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Anti p107

Manufactured by Proteintech

Anti-P107 is a lab equipment product manufactured by Proteintech. It is a primary antibody used for the detection and analysis of the P107 protein in various experimental applications.

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2 protocols using anti p107

1

Protein Extraction and Western Blot Analysis

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Protein extracts from tissues were prepared using RIPA lysis buffer (Beyotime). Tissues or cells were harvested and lysed in RIPA Buffer (50mM Tris (pH 7.4), 150mM NaCl, 1% Triton X-100, 1% sodium deoxycholate) containing proteinase inhibitors cocktail (Roche) on ice for 40 minutes. Lysates were centrifuged 40 minutes at 4°C at maximum speed (20000 rcf.) and resulting protein extracts separated by SDS–PAGE (12%). After transfer of proteins to PVDF membranes (Bio-rad), membranes were blocked with 5% skim milk in TBS containing 0.1% Tween 20 (TBS-T) for 1 hr at room temperature, followed by two washes with TBS-T. Membranes were incubated overnight at 4°C with primary antibodies followed by three 10-min washes in TBS-T, exposure to HRP-conjugated secondary antibody for 1 hr at room temperature, and 3 washes with TBS-T. Detection of HRP conjugated secondary antibody was performed with ECL (PerkinElmer). Antibodies used in supplemental experiment were anti-E2F3 (ABclonal Technology, A8811), anti-GSK3B (ABclonal Technology, A0479), Anti-P107 (Proteintech, 13354–1-AP).
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2

Protein Extraction and Western Blot Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
Protein extracts from tissues were prepared using RIPA lysis buffer (Beyotime). Tissues or cells were harvested and lysed in RIPA Buffer (50mM Tris (pH 7.4), 150mM NaCl, 1% Triton X-100, 1% sodium deoxycholate) containing proteinase inhibitors cocktail (Roche) on ice for 40 minutes. Lysates were centrifuged 40 minutes at 4°C at maximum speed (20000 rcf.) and resulting protein extracts separated by SDS–PAGE (12%). After transfer of proteins to PVDF membranes (Bio-rad), membranes were blocked with 5% skim milk in TBS containing 0.1% Tween 20 (TBS-T) for 1 hr at room temperature, followed by two washes with TBS-T. Membranes were incubated overnight at 4°C with primary antibodies followed by three 10-min washes in TBS-T, exposure to HRP-conjugated secondary antibody for 1 hr at room temperature, and 3 washes with TBS-T. Detection of HRP conjugated secondary antibody was performed with ECL (PerkinElmer). Antibodies used in supplemental experiment were anti-E2F3 (ABclonal Technology, A8811), anti-GSK3B (ABclonal Technology, A0479), Anti-P107 (Proteintech, 13354–1-AP).
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