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Genomics Redefines The Boundaries Of Fungal Genomics Product Applications Available In In Singapore
20 applications found
The modular fashion with which Affilin® ligands can be fused together makes creating multi-specific binders an easy task. Combined with varying linker lengths, composition, and orientation, plus the optional addition of further accessory modules, our Navigo experts build the designed molecules as previously planned on the drawing ...
ByNavigo Proteins GmbH based in Halle, GERMANY
Solid tumor-specific Affilin molecules are currently being evaluated as CAR-T ligands. Specifically, they were confirmed to be functionally expressed on the effector cell surface, mediate target cell-binding and effective target cell-killing in a dose-dependent fashion. Importantly they were just as effective as commonly used antibody ...
ByNavigo Proteins GmbH based in Halle, GERMANY
Oligonucleotide refers to a very short single or double-stranded fragment of nucleic acid that can be joined together to form a single-stranded biopolymers. Oligo Pools are customizable genomic research products polymerized from various oligonucleotide fragments, playing an important role in gene synthesis, next-generation sequencing, library preparation, and so ...
ByCD Biosciences - htDNA-chip® based in Shirley, NEW YORK (USA)
Meeting regulatory requirements and maintaining quality doesn’t have to take up a lot of valuable time. With the PCS, MVS, and Artel’s Services, clinical labs can streamline regulatory compliance, maximizing productivity. ...
ByArtel, Inc. by Advanced Instruments based in Westbrook, MAINE (USA)
Metagenomics is the study of all microbial genomes present in an environment, from the bottom of the sea to inside our own bodies. If you have shotgun NGS sequencing data, Partek provides powerful, easy-to-use analysis tools to characterize microbial ...
ByPartek Incorporated based in Chesterfield, MISSOURI (USA)
DNA sequencing refers to the analysis of the base sequence of specific DNA fragments, namely the arrangement of adenine (A), thymine (T), cytosine (C) and guanine (G). The emergence of rapid DNA sequencing methods can greatly promote the research and discovery of biology and medicine. At present, the lowest-cost and high-throughput next-generation sequencing is the most widely used. Next-generation sequencing technology, also known as high-throughput sequencing technology, solves the problem that first-generation ...
ByCD Biosciences - htDNA-chip® based in Shirley, NEW YORK (USA)
Copy number variation (CNV) is a type of structural variation and it encompasses duplication or deletion events that affect a considerable section of the genome. Those events may be mirrored by changes in gene expression levels and are consequently involved in pathogenesis. Partek tools enable you to start with raw data, detect amplified or deleted regions, and interpret or integrate the data with other assays such as gene expression. ...
ByPartek Incorporated based in Chesterfield, MISSOURI (USA)
In the era of global information, traditional storage technologies have been slightly tested. DNA must realize reliable information encoding. Only when DNA becomes a viable competitor of traditional storage technology is the first step for DNA to realize information storage. The most important thing is to produce nucleotide strings cheaply and quickly. For DNA, it is composed of four different monomers, consisting of a deoxyribonucleic acid having a skeleton with phosphoric acid. First, DNA is a polymer biological ...
ByCD Biosciences - htDNA-chip® based in Shirley, NEW YORK (USA)
Cancer is one of the leading causes of deaths in India and a major public health concern. It is estimated that there are around 1 million new cancer cases every year and as many as 5 lakh deaths occur annually. Around 71% of all cancer deaths in India occur in people 30 to 69 years of age, when adults are very productive. The burden of cancer is expected to further increase due to increase in life expectancy, heavy use of tobacco and other risk factors such as radiation, viruses, ...
ByinDNA Research Labs based in , INDIA
Overcome CRISPR delivery limitations with FluidFM: for multiplex genome editing and fast cell line development. The discovery of CRISPR-Cas9 for targeted gene engineering has revolutionized life sciences. Regardless of its broad introduction across many disciplines in biology, several challenges persist in editing cell lines, particularly for sensitive cells, or when multiple edits are required. FluidFM offers a unique in-vitro gene editing tool to improve the efficiency and applicability of CRISPR across a ...
ByCytosurge AG based in Glattbrugg, SWITZERLAND
Single cell RNA-Seq is revolutionizing the study of complex tissues and diseases. The powerful and easy-to-use tools in Partek® Flow® empower researchers to analyze their own single cell RNA-Seq ...
ByPartek Incorporated based in Chesterfield, MISSOURI (USA)
Gene expression is the most fundamental level at which the genotype gives rise to a phenotype. Whether you have RNA-Seq, qPCR or microarray data, Partek provides easy-to-use tools that guide you through the analysis process from start to finish within a point-and-click interface. With over 8,000 citations, see why our gene expression analysis tools are the most trusted in the genomics ...
ByPartek Incorporated based in Chesterfield, MISSOURI (USA)
At the end of 2019, a novel coronavirus was identified as the cause of a cluster of pneumonia cases in Wuhan, a city in the Hubei Province of China. The severity and rapid spread of COVID-19 (caused by SARS-CoV-2), resulted in a global pandemic declared by the World Health Organization in March 2020. The virus has spread to more than 100 countries, including the United ...
ByNovavax based in Gaithersburg, MARYLAND (USA)
Förster resonance energy transfer (FRET) is a phenomenon of non-radiative transfer of the optical excitation from an excited electronic level of one molecule, called the donor, to a resonant electronic level of another molecule, called the acceptor. In ...
ByEdinburgh Instruments - TECHCOMP Group based in , UNITED KINGDOM
Unlike conventional vaccination strategies, cancer vaccines are designed to mount responses against tumor-specific antigens, arising from somatic mutations specific to the cancer genome. They promise a highly tailored approach by targeting patient-specific ...
ByEnpicom B.V. based in s-Hertogenbosch, NETHERLANDS
Whole genome, exome, or targeted panel DNA sequencing (DNA-Seq) studies can identify genetic variants that contribute to disease and phenotypes. Partek offers powerful and easy-to-use tools for processing and analyzing your DNA sequencing data. With the latest databases and bioinformatics tools available in a point-and-click interface, variant analysis is simple. ...
ByPartek Incorporated based in Chesterfield, MISSOURI (USA)
Realize the value of global clinical and genomic data with us. We help reduce your risk, enhance your pipeline value and advance your enterprise data strategy by solving the barriers of data access and enabling rapid insight ...
ByBC Platforms based in Zürich, SWITZERLAND
Isolating edited-pluripotent stem cells with traditional sorting techniques can subject the cells to rough conditions in which gene expression, genomic stability and overall cell-health can become compromised. Microfluidic cell sorting with the WOLF, along with single cell deposition using the N1 single cell dispenser, eliminates the challenges that pluripotent stem cells face by sorting at gentle pressures without decompression shock and shear stress, and allow for efficient single cell deposition for high ...
ByNanoCellect Biomedical, Inc. based in San Diego, CALIFORNIA (USA)
Sample preparation is a significant yet underappreciated step that allows for high quality sequencing and analysis, critical to achieving breakthroughs in medicine, agriculture, and other industries. NanoCellect’s microfluidic cell sorter, the WOLF, allow the cell’s integrity to be maintained for numerous sequencing and multi-omics techniques. The WOLF’s ability to flexibly fit into any genomic researcher’s lab, make it a key step to any cell sequencing analysis workflow. 10x Genomics ...
ByNanoCellect Biomedical, Inc. based in San Diego, CALIFORNIA (USA)
Microbe Inotech Laboratories, Inc. provides a microbial genomics platform through licensed database agreements focused on the characterization of microorganisms, pathogens and anti-microbial resistance for pathogen detection, food safety inspections and issues, pharmaceutical discovery, public health surveillance, water and wastewater analysis, agriculture and microbiome analysis and comparisons. From a post-sequencingmetagenomic sample (i.e. DNA extracted from your sample) the MiL Inc. provides identification ...
ByPluton Biosciences, Inc. based in St. Louis, MISSOURI (USA)