Method and related biological material for cultivating transgenic plant of fluorescent protein mCherry labeled microtubulin
A technology of transgenic plants and fluorescent proteins, which is applied in the field of cultivating transgenic plants labeled with fluorescent protein mCherry-labeled tubulin, can solve the problems of chimeric expression, non-expression of cell expression, unstable expression of fusion protein, etc., and achieve the effect of stable expression.
- Summary
- Abstract
- Description
- Claims
- Application Information
 AI Technical Summary 
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0053] Embodiment 1, the expression vector pEarleyGate302-P used in the method for cultivating the transgenic plant of fluorescent protein mCherry labeling tubulin TUB6 :: Preparation of mCherry-TUB6 and its related biomaterials
[0054] The name shown in the artificially synthesized SEQ ID No.1 is P TUB6 :: DNA molecule of mCherry-TUB6. In SEQ ID No.1, positions 1-3004 are promoter P TUB6 ; The 3005-5074th position of SEQ ID No.1 is the mCherry-TUB6 fusion gene, the coding sequence of the mCherry-TUB6 fusion gene is the 3005-5074th position of SEQ ID No.1, encoding the fusion shown in SEQ ID No.2 Protein mCherry-TUB6; No. 3005-3712 of SEQ ID No.1 is the coding gene of mCherry, which encodes mCherry shown in No. 1 to No. 236 of SEQ ID No.2; No. 3713-3713 of SEQ ID No.2 Position 3724 is the coding gene of GA-Linker, which encodes the GA-Linker shown in the 237-240th position of SEQ ID No.2; the 3725-5074th position of SEQ ID No.2 is the coding gene of plant tubulin TUB6 , w...
Embodiment 2
[0060] Embodiment 2, the method for cultivating the transgenic plant of fluorescent protein mCherry labeling tubulin
[0061] 1.P TUB6Transfected pEarleyGate302-P that initiates the expression of mCherry-TUB6 fusion protein TUB6 :: Preparation of mCherry-TUB6 Arabidopsis (using pEarleyGate302-P TUB6 :: mCherry-TUB6 to cultivate transgenic plants with fluorescent protein mCherry-labeled tubulin)
[0062] Arabidopsis transformation was done by flower dipping method. Activated GV3101 / pEarleyGate302-P TUB6 :: mCherry-TUB6 was cultured in shake flask at 28°C for 24 hours in a final concentration of 50mg / mL kanamycin and 14mg / mL gentamicin in 5mL YEP liquid medium; after 200mL expansion culture, centrifuge at 4°C at 3600rpm for 15min to collect Bacterial cells were resuspended with 5% sucrose solution, and silwet L-77 with a volume ratio of 0.05% was added to obtain a bacterial suspension; the Colombian ecotype Arabidopsis thaliana inflorescences that had grown to the full flowe...
PUM
 Login to View More
 Login to View More Abstract
Description
Claims
Application Information
 Login to View More
 Login to View More - R&D
- Intellectual Property
- Life Sciences
- Materials
- Tech Scout
- Unparalleled Data Quality
- Higher Quality Content
- 60% Fewer Hallucinations
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2025 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com
