Sentence examples for mouse tail veins from inspiring English sources

B16F10 cells labeled with BCECF or CFSE were injected into mouse tail veins.

B16F10 cells labeled with CFSE were injected into mouse tail veins.

To determine the therapeutic dosing schedule, intratumoral distributions of N Chitosan-DMNPs in tumor-bearing mice were investigated through MR images after intravenous injection into mouse tail veins (150 μg Fe + Mn, 3 mg/kg DOX).

One million TC-1 cells in 0.1 ml FCS-free medium were injected into mouse tail veins using a 25-gauge needle.

Blood samples were obtained from adult mouse tail veins.

Adenovirus encoding Cre recombinase was purified and injected intravenously through mouse tail veins as previously described (Li et al., 2008).

Inject the sporozoite suspension i.v. into the mouse tail vein.

Vasodilate the mouse tail vein, either by soaking the tail in warm water (40 °C) for 5 min or by heating under an infrared lamp.

For the engraftment, the NSG mice were irradiated with 2.0 Gy of gamma rays followed by injection of 200,000 human CD34+ cells (n = 5 human donors) in the mouse tail vein within 24 hours after the irradiation.

Human cell engraftment was determined four months later by flow cytometry using 20 μl of mouse tail vein blood, stained with antibodies specific to human CD45, (WBC marker, clone HI30, Biolegend, San Diego, CA), human CD3 (T cell marker, clone UCHT1; Biolegend), human CD20 (B cell marker, clone 2H7; Biolegend) and mouse CD45, (WBC marker, clone 30-F11, eBioSan Diego, CADiego, CA).

After mouse placement, the mouse tail vein should be cannulated (Haney et al. 2009).