추천 제품
포장
bottle of 15 g
Quality Level
파라미터
60-225 °C temp. range
기술
gas chromatography (GC): suitable
기질
60/80 Carbopack B support
기질 활성군
SP®-1000 phase, 1%
컬럼 유형
packed GC
호환성
for analyte group halogenated organics
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일반 설명
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.
애플리케이션
SP 1000 on carbopack B packing was used for determining the carcinogenicity of inhaled 1,3-butadiene in mice at low exposure concentration.
법적 정보
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
개인 보호 장비
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
가장 최신 버전 중 하나를 선택하세요:
Analytical Measurements in Aquatic Environments.
Science, 2009, 73-73 null
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.
Cancer discovery, 9(2), 264-281 (2018-10-12)
Translation initiation is orchestrated by the cap binding and 43S preinitiation complexes (PIC). Eukaryotic initiation factor 1A (EIF1A) is essential for recruitment of the ternary complex and for assembling the 43S PIC. Recurrent EIF1AX mutations in papillary thyroid cancers are
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
Nature communications, 12(1), 366-366 (2021-01-16)
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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