Services
Providing Advanced Biological Technical Services for Researchers in Fundamental Science
Watermelon Genetic Transformation
Project Brief
Watermelon genetic transformation refers to the process of introducing exogenous genes into grapefruit cells or tissues using molecular biology techniques, enabling them to integrate into the grapefruit genome and achieve stable inheritance and expression, thereby cultivating transgenic grapefruit plants with targeted traits. This technology serves as the core means for grapefruit molecular breeding, gene function verification, and the development of related innovative applications. It can effectively break through the species barriers and cycle limitations of traditional hybrid breeding, and rapidly improve the key agronomic traits of grapefruit.
Technological Superiority
1. Efficient screening: Strict optimization of each step in genetic transformation, resulting in high transformation efficiency.
2. Full-process monitoring: From seed disinfection onwards, every stage is strictly monitored with real-time progress tracking.
3. Integrated quantitative analysis: Offers detection methods such as PCR, qPCR, and Sanger sequencing to ensure authentic transgenic outcomes.
Sample Receiving Standards
| Type | Sample Submission Standards | Conditions of carriage |
| The sequence that requires gene synthesis | nothing | nothing |
The constructed plasmid Intermediate vector plasmid | Concentration > 100 ng/ul, Volume > 20 ul; Provides carrier sequence and resistance, without contamination. | The plasmid will be sent using an ice pack. |
| Contains bacterial culture with the constructed plasmid; contains bacterial culture with the intermediate vector plasmid | Provide resistance. For bacterial solutions with a volume greater than 0.5ml and glycerol bacteria that have been stored for more than one year, the samples should be activated before submission. | The bacterial liquid is sent by dry ice. The amount of dry ice used: 1 day (5kg), 2-3 days (10-20kg), 3-5 days (20-30kg). |
| Planktonic bacteria | non-pollution | normal temperature |
Note: 1. For other types of samples, please contact our company in advance. 2. For dry ice sampling and transportation, notify our company at least 2 days before submitting the samples. | ||
Service process, Cycle and Delivery

| Species | Type of Service | Variety | Service Period | Delivery Standard (Default delivery includes resistance gene identification) |
| Watermelon | 1. Vector construction / Gene synthesis 2. Sequencing of the target gene + Vector construction 3. The target gene has been constructed into an expression vector and its sequence has been verified through sequencing. | Xishang 8 variety | ten | A. Vector Construction: The client does not provide the vector template and does not deliver it. B. Gene Synthesis: The client does not provide the vector template and does not deliver it. |
| Overexpression | 5 to 6 months | The number of T0 generation positive plants (resistant plants) is ≥ 13. | ||
| 10 to 12 months | Two T0 positive seedlings were harvested to obtain T1 mature fruits (a total of 2 samples, the exact weights are subject to actual measurement) | |||
| Single-gene knockout | 6 to 7 months | The number of T0 generation positive seedlings (resistant seedlings) is ≥ 5. | ||
| 11 to 13 months | One T0 positive seedling was harvested to produce T1 mature fruits (a total of 1 sample, the exact weight is subject to actual measurement) |
Note: Other varieties can be tested*.
Case Show

A: Preparation of explants; B: Inoculation; C: Regeneration; D: Bud induction; E: Differentiation; F: Rooting
Services Workflow
Online Consultation
01
Solution Matching
02
Service Contract
03
One-Stop-Services
04
Project Report
05
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Tel: +86 025-85205672
Email: info@pronetbio.com
Address: Building 3C, Nanjing Xianlin Zhigu,
Qixia District, Nanjing, Jiangsu, China, 210033
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