Secreted neural apoptosis inhibiting proteins
An apoptosis inhibitor protein, secreted technology, applied in the field of molecular biology
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[0175] RNA extraction: The cultured cells or tissue homogenate were lysed in 1.5 ml Trizol (Gibco, Cat. No. 15596) per 10 cm culture dish or 50 mg tissue homogenate, respectively. The lysate was pipetted multiple times to homogenize the lysate (and subsequently transfer the cell lysate to a tube). After homogenization, the lysates were incubated at 30°C for 5 minutes to completely dissociate the nucleoprotein complexes. After incubation, chloroform was added to the lysate at a ratio of 0.2 ml chloroform (Sigma, Cat. No. C53 12) per 1 ml Trizol reagent, and the tube was shaken vigorously for 15 seconds. The lysates were then incubated at 30°C for 3 minutes. After incubation, the lysates were centrifuged at 12,000 xg for 15 minutes at 4°C. After centrifugation, remove the supernatant and rinse the remaining RNA pellet with 70% ethanol. The rinsed samples were then centrifuged at 7500 xg for 10 minutes at 4°C, and the resulting supernatant was discarded. The remaining RNA pel...
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