Abstract
SYNOPSIS. The kinetoplast of L. tarentolae remains attached to the basal body upon cell rupture by detergent lysis, sonication, or hypotonic lysis in 0.02 M Tris buffer (pH 7.9) at 0–4 C. Hypotonic lysis in 0.02 M Tris‐HCl‐2 mM EDTA at 0–4 C and application of mild shearing forces bring about release of most of the swollen kinetoplasts. The kinetoplast DNA can be seen in phase contrast microscopy as a dark mass contiguous to the kinetoplast membrane directly opposite the basal body. Upon return to isotonic media, the kinetoplast shrinks; the membranes of such kinetoplasts are impermeable to added DNAase.
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Dates
Type | When |
---|---|
Created | 18 years, 3 months ago (May 13, 2007, 8:27 p.m.) |
Deposited | 1 year, 10 months ago (Nov. 1, 2023, 2:35 p.m.) |
Indexed | 1 year, 10 months ago (Nov. 1, 2023, 9:11 p.m.) |
Issued | 57 years, 7 months ago (Feb. 1, 1968) |
Published | 57 years, 7 months ago (Feb. 1, 1968) |
Published Online | 18 years, 4 months ago (April 30, 2007) |
Published Print | 57 years, 7 months ago (Feb. 1, 1968) |
@article{SIMPSON_1968, title={Behavior of the Kinetoplast of Leishmania tarentolae upon Cell Rupture*}, volume={15}, ISSN={0022-3921}, url={http://dx.doi.org/10.1111/j.1550-7408.1968.tb02097.x}, DOI={10.1111/j.1550-7408.1968.tb02097.x}, number={1}, journal={The Journal of Protozoology}, publisher={Wiley}, author={SIMPSON, LARRY}, year={1968}, month=feb, pages={132–136} }