4000-520-616
欢迎来到免疫在线!(蚂蚁淘生物旗下平台)  请登录 |  免费注册 |  询价篮
主营:主营:分子类化合物
咨询热线电话
4000-520-616
当前位置: 首页 > 产品中心 > peptide > Qiagen/Microbial DNA qPCR Arrays/330261
商品详细Qiagen/Microbial DNA qPCR Arrays/330261
Qiagen/Microbial DNA qPCR Arrays/330261
Qiagen/Microbial DNA qPCR Arrays/330261
商品编号: 330261
品牌: Qiagen
市场价: ¥0.00
美元价: 0.00
产地: 美国(厂家直采)
公司:
产品分类: 多肽合成
公司分类: peptide
联系Q Q: 3392242852
电话号码: 4000-520-616
电子邮箱: info@ebiomall.com
商品介绍

Microbial DNA qPCR Arrays

Product picture
For real-time PCR-based, application-specific microbial identification or profiling
  • Profile microbial species, virulence genes, or antibiotic resistance genes
  • Simple procedure for a variety of sample types
  • Integrated controls ensure reliability of results
Microbial DNA qPCR Arrays are collections of assays to identify and profile microbial species, virulence factorgenes or antibiotic resistance genes from a variety of sample types. Species identification assays target bacterial 16S rRNA genes and fungal ribosomal RNA genes, and each array includes controls for host DNA, presence of bacterial DNA and success of the PCR reaction. Microbial qPCR Mastermixis also included in the array kit.The simplicity of the product format and operating procedure allow routine, reliable identification or profiling of microbial species and genes from samples in any research laboratory with access to a real-time PCR instrument.What is the difference between microbial identification and profiling? Identification is determining the microbe’s presence or absence in your sample which requires running a No Template Control during your analysis. Profiling is determining the microbe’s relative expression in two or more experimental conditions for which you will need to run a reference sample and a normalizer (provided by QIAGEN).
  • Buy Products
  • Product Details
  • Product Resources

Buy Products

Cat No./ID:330261
Microbial DNA qPCR Arrays
Go to GeneGlobe
Array plate and master mix for detection of microbial species or genes
Microbial DNA qPCR Arrays are intended for molecular biology applications. These products are not intended for the diagnosis, prevention, or treatment of a disease.

Product Details

9
The Antibiotic Resistance Genes Microbial qPCR Array identified antibiotic resistance genes in sewage samples.
Municipal biosolids generated by wastewater treatment plants are significant reservoirs for antibiotic resistance genes, since they originate from fecal microbiota. The end product from the treatment plants can either be disposed of in landfills or sold as fertilizer for agricultural use, where antibiotic-resistant bacteria may be reintroduced into the food supply. To determine the diversity of antibiotic resistance genes in municipal biosolids, genomic DNA from belt-filter presscake sewage samples was isolated and analyzed for the presence of antibiotic resistance genes using the Antibiotic Resistance Genes Microbial qPCR Array (cat.no. BAID-1901Z). Raw CT values were exported into the data analysis software and identification criteria was followed. Figure [A] shows the results from the sewage sample. There were 14 antibiotic resistance genes from different resistance classifications that were present in the metagenomic sample. In addition, there were genes that gave an inconclusive result. To determine the presence/absence of the antibiotic resistance genes from the inconclusive results, the “Determination of Inconclusive Microbial DNA qPCR Array/Assay Results” protocol was followed for SHV, ACT-1 group, MIR and LAT [B]. The verification protocol determined that these genes were present in the sewage sample. This highlights the importance of increased surveillance of antibiotic resistance reservoirs to identify potential sources of antibiotic-resistant bacteria that may affect the food supply.
9
The lower limit of quantification (LLOQ) for antibiotic resistance gene detection Microbial DNA qPCR Assays reveals high sensitivity.
This chart shows the distribution of LLOQ for Microbial DNA qPCR Assays for antibiotic resistance gene detection. 95% of all antibiotic resistance gene assays have a LLOQ of <100 gene copies.
9
The lower limit of quantification (LLOQ) for microbial identification Microbial DNA qPCR Assays reveals high sensitivity.
This chart shows the distribution of LLOQ for microbial identification Microbial DNA qPCR Assays. 92% of all microbial identification assays have a LLOQ of <100 gene copies.
9
Microbial DNA qPCR Assays are highly specific.
To determine the specificity of Microbial DNA qPCR Assays, each assay was tested against 119 genomic DNA samples from different bacteria and fungi. To facilitate testing, genomic DNA from different microbial species was pooled (10 different genomic DNA samples per pool) and each assay was tested against the different pools. None of the pools contained DNA from the same genus, to facilitate identification of cross-reacting species. Each pool contained the equivalent of 2000 genome copies for each microbial species. In addition, each assay was tested against human, mouse, and rat genomic DNA. A representative example for Streptococcus pyogenes is shown. The assay for Streptococcus pyogenes gave a CT of 26.9 and 26.6 for the Staphylococcus/Streptococcus pool and complete pool [A]. Both pools contained genomic DNA for Streptococcus pyogenes. To determine which genomic DNA was detected by the Streptococcus pyogenes assay, each individual genomic DNA comprising the Staphylococcus/Streptococcus pool was tested separately [B]. Only Streptococcus pyogenes genomic DNA gave an acceptable CT call (26.8) while the others gave a CT>35. Most of the assays were specific as they did not detect unintended targets. For assays that detected other species, the list of detected targets along with in silico predictions are given in the specifications sheet.
9
Limit of detection versus lower limit of quantification.
This chart demonstrates the difference between the limit of detection (LOD) and the lower limit of quantification (LLOQ). The LOD is defined as the lowest concentration at which 95% of the positive samples are detected, whereas the LLOQ is the lowest concentration that falls within the linear range of a standard curve. LOD depends upon the precision of the assay, and requires at least 40 replicates for determination of a positive sample. For the Microbial DNA qPCR Assays, LLOQ is sufficient to determine assay sensitivity.
9
Specificity of the Antibiotic Resistance Genes Microbial DNA qPCR Array is verified by pyrosequencing.
To verify the specificity of the Antibiotic Resistance Genes Microbial DNA qPCR Array (cat no. BAID-1901Z) results from Klebsiella pneumoniae isolates, pyrosequencing assays were designed to detect for the presence and sequences of SHV-156G, SHV-156D, SHV-238G240E, SHV-238S240K, SHV-238S240E, SHV-238G240K, ermB, mefA, tetA, tetB,CTX-M-1 Group, CTX-M-2 Group, AAC(6′)-lb-cr and aadA1. For each Klebsiella pneumoniae isolate, results from the Antibiotic Resistance Genes Microbial DNA qPCR Array were confirmed by pyrosequencing. Representative pyrograms for [A] SHV-156G, [B] SHV-238/240, [C] KPC and [D] CTX-M-1 group are shown. For SHV variants, the Antibiotic Resistance Gene Microbial DNA qPCR Array was able to reliably distinguish single nucleotide polymorphisms occurring at different sites.
9
Microbial DNA qPCR Arrays generate reliably reproducible results.
To determine the reproducibility of the Microbial DNA qPCR Array, both intra-individual and inter-individual variability was tested. In this experiment, 500 ng genomic DNA isolated from belt-filter presscake sewage sample was loaded onto the Antibiotic Resistance Genes Microbial DNA qPCR Array (cat. no.BAID-1901Z). To determine intra-individual variability, the same operator ran two different PCR arrays on different days with four technical repeats. To determine inter-individual variability, two different operators ran PCR arrays with four technical repeats. The results show low inter- and intra-individual variation of the qPCR array.
9
The lower limit of quantification (LLOQ) for virulence factor gene detection Microbial DNA qPCR Assays reveals high sensitivity.
This chart shows the distribution of LLOQ for Microbial DNA qPCR Assays for virulence factor gene detection. 97% of all virulence factor gene assays have a LLOQ of <100 gene copies.
9
The lower limit of quantification (LLOQ) for all Microbial DNA qPCR Assays reveals high sensitivity.
This chart shows the distribution of LLOQ for all Microbial DNA qPCR Assays. 93% of all Microbial DNA qPCR Assays have a LLOQ of <100 gene copies.
9
The Microbial DNA qPCR Array screens gut microbiota for the presence of antibiotic resistance genes.
The human gut microbiota is known to act as a reservoir for antibiotic resistance genes, where they can be transferred horizontally to potential pathogenic bacteria. To detect the presence of antibiotic resistance genes from gut microbiota, stool samples from five healthy adults were collected and genomic DNA was isolated using QIAGEN’s QIAamp DNA Stool Mini Kit. 500 ng genomic DNA from each stool sample was analyzed for presence of antibiotic resistance genes using the Antibiotic Resistance Genes Microbial DNA qPCR Array (cat.no. BAID-1901Z). The Antibiotic Resistance Genes Microbial DNA qPCR Array contains assays for 83 antibiotic resistance genes, assays to identify methicillin-resistant Staphylococcus aureus, and control assays. ErmB, mefA, and tetA were found in all or most of the stool samples tested, showing that they may be highly prevalent in the gut. These antibiotic resistance genes have been reported to be isolated from bacterial strains originating from food, suggesting a possible source of origin. This highlights the importance of increased monitoring of antibiotic resistance reservoirs to identify potential sources of antibiotic-resistant bacteria.
9
Microbial DNA qPCR Assays display high sensitivity even in complex metagenomic samples.
To ensure that Microbial DNA qPCR Assays performed comparably in a complex sample, where there may be up to a thousand different microbial species, each assay was tested using stool, tooth plaque, and sputum samples. For each sample, synthetic template targets were spiked in and the CT was compared to synthetic template alone. PCR was performed using several sample types, which included pooled synthetic template targets alone, stool, stool plus pooled synthetic template targets, plaque, plaque plus pooled synthetic template targets, sputum, and sputum plus pooled synthetic template targets. If the CT<35 in stool, plaque, or sputum samples alone, then ΔCT was calculated (i.e., CTstool + pooled synthetictemplate targets– CTpooled synthetic template targets). This calculation was performed for all the assays. For each assay, the ΔCT<3, indicating that a complex metagenomic background does not affect the performance of each Microbial DNA qPCR Assay.
9
Vaginal samples positive for Gardnerella vaginalis also show changes in commensal and bacterial vaginosis-related microbes compared to healthy samples.
To compare any differences in the vaginal microbiome between healthy women and women with bacterial vaginosis, each sample that tested positive for Gardnerella vaginalis using the Vaginal Flora Microbial DNA qPCR Array was compared to samples from healthy women (n=3). Fold-change in microbial species abundance was calculated by the ΔΔCT method using human genomic DNA to normalize. The results show that as the relative abundance of Gardnerella vaginalis increases, the abundance of the commensal species Lactobacillus crispatus decreases. Also, an increase in Gardnerella vaginalis was associated with an increase in other bacterial vaginosis-associated microbial species. This suggests that Lactobacillus crispatus protects the vagina from bacterial vaginosis-associated microbial species.
9
The Vaginal Flora Microbial DNA qPCR Array provides accurate profiling for cervical swab samples.
The vaginal microbiota is a key component influencing women’s urogenital health. To determine what changes in the vaginal microbiota occurs during bacterial vaginosis, the Vaginal Flora Microbial DNA qPCR Array (cat. no. BAID-1902Z), which detects up to 90 different microbial species, was used to test cervical swabs from healthy individuals and from patients with bacterial vaginosis. Genomic DNA from vaginal samples originating from three patients that tested negative for bacterial vaginosis, three patients that tested positive for Candida, three patients that tested positive for Garderella vaginalis, and one patient that tested positive for Trichomonas vaginalis by BD Affirm™ VPIII Microbial Identification Test were run on the Vaginal Flora Microbial DNA qPCR Array. Genomic DNA from ThinPrep samples were isolated using QIAGEN’s QIAamp MinElute Media Kit and 500 ng genomic DNA from each sample was analyzed. After the PCR run on a Roche LightCycler 480, raw CT values were exported to the Microbial DNA qPCR data analysis software. Positive (+) / negative (blank) / inconclusive (+/-) results for each microbial species were determined using the identification criteria. The results from the Vaginal Flora Microbial DNA qPCR Array were in concordance with the BD Affirm VPIII Microbial Identification Test.
9
Linearity and sensitivity of Microbial DNA qPCR Arrays.
Linearity and sensitivity for each Microbial DNA qPCR Array was determined using synthetic templates over a 6 log serial dilution ranging from 1 copy to 1 million copies. The following are representative results for all the qPCR assays. [A] shows the real-time amplification curves of the KPC antibiotic resistance gene qPCR assay. In [B], a standard curve was prepared that shows that the primer efficiency equals 103% (calculated from slope = –3.3236) and the correlation coefficient is 0.9983, indicating optimum performance for the KPC qPCR assay. All Microbial DNA qPCR Assays have primer efficiencies between 80–120% and correlation coefficients (R)>0.995.
Performance
Linearity and dynamic range
Microbial DNA qPCR Assays display linear amplification across a range from 10 to 106 copies of DNAtemplate (see figure, Linearity and sensitivity of Microbial DNA qPCR Assays).
Lower limit of quantification (LLOQ)
The LLOQ is the lowest concentration of template that still falls into the linear range of the standard curve (see figure, Limit of detection versus lower limit of quantification). Across all Microbial DNA qPCR Assays, 93% have an LLOQ of <100 gene copies (see figure, The LLOQ for all Microbial DNA qPCR Assays reveals high sensitivity). 92% of microbial identification assays meet this LLOQ, as do 95% of virulence factor gene assays and 97% of antibiotic resistance gene assays (see figures, The LLOQ for microbial identification Microbial DNA qPCR Assaysreveals high sensitivity,The LLOQ for virulence factorgene detection Microbial DNA qPCR Assaysreveals high sensitivity, andThe LLOQ for antibiotic resistance gene detection Microbial DNA qPCR Assays reveals high sensitivity).
Specificity
Each Microbial DNA qPCR Assay is stringently tested to ensure that it detects only one target species or gene (see figure, Microbial DNA qPCR Assays are highly specific). For assays that do detect more than one target, a list of detected targets and in silico predictions is included on the product sheet.This specificity is maintained even when samples have high species complexity, such as in stool, sputum, and plaque (see figure,Microbial DNA qPCR Assays display high sensitivity even in complex metagenomic samples), and is verifiable by sequencing methods (see figure,Specificity of the Antibiotic Resistance Genes Microbial DNA qPCR Array is confirmed by pyrosequencing).
Reproducibility
Microbial DNA qPCR Assays are highly reproducible, both in intra- and inter-individual variability tests (see figure, Microbial DNA qPCR Arrays generate reliably reproducible results).
Principle
Microbial DNA qPCR Assays are designed to detect bacterial 16S rRNA gene and fungal ribosomal rRNA gene sequences for species identification, as well as detecting virulence factor genes and antibiotic resistance genes using PCR amplification primers and hydrolysis-probe detection.Microbial DNA qPCR Arrays are 96- or 384-well plates comprising related assays; for example, microbial species associated with respiratory infections, or microbes that are studied for biodefense. Controls are integrated on each plate to test for the presence of fungal DNA, bacterial DNA, host genomic DNA, and success of the PCR reaction, ensuring confidence in the results.
Procedure
The Microbial DNA qPCR Array procedure is simple and can be carried out in any laboratory with a real-time PCR instrument. DNA is isolated using the QIAamp kit that is suited for the sample type, and then mixed with the appropriate Microbial qPCR Mastermix. The mixture is aliquotted across the array plate, and real-time PCR is performed to obtain the raw CT values for each assay. The complimentary data analysis software is then used to profile genes or species in the sample.
Applications
Microbial DNA qPCR Arrays are highly suited for identification or profiling of microbial species or genes in a variety of sample types.For example, the Vaginal Flora Microbial DNA qPCR Array can be used to explore the underlying causes of bacterial vaginosis (see figures,The Vaginal Flora Microbial DNA qPCR Array provides accurate profiling for cervical swab samples andVaginal samples positive for Gardnerella vaginalis also show changes in commensal and bacterial vaginosis-related microbes compared to healthy samples), while the Antibiotic Resistance Genes Microbial DNA qPCR Array canidentify these genes insamples from the gut or from sewage (see figures,The Microbial DNA qPCR Array screens gut microbiota for the presence of antibiotic resistance genes and The Antibiotic Resistance Genes Microbial DNA qPCR Array identified antibiotic resistance genes in sewage samples).

Product Resources

You are not authorized to download the resource

Brochures & Guides (2)
  • Sort options
    • Sort alphabetically
Microbial Product Configurator
Microbial product configurator guide
Show details
Microbial DNA qPCR Arrays
For application-specific microbial identification and profiling by real-time PCR
Show details
Download Files (20)
  • Sort options
    • Sort alphabetically
Antibiotic Resistance + MRSA Microbial Identification Data Analysis
Show details
Antibiotic Resistance plus MRSA Microbial Profiling Data Analysis
Show details
Bacterial Vaginosis Microbial Identification Data Analysis
Show details
Biodefense Microbial Identification Data Analysis
Show details
Food Testing Dairy Microbial Identification Data Analysis
Show details
Food Testing Meat Microbial Identification Data Analysis
Show details
Food Testing Poultry Microbial Identification Data Analysis
Show details
Food Testing Seafood Microbial Identification Data Analysis
Show details
Food Testing Vegetable Microbial Identification Data Analysis
Show details
Determination of Inconclusive Results Microbial Identification Data Analysis
Show details
Intestinal Infections Microbial Identification Data Analysis
Show details
Metabolic Disorders Microbial Identification and Profiling Data Analysis
Show details
Respiratory Infections Microbial DNA qPCR Array Microbial Identification Data Analysis
Show details
Respiratory Viral Infections Microbial DNA qPCR Array Microbial Identification Data Analysis
Show details
Sepsis Microbial DNA qPCR Array Microbial Identification Data Analysis
Show details
Sepsis Microbial DNA qPCR Array Microbial Profiling Data Analysis
Show details
Urinary Tract Infection Microbial DNA qPCR Array Microbial Identification Data Analysis
Show details
Vaginal Flora Microbial DNA qPCR Array Microbial Identification Data Analysis
Show details
Vaginal Flora Microbial DNA qPCR Array Microbial Profiling Data Analysis
Show details
Water Analysis Microbial DNA qPCR Array Microbial Profiling Data Analysis
Show details
Analysis Software (1)
  • Sort options
    • Sort alphabetically
Microbial Custom PCR Array Universal Patch
Show details
FAQs (19)
  • Sort options
    • Sort alphabetically
What are the minimum sample requirements for Microbial DNA qPCR kits?
FAQ ID— 3393
View
What are the storage conditions for the Microbial DNA qPCR products?
FAQ ID— 3394
View
Which Microbial qPCR Mastermix should I use?
FAQ ID— 3395
View
What is the expected amplicon size of the Microbial DNA qPCR Assays?
FAQ ID— 3396
View
What is the difference between Positive PCR Control (PPC) and Microbial DNA Positive Control?
FAQ ID— 3397
View
Can I use the Microbial DNA-Free Water and Microbial qPCR Mastermix if they have been opened more than 3 times?
FAQ ID— 3398
View
What sample types can be tested on the arrays/assays?
FAQ ID— 3399
View
Are the assays species-specific?
FAQ ID — 3400
View
What is LLOQ?
FAQ ID— 3401
View
What is the difference between LLOQ and LOD?
FAQ ID— 3402
View
What sequences are used to design the Microbial DNA qPCR Assays?
FAQ ID— 3403
View
Can I measure antibiotic resistance gene expression?
FAQ ID— 3404
View
Can I measure virulence factor gene expression?
FAQ ID— 3405
View
Are the Microbial DNA qPCR Assays wet-lab verified?
FAQ ID— 3406
View
Which probe labels are available for the Microbial DNA qPCR Assays?
FAQ ID— 3407
View
What is the sensitivity for the Microbial DNA qPCR kits?
FAQ ID— 3409
View
How can I calculate the number of bacterial cells that are present in a sample using the Microbial DNA qPCR Assays?
FAQ ID — 3411
View
What species are detected by the Pan Bacteria 1 and Pan Bacteria 3 Assays?
FAQ ID - 3427
View
Is the Microbial qPCR mastermix used in the Microbial DNA assay and in the Microbial DNA arrays free of genomic bacterial DNA?
FAQ ID - 3535
View
Kit Handbooks (1)
  • Sort options
    • Sort alphabetically
Microbial DNA qPCR Handbook
New version – For real-time PCR-based profiling/detection of microbial species, antibiotic resistance genes or virulence factor genes
Show details
Webinars (1)
  • Sort options
    • Sort alphabetically
Exploring the temperate leaf microbiome: From natural forests to controlled experiments and urban environments
The work presented here thus offers an original assessment of the dynamics at play in the tree phyllosphere.
Show details
Scientific Posters (1)
  • Sort options
    • Sort alphabetically
Detection and Surveillance of Antibiotic Resistance Genes From Food and Fertilizer Sources Using qPCR Technology
Show details
Supplementary Protocols (4)
  • Sort options
    • Sort alphabetically
Microbial DNA qPCR Array ABI7500 Instrument Setup
Show details
Microbial DNA qPCR Array ABI7900 Instrument Setup
Show details
Microbial DNA qPCR Array Rotor-Gene Q Instrument Setup
Show details
Microbial DNA qPCR Array ViiA7 Instrument Setup
Show details
Technical Information (2)
  • Sort options
    • Sort alphabetically
Microbial DNA qPCR Assay/Assay Kits
Show details
Antibiotic Resistance Gene Resource and Assay List
Show details
Safety Data Sheets (1)
  • Sort options
    • Sort alphabetically
MSDS Microbial DNA qPCR Arrays
fragment fix placeholder

Customers who bought these products also bought

  • Cat No./ID:330033
    /us/products//discovery-and-translational-research/pcr-qpcr-dpcr/qpcr-assays-and-instruments/microbial-dna-qpcr-assays-and-panels/microbial-dna-qpcr-assay-kits/

    Microbial DNA qPCR Assay Kit

    One 20 µl tube of Microbial DNA qPCR Assay, 1 tube Positive PCR Control (20 µl), 1 tube Microbial DNA Positive Control (50 µl), 1 tube Microbial DNA-Free Water (1.35 ml), and 1 tube Microbial qPCR Mastermix (1.35 ml)
    Select Targets
  • Cat No./ID:13000-V1-50
    /us/products//instruments-and-automation/accessories/vortex-adapter/

    Vortex Adapter for 2 (50 ml) tubes

    For vortexing 50 ml tubes using the Vortex-Genie 2 Vortex.
    $112.00
    Add To Cart
  • Cat No./ID:338135
    /us/products//discovery-and-translational-research/pcr-qpcr-dpcr/qpcr-assays-and-instruments/microbial-dna-qpcr-assays-and-panels/microbial-dna-positive-control/

    Microbial DNA Positive Control V2

    One 50 µl tube at 10x concentration of all the assays

    $66.40
    Add To Cart
  • Cat No./ID:978746
    /us/products//discovery-and-translational-research/epigenetics/dna-methylation/pyrosequencing/consumables/pyromark-q24-advanced-accessories-and-reagents/

    PyroMark CpG Assay (200)

    PCR and sequencing primers for Pyrosequencing analysis of gene-specific CpG methylation after DNA bisulfite conversion (200 reactions; tube format)
    Select Targets
  • Cat No./ID:19301
    /us/products//discovery-and-translational-research/lab-essentials/plastics/powerbead-tubes/

    PowerBead Pro Tubes (2 ml) (50)

    Bead tubes ready for rapid and reliable biological sample lysis from a wide variety of starting materials, 2 ml
    $196.00
    Add To Cart
  • Cat No./ID:13000-V1-5
    /us/products//instruments-and-automation/accessories/vortex-adapter/

    Vortex Adapter for 6 (5 ml) tubes

    For vortexing 5 and 15 ml tubes using the Vortex-Genie 2 Vortex.
    $126.00
    Add To Cart
  • Cat No./ID:19092
    /us/products//discovery-and-translational-research/lab-essentials/buffers-reagents/pathogen-lysis-tubes/

    Pathogen Lysis Tubes L

    50 Pathogen Lysis Tubes with large beads, 1 vial of Reagent DX
    $262.00
    Add To Cart
  • Cat No./ID:338162
    /us/products//discovery-and-translational-research/lab-essentials/plastics/rt2-pcr-array-loading-reservoir/

    RT2 PCR Array Loading Reservoir (12)

    12 x 5 ml capacity, irradiation-sterilized RT2 PCR Array Loading Reservoirs
    $24.90
    Add To Cart
  • Cat No./ID:338132
    /us/products//discovery-and-translational-research/lab-essentials/buffers-reagents/microbial-dna-free-water/

    Microbial DNA-Free Water

    12 tubes of 1.35 ml each
    $80.00
    Add To Cart
  • Cat No./ID:50214
    /us/products//diagnostics-and-clinical-research/sample-processing/qiaamp-ucp-pathogen-mini-kit/

    QIAamp UCP Pathogen Mini Kit

    50 QIAamp UCP Mini Columns, Collection Tubes (2 ml), Tube Extenders (20 ml), Elution Tubes, VacConnectors, Buffers, and Proteinase K
    $345.00
    Add To Cart
  • Cat No./ID:14900-50-NF
    /us/products//discovery-and-translational-research/dna-rna-purification/dna-purification/microbial-dna/dneasy-powerwater-kit/

    DNeasy PowerWater Kit (50)

    For the isolation of genomic DNA from filtered water samples, including turbid water
    $529.00
    Add To Cart
  • Cat No./ID:19088
    /us/products//discovery-and-translational-research/lab-essentials/buffers-reagents/reagent-dx/

    Reagent DX (1 ml)

    1 ml Antifoaming Reagent for QIAGEN Lysis Buffers
    $55.90
    Add To Cart
  • Cat No./ID:69204
    /us/products//new-products/dneasy-plant-pro-kit/

    DNeasy Plant Pro Kit (50)

    Tissue Disruption Tubes, MB Spin Columns, Buffers, Collection Tubes (1.5 and 2 ml), for 50 preps
    $248.00
    Add To Cart
  • Cat No./ID:47014
    /us/products//discovery-and-translational-research/dna-rna-purification/dna-purification/microbial-dna/dneasy-powersoil-pro-kit/

    DNeasy PowerSoil Pro Kit (50)

    For the isolation of microbial genomic DNA from all soil types.
    $357.00
    Add To Cart
品牌介绍
QIAGEN是一家专业化致力于生物分子样品制备解决方案的跨国经营企业,总部位于德国。1984年,QIAGEN在德国成立,1996年在美国纽约纳斯达克上市。QIAGEN拥有超过1000项专利和认可证明,在18个国家设立了分公司,代理商服务国超过40个,在全球有超过400000的用户。QIAGEN提供的产品超过500类,包括各种试剂,耗材和自动化纯化工作站。这些产品用于样品采集,稳定,核酸或蛋白的分离,纯化和检测中,不仅广泛的应用于科研领域的各个方面,在生物技术,制药,法医研究,食品安全检测,畜牧业和分子诊断领域也得到了广泛的应用。QIAGEN产品的卓越品质和在应用中的出色表现使得其成为样品处理中标准的代名词。