Amplicon Biotech Services
Amplicon Biotech provides the following Custom Services which will make difference for thousand of researchers over the period of time. As the most trusted company, we're proud to provide flexible and reliable services to accelerate your research in collaboration with the world leaders.
The Most preferable and useful services for research are:-
- Protein & Peptide Synthesis.
- Gene synthesis & Gene Cloning
- Primer synthesis
- Probe designing
- Antibody Customization
- NGS(Next Generation Sequencing)
A primer is a short single strand of RNA or DNA (generally about 18-22 bases) that serves as a starting point for DNA synthesis. It is required for DNA replication because the enzymes that catalyze this process, DNA polymerizes, can only add new nucleotide to an existing strand of DNA. The polymer starts replication at the 3′-end of the primer, and copies the opposite strand.
In molecular biology, a hybridization probe is a fragment of DNA or RNA of variable length (usually 100–1000 bases long) which can be radioactively labeled. It can then be used in DNA or RNA samples to detect the presence of nucleotide sequences (the DNA target) that are complementary to the sequence in the probe. We have collaboration with the world leaders in probe designing services and provide the best solutions to all the research institutes in India.Ask for Price
Antibody Customization in the development of thousands of products and reagents is your assurance that we can provide you with the results.Antibody Customization many customization options are available, such as antibody conjugation, nationalization, custom via ling & allotting, and antibody validation by Western blot, ELISA, or precipitation.We offer expert consulting as well as molecular assay, antibody.
Next generation sequencing (NGS), massively parallel or deep sequencing are related terms that describe a DNA sequencing technology which has revolutionized genomic research. Using NGS an entire human genome can be sequenced within a single day. In contrast, the previous Sanger sequencing technology, used to decipher the human genome, required over a decade to deliver the final draft By understanding the sequence of DNA, researchers have been able to elucidate the structure and function of proteins as well as RNA and have gained an understanding of the underlying causes of disease. Next Generation Sequencing (NGS) is a powerful platform that has enabled the sequencing of thousands to millions of DNA molecules simultaneously. This powerful tool is revolutionizing fields such as personalized medicine, genetic diseases, and clinical diagnostics by offering a high throughput option with the capability to sequence multiple individuals at the same time.Ask for Price