おすすめの製品
品質水準
形状
liquid
特徴
DNA free
テクニック
DNA extraction: suitable
DNA sequencing: suitable
PCR: suitable
輸送温度
ambient
保管温度
room temp
詳細
Microbial DNA-free water is filter-sterilized and UV- treated. It undergoes stringent quality control testing to ensure that it is free of any detectable levels of DNA. The quality tests guarantee the absence of detectable levels of contaminating DNA using 35 cycles PCR amplification of 16S and 18S rDNA using universal primer sets.
Provided in 10 vials of 1.5 ml, enabling use of 1 tube per PCR setup to avoid contamination of your master stock.
Progression in Next Generation Sequencing (NGS) technology now allows identification and sequencing of microbes in relatively low quantities and in complex samples. Therefore, NGS is the method of choice for population identification in microbiome samples, as most of them include large variety of microbes and in some cases also host cells. Still, biases and errors are common in this workflow and can be introduced in different steps along this process. Reagents used must be free of any microbial contaminant to avoid introduction of exogenous error to the samples especially these with relatively low microbial counts
Provided in 10 vials of 1.5 ml, enabling use of 1 tube per PCR setup to avoid contamination of your master stock.
Progression in Next Generation Sequencing (NGS) technology now allows identification and sequencing of microbes in relatively low quantities and in complex samples. Therefore, NGS is the method of choice for population identification in microbiome samples, as most of them include large variety of microbes and in some cases also host cells. Still, biases and errors are common in this workflow and can be introduced in different steps along this process. Reagents used must be free of any microbial contaminant to avoid introduction of exogenous error to the samples especially these with relatively low microbial counts
アプリケーション
Microbial DNA-free water is suited for use in PCR assays as a negative PCR template control (1). It has been used to dilute genomic DNA template in qPCR assay to detect and quantify microbial load in water and other environmental samples and for downstream applications, such as sanger sequencing and next-generation sequencing.(2, 3) It may be used in the preparation of PCR master mixes and reagents to prevent DNA contamination problems leading to false-positive signals in real-time polymerase chain reaction detection of bacterial pathogens in biological samples. (4)
特徴および利点
DNA-free Water: Filter-sterilized and UV-treated to ensure the water is completely free of DNA microbial contaminant to avoid introduction of exogenous error
Highest quality: Strict quality control testing for absence of detectable levels of contaminating microbial DNA
Convenient: 1 tube per PCR setup for avoiding master stock contamination
Highest quality: Strict quality control testing for absence of detectable levels of contaminating microbial DNA
Convenient: 1 tube per PCR setup for avoiding master stock contamination
保管分類コード
12 - Non Combustible Liquids
WGK
nwg
引火点(°F)
Not applicable
引火点(℃)
Not applicable
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
Jan Code
MBD0025-1.5ML:
MBD0025-BULK:
MBD0025-VAR:
MBD0025-10X1.5ML-C:
MBD0025-1ML-PW:
MBD0025-10X1.5ML:
MBD0025-1.5ML-PW:
試験成績書(COA)
製品のロット番号・バッチ番号を入力して、試験成績書(COA) を検索できます。ロット番号・バッチ番号は、製品ラベルに「Lot」または「Batch」に続いて記載されています。
Activity and DNA contamination of commercial polymerase chain reaction reagents for the universal 16S rDNA real-time polymerase chain reaction detection of bacterial pathogens in blood
Diagnostic Microbiology and Infectious Disease, 66, 41-49 (2010)
Fishing in the water: effect of sampled water volume on environmental DNA-based detection of macroinvertebrates
Environmental Science & Technology, 50.1, 305-312 (2016)
Development of a sensitive and false-positive free PMA-qPCR viability assay to quantify VBNC Escherichia coli and evaluate disinfection performance in wastewater effluent
Journal of Microbiological Methods, 132, 139-147 (2017)
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