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Merck
CN

24-0370

石蜡

SAJ first grade, mp 50-52 °C

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化学文摘社编号:
UNSPSC Code:
41115710
EC Number:
232-315-6
MDL number:
Grade:
SAJ first grade
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dilution

(for analytical testing)

InChI key

JWHAUXFOSRPERK-UHFFFAOYSA-N

grade

SAJ first grade

form

solid

availability

available only in Japan

mp

50-52 °C

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wgk

nwg

flash_point_f

602.6 °F - Pensky-Martens closed cup

flash_point_c

317 °C - Pensky-Martens closed cup

ppe

Eyeshields, Gloves, type N95 (US)

存储类别

11 - Combustible Solids

法规信息

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Roman Zimmermann et al.
Plant physiology, 152(1), 356-365 (2009-11-21)
In an approach to study lateral root development in monocots, genome-wide searches for homologs of the Gibberellic Acid Stimulated Transcript-like (GAST-like) gene family in rice (Oryza sativa) and maize (Zea mays) were carried out. Six novel GAST-like genes in rice
Wisam Al-Faqheri et al.
PloS one, 8(3), e58523-e58523 (2013-03-19)
This paper introduces novel vacuum/compression valves (VCVs) utilizing paraffin wax. A VCV is implemented by sealing the venting channel/hole with wax plugs (for normally-closed valve), or to be sealed by wax (for normally-open valve), and is activated by localized heating
Haohao Zhong et al.
Diagnostic molecular pathology : the American journal of surgical pathology, part B, 22(1), 52-58 (2013-02-02)
We report a hydrothermal pressure method (pressure cooking) for simultaneous deparaffinization and lysis of formalin-fixed paraffin-embedded tissue followed by conventional chaotropic salt column purification to obtain high-quality DNA. Using this method, the release of DNA occurred within the first minute
André Luis Costa-da-Silva et al.
PloS one, 8(1), e53816-e53816 (2013-01-24)
Aedes aegypti, the main vector of dengue virus, requires a blood meal to produce eggs. Although live animals are still the main blood source for laboratory colonies, many artificial feeders are available. These feeders are also the best method for
Linda A Cannizzaro
Methods in molecular biology (Clifton, N.J.), 946, 61-83 (2012-11-28)
In the past decade, fluorescent in situ hybridization (FISH) has been used routinely in detecting molecular abnormalities in the interphase and metaphase stages of the cell cycle. Many of the molecular anomalies which are detected in this manner are diagnostic

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