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doi: 10.1210/er.2007-0006

2B due to the difference in flow rate within the employed methods (0.4 mL min 1 for SEC HPLCMS compared to 0.8 mL min 1 for SEC HPLCUV)

Generation of Gstt1-mCherry Cell Line, FACS and RNA Sequencing Endogenous tagging of murine Gstt1 To create Gstt1-mCherry tagged cell lines, we generated an integration donor made of two 750 bp homology arms flanking the stop codon of murine GSTT1 followed by a selection cassette containing GFP and hygromycin

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Does the type of GnRH analogue used, affect live birth rates in women with endometriosis undergoing IVF/ICSI treatment, according to the rAFS stage