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Merck
모든 사진(4)

주요 문서

E7023

Sigma-Aldrich

Ethyl alcohol, Pure 200 proof

greener alternative

≥99.45%, for molecular biology, 200 proof, suitable for RNA extraction and DNA extraction

동의어(들):

Ethyl alcohol, Pure, Ethanol, absolute alcohol, non-denatured ethanol

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About This Item

Linear Formula:
CH3CH2OH
CAS Number:
Molecular Weight:
46.07
EC Number:
MDL number:
UNSPSC 코드:
15101802
PubChem Substance ID:
NACRES:
NA.21
bp:
78.3 °C

제품명

Ethyl alcohol, Pure 200 proof, for molecular biology

Grade

Molecular Biology
for molecular biology

Quality Level

vapor density

1.59 (vs air)

분석

≥99.45%

양식

liquid

expl. lim.

3.1-27.7 %

환경친화적 대안 제품 특성

Safer Solvents and Auxiliaries
Use of Renewable Feedstocks
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

농도

200 proof

기술

DNA extraction: suitable
RNA extraction: suitable

불순물

≤0.2% (water)

pH

7.0 (20 °C, 10 g/L)

bp

78.3 °C

mp

-114 °C

density

0.789 g/mL at 20 °C

응용 분야

agriculture

환경친화적 대안 카테고리

SMILES string

OCC

InChI

1S/C2H6O/c1-2-3/h3H,2H2,1H3

InChI key

LFQSCWFLJHTTHZ-UHFFFAOYSA-N

유전자 정보

유사한 제품을 찾으십니까? 방문 제품 비교 안내

일반 설명

This product is 200proof, non-denatured absolute ethanol (100%). This is a molecular biology grade product and is tested for the RNase and Dnase.
We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. Ethanol is environmentally preferable green solvent and thus it aligns with "Safer Solvents and Auxiliaries" and "Use of Renewable Feedstocks". 

애플리케이션

Pure ethyl alcohol (ethanol) has been used in the following process:
  • DNA and RNA extraction
  • array hybridization
  • ethanol sedation assay
Suitable for use in the precipitation of nucleic acids

생화학적/생리학적 작용

Positive allosteric modulator of GABAA receptors, and negative allosteric modulator of NMDA glutamate receptors.

기타 정보

Sales restrictions may apply

픽토그램

FlameExclamation mark

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point (°F)

55.4 °F - closed cup

Flash Point (°C)

13 °C - closed cup


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시험 성적서(COA)

Lot/Batch Number

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문서 라이브러리 방문

Derek J Stefanik et al.
Nature protocols, 8(5), 892-899 (2013-04-13)
Among marine invertebrates, the starlet sea anemone Nematostella vectensis has emerged as an important laboratory model system. One advantage of working with this species relative to many other marine invertebrates is the ease of isolating relatively pure DNA, RNA and
Jaishree Garhyan et al.
BMC research notes, 6, 72-72 (2013-03-01)
Hybridization based assays and capture systems depend on the specificity of hybridization between a probe and its intended target. A common guideline in the construction of DNA microarrays, for instance, is that avoiding complementary stretches of more than 15 nucleic
Ran Lin et al.
PLoS genetics, 11(8), e1005366-e1005366 (2015-08-05)
The heavy consumption of ethanol can lead to alcohol use disorders (AUDs) which impact patients, their families, and societies. Yet the genetic and physiological factors that predispose humans to AUDs remain unclear. One hypothesis is that alterations in mitochondrial function
Ross B Mounsey et al.
Experimental neurology, 273, 36-44 (2015-08-06)
Parkinson's disease (PD) is a common chronic neurodegenerative disorder, usually of idiopathic origin. Symptoms including tremor, bradykinesia, rigidity and postural instability are caused by the progressive loss of dopaminergic neurons in the nigrostriatal region of the brain. Symptomatic therapies are
Gian Marco Leggio et al.
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 39(8), 2017-2028 (2014-03-04)
Mesolimbic dopamine (DA) controls drug- and alcohol-seeking behavior, but the role of specific DA receptor subtypes is unclear. We tested the hypothesis that D3R gene deletion or the D3R pharmacological blockade inhibits ethanol preference in mice. D3R-deficient mice (D3R(-/-)) and

프로토콜

Whole genome amplification (WGA) of plasma and serum DNA presents a unique challenge due to the small amount of nucleic acid in such samples.

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