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Virus-Induced Gene Silencing (VIGS) of Plant Genes

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Introductions

Virus-Induced Gene Silencing (VIGS) -Lifeasible

Virus induced gene silencing (VIGS) is a new technology suitable for rapid and high-throughput research and identification of plant gene functions. Its principle is to use the natural defense mechanism of plants against viruses. When the endogenous target gene of the plant is loaded into the plant virus vector and the plant is inoculated, the virus infects the plant systemically, spreads to the whole plant, and simultaneously expresses the double-stranded RNA (dsRNA) of the target gene. This dsRNA will trigger the RNAi mechanism in plants to degrade the endogenous transcription of the target gene in the plant to produce mRNA, resulting in the down-regulation or inhibition of the function of the target gene, so as to understand the function of the target gene through combined analysis with plant phenotypic changes.

Services

Lifeasible has established plant VIGS technology platform, used to serve research workers who need VIGS to assist research. Once the VIGS technology system is established, it is regarded as a powerful tool for studying plant gene functions, and has been in-depth research and widely used. It has been used in tobacco, tomato and other plants to study the functional genes of disease resistance, growth and development and metabolic regulation. We uphold the customer-centric tenet and are committed to providing better services, saving customers a lot of time and energy.

Service content and process

Service Content and Process of Virus-Induced Gene Silencing (VIGS) - Lifeasible

Service requirements

  • Target gene sequence or accession number
  • Required vector
  • Plant variety and name. If it is a rare plant, the customer needs to prepare it

Feedback to customers

  • Sequencing report of constructed vector.
  • The plasmid and bacteria of the constructed vector.
  • Complete experimental methods, original experimental records, instrument parameters, reagents and consumables information.
  • Phenotype and gene function analysis pictures (customized according to requirements).

Project cycle

  • It takes about 4 months.

Advantages

  • Stable and easy. The target gene fragment can be assembled by cloning directly into a viral vector without assembling the inverted repeat sequence, and the inverted repeat sequence may be unstable when propagating in a bacterial host.
  • Simple and fast. VIGS vectors are usually introduced into plants by Agrobacterium-mediated methods or bio bombardment methods, and the VIGS phenotype develops within 1 or 2 weeks.
  • The cost is lower. The cost of VIGS experiments is relatively low, and high-throughput screening research can be achieved.
  • We have many newly developed virus-derived vectors, such as tobacco mosaic virus (TMV), potato X virus (PVX), tobacco rattle virus (TRV), tomato golden mosaic virus (TGMV), African cassava mosaic virus (ACMV).
  • There are also many mature plant transformation platforms, such as tobacco, Arabidopsis, rice, wheat, corn, soybean, cotton, etc.

※ For research or industrial use.

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