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Anti-Claudin 18.1 antibody
WB:1:500-1:1,000
FC:1:50-1:100
Fig1: Western blot analysis of Claudin18 on different lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody ( was used in 5% BSA at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:5,000 dilution was used for 1 hour at room temperature.
Positive control:
Lane 1: human stomach tissue lysate
Lane 2: AGS cell lysate
Fig2: Flow cytometric analysis of Claudin18 was done on F9 cells. The cells were fixed, permeabilized and stained with the primary antibody ((red). After incubation of the primary antibody at room temperature for an hour, the cells were stained with a Alexa Fluor 488-conjugated Goat anti-Rabbit IgG Secondary antibody at 1/1000 dilution for 30 minutes.Unlabelled sample was used as a control (cells without incubation with primary antibody; black).
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