新配方电泳转印缓冲液，电泳时间可从2小时缩减至20分钟，转印可在10分钟内完成，保持条带清晰锐利。与常规方法兼容。New protein separation and western blot transfer buffers are modified formulations that perform just like tris-glycine, but significantly accelerate run and transfer times without compromising results. Tris-glycine SDS buffers have been recognized as the gold standard for analyzing proteins by PAGE, for decades. Now, the standard 2-hour method for protein separation and transfer can be reduced to less than 30 minutes with these buffers:
Benefits
– Separation in 10–20 minutes
– Transfer in 10 minutes
– Compatibility with standard gel systems and protocols
– Razor sharp resolution
For mounting and preservation of fluorescence-stained tissues and cellsProvides superior anti-fade and anti-photobleaching propertiesCan be used for in situ hybridization techniques or for other procedures requiring fluorescent labeling of DNASupplied as a 10 ml aqueous solutionInhibits photobleaching of probes containing fluorescein, Texas Red, Rhodamine and other fluorochromes including CruzFluor™ (CFL) fluorescent dyesContains 1.5 µg/ml 4',6-diamidino-2-phenylindole (DAPI) (sc-3598) for DNA counterstaining. DAPI produces a blue fluorescence with ex = 360 nm and em = 460 nm when bound to DNAMounted sections retain fluorescence during prolonged storage if permanently sealed around perimeter with nail polish or a plastic sealantStore mounted slides at 4° C protected from lightStable for 6 months from date of purchase
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