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Volumn 3, Issue 11, 2007, Pages 1894-1899

Exploring a nanotube dispersion mechanism with gold-labeled proteins via cryo-TEM imaging

Author keywords

Carbon nanotubes; Dispersion; Gold; Proteins; Transmission electron microscopy

Indexed keywords

CARRIER CONCENTRATION; DISPERSIONS; GOLD; MOLECULAR STRUCTURE; MONOMERS; PROTEINS; TRANSMISSION ELECTRON MICROSCOPY;

EID: 36048972401     PISSN: 16136810     EISSN: 16136829     Source Type: Journal    
DOI: 10.1002/smll.200700124     Document Type: Article
Times cited : (37)

References (58)
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    • The imaged GNP-GNP distance is much longer than the GNP's diameter (8 nm). Therefore, we expect that the BSA-BSA distance (≈40 nm) is not affected (see Figures 1D and 2B). Moreover, the calculated Debye length in our system is 3 nm (i.e., Columbic interactions are screened above this value), again, much shorter than the imaged length density distance.
    • The imaged GNP-GNP distance is much longer than the GNP's diameter (8 nm). Therefore, we expect that the BSA-BSA distance (≈40 nm) is not affected (see Figures 1D and 2B). Moreover, the calculated Debye length in our system is 3 nm (i.e., Columbic interactions are screened above this value), again, much shorter than the imaged length density distance.
  • 42
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    • The protein itself cannot be resolved by AFM in the presence of GNP since it is masked by the GNP-AFM tip Interactions. Therefore we carried out more AFM scans on the BSA-SWNT system In the absence of GNP
    • The protein itself cannot be resolved by AFM in the presence of GNP since it is masked by the GNP-AFM tip Interactions. Therefore we carried out more AFM scans on the BSA-SWNT system In the absence of GNP.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.