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GB111556 is a laboratory centrifuge designed for general-purpose applications. It is capable of separating samples through centrifugal force. The core function of this product is to facilitate the separation and isolation of different components within a liquid sample.

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2 protocols using gb111556

1

Immunofluorescent Staining of Cardiac Myocytes

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Immunofluorescence staining was performed on NRCMs grown on coverslips. NRCMs were fixed with 4 % paraformaldehyde for 15 min and blocked with 3 % BSA in PBS for 30 min at room temperature. For α-actinin staining, NRCMs were incubated at 4 °C for overnight with a rabbit anti-α-actinin antibody (GB111556, Servicebio, Wuhan, China) and a corresponding anti-rabbit Cy3 antibody (GB21302, Servicebio, Wuhan, China) for 1 hour at room temperature. The image was obtained via the fluorescence microscope. The surface area of NRCMs were depicted using Image J. For co-localization of USP38 and TBK1, NRCMs were incubated with rabbit anti-USP38 at 4 °C for overnight, then incubated with corresponding anti-rabbit HRP-labled antibody for 1 hour, followed by Cy3-Tyramide (GB1223, Servicebio, Wuhan, China) for 1 hour at room temperature. Subsequently, NRCMs were incubated with rabbit anti-TBK1 antibody at 4 °C for overnight, then incubated with anti-rabbit Alexa Fluro 488 antibody (GB25303, Servicebio, Wuhan, China) for 1 hour at room temperature. The nucleus was stained with DAPI (GB1012, Servicebio, Wuhan, China) for 10 min. The image was obtained via the confocal scanning microscope (NIKON Eclipse TI, Tokyo, Japan).
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2

Macrophage Polarization and Cardiomyocyte Gap Junctions

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We selected a TSA-compatible double-color immunostaining protocol using primary antibodies from the same host species. Microwave heat repair and incubation with 3% hydrogen peroxide solution were the same as before. Sections were blocked with 3% BSA for 30 minutes and then incubated with F4/80 (Servicebio, GB113373, 1:400 dilution, China) and inducible nitric oxide synthase (iNOS) (Servicebio, GB11119, 1:500 dilution, China) to evaluate macrophage polarization. Other sections were incubated with connexin 43 (Cx43) (Proteintech, 26980-1-AP, 1:300 dilution, China) and α-actinin (Servicebio, GB111556, 1:500 dilution, China) to assess cardiomyocyte gap junctions. The tissues were incubated with TSA-FITC and TSA-CY3 separately and labeled green and red, respectively. Images were captured with an inverted laser confocal microscope (ZEISS, LSM710, Germany).
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