GF63273731
Terbium
rod, 100mm, diameter 6.35mm, cast, 99%
Synonym(s):
Terbium, TB007910
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About This Item
Empirical Formula (Hill Notation):
Tb
CAS Number:
Molecular Weight:
158.93
MDL number:
UNSPSC Code:
12141614
PubChem Substance ID:
NACRES:
NA.23
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Assay
99%
form
rod
manufacturer/tradename
Goodfellow 632-737-31
resistivity
116 μΩ-cm, 20°C
L × diam.
100 mm × 6.35 mm
bp
3230 °C (lit.)
mp
1356 °C (lit.)
density
8.234 g/mL at 25 °C (lit.)
SMILES string
[Tb]
InChI
1S/Tb
InChI key
GZCRRIHWUXGPOV-UHFFFAOYSA-N
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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
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
Xavier Sainsily et al.
Biochemical pharmacology, 92(2), 280-288 (2014-09-02)
The vasoactive urotensin-II (UII), a cyclic undecapeptide widely distributed in cardiovascular, renal and endocrine systems, specifically binds the UII receptor (UT receptor), a G protein-coupled receptor (GPCR). The involvement of this receptor in numerous pathophysiological conditions including atherosclerosis, heart failure
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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