A zinc finger protein gene osrlzp controlling rice leaf shape and its application
A zinc finger protein, rice technology, applied in the application, genetic engineering, plant genetic improvement and other directions, can solve the problems such as the inability to completely and clearly outline the molecular regulatory network, the lack of in-depth research on the relationship between genes, etc., to achieve easy access and safety. high performance effects
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Embodiment 1
[0021] Embodiment 1: Cloning of rice OsRLZP gene
[0022] 1. Reagents
[0023] RNA extraction reagent Trizol was purchased from Invitrogen; reverse transcriptase ReverTraAce was purchased from Toyobo; high-fidelity DNA polymerase PrimeStar was purchased from TaKaRa; cloning vector pEASY TM -BluntSimpleCloningVector was purchased from Beijing Quanshijin Biotechnology Co., Ltd.; primers were synthesized by Shanghai Yingjun Biotechnology Co., Ltd., and the rest of the reagents were imported or domestic analytically pure products.
[0024] 2. E. coli strains and plant material
[0025] Escherichia coli (Escherichiacoli) strain DH5α was purchased from Beijing Quanshijin Biotechnology Co., Ltd.; rice japonica variety Nipponbare (OryzasativeL.ssp.japonicacv.Nipponbare) seeds were provided by Sichuan Academy of Agricultural Sciences.
[0026] 3. Medium and solution
[0027] LB medium: tryptone 10g / L, yeast powder 5g / L, NaCl 10g / L. Adjust the pH to 7.0 with NaOH and autoclave.
[...
Embodiment 2
[0071] Embodiment 2: Construction of rice OsRLZP gene overexpression recombinant plasmid
[0072] 1. Reagents
[0073] The plasmid extraction kit EasyPurePlasmidMiniPrepKit was purchased from Beijing Quanshijin Biotechnology Co., Ltd.; the agarose gel recovery kit EasyPureQuickGelExtraction Kit was purchased from Beijing Quanshijin Biotechnology Co., Ltd.; restriction enzymes HindIII, SacI, and T4 ligase were purchased from TaKaRa Company .
[0074] Other imported sub-packages and conventional reagents are the same as in Example 1.
[0075] 2. Agrobacterium strains and plant expression vectors
[0076] The Agrobacterium tumefaciens strain EHA105 used for transgenesis was purchased from Clontech; the eukaryotic expression vector pHB was constructed by the laboratory of Professor Hongquan Yang of Shanghai Jiaotong University (Mao et al., ProcNatlAcadSciUSA, 2005).
[0077] 3. Medium
[0078] YEB medium: yeast extract 1g / L, beef extract 5g / L, egg white 5g / L, sucrose 5g / L, MgS...
Embodiment 3
[0120] Embodiment 3: Obtaining of rice OsRLZP overexpression transgenic plants
[0121] 1. Reagents
[0122] RNA extraction reagent Trizol was purchased from Invitrogen; reverse transcriptase ReverTraAce was purchased from Toyobo; real-time quantitative PCR reagent TransStart TM GreenqPCRSuperMix was purchased from Beijing Quanshijin Biotechnology Co., Ltd. Other reagents are imported sub-packages or domestic analytically pure products.
[0123] 2. Medium
[0124] Plant tissue culture medium:
[0125]
[0126]
[0127] (1) Induction medium: NB+2mg / L2, 4-D, pH5.8~5.9; (2) Co-cultivation medium: NB+2mg / L2, 4-D+100μmol / L acetosyringone, pH5. 2; (3) Screening medium: NB+2mg / L2, 4-D+250mg / L carbenicillin+30~50mg / L hygromycin, pH5.8~5.9; (4) Differentiation medium: NB+ 10mg / LKT+0.4mg / LNAA+250mg / L carbenicillin, pH5.8~5.9; (5) Rooting medium: 1 / 2MS, pH5.8~5.9.
[0128] 3. Method
[0129] 3.1 Agrobacterium-mediated transformation of rice
[0130] 3.1.1 Induction and subc...
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