推荐产品
描述
13C-depleted
质量水平
同位素纯度
99.9 atom % 12C
表单
solid
mp
132-135 °C (lit.)
质量偏移
depleted
SMILES字符串
N[12C](N)=O
InChI
1S/CH4N2O/c2-1(3)4/h(H4,2,3,4)/i1+0
InChI key
XSQUKJJJFZCRTK-IGMARMGPSA-N
基因信息
human ... CA1(759) , CA2(760) , EPHX2(2053)
mouse ... Ephx2(13850)
rat ... Ppm1a(24666)
正在寻找类似产品? 访问 产品对比指南
包装
This product may be available from bulk stock and can be packaged on demand. For information on pricing, availability and packaging, please contact Stable Isotopes Customer Service.
储存分类代码
11 - Combustible Solids
WGK
WGK 1
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
Julian Wampfler et al.
Journal of leukocyte biology, 98(3), 357-363 (2015-05-21)
Successful myeloid differentiation depends on the expression of a series of miRNAs. Thus, it is hardly surprising that miRNAs are globally repressed in AML, a disease mainly characterized by a block in cellular myeloid differentiation. Studies investigating the mechanisms for
Giora van Straten et al.
PloS one, 9(6), e100077-e100077 (2014-06-20)
The detoxification of ammonia occurs mainly through conversion of ammonia to urea in the liver via the urea cycle and glutamine synthesis. Congenital portosystemic shunts (CPSS) in dogs cause hyperammonemia eventually leading to hepatic encephalopathy. In this study, the gene
Stephanie Dille et al.
PloS one, 9(7), e103220-e103220 (2014-07-30)
Chlamydia grows inside a cytosolic vacuole (the inclusion) that is supplied with nutrients by the host through vesicular and non-vesicular transport. It is unclear in many respects how Chlamydia organizes this transport. One model posits that the Chlamydia-induced fragmentation of
Anne-Roos S Frenay et al.
PloS one, 10(6), e0129732-e0129732 (2015-06-11)
Some diseases associated with a temporary deterioration in kidney function and/or development of proteinuria show an apparently complete functional remission once the initiating trigger is removed. While it was earlier thought that a transient impairment of kidney function is harmless
Hannah M Kaneb et al.
Human molecular genetics, 24(5), 1363-1373 (2014-10-26)
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder characterized by the selective death of motor neurons. Causative mutations in the global RNA-processing proteins TDP-43 and FUS among others, as well as their aggregation in ALS patients, have identified defects
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系技术服务部门