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T4904

Supelco

Tris-Glycine Buffer 10× Concentrate

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Synonym(s):
running buffer
EC Number:
NACRES:
NA.25

sterility

0.2 μm filtered

Quality Level

foreign activity

Protease, none detected

storage temp.

2-8°C

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This Item
T7777T1165SRE0062
foreign activity

Protease, none detected

foreign activity

-

foreign activity

-

foreign activity

-

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

room temp

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

500

Application

Tris-Glycine buffer 10× concentrate has been used as a transfer buffer for Western blotting.

Biochem/physiol Actions

For Western blotting and gel electrophoresis. Tris-glycine buffer is used to make a Tris-glycine-methanol transfer buffer, which is the most common protein transfer buffer for wet blot transfers. The methanol prevents the gel from swelling during the transfer and enhances the protein binding to nitrocellulose.The 10× Tris-glycine buffer is diluted to 1× with methanol and water to make a solution containing 25 mM Tris, 192 mM glycine, and 20% methanol. A sufficient amount of transfer buffer should be made to cover the electrode wires in the wet blot transfer unit and to soak the gel, membrane and blotting paper.

Other Notes

0.25 M Tris, 1.92 M glycine, pH approx. 8.3
Contains no methanol.

related product

Product No.
Description
Pricing

Storage Class Code

12 - Non Combustible Liquids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Multiple tandem epitope tagging for enhanced detection of protein expressed in mammalian cells.
Zhang L, et al.
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Immunoblotting and dot blotting.
D I Stott
Journal of immunological methods, 119(2), 153-187 (1989-05-12)
H Towbin et al.
Proceedings of the National Academy of Sciences of the United States of America, 76(9), 4350-4354 (1979-09-01)
A method has been devised for the electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets. The method results in quantitative transfer of ribosomal proteins from gels containing urea. For sodium dodecyl sulfate gels, the original band pattern was

Protocols

Western Blotting Protocol - Immunoblotting or Western Blot Protocol

Western blot protocol with workflow steps for different blot procedures, describing the electrophoretic transfer of proteins from SDS polyacrylamide gels to sheets of nitrocellulose. Also known as Immunoblotting protcol.

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