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AmniSure ROM Test RPT (25) Multilang 1
For the detection of PAMG-1 in amniotic fluid found in vaginal discharge of pregnant women
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QIAGEN OneStep Ahead RT-PCR kit
For faster one-step RT-PCR with high sensitivity, specificity and fidelity
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S_9747_QuantiNova_LNA_PCR_Custom_Assay
For in-depth, accurate and reliable gene expression analysis using LNA-enhanced SYBR® Green-based PCR
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Custom 96- and 384-well plates of LNA-enhanced, SYBR® Green-based miRNA qPCR assays
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For exceptionally sensitive and specific miRNA profiling using LNA-enhanced, SYBR® Green-based miRNA qPCR
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For quick and easy quality control of miRNA samples prior to SYBR® Green-based qPCR profiling
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For quality control of the RNA isolation and cDNA synthesis steps of miRCURY LNA miRNA PCR experiments
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For exceptionally sensitive and specific miRNA profiling using LNA-enhanced, SYBR® Green-based miRNA qPCR
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For setup and optimization of miRNA quantification experiments using SYBR® Green-based qPCR
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For extremely sensitive and accurate quantification of mature miRNA using LNA-enhanced, probe-based qPCR
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For extremely sensitive and specific miRNA quantification using LNA-optimized, SYBR® Green-based miRNA PCR
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For in-depth pathway- or disease-specific gene expression analysis using LNA-enhanced, SYBR® Green-based PCR
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For in-depth pathway- or disease-specific gene expression analysis using LNA-enhanced, SYBR® Green-based PCR
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For accurate and reliable lncRNA quantification using LNA-enhanced, SYBR® Green-based PCR
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For in-depth pathway- or disease-specific gene expression analysis using LNA-enhanced, SYBR® Green-based PCR
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For high-performance PCR with the miRCURY LNA miRNA Probe PCR System
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For setup and optimization of miRNA in situ hybridization (ISH) experiments
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For ultra-sensitive and specific miRNA detection by in situ hybridization (ISH) or Northern blotting
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For ultra-sensitive and specific detection of novel miRNA sequences by in situ hybridization (ISH) or Northern blotting
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For studying the effects of an individual miRNA on a single target site
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For real-time PCR-based microbial detection; includes one assay and everything required for a successful qPCR run for 20 reactions
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For real-time PCR-based microbial detection; includes one assay with Microbial qPCR Mastermix for 100 reactions
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For real-time PCR-based, application-specific microbial identification or profiling
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Investigator STAR Lyse&Prep Kit (400)
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Forensic, human identity, biosecurity application을 하기 위한 BioRobot EZ1 시스템과 BioRobot EZ1 Advanced 시스템을 이용하여 DNA를 자동으로 분리 정제할 수 있습니다
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For buccal and saliva samples
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QuantiNova Pathogen +IC Kit (500)
For ultrafast, simultaneous detection of viral RNA/DNA and bacterial DNA, including internal control
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For efficient collection and recovery of DNA including crime scene trace and epithelial cells
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To aid in the diagnosis of preterm labor (PTL)
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therascreen EGFR Plasma RGQ PCR Kit 24, V1
For sensitive detection of clinically proven somatic mutations in the EGFR oncogene, on cfDNA (circulating-free DNA) extracted from plasma samples
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For sequencing-based detection and quantitation of cancer-related gene mutations in the NRAS gene
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For quantitative detection of cytomegalovirus DNA using real-time PCR
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In vitro diagnostic를 목적으로 사용하기 위해 human plasma와 serum에서 viral nucleic acid를 분리정제할 수 있습니다
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therascreen EGFR 29 RGQ PCR Kit (24)
For the confident detection of mutations in the EGFR oncogene
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For targeted sequencing of established autosomal and Y-STR markers
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OEM by QIAGEN offers bulk manufacturing of Exonuclease I in custom formulations.
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OEM by QIAGEN offers bulk manufacturing of E. coli Pyrophosphatase in custom formulations.
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Messophilic, highly processive, replicative DNA Polymerase
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For effectively hydrolyzing inorganic pyrophosphate (PPi), helping maintain the enzymatic activity
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For estimation of appearance and biogeographic ancestry with community-approved SNPs
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For exceptionally high synthesis and replication fidelity rates due to highly processive DNA polymerase
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For binding and stabilizing single-stranded DNA (ssDNA) during various DNA polymerase-mediated reactions
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For fast, targeted whole genome library preparation of SARS-CoV-2 for genomic surveillance and variant detection
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For removal of single-stranded primers in PCR reactions
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S_0659_IAS_QSYM
다양한 종류의 샘플에서 6xHis-tagged recombinant protein 또는 nucleic acid를 전자동으로 분리 정제할 수 있습니다
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OEM by QIAGEN offers bulk manufacturing of Terminal Deoxynucleotidyl Transferase (TdT) in custom formulations.
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S_2522_IS_theraMGMTPyro_16x9
For quantitative measurements of methylation status in exon 1 of the human MGMT gene
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For sequencing-based detection and quantitation of cancer-related gene mutations in the KRAS gene
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For sequencing-based detection and quantitation of cancer-related gene mutations in the BRAF gene
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For sequencing-based detection and quantitation of cancer-related gene mutations in the EGFR gene
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OEM by QIAGEN offers bulk manufacturing of T4 RNA Ligase 2 in custom formulations.
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OEM by QIAGEN offers bulk manufacturing of T4 RNA Ligase 1 in custom formulations.
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S_1260_4_LS_HID_QIAcard_FTA_Elute_Buffer
For the selective lysis of erythrocytes from human blood and bone marrow aspirates
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For collection of whole blood samples and stabilization of circulating cell-free DNA (ccfDNA) from plasma and genomic DNA (gDNA) from the nucleated cellular fraction
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For the ligation of single-stranded or double-stranded RNA molecules, as well as RNA-DNA hybrids
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For the ligation of RNA molecules, facilitating the joining of RNA fragments or the addition of RNA adapters
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For joining or ligation of DNA fragments, particularly in DNA sequencing and cloning techniques
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For facilitating the labeling of DNA probes and tailing of DNA fragments
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For dye-based one-step RT-PCR on the QIAcuity digital PCR instruments
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For in vitro transcription and synthesizing RNA from a DNA template
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For the hands-free isolation of DNA from soil and stool using your automation workflow of choice
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S_9474_Investigator26plexQS
For multiplex amplification of all Chinese National database loci and CODIS-required markers with an innovative Quality Sensor
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For efficient digestion of proteins in biological samples and for eliminating DNases and RNases during nucleic acid isolation
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S_1084_7_GEN_Boxblue_cmyk_disclaimer
NeuMoDx respiratory assays are intended for in vitro diagnostic use. Product availability may vary from country to country. Contact your country representative for further details.
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Comprehensive oncology profiling combining gene fusion detection, gene expression analysis and single nucleotide variant (SNV) calling in just one assay
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Comprehensive oncology profiling combining gene fusion detection, gene expression analysis and single nucleotide variant (SNV) calling in just one assay
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For preparing libraries from unidentified persons and remains samples
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S_1084_7_GEN_Boxblue_cmyk_disclaimer
The NeuMoDx system and assays are intended for in vitro diagnostic use. Product availability may vary from country to country. Contact your country representative for further details.
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For rapid rRNA removal for RNA-seq library preparation from Caenorhabditis elegans (worm) samples
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For rapid rRNA removal for RNA-seq library preparation from fish total RNA samples
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For rapid rRNA removal for RNA-seq library preparation from Drosophila melanogaster (fly) samples
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S_1084_7_GEN_Boxblue_cmyk_disclaimer
To support customers developing in-house assays using real-time PCR molecular testing
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In this webinar, we will take a look at a large-scale SNP-based forensic identification panel for DNA analysis with massively parallel sequencing (MPS). The panel was specifically designed for the challenges of identifying missing persons; where DNA is frequently highly degraded, and relationship tests may involve reference samples from across several generations and in a deficient pedigree.
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The FBI CODIS Core Loci Working Group have published the recommendation that the CODIS core loci should be expanded, and a combination of STR markers from the Combined DNA Index System (CODIS), the European Network of Forensic Science Institutes (ENFSI), and the European DNA Profiling Group (EDNAP) should be used to improve the accuaracy of forensic testing. QIAGEN has developed new kits — Investigator 24plex Kits — that coamplify all 23 recommended markers. The kits use novel 6-dye technology to keep the amplicon length of markers short while avoiding overlapping of markers. Kits are available for purified DNA from casework and for reference samples. This webinar will outline the benefits of the Investigator 24plex Kits and highlight the improved workflow, which saves unnecessary re-runs of a sample by use of an internal “Quality Sensor” control. This unique Quality Sensor can distinguish: Successful amplification Degraded DNA Inhibited DNA No DNA Failed PCR amplification Join us to learn how to improve results and streamline your forensic STR analysis with the new Investigator 24plex Kits.
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The core short tandem repeats (STRs) in worldwide use have served the forensic analyst very well for many years. Further, recent expansions of European Standard STR sets plus ongoing discussions to extend CODIS have brought powerful upgrades to the battery of core markers available. However, there are still scenarios when supplementary STRs could enhance the data necessary for interpreting complex forensic patterns: making safer inferences about relatedness across distant relationships in deficient pedigrees, and in the not too distant future, improving the specificity of familial searching or expanding the points of reference to better interpret mixed profiles. The QIAGEN HDplex Kit contains 9 completely novel STRs in addition to ESS or CODIS D12S39, D18S51 and SE33 markers. On an average, these 9 novel STRs provide higher powers of discrimination than kits using the core loci alone. This webinar will outline the completed studies on worldwide patterns of variability in the 12 novel HDplex STRs and their ability to enhance the power of paternity analyses when combined with existing markers. It will also describe the upgraded pop.STR allele frequency browser which provides data for 23 core STRs plus a total of 28 supplementary STRs in 56 global populations. Join us to learn more on: Enhancing data necessary for interpreting complex forensic patterns with supplementary STRs Making safer inferences about relatedness across distant relationships in deficient pedigrees Improving the specificity of familial searching to better interpret mixed profiles
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