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表单
liquid
存货情况
available only in Japan
浓度
3.2 mM
SMILES字符串
Cl[Ca]Cl
InChI
1S/Ca.2ClH/h;2*1H/q+2;;/p-2
InChI key
UXVMQQNJUSDDNG-UHFFFAOYSA-L
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Warning
危险声明
预防措施声明
危险分类
Eye Irrit. 2
储存分类代码
10 - Combustible liquids
WGK
WGK 1
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Dino Demirovic et al.
Journal of cell communication and signaling, 8(4), 333-339 (2014-09-07)
Repeated exposure to mild heat shock (HS) has been shown to induce a wide range of health promoting hormetic effects in various biological systems, including human cells undergoing aging in vitro. In order to understand how cells distinguish between mild
Kaisa Kyöstilä et al.
PLoS genetics, 11(4), e1005169-e1005169 (2015-04-16)
Inherited neurodegenerative disorders are debilitating diseases that occur across different species. We have performed clinical, pathological and genetic studies to characterize a novel canine neurodegenerative disease present in the Lagotto Romagnolo dog breed. Affected dogs suffer from progressive cerebellar ataxia
Shigeru Komaba et al.
PloS one, 10(9), e0138012-e0138012 (2015-09-12)
Amino acid transporters (AATers) in the brush border of the apical plasma membrane (APM) of renal proximal tubule (PT) cells mediate amino acid transport (AAT). We found that the membrane-associated class I myosin myosin 1b (Myo1b) localized at the apical
Konstantinos Malliaras et al.
EMBO molecular medicine, 6(6), 760-777 (2014-05-07)
Controversy surrounds the identity, origin, and physiologic role of endogenous cardiomyocyte progenitors in adult mammals. Using an inducible genetic labeling approach to identify small non-myocyte cells expressing cardiac markers, we find that activated endogenous cardioblasts are rarely evident in the
Francesca Maltecca et al.
The Journal of clinical investigation, 125(1), 263-274 (2014-12-09)
Spinocerebellar ataxia type 28 (SCA28) is a neurodegenerative disease caused by mutations of the mitochondrial protease AFG3L2. The SCA28 mouse model, which is haploinsufficient for Afg3l2, exhibits a progressive decline in motor function and displays dark degeneration of Purkinje cells
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