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Merck
모든 사진(1)

문서

11691112001

Roche

Human Genomic DNA

from human blood (buffy coat)

동의어(들):

dna, human, homo sapiens dna

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About This Item

UNSPSC 코드:
41106310

생물학적 소스

human blood

Quality Level

형태

solution

포장

pkg of 100 μg

제조업체/상표

Roche

농도

0.2 mg/mL

색상

colorless

solubility

water: miscible

저장 온도

2-8°C

일반 설명

DNA is composed of units called nucleotides arranged into two long polynucleotide chains, resulting in a double helical structure. Nucleotides contain a phosphate group, a sugar group and a nitrogen base. There are four types of nitrogen bases namely adenine (A), thymine (T), guanine (G) and cytosine (C). The arrangement of these bases establishes the genetic codon. The difference in the nucleotide sequences is the reason why organisms differ from one another. In eukaryotic cell, the DNA is localized to the nucleus.
High molecular weight (>50kb) genomic DNA isolated from human blood (buffy coat) by the method of Sambrook et al..

애플리케이션

Human Genomic DNA is suitable for:
  • Southern hybridization analysis
  • genomic library construction
  • the amplification of large DNA targets by the Expand System
  • to assess the quality or integrity of DNA sample using qPCR or real time (RT) PCR and as a control during DNA sequencing
The amplification of very long fragments of genomic DNA requires template DNA of very high quality. In some cases, amplification failure may be due to poor template quality. This particular quality of genomic DNA is prepared to ensure reliable amplification of long DNA fragments.

생화학적/생리학적 작용

DNA is an essential component of the mechanism for heredity. The nucleotide sequences carry information regarding different biological processes. The genetic codons encode proteins essential for biological function. This genetic information is transmitted to the next generation during cell division. The amplification of very long fragments of genomic DNA requires template DNA of very high quality. In some cases, amplification failure may be due to poor template quality. This particular quality of genomic DNA is prepared to ensure reliable amplification of long DNA fragments.

품질

Molecular weight: The preparation is electrophoretically separated on a 0.5% agarose gel and the gel is stained with ethidium bromide. The molecular weight of the purified genomic DNA is greater than 50kb.
Function test: The preparation is used as template in a PCR with the Expand PCR System and appropriate primers from the human tPA Control Primer Set. Amplification products up to 27kb long are obtained.
Absence of contaminating organisms: The serum used for this preparation was tested for HBs antigen and the presence of antibodies to HIV-1, HIV-2, HCV. All tests were negative.

물리적 형태

Solution in 10 mM Tris HCl, 1 mM EDTA, pH 8.0

기타 정보

For life science research only. Not for use in diagnostic procedures.

면책조항

RESEARCH USE ONLY. This product is regulated in France when intended to be used for scientific purposes, including for import and export activities (Article L 1211-1 paragraph 2 of the Public Health Code). The purchaser (i.e. enduser) is required to obtain an import authorization from the France Ministry of Research referred in the Article L1245-5-1 II. of Public Health Code. By ordering this product, you are confirming that you have obtained the proper import authorization.

Storage Class Code

12 - Non Combustible Liquids

WGK

nwg

Flash Point (°F)

No data available

Flash Point (°C)

No data available


시험 성적서(COA)

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문서 라이브러리 방문

M Y Balkhi et al.
Science signaling, 6(286), ra63-ra63 (2013-08-01)
In sarcoma, the activity of NF-κB (nuclear factor κB) reduces the abundance of the microRNA (miRNA) miR-29. The tumor suppressor A20 [also known as TNFAIP3 (tumor necrosis factor-α-induced protein 3)] inhibits an upstream activator of NF-κB and is often mutated
Alberts B, et al.
Molecular Cell Biology. 4th edition. (2002)
Sinden RR, et al.
DNA (2012)
L M Rice et al.
Journal of applied microbiology, 115(3), 818-827 (2013-06-19)
The goal of this study was to develop a molecular diagnostic multiplex assay for the quantitative detection of microbial pathogens commonly responsible for ventilator-associated pneumonia (VAP) and their antibiotic resistance using linear-after-the-exponential polymerase chain reaction (LATE-PCR). This multiplex assay was
Ioannis G Fatouros et al.
Clinical chemistry, 52(9), 1820-1824 (2006-07-15)
Circulating free plasma DNA is implicated in conditions associated with tissue injury, including exercise-induced inflammation, and thus is a potential marker for athletic overtraining. We measured free plasma DNA along with C-reactive protein (CRP), creatine kinase (CK), and uric acid

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