Editing
LCC 500-501 Operation
(section)
Jump to navigation
Jump to search
Warning:
You are not logged in. Your IP address will be publicly visible if you make any edits. If you
log in
or
create an account
, your edits will be attributed to your username, along with other benefits.
Anti-spam check. Do
not
fill this in!
== Operation <br>Start-up <br> == 1. Check that all components are correctly installed 2. Turn on the pumps, monitors, recorder and fraction collector. 3. Set the flow rate on the pumps to zero and press the RUN button (E-50, P-500, P-6000). 4. Set the three chart speed selection buttons on the recorder to 10, mm/sec and "ext". Set the input range selection buttons for the channel connected to GRADIENT 1 V on the LCC-501 Plus to 1 V (10x100 mV) and the buttons for die channel connected to the monitor to the appropriate voltage. Press the input range selection button 0 on both channels to adjust both pens to zero with the zero control knob. Release both input range selection buttons 0 (REC-102). 5. Set the appropriate sensitivity with the sensitivity range selector on the UV monitor and adjust the baseline with the baseline knob or press "AUTO ZERO" on the UV-M II. 6. Turn On the LCC-501 Plus. <br> 7. Enter the Calibration block and check the kalor for method base and calibration values for the pumps, recorder etc. <br> 8. Program the fraction collector and set it in the start position. <br> 9. Check that the pumps are filled with the correct buffers by activating the wash program in the Manual block. <br> 10. To get started as fast as possible there are 9 different preprogrammed methods within the sminvare of the LCC-501 Plus. They am easily copied into Method banks in methods 0~8 with the command a CLEAR MEMORY 501. The methods are for specific columns sizes and techniques, to optimise your methods follow the instructions included with the columns. <br> Note The preprogrammed methods wiil not write over existing methods. 11. If the method is to be programmed before starting the run, it is convenient to equilibrate the column during this period by setting the initial conditions through the Manual block. <br> 12. Program the method. <br> 13. Check the method in the Review block or by listing it on the printer. <br> 14. Run the method. <br>
Summary:
Please note that all contributions to ELN may be edited, altered, or removed by other contributors. If you do not want your writing to be edited mercilessly, then do not submit it here.
You are also promising us that you wrote this yourself, or copied it from a public domain or similar free resource (see
ELN:Copyrights
for details).
Do not submit copyrighted work without permission!
Cancel
Editing help
(opens in new window)
Navigation menu
Personal tools
Not logged in
Talk
Contributions
Create account
Log in
Namespaces
Page
Discussion
English
Views
Read
Edit
View history
More
Search
Navigation
Category:
Main page
To Do
Tasks
My ELN
Weekly Reports
Buffer Recipe
SOP
Protocols
Inventories
Projects
Products
Customers
Contacts
Suppliers
Vectors
Vector Map
Clones
Cloning
Sequencing
NGS
Protein Expression
Purchaseing
QC
293 Expression
CHO Expression
Sf9 Expression
Protein Purification
Stem Cells
Cytokines
Protein Kinases
GPCR
Cell Lines
Competent Cells
Viral Proteins
VLP
Baculovirus
AAV
Adenovirus
Lentivirus
Virus Titering
Antibodies
Transfection
ELISA
qPCR RT-PCR
ImmunoAssay
Multiplex BioAssa
Lateral_Flow
Conjugation
Compounds Synthesis
BioEngineering
GenomeEngineering
Services
Software
Ideas
Links
Knowledgebase
Employees
Company
Tools
What links here
Related changes
Page information
Navigation
Special pages