5 mM, and after induction at 37 C for 6 h, the E coli was harves

5 mM, and after induction at 37 C for 6 h, the E. coli was harvested by centrifugation at 3000 rpm. rECP and mECP were collected from inclu sion bodies that were refolded by dialysis in refolding buffer. The purified rECP and mECP were concentrated by Amicon Ultra 15 and stored in phosphate buffered saline at 80 C until use. After purification, we used Endotoxin new product Removing Gel to remove LPS before rECP storage and also checked LPS residual level by HEK Blue LPS Detection Kit before each treatment. MTT cell viability assay The toxicity effect of rECP on cell viability was deter mined by a colorimetric assay using 3 2,5 diphenyltertrazolium bromide as described. Briefly, cells were seeded in 96 well plate and incu bated overnight at 37 C, 5% CO2. The cells were treated with the indicated concentration of rECP.

After treatment with rECP for 48 h, 10 ul MTT was added to 90 ul of culture medium well Inhibitors,Modulators,Libraries for 4 h. Levels of MTT were determined by measuring the absorbance at 570 nm. Detection of chromatin condensation Hoechst 33342 was added 20 min prior to the end of the incubation period in the dark. The cells were washed with cold PBS twice and fixed with 3. 7% formaldehyde for 15 min. The nuclei of apoptotic cells were observed by fluorescence microscopy. Detection of apoptosis by sub G1 fractions and Annexin V FITC To determine the sub G1 fractions, detached BEAS 2B cells were fixed in 75% ethanol at 20 C overnight and centrifuged at 1000 g for 5 min to remove ethanol, followed by treatment with 50 ug ml RNase A and staining with Inhibitors,Modulators,Libraries 50 ug ml propidium iodide on ice for 30 min in the dark.

The stained cells were analyzed by fluorescence activated cell sorting according to the manufac turers instructions. The Inhibitors,Modulators,Libraries levels of early apoptosis were determined using the Annexin V FITC Apoptosis Detection Inhibitors,Modulators,Libraries kit. The method was per formed as described with minor modification. After trypsinization, BEAS 2B cells were washed twice with cold PBS and resuspended in 1�� binding buffer. The cell suspension was transferred to 5 ml tubes, and 5 ul annexin V was added. After incubation with annexin V for 5 min at 4 C, 5 ul PI was added. The cells were incubated at 4 C in the dark for 15 min, and 800 ul of binding buffer was added before FACS analysis. Detection of mitochondrial membrane potential Inhibitors,Modulators,Libraries To determine MMP, the detached BEAS 2B cells were stained with 100 nM MitoTracker Red CMXRos in RPMI medium for 20 min at 37 C in the dark. After typsinization, kinase inhibitor Erlotinib the stained cells were ana lyzed by FACS. Fluorescence of PI was collected in the FL2 or FL3 detector, and fluorescence of MitoTracker was collected in the FL3 detector. All data were evalu ated using Cell Quest software.

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