GF77306182
Terbium
rod, 50mm, diameter 6.35mm, cast, 99%
Synonym(s):
Terbium, TB007910
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1 EA
$2,050.00
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
$2,050.00
Usually ships in 1 week. (Orders outside of US and Europe, please allow an additional 1-2 weeks for delivery)
Request a Bulk Order
Recommended Products
assay
99%
form
rod
manufacturer/tradename
Goodfellow 773-061-82
resistivity
116 μΩ-cm, 20°C
L × diam.
50 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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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
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
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
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
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
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