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Pb9249

Manufactured by Boster Bio
Sourced in United States

The PB9249 is a multi-channel pipette manufactured by Boster Bio. It is designed to accurately and precisely transfer small volumes of liquids. The core function of the PB9249 is to enable efficient liquid handling in laboratory settings.

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2 protocols using pb9249

1

Immunofluorescent Analysis of Liver PD-1 and CD8

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Immunofluorescence staining of paraffin-embedded human liver tissue sections was performed using anti-PD-1/CD279 (66220-1-Ig, Proteintech, Rosemont, IL, United States) and anti-CD8α (PB9249, Boster Bio, Pleasanton, CA, United States) antibodies. Antigen retrieval was performed with EDTA buffer (AR0023, Boster Bio). Tissue sections were blocked with 10% goat serum (AR1009, Boster Bio), and then incubated with rabbit anti-CD8α antibody (1:200 dilution) and mouse anti-PD-1 antibody (1:4000 dilution) at 4 °C overnight. Secondary antibodies including DyLight594 fluorescein goat anti-mouse (BA1141, Boster Bio) and fluorescein DyLight488 goat anti-rabbit (BA1127, Boster Bio) IgGs were then added and incubated for 45 min at 37 °C. DAPI staining solution (AR1176, Boster Bio) was used for counterstaining at room temperature for 3 min, and then washed with PBS (pH 7.2-7.6) (AR0030, Boster Bio). Slides were mounted using anti-fluorescent quench mounting medium (AR1109, Boster Bio). Finally, whole-slide scanning (APERIOVERSA8, Leica, Wetzlar, Germany) and image acquisition (BX51, Olympus, Tokyo, Japan) were performed.
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2

Quantifying PD-L1 and ANLN in BLCA Tissues

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In total, 21 BLCA tissue samples were acquired from patients who had undergone curative surgery at the Second Affiliated Hospital of Wenzhou Medical University. Ethical approval was obtained from the Second Affiliated Hospital of Wenzhou Medical University Research Ethics Committee. Antibodies against anillin (ANLN) (DF13590, 1 : 200; Affinity Biosciences), CD8 (PB9249, 1 : 200; BOSTER), and PD-L1 (66248-1-lg, 1 : 5000; Proteintech) were used for the immunohistochemical (IHC) staining of these proteins in the tissue samples, which was performed according to previously published methods [17 (link)]. For the IHC analysis, the H-score was applied to assess the expression levels of PD-L1 and ANLN [18 (link)]. The number of CD8+ cells was counted using the ImageJ software.
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