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1 Introduction 1.1 Intended use The smart Blood DNA Midi prep (m) has been designed for manual isolation of high molecular weight genomic DNA from peripheral blood mononuclear cells (PBMC) derived from fresh or frozen blood stabilized with EDTA, citrate or heparin. The kit utilizes the new SmartExtraction technology invented by Analytik Jena (patent ...
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1 Introduction 1.1 Intended use The smart DNA prep (m) kit has been designed for the manual isolation of high molecular weight genomic DNA (200 kb - > 500 kb) from tissue samples, eukaryotic cells, rodent tails, bacteria and ...
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1. Introduction Automation of library preparation is very important to reduce opportunities for error, increase reproducibility, and reduce the amount of hands-on time allowing researchers to generate sequence data from DNA more efficiently. By utilizing the CyBi-FeliX, a benchtop instrument for a variety of automated liquid handling tasks, the HaloPlex Target Enrichment System Kit for NGS ...
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1. INTRODUCTION Analytik Jena's blackPREP FFPE DNA Kit is optimized for DNA extraction from a variety of FFPE (formalin-fixed, paraffin-embedded) tissue sample, e.g. adipose tissue, pancreatic tissue or placenta as starting ...
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1 Introduction 1.1 Intended use The kit has been designed as a tool for very fast and efficient isolation of genomic DNA from small amounts of different types of forensic samples like, hairs or hair roots; stains of blood, saliva or sperm; finger nails; cigarette butts; bubble gum; buccal swabs; stamps and envelopes as well as fingerprints on different surfaces. The kit is intended for use by ...
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Background information The only effective way to combat a disease like cancer is to understand it. And as we work to understand cancer, analyzing DNA methylation has come to play an increasingly important role, providing more meaningful information on tumorigenesis, tumor progression and metastasis. Malignant tumors exhibit abnormal DNA methylation - following a pattern differing significantly ...
CD Genomics provides a complete list of transcriptomics sequencing to meet the needs and budgets of our clients. Transcriptomic sequencing can be used for differential expression analysis, detection of mutations (SNPs/InDels), and functional annotation. This is a brief overview of our transcriptomic services. Visit https://www.cd-genomics.com/Transcriptomics.html for more facts. ...
Transposase is an enzyme that binds to the end of a transposon and catalyzes its movement to another part of the genome by a “cut and paste” mechanism or a replicate transposition mechanism. Tn5 Transposase (Tnp) is a member of the RNase superfamily of proteins which includes retroviral integrases. ...
The µ-Grinder 96 is a grinder developed to carry out varietal selection of plants by molecular markers from grains. It is characterized in particular by its pestle-mortar technique specially designed to grind plant matrices in very small ...
iGene Labserve Pvt. Ltd. is gaining recognition by offering resilient, innovative solutions in laboratory instrumentation across healthcare, genomics, drug discovery, biopharma, and food & beverage sectors. We strive to enhance lab efficacy and reduce challenges through advanced technologies and a diverse product portfolio tailored to our customers’ needs. ...
CD Genomics provides a complete list of transcriptomics sequencing to meet the needs and budget of our clients. Transcriptomic sequencing can be used for differential expression analysis, detection of mutations (SNPs/InDels), and functional annotation. This is a brief overview of our transcriptomic services. Visit https://www.cd-genomics.com/Transcriptomics.html for more facts. ...
Invitrogen and Gibco TrueCut Cas9 proteins are designed to deliver consistently higher editing efficiency across a wide range of gene targets and cell types. We now offer three versions of our leading Cas9 protein to better meet your genome editing ...
CD Genomics provides a wide range of epigenomics sequencing services to meet the needs and budget of our clients. They can be used for many purposes, including detection of various methylations, elucidation of mechanisms of complex disease, disease diagnosis, and translational discovery. ...
Clinical interpretation has been one of the most complex and time-consuming aspects of transforming genomic data into meaningful results, until now. ...
CD Genomics provides a wide range of epigenomics sequencing services to meet the needs and budget of our clients. They can be used for many purposes, including detection of various methylations, elucidation of mechanisms of complex disease, disease diagnosis, and translational discovery. https://www.cd-genomics.com/Epigenomics.html ...
To complement our SGS solutions, CD Genomics offers PacBio SMRT sequencing and Oxford Nanopore sequencing. We provide advanced solutions for genomic, transcriptomic, and epigenetic studies by utilizing long-read single-molecular sequencing. Our highly skilled and knowledgeable team can assist you with any procedure to ensure accurate and unbiased findings. ...
FUSION GENOMICS ONETest platform offers a complete 12 hours “Benchtop to Desktop” solution for next generation sequencing based diagnostic testing of infectious diseases. The ONETest platform comprises our patent pending and proprietary UNIPrep, QUANTUMProbes and the FUSIONCloud with 1000X the sensitivity over PCR and up to 9000X target enrichment over metagenome sequencing. The ...