11815
Coated GC Packing
phase SP®-1000, 1%, matrix 60/80 Carbopack B support, bottle of 15 g
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About This Item
EC Number:
UNSPSC Code:
23151817
Recommended Products
packaging
bottle of 15 g
Quality Level
parameter
60-225 °C temp. range
technique(s)
gas chromatography (GC): suitable
matrix
60/80 Carbopack B support
matrix active group
SP®-1000 phase, 1%
column type
packed GC
compatibility
for analyte group halogenated organics
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General description
The choice of coating material is based on the stationary phase of the GC.
Ready-to-use coated packing for those wanting to pack their own columns.
Application
SP 1000 on carbopack B packing was used for determining the carcinogenicity of inhaled 1,3-butadiene in mice at low exposure concentration.
Legal Information
SP is a registered trademark of Sigma-Aldrich Co. LLC
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Analytical Measurements in Aquatic Environments.
Namiesnik J and Szefer P.
Science, 2009, 73-73 null
R L Melnick et al.
Cancer research, 50(20), 6592-6599 (1990-10-15)
The carcinogenicity of inhaled 1,3-butadiene was evaluated in C57BL/6 x C3H F1 mice exposed to concentrations of this gas ranging from 6.25 to 625 ppm. Butadiene is a high production volume chemical, used mainly in the manufacture of synthetic rubber.
Gnana P Krishnamoorthy et al.
Cancer discovery, 9(2), 264-281 (2018-10-12)
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Marte Molenaars et al.
Cell metabolism, 31(3), 549-563 (2020-02-23)
Slowing down translation in either the cytosol or the mitochondria is a conserved longevity mechanism. Here, we found a non-interventional natural correlation of mitochondrial and cytosolic ribosomal proteins (RPs) in mouse population genetics, suggesting a translational balance. Inhibiting mitochondrial translation
Mylène Tajan et al.
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Many tumour cells show dependence on exogenous serine and dietary serine and glycine starvation can inhibit the growth of these cancers and extend survival in mice. However, numerous mechanisms promote resistance to this therapeutic approach, including enhanced expression of the de
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