Scientist Solutions: Life Science Discussions
 Refer a Friend    Link To Us    Bookmark Us       

      
 » Home » Lab Automation/High-Throughput Screening  » General Discussion » Beckman Coulter Biomek NXp

Other Topics
3/25/2008 01:27 PM
qPCR NEWS March 2008 - qP ...
3/8/2008 09:58 PM
Thermo Fisher Scientific ...
2/7/2008 06:13 PM
STUBLI CONNECTORS TO HIRE ...
2/7/2008 06:27 PM
STUBLI CONNECTORS TO HIRE ...
11/13/2007 09:15 PM
ALA and FIRST Enter Into ...
9/14/2007 06:30 AM
Automation Systems Engine ...
9/6/2007 02:54 AM
Extreme Pipetting Expedit ...
8/2/2007 04:37 PM
ALA Expands Innovation Av ...
7/12/2007 09:55 PM
Spotlight Series - Puttin ...
7/1/2007 07:16 AM
LABSNAP - A Fast Read on ...
Subscribet to topic
Add Reply  Add New Topic  Add New Poll
bottom of page RSS Feed 

Topic Feed

 

Beckman Coulter Biomek NXp

 [View Printable]
Response

Frog Egg

See
Similar
Scientists





Group: Member
Posts: 1
Joined: Oct 08, 2007







 Send a personal messsage to Response Reply with a quote from this post Go to the top of the page

I currently have a Biomek NXp from Beckman Coulter. I want to determine that the volumes being dispensed are correct. If anyone has any ideas on how to confirm this I would be greatful

.........................

Posted Oct 08, 2007, 12:04 PM
roboteer@pa

Frog Egg

See
Similar
Scientists





Group: Member
Posts: 2
Joined: Feb 04, 2008







 Send a personal messsage to roboteer@pa Reply with a quote from this post Go to the top of the page

You might be able to locate a protocol if you check Beckman FX user groups (I'm told they exist). Alternatively, you can do a weighing excercise as well. Here is what is involved. 1st, take a standard 96 well microplate, clean and dry from a shipping bag. 2nd, weigh it on a top loading balance to +/- 1mg. Then place it on the NX and have the NX dispense 50 uL / well into a column of wells (say the "1" column). 3rd, THen repeat with three more columns on themicrplate. 4th- Now promptly reweigh (without spilling) the filled microplate. Divide the total weight gain (in mg) by 32. If you wish, correct for density as well. Be sure to use pure water as the pipetted liquid. You should observe a weight very close to 50 mg. If not, that represents the bias. 5th - repeat these steps (#1-4) for larger volumes such as 75 uL, 100uL. You should now see whether there is a net bias in the delivery of the pipetting system. If you do a regression equation using these (specified voumes vs observed volume), you can see the correction needed to get the system to deliver an accurate volume (or so that is the way it is supposed to work). Happy pipetting!

.........................

Posted Feb 04, 2008, 21:42 PM
top of page Add Reply  Add New Topic  Add New Poll

Forum Jump