|
| |
|
|
| [ 文章来源： | 文章作者：
| 发布时间：2007-08-28|
字体：
[大
中
小]
| |
|
Preparation of Slides
| | Qty | Order info Glass microscope slides 60 Gold Seal #3010 Slide rack 2 Shandon Lipshaw #121 (800-245-6212) <= Each rack holds 30 slides Slide chamber 6 Shandon Lipshaw #121 <= Each chamber holds 350 mL ddH2O ~5 L NaOH 70 g 95% Ethanol 420 mL Poly-L-lysine 70 mL Sigma #P 8920 70 mL Vacuum oven (45C) Slide box (plastic only) 1 VWR #48443-806
1. Place slides in slide racks. Place racks in chambers. 2. Prepare CLEANING SOLUTION: Dissolve 70 g NaOH in 280 mL ddH2O. Add 420 mL 95% ethanol. Total volume is 700 mL (= 2 X 350 mL); stir until completely mixed. If solution remains cloudy, add ddH2O until clear. 3. Pour solution into chambers with slides; cover chambers with glass lids. Mix on orbital shaker for 2 hr. Once slides are clean, they should be exposed to air as little as possible. Dust particles will interfere with coating and printing. 4. Quickly transfer racks to fresh chambers filled with ddH2O. Rinse vigorously by plunging racks up and down. Repeat rinses 4X with fresh ddH2O each time. It is critical to remove all traces of NaOH-ethanol. 5. Prepare POLYLYSINE SOLUTION: 70 mL poly-L-lysine 70 mL tissue culture PBS in 560 mL water. Use plastic graduated cylinder and beaker. 6. Transfer slides to polylysine solution and shake 15 min. - 1 hr. 7. Transfer rack to fresh chambers filled with ddH2O. Plunge up and down 5X to rinse. 8. Centrifuge slides on microtiter plate carriers (place paper towels below rack to absorb liquid) for 5 min. @ 500 rpm. Transfer slide racks to empty chambers with covers for transport to vacuum oven. 9. Dry slide racks in 45C vacuum oven for 10 min. (Vacuum is optional.) 10. Store slides in closed slide box (plastic only, without rubber mat bottom) 11. BEFORE PRINTING ARRAYS: Check that polylysine coating is not opaque.
上一篇：DNA Samples Preparation 下一篇：Protocol for Reverse Transcription and Amino-allyl Coupling of RNA
|
|
DNA Samples Preparation