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ใƒžใ‚ฆใ‚น่ƒŽๅ…ใฎ่„ณใฎใƒˆใƒฌใƒผใ‚นๆกไปถไป˜ใ้บไผ็ตŒใ‚ทใƒŠใƒ—ใ‚น
JoVE ์‹ ๋ฌธ
์‹ ๊ฒฝ๊ณผํ•™
JoVE ๋น„๋””์˜ค๋ฅผ ํ™œ์šฉํ•˜์‹œ๋ ค๋ฉด ๋„์„œ๊ด€์„ ํ†ตํ•œ ๊ธฐ๊ด€ ๊ตฌ๋…์ด ํ•„์š”ํ•ฉ๋‹ˆ๋‹ค.  ์ „์ฒด ๋น„๋””์˜ค๋ฅผ ๋ณด์‹œ๋ ค๋ฉด ๋กœ๊ทธ์ธํ•˜๊ฑฐ๋‚˜ ๋ฌด๋ฃŒ ํŠธ๋ผ์ด์–ผ์„ ์‹œ์ž‘ํ•˜์„ธ์š”.
JoVE ์‹ ๋ฌธ ์‹ ๊ฒฝ๊ณผํ•™
Conditional Genetic Transsynaptic Tracing in the Embryonic Mouse Brain
DOI:

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11:03 min

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December 22, 2014

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Chapters

  • 00:05Title
  • 01:29Preparing and Fixing Tissues
  • 03:04Freezing and Cryosectioning
  • 04:26Tyramide Signal Amplification (TSA) for Tracer Visualization
  • 08:14Development of the Neural Circuits Controlling the Reproductive Axis
  • 10:06Conclusion

Summary

์ž๋™ ๋ฒˆ์—ญ

Capitalizing on a binary genetic strategy we provide a detailed protocol for neural circuit tracing in mice that express complementary transsynaptic tracers after Cre-mediated recombination. Because cell-specific tracer production is genetically encoded, our experimental approach is suitable to study the formation and maturation of neural circuitry during murine embryonic brain development at a single cell resolution.

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