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Tris acetate page and bis tris gels

Manufactured by Thermo Fisher Scientific
Sourced in United States

Tris-Acetate PAGE and Bis-Tris gels are laboratory equipment used for the separation and analysis of proteins. These gels facilitate the electrophoretic separation of proteins based on their molecular weight and charge. The Tris-Acetate PAGE gel system utilizes a Tris-Acetate buffer, while the Bis-Tris gel system employs a Bis-Tris buffer. Both systems provide reliable and reproducible protein separation for various applications in biochemistry and molecular biology.

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2 protocols using tris acetate page and bis tris gels

1

Immunoblotting with Tris-Acetate and Bis-Tris Gels

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Cell-extract proteins were resolved by Tris-Acetate PAGE and Bis-Tris gels (Invitrogen, Carlsbad, CA, USA) and transferred onto polyvinylidene difluoride membranes (PVDF), blocked in 5% milk in PBST, and incubated overnight with indicated antibodies. Membranes were washed and incubated with HRP-conjugated antirabbit IgG or antimouse IgG (Cell Signaling Technology, Danvers, MA, USA), followed by detection using BioRad Gel Doc. For Coomassie staining, proteins were resolved on PAGE gels (Invitrogen, Carlsbad, CA, USA) followed fixation and staining with Bio-Safe Coomassie G-250 stain (Bio-Rad Laboratories, Hercules, CA, USA) according to manufacturer’s instructions.
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2

Protein Separation and Immunoblotting

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Cell extract proteins were resolved by Tris-Acetate PAGE and Bis-Tris gels (Invitrogen, Carlsbad, CA, USA) and transferred onto polyvinylidene difluoride membranes, which were incubated overnight with primary antibodies, washed, and incubated with HRP-conjugated anti-rabbit Ig or anti-mouse Ig (Amersham Biosciences, Little Chalfont, UK) for 1 h.
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