The purified Sp17-ICG-Der-02 conjugates were stored

at 4°C in the dark for future use. ELISA for immunological activity of ICG-Der-02 labeled anti-Sp17 Recombinant human sperm protein 17 produced in our laboratory [14] at 1 μg/ml in coating buffer were added to 96-well plates (100 μl/well) and incubated overnight at 4°C. The plates were then washed with 0.05% Tween 20/PBS and blocked with 100 μl/well of 5% fetal calf serum/PBS for 1 h at 37°C. After washing, ICG-Der-02 labeled or naked anti-Sp17 (100 μl/well), serially diluted with 5% fetal calf serum/PBS, was added and the plates were incubated for 1 h at 37°C. After a third washing, 1:2000 diluted goat anti-mouse IgG labeled with horseradish peroxidase (100 μl/well) was NVP-LDE225 datasheet added and the plates were incubated for 1 h

at 37°C. After another washing substrate TMB solution was added to each well and the plates were incubated for 10 min at 37°C. Finally, 2 mol/L H2SO4 was added and the plates were read at 450 nm using a Benchmark microplate reader Proteasomal inhibitor (BIO-RAD, Hercules, CA, USA). In vivo and in vitro NIR Imaging In vivo NIR imaging was performed using a self-built NIR imaging system. This NIR imaging system has been introduced in detail in our previous work [18]. In brief, a helium-neon laser (1 = 765.9 nm) is defocused to provide a broad spot with even optical density, and another 808 nm laser is supplied as background light. High sensitivity CCD camera detects the reflected light, endogenously generated luminescence or fluorescence emission. An 800 nm long pass filter could blocked the laser light (765 nm) efficiently. Nine tumor-bearing nude mice were randomly MAPK inhibitor divided into two groups. The experimental group (group A, n = 5) and control group (group B, n = 4) were both administrated anti-Sp17-ICG-Der-02 and free

Demeclocycline ICG-Der-02 through caudal vein injection. The dose for each animal was 5 μg, calculated as the amount of ICG-Der-02. The subjected mouse was anesthetized in an isoflurane chamber and immobilized in a Lucite jig before whole-body imaging at predetermined intervals (1 h, 2 h, 4 h, 6 h, 1 day, 2 days, and 3 days) post-injection. Two animals from the experimental group were observed until 7 d post-injection. Other animals were killed at 1 day and 3 days post-injection, and the tumor and major organs were taken out for ex vivo optical imaging examinations. All fluorescence images were acquired with 1 s exposure (f/stop = 4). Results Overexpression of Sp17 in hepatocellular carcinoma cells Through immunocytochemistry and immunohistochemistry, strong positive staining was observed in the human hepatocellular carcinoma cell line SMMC-7721 and its tumor xenografts tissues (Figure 1). We found Sp17 mainly localized on the cell surface of in vitro cultured cells and both surface and cytoplasm of xenografts tissues.