Date: Wed, 23 May 2007 08:57:32 -0700 From: "Chang Shi" <cshi@mclab.com> To: "'ABRF Discussion List'" <ABRF@list.abrf.org> Subject: RE: 3730 capillary regenerationHI, Ashwani, MCLAB has a product (CARE solution) for regenerating capillary Array (including 50 cm), which can be used on the sequencer machine. Any abrf member can send a email (mclab@mclab.com) to get free bottles of the solution (the offer ends 6/30/07). 1).No need to remove the capillary for treatment 2).the resolution loss can be recovered after the treatment 3).To remove the background noise, e.g. yellow haze, and keep the baseline low 4).It is easy to use. Whenever there is dirty background or resolution loss, we use it to clean the gel block and capillary. It has been two years now. The highest number of runs is 3074 (it is still on the 3730xl, has not reach Glen Byrns's 9000 record).
Hope it helps. Changping Shi, PH.D. MCLAB 384 Oyster Point Blvd, Suit 15 South San Francisco, CA 94080 Tel: (650)872-0245 Fax:(650)872-0253 -----Original Message----- From: Ashwani Kumar Sent: Tuesday, May 22, 2007 8:47 PM To: 'ABRF Discussion List' Subject: RE: 3730 capillary regeneration Did anyone had any luck with 50cm array regeneration for sequencing on ABI 3730? We on an average use 50 cm arrays for 1500 runs, after which many of the capillaries start showing resolution loss of the peaks in many of the capillaries. Ashwani In-Charge, Sequencing Facility, TCGA
-----Original Message----- From: grbyrns@ucdavis.edu Sent: 23 May 2007 02:05 To: ABRF@list.abrf.org Subject: 3730 capillary regeneration Just a quick update to those using the AB3730 sequencer. We now get an average of about 5000 runs per 36cm array. Our highest is over 9000 runs. Most for fragment analysis, maybe 5% sequencing. Our wash technique is to use the syringe to empty the array of polymer while it stands on a paper towel. Then, 1M Nitric acid is syringed into the array and allowed to stand for 5 minutes. It is then replaced with 1N NaOH, left for 5 minutes. Finally, at least 10 syringe-loads of hot ddH2O is washed through the array before remounting. The bubble wizard is used to fill the array, followed by the spatial (with fill) calibration. The two fills give time for the polymer re-coating of the stripped capillaries. Again, DO NOT TRY THIS, if you don't have a good way to move the liquids under high pressure into and out of the array. An exploding syringe of nitric acid will ruin your day. Glen Byrns Veterinary Genetics Laboratory UC Davis |