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Research Article Open access CC BY 4.0

Tissue Specific Genomic and Proteomic Profiling in Albino Wistar Rat

Raja Saha, Tuhin Khaddar, Sanchari Pal, Arpita Singha, Anirban Chakraborty, Riya Samai, Ipsita Koley, Santashree Maity, Tiyasa Roy, Rajashree Panda, Rimpi Samanta, Arijit Chakraborty, Mitusi Koley, Debojyoti Pradhan, Mousumi Shit, Santipriya Maity, Sunanda Shit, Taslima Nasrin, Daliya Panja, Priti Roy, Sangita Maiti Dutta

Asian Journal of Biochemistry, Genetics and Molecular Biology · pp. 10–19 · Published 1 May 2026

10.9734/ajbgmb/2026/v18i5538

Abstract

Animal tissues from Albino Wistar rats provide a valuable model to compare uniform genomic DNA with tissue-specific protein expression, enabling baseline molecular profiling across organs. This study aimed to isolate high-quality genomic DNA and characterize tissue-specific protein expression profiles from liver, kidney, lung, and brain tissues of albino Wistar rat (Rattus norvegicus). Genomic DNA was extracted using the phenol-chloroform method and evaluated by spectrophotometric analysis and agarose gel electrophoresis. All samples exhibited high purity (A260/A280: 1.80-1.97) and intact high-molecular-weight DNA bands with minimal degradation. Total protein was quantified using the Lowry method, demonstrating tissue-dependent variation, with the highest concentration observed in liver (93 µg/mL), followed by kidney (86 µg/mL), lung (78.6 µg/mL), and brain (76.5 µg/mL). SDS-PAGE analysis revealed distinct and complex banding patterns across tissues, reflecting differential protein expression profiles. Despite uniform genomic integrity across tissues, proteomic heterogeneity was evident, consistent with organ-specific functional specialization. This study provides baseline comparative molecular profiling across rat tissue and establishes reliable protocols for simultaneous genomic and proteomic analysis and provides baseline molecular data for future biomedical and toxicological investigations.

Rattus norvegicus genomic DNA isolation protein estimation SDS-PAGE electrophoresis

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