Brightness” button (as box 1), then use the scrollbar (as box 2) to adjust the brightness level.
  • Page 49 Section 4 4.3 Image Analysis: Using “Gel Positive/Gel Negative” to analyze the sample Step4-1 The result of Brightness is shown below. Press “!” to proceed or press “ ” to cancel. : Confirm action : Cancel Step5 Contrast: Adjusting the contrast level of the image by pressing the “Contrast”...
  • Page 50 Section 4 4.3 Image Analysis: Using “Gel Positive/Gel Negative” to analyze the sample “ ” to cancel. : Confirm action : Cancel Step6 Negative: To reverse the image between black and white by pressing on the “Negative” button (as box 1). If you don’t want to negative the image, you can press the “Negative”...
  • Page 51 Section 4 4.3 Image Analysis: Using “Gel Positive/Gel Negative” to analyze the sample the image, press the ”+” button (as box 2). If you want to zoom out the image, press the “-“ button (as box 2). Press “EXIT” to finish. This feature simply lets you zoom in and zoom out of the image but will not make any changes to the image file.
  • Page 52 Section 4 4.3 Image Analysis: Using “Gel Positive/Gel Negative” to analyze the sample : Change the font type : Change the font size. : Move the text to the desired location by moving the mouse cursor to the desired location on the image and click the left button of the mouse.
  • Page 53 Section 4 4.3 Image Analysis: Using “Gel Positive/Gel Negative” to analyze the sample Step9 Original: This is the master undo button. It will undo ALL the changes you made to the image and revert it back to the original image. A massage will pop up to ask for confirmation once you press the “Original”...

  • Page 54: Selecting The Image Lane

    Section 4 4.3 Image Analysis: Using “Gel Positive/Gel Negative” to analyze the sample 4.3.3 Selecting the Image Lane Step1 Add Lane: Selecting your lane by creating a long rectangular box along the lane. Press “Add Lane” button (as box 1) and then hold and drag the rectangular box to the area you want.

  • Page 55: Lane Analysis

    Section 4 4.3 Image Analysis: Using “Gel Positive/Gel Negative” to analyze the sample Step2 Delete Lane: Press “Del Lane” button (as box 1), and then click the center of rectangular box you want to delete. After selecting all lanes, click “Next Step” button (as box 2) to move forward. Note: Make sure your bands are straight and enclosed inside the rectangular box.
  • Page 56 Section 4 4.3 Image Analysis: Using “Gel Positive/Gel Negative” to analyze the sample Step1 Auto Find: Click on the “Auto Find” button (as box 1), the software will allow you to adjust the sensitivity level according to your needs. Sensitivity level (as box 2) is ranged from 1 to 10. Select a number appropriate to your image.
  • Page 57 Section 4 4.3 Image Analysis: Using “Gel Positive/Gel Negative” to analyze the sample Step1-2 If the density of band (as box 1) is not clear, the Auto Find (as box 2) function cannot find any peaks. Step1-3 The warning dialog will pop up on the screen.
  • Page 58 Section 4 4.3 Image Analysis: Using “Gel Positive/Gel Negative” to analyze the sample Step2 Add Peak: Click “Add Peak” button (as box 1), choose two points which covers the range of the peak from the screen (select one point from the left side and a second point from the right side of the desired peak) to add a peak (as box 2) and then click the “!”.
  • Page 59 Section 4 4.3 Image Analysis: Using “Gel Positive/Gel Negative” to analyze the sample Step3 Delete Peak: Press “Delete Peak” button (as box1), click on that peak (as box 2), the peak will turn gray and then click “!” to finished. Step3-1 The peak will turn white.
  • Page 60 Section 4 4.3 Image Analysis: Using “Gel Positive/Gel Negative” to analyze the sample calculation. The order of the peaks will be rearranged. Step4 Base Line: This feature is used to help you increase (or cut off) the peaks you want (or do not want) to include in the quantification step. Press “Base Line”...

  • Page 61: Image Summarization

    Section 4 4.3 Image Analysis: Using “Gel Positive/Gel Negative” to analyze the sample There were three lanes selected (as box 1) in this example, so you need to press on the “Next Lane” button (as box 2) go to select peaks for lane3 before proceeding to summarizing the data.
  • Page 62 Section 4 4.3 Image Analysis: Using “Gel Positive/Gel Negative” to analyze the sample known marker size. After key in the first value, the system will show a dialog to remind you to key in the second value. Note: The “concentration” values of marker are provided by marker manufactuerer.
  • Page 63 Section 4 4.3 Image Analysis: Using “Gel Positive/Gel Negative” to analyze the sample image a file name (as box 2) and press “Save” (as box 3) to finish. Step5 Click on the “Export Data” button (as box1), a window pops up to ask you to select a destination location to save your file.
  • Page 64 Section 4 4.3 Image Analysis: Using “Gel Positive/Gel Negative” to analyze the sample quantification analysis by calculating the molecular weight. Step2 Key in the respective molecular weight values of the marker in this page. Note: The ”Mol weight” values of marker are provided by marker manufacturer.
  • Page 65 Section 4 4.3 Image Analysis: Using “Gel Positive/Gel Negative” to analyze the sample Step4 Click “Save image” button (as box 1) to store this image from the screen. Choose a destination location to save your image. Give the image a file name (as box 1) and press “Save” (as box 2) to finish. Step5 When clicking the “Mol Weight Calc.”...
  • Page 66 Section 4 4.3 Image Analysis: Using “Gel Positive/Gel Negative” to analyze the sample software will calculate the unknown “Mol weight” based on the input marker values. Press the “Export Data” button (as box 2), the software will export the data to a CSV file sheet. Step6 Choose a destination location to save your export.

  • Page 67: Image Analysis: Using "Dot Blot Positive/ Dot Blot Negative" To Analyze The Sample

    Section 4 4.4 Image Analysis: Using “Dot blot positive/ Dot blot negative” to analyze the sample 4.4 Image Analysis: Using “Dot blot positive/ Dot blot negative” to analyze the sample 4.4.1 Load the image Step1 Press “Analysis” (as box 1) to select the image you wish to analyze. You may select the image file from the hard drive or the USB drive.

  • Page 68: Processing The Image File

    Section 4 4.4 Image Analysis: Using “Dot blot positive/ Dot blot negative” to analyze the sample 4.4.2 Processing the Image File You will be directed to the image processing tool box as shown below. Step1 Crop: Crop the image by press the “Crop” button (as box 1). In order to select the cropping area of the image, hold and drag the cursor to select the area you want (as box 2).
  • Page 69 Section 4 4.4 Image Analysis: Using “Dot blot positive/ Dot blot negative” to analyze the sample Step2 Rotate: To rotate the image, first select the “Rotate” button (as box1) and the toolbar (as box 2) will pop up. Toolbar: : Rotate counter-clock wise : Rotate clock wise : Confirm action : Cancel...
  • Page 70 Section 4 4.4 Image Analysis: Using “Dot blot positive/ Dot blot negative” to analyze the sample Step2-1 You may rotate the image counter-clock wise or clock wise in two ways: a. Using the toolbar labelled as box 1, press "!" to confirm action. b.
  • Page 71 Section 4 4.4 Image Analysis: Using “Dot blot positive/ Dot blot negative” to analyze the sample : Invert the image from left to right. : Confirm action : Cancel Step4 Brightness: Adjusting the brightness of the image by pressing on the “Brightness”...
  • Page 72 Section 4 4.4 Image Analysis: Using “Dot blot positive/ Dot blot negative” to analyze the sample Step4-1 The result of Brightness is shown below. Press “!” to proceed or press “ ” to cancel. : Confirm action : Cancel Step5 Contrast: Adjusting the contrast level of the image by pressing the “Contrast”...
  • Page 73 Section 4 4.4 Image Analysis: Using “Dot blot positive/ Dot blot negative” to analyze the sample “x” to cancel. : Confirm action : Cancel Step6 Negative: To reverse the image between black and white by pressing on the “Negative” button (as box 1). If you don’t want to negative the image, you can press the “Negative”...
  • Page 74 Section 4 4.4 Image Analysis: Using “Dot blot positive/ Dot blot negative” to analyze the sample button (as box 1) and then a toolbar will pop out. If you want to zoom in the image, press the ”+” button (as box 2). If you want to zoom out the image, press the “-“button (as box 2).
  • Page 75 Section 4 4.4 Image Analysis: Using “Dot blot positive/ Dot blot negative” to analyze the sample text using this toolbar. The toolbar functions are explained as below. : Change the font type : Change the font size. : Move the text to the desired location by move the mouse cursor to the desired location on the image and click the left button of the mouse.
  • Page 76 Section 4 4.4 Image Analysis: Using “Dot blot positive/ Dot blot negative” to analyze the sample Step9 Original: This is the master undo button. It will undo ALL the changes you made to the image and revert it back to the original image. A massage will pop up to ask for confirmation once you press the “Original”...

  • Page 77: Selecting The Image Dot

    Section 4 4.4 Image Analysis: Using “Dot blot positive/ Dot blot negative” to analyze the sample 4.4.3 Selecting the Image Dot Press “Dot blot Positive” button and the software will automatically analyze the dot-blot samples from the image. Step1 Add Dot: Click “Add Dot” button (as box 1) to add one sample. Use the mouse to select the sample (as box 2) from the screen.
  • Page 78 Section 4 4.4 Image Analysis: Using “Dot blot positive/ Dot blot negative” to analyze the sample Step1-1 The image will be shown below as you have selected. Step2 Delete Dot: Press “Del Dot” button (as box 1), and then select the dot (as box 2) you want to delete.

  • Page 79: Calculating The Density

    Section 4 4.4 Image Analysis: Using “Dot blot positive/ Dot blot negative” to analyze the sample 4.4.4 Calculating the density Step1 Double click on the “Dot concentration” blank boxes to input the real density of each sample. (You will need at least one value in order to calculate the rest of the numbers.) Step2 Enter the value of known concentration.
  • Page 80 Section 4 4.4 Image Analysis: Using “Dot blot positive/ Dot blot negative” to analyze the sample Step3 Click “Save image” button (as box 1) to store this image from the screen. Choose a destination location to save your image. Give the image a file name (as box 2) and press “Save”...

  • Page 81: Troubleshooting Guide

    Section 5 Section 5 Troubleshooting Guide Many operating problems may be solved by carefully reading and following the instructions in this manual accordingly. Some suggestions for troubleshooting are given below. Should these suggestions not resolve the problem, please contact our SERVICE DEPARTMENT or a distributor in your region for assistance.

  • Page 82: Maintenance

    Never use abrasive cleaners, solvent based cleaners or scouring pads. The housing may be cleaned with a moist cloth containing a mild soap solution. Always disconnect the OmniDOC Pro Gel Documentation System from the electrical power prior to cleaning.

  • Page 83: Adjust The Scientific Grade Camera For Clearer Image

    Section 6 6.2 Adjust the scientific grade camera for clearer image 6.2 Adjust the scientific grade camera for clearer image Tool: 2.5 mm hex wrench (not provided) Step1 Open scientific grade camera door. Remove the filter to a stable place.
  • Page 84 Section 6 6.2 Adjust the scientific grade camera for clearer image Step2 Use 2.5mm hex wrench to loosen the screws of camera holder and hold the scientific grade camera to prevent damage to the lens. Step3 Pull out the scientific grade camera gently.
  • Page 85 Section 6 6.2 Adjust the scientific grade camera for clearer image Step4 Disconnect the USB port with scientific grade camera. Step5 Separate the camera with darkroom, you could use general camera cleaning kit to clean the lens and then reinstall the camera on the camera holder for more clear image.

  • Page 86: Replacing Amber Filter Onto Viewing Window

    Section 6 6.3 Replacing Amber Filter onto Viewing Window 6.3 Replacing Amber Filter onto Viewing Window Two filters (transparent filter and amber filter) are installed as default, if you did not purchase the blue light module and would like to remove the amber filter, please follow the steps below.
  • Page 87 Section 6 6.3 Replacing Amber Filter onto Viewing Window Step1 Loosen 4 nuts from the corners. Remove the transparent filter. Step2 There are no screw holes on the amber filter, please put the amber filter on the inside of the bolt.
  • Page 88 Section 6 6.3 Replacing Amber Filter onto Viewing Window Step3 Cover the transparent filter on the amber filter, put the nuts of four corners and then use the socket wrench to tighten the nuts. Step4 Confirm the amber filter is be fixed in the center of the viewing window.

  • Page 89: Adjust The Scientific Camera When Out Of Focus

    6.4 Adjust the scientific camera when out of focus 6.4 Adjust the scientific camera when out of focus Adjust the scientific camera for out of focus only under OmniDOC Gel Documentation System pc version to operate, please refer to OmniDOC Gel Documentation System pc version instruction manual to install the software on your computer.
  • Page 90 Section 6 6.4 Adjust the scientific camera when out of focus Step2 Put fluorescent ruler on the UV table again. Turn on the UV light and press “Actual Size” button (as box 1) to make sure the picture is clear and focus on.

  • Page 91: Warranty

    This warranty excludes damages resulting from shipping, misuse, carelessness, or neglect. Consumable parts (UV lamp and UV filter) are not covered by our warranty. Cleaver Scientific’s liability under the warranty is limited to the receipt of reasonable proof by the customer that the defect is embraced within the terms of the warranty.

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