Your privacy, your choice

We use essential cookies to make sure the site can function. We also use optional cookies for advertising, personalisation of content, usage analysis, and social media.

By accepting optional cookies, you consent to the processing of your personal data - including transfers to third parties. Some third parties are outside of the European Economic Area, with varying standards of data protection.

See our privacy policy for more information on the use of your personal data.

for further information and to change your choices.
Skip to main content
Fig. 1 | Cellular & Molecular Biology Letters

Fig. 1

From: Hsp70-Bim interaction facilitates mitophagy by recruiting parkin and TOMM20 into a complex

Fig. 1

S1g-2 and S1 modulate a variety of stress-induced autophagy in opposite ways. A Chemical structures of S1g-2, S1, S1n, S1g-2-probe, S1-probe and S1n-probe. B Western blot analysis of the levels of LC3 and p62 in HEK293T cells treated with 0.5 mM H2O2, 34 μM VP-16 or HBSS in the presence or absence of 10 μM S1g-2, 10 μM S1 and 10 μM S1n respectively for 4 h, using β-actin as a loading control. An equivalent of DMSO were added to the compound untreated group as vehicle control. The graphs show (mean ± SD, n = 3 biologically independent experiments) LC3-II/LC3-I ratios of each treatment normalized to the LC3-II/LC3-I ratio of control cells. **P < 0.01 (one-way ANOVA test); n.s. indicates no significance between HBSS + S1n and HBSS group

Back to article page

Cellular & Molecular Biology Letters

ISSN: 1689-1392

Contact us