10.22376/ijpbs.2019.10.1.p1-12 Volume 5 Issue 3 2014 (July- September) Isolation of high quality of RNA is prerequisite for functional genomics studies. It is quite difficult to get quality RNA from recalcitrant tissues, due to large amounts of secondary metabolites and other interfering compounds. We have encountered this problem in isolation of RNA from the lessThan i greaterThan Ziziphus mauritiana lessThan /i greaterThan Lam which is a xerophytic plant. To overcome this problem, we have developed an improved CTAB-PVPP-LiCl method. In this protocol we have used insoluble PVPP for removal of polysaccharides and phenolic compounds and acidic phenol for efficient partition of RNA. In addition to these two modifications, 8M LiCl precipitation step was included for preferential precipitation of RNA. The RNA isolated was found to be of high quality from both roots and leaves of normal and abiotic stressed plants as evidenced from the downstream applications such as RT-PCR and qRT-PCR. SRAVANI KONDURU, CHANDRA OBUL REDDY PULI, JAYANNA NAIK BANAVATH, VARAKUMAR PANDIT, KRISHNA KUMAR GUDURU AND CHANDRA SEKHAR AKILA Ziziphus mauritiana, Polysaccharides, Polyphenols, RNA isolation, RT-PCR, qRT-PCR 658-665