GF62438520
Iron
rod, 200mm, diameter 25mm, as drawn, 98+%
Synonyme(s) :
Iron, FE007965
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About This Item
Produits recommandés
Pureté
98%
Forme
rod
Fabricant/nom de marque
Goodfellow 624-385-20
Résistivité
9.71 μΩ-cm
L × diam.
200 mm × 25 mm
Point d'ébullition
2750 °C (lit.)
Pf
1535 °C (lit.)
Densité
7.86 g/mL at 25 °C (lit.)
Chaîne SMILES
[Fe]
InChI
1S/Fe
Clé InChI
XEEYBQQBJWHFJM-UHFFFAOYSA-N
Description générale
For updated SDS information please visit www.goodfellow.com.
Informations légales
Product of Goodfellow
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50 years ago in the Journal of Pediatrics: Iron metabolism in premature infants: II. Prevention of iron deficiency.
The Journal of pediatrics, 164(4), 768-768 (2014-03-22)
Infection and immunity, 82(6), 2356-2367 (2014-03-26)
Hypervirulent (hypermucoviscous) Klebsiella pneumoniae (hvKP) strains are an emerging variant of "classical" K. pneumoniae (cKP) that cause organ and life-threatening infection in healthy individuals. An understanding of hvKP-specific virulence mechanisms that enabled evolution from cKP is limited. Observations by our
Nature, 509(7498), 105-109 (2014-04-04)
Autophagy, the process by which proteins and organelles are sequestered in double-membrane structures called autophagosomes and delivered to lysosomes for degradation, is critical in diseases such as cancer and neurodegeneration. Much of our understanding of this process has emerged from
Biochemistry, 53(14), 2232-2241 (2014-04-01)
From an evolutionary point of view, plant and animal ferritins arose from a common ancestor, but plant ferritin exhibits different features as compared with the animal analogue. One major difference is that the 4-fold channels naturally occurring in plant ferritin
Proceedings of the National Academy of Sciences of the United States of America, 111(17), E1695-E1704 (2014-04-16)
Eukaryotic ribonucleotide reductases (RNRs) require a diferric-tyrosyl radical (Fe(III)2-Y•) cofactor to produce deoxynucleotides essential for DNA replication and repair. This metallocofactor is an important target of RNR-based therapeutics, although mechanisms of in vivo cofactor assembly, inactivation, and reactivation are poorly
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