Medical Genomics Downloads
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BEC - Model SARS-CoV-2 RT - Lamp Kit brochure
BEC SARS-CoV-2 RT-LAMP system is designed for the rapid detection of SARS-CoV-2 genome on the field. It is composed of reagent kits and a dedicated reading instrument. The tests have been developed by Bertin Technologies and Enalees to allow a fast and easy molecular testing solution during the Covid-19 ...
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Hanabi - Model PV - Mini Metaphase Spreader - Brochure
HANABI-PV Metaphase AutoSpreader mini is the automatic compact equipment for the chromosome metaphase specimen slide of the ideal spreader for the chromosome analysis such as FISH, CGH, and G-banding HANABI PV Metaphase Auto-Spreader is chromosome metaphase specimen making device that succeeded the structure of chromosome metaphase spread device "HANABI" admitted in the world. Samples number 48 ...
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Croyez - Model His-SUMO tag, HEK293 - Human Coronavirus (NL63) Nucleocapsid Protein - Brochure
Nucleocapsid protein (NP) packages the positive strand viral genome RNA into a helical ribonucleocapsid (RNP) and plays a fundamental role during virion assembly through its interactions with the viral genome and membrane protein M. NP also plays an important role in enhancing the efficiency of sub-genomic viral RNA transcription as well as viral replication. This product is composed of a DNA ...
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Beyond Sequencing CRISPR Gene Editing Assessment and Quality Control Using Next-Generation Sequencing
Sequencing-based genome editing validation can detect whether alleles of a gene have been edited correctly, identify insertion and deletion sites at the whole-genome level, and screen and identify monoclonal cell lines. In addition,it is an excellent way to study the off-target effects of CRISPR gene editing. ...
By CD Genomics
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The Broad Prospects of miRNA Research
The use of the latest high-throughput technologies, such as miRNA microarrays and miRNA-Seq, allows further in-depth research on the mechanism by which miRNA functions. CD Genomics excels at providing a comprehensive portfolio of sequencing services. Our miRNA-Seq and miRNA microarray will help you study the role of miRNAs in cell differentiation, biological development, disease development, and ...
By CD Genomics
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The Time is Now for Bacteriophage Research
Sequencing technologies, genomics,and bioinformatics are rapid and effective tools to study phage genomics. In addition, further analysis,including transcription,translation, regulation, and modification, is also emerging as a technique that is extremely helpful in exploring the life cycle, specificity, lytic ability, and lysogenicity of phages. ...
By CD Genomics
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Model V-130-50/V-130-250 - Blood & Tissue Genomic DNA Extraction System - Datasheet
GSI Blood & Tissue Genomic DNA Extraction System provides a simple and fast way to purify genomic DNA (including viral or mitochondrial DNA) from various sources such as blood, plasma, serum, buffy coat, lymphocytes and body fluids. A simple spin column procedure can purify pure DNA (approximately 20-30 kb fragment) for PCR, enzymatic reactions, and other downstream applications. 0.2 ml whole ...
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Clean Genome E. coli Electrocompetent Cell Protocol - Datasheet
Transformation efficiency is tested using pUC19 Control DNA, in duplicate. Transformed cells are plated onto LB plates containing 50 µg/mL carbenicillin. Transformation efficiency is > 5 x 109 cfu/µg DNA for the core Clean Genome® E. coli strain, but may be lower for strains carrying mutations that reduce recombination and or mutation ...
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Microbiome and Metabolome Research
Gut microbes provide energy to microbiota by digesting food residues and releasing metabolites for the gut, affecting the host if they enter the host's circulatory system. Conversely, intestinal metabolites can influence the composition, gene expression, and gut microbiota-derived metabolites. ...
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Characterizing Complete Plasmid DNA Sequencing Analysis from P. larvae tetracycline-resistant Strains
Plasmid-mediated gene transfer plays an important role not only in the mobilization and dissemination of antibiotic resistance and virulence genes but also in microbial population evolution.CD Genomics offers complete plasmid DNA sequencing services and improved bioinformatics pipelines that deliver reliable and accurate data. https://www.cd-genomics.com/complete-plasmid-dna-sequencing.html ...
By CD Genomics
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Gexscope - Single Cell V(D)J Kit - Brochure
GEXSCOPE Single Cell V(D)J Kit enables simultaneous detection of T-cell or B-cell receptor gene expression, together with whole transcriptome expression at single-cell level. ...
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Model VPK-401 - AAV-1 Helper Free Packaging System - Manual
Adeno-associated viruses (AAVs) are derived from defective parvoviruses, which depend on essential helper functions provided by other viruses, such as adenovirus and herpes virus, for efficient viral replication and propagation. AAV has no etiologic association with any known diseases and has been successfully used to establish efficient and long-term gene expression in vivo in a variety of ...
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AtlasXomics - Model DBiT-seq - Spatial Multi-Omics Platform Technology with Cellular Resolution - Brochure
The DBiT-seq discovery platform combines microfluidics with next generation sequencing. The process starts by adding multi-omic probes (e.g., for mRNA, genomic DNA, or proteins) directly to a tissue section. Sequentially and orthogonally applied microfluidics chips deliver x-barcodes and y-barcodes, creating an in situ x-y coordinate system in tissue. Each intersection area between a ...
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Beyond Sequencing CRISPR Gene Editing Assessment and Quality Control Using Next-Generation Sequencing
Sequencing-based genome editing validation can detect whether alleles of a gene have been edited correctly, identify insertion and deletion sites at the whole-genome level, as well as screen and identify monoclonal cell lines. In addition, it is an excellent way to study the off-target effects of CRISPR gene editing. NGS is a massively parallel sequencing strategy that allows for higher ...
By CD Genomics
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High-Throughput Genotyping Paves the Way in Genomics
Single-nucleotide polymorphisms (SNPs) are found in both coding and non-coding regions of genes, one of the most common types of variation; single nucleotide variants (SNVs) are characterized by changes in a single position within the DNA sequence, including conversions, reversals, insertions or deletions, with a variable frequency of >1%. In humans, approximately 3 ×10° SNPs were found, with an ...
By CD Genomics
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High-Throughput Genotyping Paves the Way in Genomics
Single-nucleotide polymorphisms (SNPs) are found in both coding and non-coding regions of genes, one of the most common types of variation; single nucleotide variants (SNVs) are characterized by changes in a single position within the DNA sequence, including conversions, reversals, insertions or deletions, with a variable frequency of >1%. In humans, approximately 3 ×10° SNPs were found, with an ...
By CD Genomics
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Sequencing Approach Enables More In-depth Phageome Investigation
CD Genomics, an advanced sequencing service provider equipped with extensive technologies and knowledge in phageome, is now ready to provide comprehensive Phage Genome Sequencing and Metagenomics Services. https://www.cd-genomics.com/Microbial-Whole-Genome-Sequencing.html ...
By CD Genomics
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Unchained - Model Lunatic - Protein and Nucleic Acid Quantification System Datasheet
Lunatic, our next-gen UV/Vis absorbance spectrometer, makes batch quantification of protein, DNA and RNA a no-brainer. All you need is 2 μL and 10 minutes to measure up to 96 samples. Run them straight-up, even at high concentrations, without ever diluting. Lunatic gets biologics and genomics UV/Vis quantification on the money every time. Just drop, load and read. ...
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Genomic DNA - Brochure
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