解决
发表于 2025-3-25 06:10:46
Kan WangIncludes cutting-edge methods and protocols.Provides step-by-step detail essential for reproducible results.Contains key notes and implementation advice from the experts
Multiple
发表于 2025-3-25 09:27:42
Methods in Molecular Biologyhttp://image.papertrans.cn/a/image/151689.jpg
esthetician
发表于 2025-3-25 12:00:27
Agrobacterium Protocols978-1-4939-1658-0Series ISSN 1064-3745 Series E-ISSN 1940-6029
Nonporous
发表于 2025-3-25 16:13:57
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暴行
发表于 2025-3-25 21:09:41
Philippe Major,Milan Matthiesenformation: tetraploidy, chimeras, and escape. Using a liquid culture system for somatic embryogenesis, Akasaka-Kenedy et al. (Plant Sci 166: 763–769, 2004) overcame these problems and established an efficient transformation system; the protocol introduced in this chapter is based on this method.
Confess
发表于 2025-3-26 01:54:00
1064-3745 ation advice from the experts.Rapid changes and significant progress have been made in the .Agrobacterium. field, such as genetically transforming plants for both basic research purposes and agricultural development. In .Agrobacterium Protocols, Third Edition, Volumes 1 .and. 2., a team of leading e
GORGE
发表于 2025-3-26 07:37:57
Dao Companion to Korean Confucian Philosophy cocultivation medium; selection and regeneration of transformed shoots are carried out on selection medium containing 50 mg/L kanamycin (Km) and 250 mg/L timentin (or cefotaxime) for 3–5 months. In this protocol, the optimal media for shoot proliferation and shoot regeneration from leaf explants are genotype dependent.
opinionated
发表于 2025-3-26 11:22:15
Cherry cocultivation medium; selection and regeneration of transformed shoots are carried out on selection medium containing 50 mg/L kanamycin (Km) and 250 mg/L timentin (or cefotaxime) for 3–5 months. In this protocol, the optimal media for shoot proliferation and shoot regeneration from leaf explants are genotype dependent.
拍下盗公款
发表于 2025-3-26 16:18:05
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Neuropeptides
发表于 2025-3-26 16:57:00
Melon (,)formation: tetraploidy, chimeras, and escape. Using a liquid culture system for somatic embryogenesis, Akasaka-Kenedy et al. (Plant Sci 166: 763–769, 2004) overcame these problems and established an efficient transformation system; the protocol introduced in this chapter is based on this method.