推荐产品
等级
NMR reference standard
质量水平
表单
solution
浓度
90% in DMSO-d6 (99.9 atom % D)
技术
NMR: suitable
NMR管尺寸
10 mm × 8 in.
SMILES字符串
NC=O
InChI
1S/CH3NO/c2-1-3/h1H,(H2,2,3)
InChI key
ZHNUHDYFZUAESO-UHFFFAOYSA-N
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特点和优势
15N 灵敏度
数量
10 mm O.D. tube contains 3.175 mL.
警示用语：
Danger
危险声明
危险分类
Carc. 2 - Repr. 1B - STOT RE 2 Oral
靶器官
Blood
储存分类代码
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 2
闪点(°F)
190.0 °F
闪点(°C)
87.8 °C
Min Chen et al.
Prenatal diagnosis, 35(6), 534-543 (2015-02-03)
To develop a single-tube multi-marker assay for improved preimplantation genetic diagnosis (PGD) of deletional and/or non-deletional Hb Bart's hydrops fetalis syndrome, providing haplotype confirmation of deletional status, and maximization of linkage informativity. We performed in silico mining to identify novel
A Touati et al.
Journal of clinical microbiology, 53(10), 3182-3194 (2015-07-24)
Molecular typing of Mycoplasma pneumoniae is an important tool for identifying grouped cases and investigating outbreaks. In the present study, we developed a new genotyping method based on single nucleotide polymorphisms (SNPs) selected from the whole-genome sequencing of eight M.
J Veenemans et al.
Journal of clinical microbiology, 52(7), 2454-2460 (2014-05-03)
Next-generation sequencing (NGS) has the potential to provide typing results and detect resistance genes in a single assay, thus guiding timely treatment decisions and allowing rapid tracking of transmission of resistant clones. We evaluated the performance of a new NGS
Vishnu Priya Bollampalli et al.
PLoS pathogens, 11(10), e1005206-e1005206 (2015-10-07)
The transport of antigen from the periphery to the draining lymph node (DLN) is critical for T-cell priming but remains poorly studied during infection with Mycobacterium bovis Bacille Calmette-Guérin (BCG). To address this we employed a mouse model to track
Björn Heindryckx et al.
Mitochondrion, 18, 12-17 (2014-08-28)
To investigate the applicability of preimplantation genetic diagnosis (PGD), we used trophectoderm (TE) biopsy to determine the mutation load in a 35-year-old female with mitochondrial encephalopathy, lactic acidosis and stroke-like syndrome (MELAS). Transfer of a mutation-free blastocyst gave birth to
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