T1165
Tris-Tricine-SDS Buffer 10× Concentrate
Synonyme(s) :
10X TTS Buffer, 10X Tris Tricine SDS running buffer, Tris Tricine SDS transfer buffer
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A propos de cet article
NACRES:
NA.25
UNSPSC Code:
41105319
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Laissez-nous vous aidersterility
0.2 μm filtered
form
liquid
pH
8.05-8.30 (25 °C in water, high purity, 1:10)
application(s)
diagnostic assay manufacturing
storage temp.
2-8°C
Quality Level
Catégories apparentées
General description
Tris-Tricine-SDS (TTS) running buffer is the cathode (upper reservoir) buffer for SDS−polyacrylamide gel electrophoresis of proteins using the Schagger and von Jagow method. The Schagger and von Jagow method is designed for the separation of small molecular weight proteins. It differs from the Laemmli method in that the glycine is replaced with tricine and the gel contains 1M Tris-HCl, pH 8.45 instead of 0.375 M Tris-HCl, pH 8.9. Dilution of the 10X TTS buffer produces a 1X cathode buffer containing 100 mM Tris, 100 mM tricine and 0.1% SDS. Recommended running conditions is 125 volts.
Application
Tris-Tricine-SDS Buffer 10× Concentrate is suitable for use as a running buffer for polyacrylamide based separation of bronchoalveolar lavage fluid (BALF).
Analysis Note
Tested for use as a cathode buffer for Tris-Tricine gel electrophoresis to separate low molecular weight proteins.
Other Notes
1M Tris, 1M Tricine, 1% (w/v) SDS, pH approx. 8.2.
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We describe a microfluidic Western blot assay (μWestern) using a Tris tricine discontinuous buffer system suitable for analyses of a wide molecular mass range (6.5-116 kDa). The Tris tricine μWestern is completed in an enclosed, straight glass microfluidic channel housing
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