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why I can see my band dyed in proceau S on PDFC? Since your technique works in for NC then obviously something is wrong with your PVDF. Have you hydrated your PVDF in methanol before transfer? This might a source of the problem -----Original Message----- From: [Only registered and activated users can see links. Click Here To Register...] [mailto:[Only registered and activated users can see links. Click Here To Register...].indiana.edu] On Behalf Of [Only registered and activated users can see links. Click Here To Register...] Sent: Saturday, November 25, 2006 7:01 PM To: [Only registered and activated users can see links. Click Here To Register...] Subject: Proteins Digest, Vol 18, Issue 13 Send Proteins mailing list submissions to [Only registered and activated users can see links. Click Here To Register...] To subscribe or unsubscribe via the World Wide Web, visit [Only registered and activated users can see links. Click Here To Register...] or, via email, send a message with subject or body 'help' to [Only registered and activated users can see links. Click Here To Register...] You can reach the person managing the list at [Only registered and activated users can see links. Click Here To Register...] When replying, please edit your Subject line so it is more specific than "Re: Contents of Proteins digest..." Today's Topics: 1. why I can see my band dyed in proceau S on PDFC? (=?GB2312?B?veDV1A==?=) ---------------------------------------------------------------------- Message: 1 Date: Sat, 25 Nov 2006 10:57:51 +0800 From: "=?GB2312?B?veDV1A==?=" <[Only registered and activated users can see links. Click Here To Register...]> Subject: [Protein-analysis] why I can see my band dyed in proceau S on PDFC? To: [Only registered and activated users can see links. Click Here To Register...] Message-ID: <4d0022c90611241857v48f5c87dj34e2c08f2df449ac@mail .gmail.com> Content-Type: text/plain; charset=ISO-8859-1; format=flowed sir/madam: I have been trying to blot proteins of brain from an 8% SDS PAGE toBioRad PVDF membrane. I thought that my blot was unsuccessful afterattempting to visualize by Ponceau S. I could not even detect my MWstandards.but the same process worked well in NCmembrane,where the band showed clearly.. Any clues as to why my ponceau S did not work? I diluted a fresh Sigam concentrate (20 mL) into 180 mL ofdeionized water. I stained for 5 min and watch as the membrane destained in 1% AcOH. At no time did I see anything resembling a protein band. This problem has occured for the past two consecutive times that I have tried the technique. Your comments are appreciated. ------------------------------ _______________________________________________ Proteins mailing list [Only registered and activated users can see links. Click Here To Register...] [Only registered and activated users can see links. Click Here To Register...] End of Proteins Digest, Vol 18, Issue 13 **************************************** |
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