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wenjie

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Western Blot Analysis
Cytosol proteins from lung (50 ug) and liver
(10 g) were separated on a 12% (w/v) polyacrylamide
gel in an electrophoresis system (Novex, San
Diego, CA) . After running at 200 V, the protein
bands were transferred overnight at 40 V onto a nitrocellulose
membrane. All membranes were blocked in
TBST (50 mM Tris, pH 7.5, 150 mM NaCl, 0.05% (v/v)
Tween-20) containing 5% (w/v) dry milk for 1 h on
a shaker at room temperature. Membranes were incubated
with either rabbit anti-AST IV or rabbit anti-
STa (1:5000) in TBST containing 5% (w/v) dry milk for
2 h on a shaker at room temperature. After incubation,
membranes were washed with TBST for 4 ¡Á 15 min
and incubated with secondary antibody (horseradish
peroxidase-conjugated immuno-pure goat anti-rabbit
IgG; H+L) at 1:5000 dilutions in the same buffer for
2 h. The membranes were washed with TBST for 4¡Á
15 min and then with Tris buffered saline (TBS) 3 ¡Á
5 min. Fluorescent bands were developed with 1mL of
substrate containing same volume of each Super Signal
West Pico Luminol Enhancer solution and Super Signal
West Pico Stable Peroxidase solution at room temperature
for 5 min. The X-ray films were exposed to the
membrane and then developed. Films were scanned
and the densitometry analysis was performed with
AAB software in a Gel Documentation and Analysis System from Advanced American Biotechnology
   Determination of Nonprotein Soluble Thiol(NPSH)
  Total nonprotein soluble thiol in lung and liver cytosol
was determined by the standard DTNB (Ellman¡¯s
reagent, 5,5`-dithiobis-2-nitrobenzoic acid) method
with a slight modification. Lung and liver tissues were
homogenized with 50 mM Tris buffer, pH 7.5, containing
250 mM sucrose and 5 mM EDTA. Homogenates
were centrifuged at 100,000g for 1 h. Equal volume of
5% (w/v) sulfosalisialic acid was used to precipitate all
proteins from the tissue cytosols. After mild vortexing
and centrifugation at 4000g, 80 uL of transparent sample
supernatant was added to 720 uL of 0.1 M potassium
phosphate buffer containing 5 uM DTNB. The
absorbance was measured after 5 min at 412 nm in a
UV-spectrophotometer. The steady state of the reaction
kinetics was checked up to 7 min. A standard curve
was generated using GSH and individual sample values
were determined from this standard curve

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ringzhu(½ð±Ò+2): ¹þ¹þ ÇóÖúµÄÄÇÈË¿ÉÕæ¹»ÀÁµÄ Á¬ÕûÀí¶¼²»ÕûÀí ¨r(¨s¨Œ¨t)¨q ÉñÂíÈ˶¼ÓÐ~~~ 2011-05-24 11:27:41
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Originally posted by wenjie at 2011-05-21 15:08:23:
Western Blot Analysis
Cytosol proteins from lung (50 ug) and liver
(10 g) were separated on a 12% (w/v) polyacrylamide
gel in an electrophoresis system (Novex, San
Diego, CA) . After running a ...

It seems very easy try to translate by yourself. I believe Iyou can do it very well.
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