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Non-invasive imaging of XBP-1-venus fusion protein in ERAI mouse retina in vivo. Twenty-four hours after intravitreal injection of either tunicamycin at 0.1 μg/eye or N-methyl-D-aspartate (NMDA) at 40 nmol/eye, the fluorescence intensity arising from XBP-1-venus fusion protein was visualized in the retinas of anesthetized animals using an ophthalmoscope fitted with a fluorescence filter.
