Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Roland Stracke"'
Publikováno v:
Electromagnetic Biology and Medicine. 24:319-330
The effects of both constant (up to 2 × 103 V/m) and high-frequency alternating fields (up to 2.1 × 105 V/m, 200 kHz to 2 MHz) on suspended microtubules are investigated. At pH 6.8 and 120 mM ionic strength, constant fields cause a motion of microt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d9e6c8443847e988f6e5584f5fcc2929
https://doi.org/10.1080/15368370500380010
https://doi.org/10.1080/15368370500380010
Publikováno v:
Nanotechnology. 12:238-244
Conventional kinesin is a motor protein which translocates organelles from cell centre to cell periphery along specialized filamentous tracks, called microtubules. The direction of translocation is determined by microtubule polarity. This process of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e6909d2ecf826ab51d6cf5f4875082f2
https://doi.org/10.1088/0957-4484/12/3/307
https://doi.org/10.1088/0957-4484/12/3/307
Publikováno v:
Cell Biology International. 24:335-341
So far, there has been a discrepancy between the velocities of kinesin-dependent microtubule motility measured in vitro and within cells. By changing ATP, Mg(2+), and kinesin concentrations, pH and ionic strength, we tried to find conditions that fav
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da5739e7320b888910e3d89c6543598d
https://doi.org/10.1006/cbir.1999.0515
https://doi.org/10.1006/cbir.1999.0515
Publikováno v:
Nanotechnology. 11:52-56
Kinesin is a microtubule-associated protein, converting chemical into mechanical energy. Based on its ability to also work outside cells, it has recently been shown that this biological machinery might be usable for nanotechnological developments. Po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3cf956a4fecec7021b76e73d445662b3
https://doi.org/10.1088/0957-4484/11/2/302
https://doi.org/10.1088/0957-4484/11/2/302
Publikováno v:
Cell biology international. 27(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85e7d1aff9b8c5da84dec2ffbe314139
https://pubmed.ncbi.nlm.nih.gov/12681326
https://pubmed.ncbi.nlm.nih.gov/12681326
Publikováno v:
Biochemical and biophysical research communications. 293(1)
By video contrast microscopy, individual microtubules formed from pure tubulin in the presence of taxol were studied in constant electric fields. At nearly physiological conditions, i.e., in a buffer at pH 6.8 and 120 mM ionic strength, suspended mic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a65483c6b412756894826c1c8de16d6
https://pubmed.ncbi.nlm.nih.gov/12054645
https://pubmed.ncbi.nlm.nih.gov/12054645
Publikováno v:
FEBS letters. 466(1)
DeCuevas et al. [J. Cell Biol. 116 (1992) 957-965] demonstrated by circular dichroism spectroscopy for the kinesin stalk fragment that shifting temperature from 25 to 30 degrees C caused a conformational transition. To gain insight into functional co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7567320f0681372298e867ba0df6e1d6
https://pubmed.ncbi.nlm.nih.gov/10648812
https://pubmed.ncbi.nlm.nih.gov/10648812
Publikováno v:
Journal of Microscopy. 121:185-189
SUMMARY In the course of preparing specimens for scanning electron microscopy, both glutaraldehyde and OsO4-fixed cells exhibit a considerable shrinkage with a reduction of the mean cellular diameter of about 45% after critical point drying. However,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6db2f8ba3e62fe2efd8b2eafd0c2234
https://doi.org/10.1111/j.1365-2818.1981.tb01211.x
https://doi.org/10.1111/j.1365-2818.1981.tb01211.x
Autor:
Roland Stracke, Karl-Hermann Schmidt
Publikováno v:
Zentralblatt fur Bakteriologie, Mikrobiologie, und Hygiene. Series A, Medical microbiology, infectious diseases, virology, parasitology. 262(4)
A simple semiquantitative method for determination of IgG-binding structures on bacteria by direct fluorescence technique is described. The fluorescence of bacterial bound IgG-FITC-conjugate was measured in a paste-like bacterial sediment by using a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16d50e551657ffc1942e5a05de924aa3
https://pubmed.ncbi.nlm.nih.gov/3799093
https://pubmed.ncbi.nlm.nih.gov/3799093