With all the necessary tools, we provide a variety of carefully formulated nucleic acid purification and isolation kits that make it simple, quick, and highly sensitive to extract DNA and RNA from tissue and cell samples.
Genomic sequencing has been implemented into clinical practise with the help of next generation sequencing (NGS). Clinically relevant target sequences have been incorporated into NGS-based gene panel assays, creating useful diagnostic tools that allow for tailored cancer patient care.
Numerous widely used molecular biology tools, include DNA/RNA extraction kits, ribosomal RNA removal tools, and PCR tools.
A semi-quantitative method called MLPA is used to find copy number variations linked to diseases. It was created as a proprietary method for the detection of copy number variations, which is currently used all over the world to investigate tumours and genetic diseases and is regarded as the gold standard in this field.
The study of chromosome composition, placement, and capacity in a cell is known as cytogenetics, and it entails looking at chromosome quantity and appearance, the precise locations of genes on chromosomes, and chromosomal behaviour during cycles of cell division. Chromosome abnormalities can be detected through hereditary material expansion, deletion, rearrangement, or correction. Chromosome analysis rules out the possibility that these aberrations are a sign of phenotypic abnormalities in the patient or their infectious states.
The parallel processing sequencing technology known as “next-generation sequencing” (NGS) provides extremely high throughput, scalability, and speed. Using this approach, the nucleotide sequence of entire genomes or specific DNA or RNA portions can be ascertained. The biological sciences have undergone a revolution thanks to NGS, which enables laboratories to carry out a wide range of tasks and investigate biological systems at a depth never before imaginable.
Devices and systems used to identify, treat, or prevent diseases are known as IVD products. They are intended for use in gathering and analysing biological samples like blood, saliva, or tissue. Samples may be drawn from a vein, a fingerstick, the back of the throat, the inside of the nose, or other locations.
The development of Next Generation Sequencing (NGS) technology and the corresponding decrease in sequencing prices have made it possible to profile biological systems at unprecedented throughputs while also saving money.
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