推薦產品
化驗
99%
形狀
foil
製造商／商標名
Goodfellow 163-133-74
電阻係數
116 μΩ-cm, 20°C
尺寸 × 厚度
25 x 25 mm × 0.1 mm
bp
3230 °C (lit.)
mp
1356 °C (lit.)
密度
8.234 g/mL at 25 °C (lit.)
SMILES 字串
[Tb]
InChI
1S/Tb
InChI 密鑰
GZCRRIHWUXGPOV-UHFFFAOYSA-N
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一般說明
For updated SDS information please visit www.goodfellow.com.
法律資訊
Product of Goodfellow
Kamal P Mani et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 148, 412-419 (2015-04-29)
Terbium molybdate nanophosphors were synthesized through a facile sol-gel route. The structure of the phosphors was characterized by X-ray diffraction, Raman spectra and Fourier transform infrared spectroscopy analysis. The X-ray diffraction studies revealed that the structure of the nanophosphor gradually
Zhi Shi et al.
Cancer research, 75(1), 147-158 (2014-11-02)
Cables1 is a candidate tumor suppressor that negatively regulates cell growth by inhibiting cyclin-dependent kinases. Cables1 expression is lost frequently in human cancer but little is known about its regulation. Here, we report that Cables1 levels are controlled by a
Lei Rao et al.
International journal of food microbiology, 205, 73-80 (2015-04-19)
The objective of this study was to investigate the inactivation of the Bacillus subtilis spores by high pressure CO2 combined with high temperature (HPCD+HT) and to analyze the clumping effect of the spores on their HPCD+HT resistance. The spores of
Dinari A Harris et al.
Current protocols in nucleic acid chemistry, Chapter 6, Unit 6-Unit 6 (2008-04-23)
The function of an RNA molecule is determined by its overall secondary and tertiary structure. The tertiary structure is facilitated and stabilized by the interaction with metal ions. The current chapter offers a detailed protocol on the use of the
Cédric Brulé et al.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 28(12), 5148-5162 (2014-09-04)
Biased agonism by G-protein-coupled receptor ligands has opened up strategies for targeted physiological or therapeutic actions. We hypothesized that urotensin II (UII)-derived peptides displayed unexpected physiological effects because of such biased signaling on the UII human urotensin (hUT) receptor. We
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