Molecular Diagnostics Product

Convenient storage: 

The samples in the Cell Free DNA blood collection tube can remain stable for up to 14 days at 6 °C to 37 °C, making sample collection, transportation and storage more convenient.

Stable storage: 

The collection tube contains unique anticoagulation and preservation reagents, which can stabilize nucleated blood cells, prevent the release of cellular genomic DNA, inhibit the nuclease-mediated degradation of free DNA, and contribute to the overall stability of free DNA.

NeoMag DNA extraction kit  contains all the necessary reagents and materials required for magnetic DNA extraction, making the process easier and more efficient. The kit is designed to simplify DNA extraction from various sample types, including blood, tissue, cells, saliva, and more.

NeoMag magnetic bead cell-free DNA (cfDNA) extraction kit is specifically designed to isolate cell-free DNA from biological samples such as plasma or serum. Cell-free DNA refers to fragmented DNA that circulates freely in bodily fluids, often originating from apoptotic or necrotic cells. The kit utilizes magnetic beads coated with molecules that bind specifically to cfDNA, enabling efficient isolation and purification of cfDNA from complex sample matrices.

• High Yield of Pure DNA:
  • NeoTyper       Silica column technology efficiently captures and binds DNA, resulting in       a high yield of pure DNA. This is crucial in diagnostic labs where the       quantity and quality of DNA are often limited.
• Versatility Across Sample Types
  • NeoTyper       Silica column-based DNA extraction kits are versatile and can be used       with various sample types including blood, saliva and swabs.

The NeoBead NGS Purification system is based on paramagnetic bead technology, designed for efficient purification of nucleic acid fragments as well as a single- or double-sided size selection of libraries following the fragmentation, ligation, and PCR steps in the next-generation sequencing (NGS) library preparation workflow.

Highly reproducible selection of the user-defined fragment range excellent recovery of fragments and efficient 

NeoDye Terminator Cleanup is an advanced paramagnetic bead-based system

designed to eliminate unincorporated dye terminators from Sanger sequencing

reactions.The process involves three simple steps:

1. Binding

2. Washing and

3. Elution.

Key Features

1. Efficient elimination of sequencing reaction contaminants

2. 28 Long Phred 20 read lengths averaging over 800 bps

3. Pass rates more than 85%

Exo SAP is commonly used in molecular biology and genetics research for the removal of excess primers and dNTPs from PCR reactions before further analysis, such as sequencing or genotyping. 

After performing PCR to amplify specific DNA fragments, there are often residual primers and nucleotides (dNTPs) in the reaction mixture. 

NeoZyme Exo SAP Kit contains a combination of two enzymes – Exonuclease 1 and Shrimp Alkaline Phosphatase (SAP). These enzymes work together to remove unincorporated prim

NeoDye terminator kit is a highly flexible and robust dye terminator chain reaction kit to give uniform peaks and is compatible to give high quality results on all the available genetic analyzer platforms in the market.

NeoDye terminator Kit generates sequencing data with 

● Uniform Peak Heights

● Optimized Signal Balance

● High Quality Reads

● Highly Accurate Base Assignments 

NeoTyper Y chromosome microdeletion STR (Short Tandem Repeat) kit is a molecular diagnostic tool designed to identify deletions within the Y chromosome. This kit is used in the field of reproductive medicine to assess male infertility, as Y chromosome microdeletions can be associated with impaired sperm production.he targeted regions often include the AZF (Azoospermia Factor) regions, namely AZFa, AZFb, and AZFc

Unlock the potential of genetic analysis with our cutting-edge STR Kit. Short Tandem Repeats (STRs) are key markers in DNA, providing unparalleled accuracy in paternity testing and chimerism STR typing. Our STR Kit is designed to deliver precise results, making it an indispensable tool for diagnostic labs. 

NEOTYPER AUTOSOMAL STR Kit is a 6-dye STR amplificaNon system that simultaneously amplifies 23 autosomal STR loci, 3 Y chromosome STR loci, Amelogenin and one Yindel.
 

FMR1 (Fragile X Mental Retardation 1) is a gene located on the X chromosome, and mutations in this gene can lead to Fragile X syndrome, which is a genetic disorder associated with intellectual and developmental disabilities. Sanger sequencing can is used for detecting mutations or expansions of the FMR1 gene.

Microsatellite instability (MSI) is a molecular phenotype that is often associated with certain types of cancer, including colorectal cancer. MSI is characterized by changes in the length of microsatellite repeat sequences within the genome, resulting from DNA replication errors. Detection of MSI is important for cancer diagnosis and prognosis, as it can influence treatment decisions and patient outcomes.

SMN1 (Survival Motor Neuron 1) is a gene associated with spinal muscular atrophy (SMA), a genetic disorder that affects motor neurons in the spinal cord and leads to muscle weakness and atrophy. Detecting mutations or variations in the SMN1 gene using Sanger sequencing is an important diagnostic approach for SMA.

The iSeq 100 Sequencing System makes next-generation sequencing easier and more affordable than ever. Designed for simplicity, it allows labs of all sizes to sequence DNA and RNA at the push of a button. Discover more without the cost.

The MiniSeq System offers a simple, affordable solution. Advance your research with proven Illumina NGS technology. Perform a broad range of targeted DNA and RNA applications in your own lab on your own schedule.

Access focused applications such as targeted resequencing, metagenomics, small genome sequencing, targeted gene expression profiling, and more. MiSeq reagents enable up to 15 Gb of output with 25 million sequencing reads and 2 × 300 bp read lengths.

Explore current and emerging applications with higher efficiency and fewer restraints.

• Flexibility and scalability to expand the breadth of applications you can perform on a benchtop system. 

• Operational simplicity with load-and-go cartridges and integrated onboard informatics.

• Improved run economics with high output to support larger studies and data-intensive methods.

• With fast, accurate results, extensibility from 10 gb up to 360 Gb,

The NovaSeq X and NovaSeq X Plus Sequencing Systems deliver extraordinary throughput and accuracy to perform data-intensive applications at production scale.

Scale your studies with three flow cell types and up to 16 Tb output per run on the dual flow cell NovaSeq X Plus system or up to 8 Tb on the single flow cell NovaSeq X system. Ultra-high-density flow cells and ultra-high-resolution optics enable output of up to 26 billion single reads per flow cell.