![]() |
|
![]() |
||||
Thread | Thread Starter | Forum | Replies | Last Post |
Good Beads / Best Beads | paolo.kunder | SOLiD | 2 | 03-27-2013 03:12 PM |
no enrichment of beads --> any ideas why? | lichtfaengerin | 454 Pyrosequencing | 1 | 08-11-2011 03:45 AM |
Calibration beads | mestro2 | Sample Prep / Library Generation | 1 | 11-30-2010 08:59 AM |
mag beads? | link1 | Sample Prep / Library Generation | 1 | 08-13-2010 07:34 AM |
Beads/slide | Katsu | SOLiD | 1 | 09-22-2009 02:14 PM |
![]() |
|
Thread Tools |
![]() |
#1 |
Member
Location: Slovakia Join Date: Apr 2012
Posts: 10
|
![]()
Hello everybody,
can anyone tell me whether the concentration of P1 beads within P1 reagent (Box 2, SOLiD EZ Bead Emulsifier) is the same as that of P1 beads of ePCR Kit V2, that should be 10,000,000 beads /ul? As far as we use the EZ Bead system and not the IKA shaker we´ve got only 3 boxes for emulsifier (P1 beads included for DNA enrichment and not separate P1 beads for calculation of enriched P1beads conc.). Can I prepare the calibration curve from the remaining P1 beads assuming 10 mil.beads/ul concentration, too?thanks. |
![]() |
![]() |
![]() |
#2 |
Senior Member
Location: Wales Join Date: May 2008
Posts: 114
|
![]()
I'm not sure why you want to prepare a calibration curve? the EZ bead system doesn't require one?
I realise this is not really the answer you are looking for but you can easily find the concentration of a give tube, just prepare a serial dilution then your usual method for bead counting....I'd recommend using a nanodrop rather than the "colour chart". JPC |
![]() |
![]() |
![]() |
#3 |
Member
Location: Houston Join Date: Mar 2012
Posts: 10
|
![]()
As my calculate, i think that is true, 10millinon/ul, EZ80 usually use 1430ul x 10millions. method should be same like IKA utilized, which apply 160ul same concentration beads. AB maybe give you more information for this question.
|
![]() |
![]() |
![]() |
Thread Tools | |
|
|