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浓度
~30% in H2O
质量水平
折射率
n20/D 1.374
密度
1.02 g/mL at 25 °C
SMILES字符串
N.CCCCCCCCCCCCOS(O)(=O)=O
InChI
1S/C12H26O4S.H3N/c1-2-3-4-5-6-7-8-9-10-11-12-16-17(13,14)15;/h2-12H2,1H3,(H,13,14,15);1H3
InChI key
BTBJBAZGXNKLQC-UHFFFAOYSA-N
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此商品 | 239267 | 381926 | 216135 |
|---|---|---|---|
| form powder | form chips, powder, crystals or chunks, solid | form - | form powder |
| Quality Level 200 | Quality Level 200 | Quality Level - | Quality Level 100 |
| composition Dye content, 97% | composition - | composition Dye content, 85% | composition - |
警示用语：
Warning
危险声明
危险分类
Aquatic Chronic 3 - Eye Irrit. 2 - Skin Irrit. 2
储存分类代码
10 - Combustible liquids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
常规特殊物品
含少量动物源组分生物产品
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Ramkumar P, et al.
The Journal of Biological Chemistry (2015)
New protein?protein interactions of mitochondrial connexin 43 in mouse heart.
Denuc A, et al.
Journal of Cellular and Molecular Medicine, 20(5), 794-803 (2016)
Targeting CPT1A-mediated fatty acid oxidation sensitizes nasopharyngeal carcinoma to radiation therapy.
Tan Z, et al.
Theranostics, 8(9), 2329-2329 (2018)
Ivan Duran et al.
Human molecular genetics, 24(7), 1918-1928 (2014-12-17)
Osteogenesis imperfecta (OI) is a genetic disorder that results in low bone mineral density and brittle bones. Most cases result from dominant mutations in the type I procollagen genes, but mutations in a growing number of genes have been identified
Roberto Di Maio et al.
Science translational medicine, 10(451) (2018-07-27)
Missense mutations in leucine-rich repeat kinase 2 (LRRK2) cause familial Parkinson's disease (PD). However, a potential role of wild-type LRRK2 in idiopathic PD (iPD) remains unclear. Here, we developed proximity ligation assays to assess Ser1292 phosphorylation of LRRK2 and, separately
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