Mutations present in a small subset of DNA templates is critical to advances in several areas of biomedical research and healthcare.

Mutation analysis is the process of finding variations in DNA sequences that could be connected to drug reactions, malignancies, or hereditary illnesses. Determining whether these mutations are acquired or inherited is essential for diagnosis, treatment, and prevention.

Research Area:

» Diagnose genetic diseases
» Identify cancer-driving mutations
» Precision Medicine plans
» Predict drug response
» Reproductive decisions and carrier screening
» Assess hereditary disease risk in families

Mutations are genetic changes acquired in germ cells or non-germ (somatic) cells. Mutations can be expressed as insertions, deletions, or base pair changes in coding or non-coding regions..

- ARMS-PCR
- Southern blot
- Next-Generation Sequencing (NGS)

Sanger Sequencing: The gold standard for identifying specific gene mutations, especially when a particular mutation is suspected.

WE SERVE FOR

- Pharmaceuticals – for screening drug candidates
- Cancer Research
- Cosmetics – for in vitro toxicity testing
- Regenerative Medicine and Stem Cell Research
- Toxicology & Safety Testing
- Academic labs – outsourcing time-consuming culture work
- Biomanufacturing

Note : Our custom analysis will provide valid solutions and guarantee a high-quality report for your research. Kindly share the technical details of work for quotation and lead time.

Contact: + 91-9891179928|  E.mail: info@chemgeneics.org