Sanger Sequencing has been extensively used to advance the field of functional and comparative genomics, evolutionary genetics and complex disease research. This method was first employed in sequencing the first human genome in 2002.Its suitability for routine validation of cloning experiments and PCR fragments, Sanger Sequencing remains a popular technique in most laboratories across the world. Experience the quality services with e-nnovation Life Sciences.
Key advantages of Sanger Sequencing are:
- Targeting smaller genomic regions in a larger number of samples
- Sequencing of variable regions
- Validating results from next-generation sequencing (NGS) studies
- Verifying plasmid sequences, inserts, mutations
- HLA typing
- Genotyping of microsatellite markers
- Identifying single disease-causing genetic variants
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