๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

PRODUCTION OF GERMLINE CHIMERIC CHICKENS BY TRANSFER OF CULTURED PRIMORDIAL GERM CELLS

โœ Scribed by IL-KUK CHANG; DONG KEE JEONG; YEONG HO HONG; TAE SUB PARK; YANGHA KIM MOON; TADAO OHNO; JAE YONG HAN


Book ID
102565767
Publisher
Elsevier Science
Year
1997
Tongue
English
Weight
144 KB
Volume
21
Category
Article
ISSN
1065-6995

No coin nor oath required. For personal study only.

โœฆ Synopsis


Primordial germ cells (PGCs) from stage 27 (5.5-day-old) Korean native ogol chicken embryonic germinal ridges were cultured in vitro for 5 days. As in in vivo culture, these cultured PGCs were expected to have already passed beyond the migration stage. Approximately 200 of these PGCs were transferred into 2.5-day-old white leghorn embryonic blood stream, and then the recipient embryos were incubated until hatching. The rate of hatching was 58.8% in the manipulated eggs. Six out of 60 recipients were identified as germline chimeric chickens by their feather colour. The frequency of germline transmission of donor PGCs was 1.3-3.1% regardless of sex. The stage 27 PGCs will be very useful for collecting large numbers of PGCs, handling of exogenous DNA transfection during culture, and for the production of desired transgenic chickens.


๐Ÿ“œ SIMILAR VOLUMES


Germ line chimera produced by transfer o
โœ Il-Kuk Chang; Atsushi Yoshiki; Moriaki Kusakabe; Atsushi Tajima; Tateki Chikamun ๐Ÿ“‚ Article ๐Ÿ“… 1995 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 679 KB

## Abstract Intrinsic primordial germ cells (PGCs) from stage 27 (5โ€dayโ€old) chick embryonic germinal ridges were cultured in vitro for a further 5 days, and shown to proliferate on stroma cells derived from the germinal ridge. To determine whether these cultured PGCs could colonize and contribute

Production of germ-line chimeras by tran
โœ Tajima, Atsushi; Naito, Mitsuru; Yasuda, Yoshiaki; Kuwana, Takashi ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 69 KB ๐Ÿ‘ 2 views

Gonadal primordial germ cells (gPGCs) were collected from gonadal anlage of 5day-old White Leghorn (WL) embryos. Collected gPGCs were suspended in freezing medium containing 10% dimethyl sulphoxide (DMSO). The cell-suspension was frozen at 1ยฐC/min until the temperature reached -80ยฐC; cells were then