Gene Synthesis

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Gene synthesis is a sophisticated biotechnological process that involves the artificial construction of custom DNA sequences based on specified genetic information. Gene synthesis plays a crucial role in various fields such as genetic engineering, synthetic biology, drug development, and protein expression studies.

Tsingke is a premier gene synthesis service provider, offering high-quality services with fast turnaround time. We have established the autonomous research and development, automated self-aggregation TSINGKE Gene Factory synthesis platform, equipped with advanced Tsynth™ synthesis technology. Based on TSINGKE HELIXTECH, we integrate synthetic materials, synthetic equipment, and synthesis processes in the gene synthesis elements, achieving a highly intelligent production system. Continuous research and upgrades to our synthesizers and materials ensure the production of highly accurate oligos, enabling stable and efficient gene synthesis with timely delivery. For quality assurance, all Tsingke-constructed plasmids undergo rigorous NGS and Sanger sequencing validation, ensuring 100% sequence accuracy.
Achieved construction of 200kb plasmid
Achieved construction of 200kb plasmid
Proficient in synthesizing large sequences
Choose from 160+ commercial vectors at no extra cost, and enjoy free codon optimization
Fast Turnaround Time
Fast Turnaround Time
As fast as 5 days for standard gene synthesis
Unique Intelligent Splitting Algorithm
Unique Intelligent Splitting Algorithm
Rapidly and scientifically designs oligos for each gene
Service Type

Tsingke offers a comprehensive suite of gene synthesis services to cater to diverse research needs, such as Standard Gene Synthesis, ssDNA, etc. Tsingke leverages cutting-edge technologies and a highly intelligent production system to ensure accuracy, efficiency, and timely delivery. Also, tsingke is committed to delivering reliable and efficient gene synthesis solutions to researchers and biotechnologists worldwide. Contact us now for more details or to get started on your project.

Service Details
Standard Gene Synthesis & ProLongGene
- Highly Customized: From simple sequences to complex sequences
- Gene Length: Up to 200 kb
- Standard Deliver 1~4 μg plasmid
- Fast Turnaround: As fast as 5 business days
DNA Fragment
- From 100 bp to 1.2 kb
- Deliver 500 ng or 1 μg PCR products
- Efficient turnaround time of 2 to 5 business days
Single-stranded DNA (ssDNA)

- From 100 nt to 6000 nt
- Deliver lyophilized product powde
Plasmid Preparation
- Research grade
- Industrial grade
- Endotoxin <0.1 Eu/μg, <0.01 Eu/μg, <0.005 Eu/μg
PCR Cloning & Subcloning 
-100% Sequence Accuracy: Guaranteed with Sanger sequencing and NGS
-Not limited by restriction enzyme cutting sites
-Customizable: Clone target gene fragment at any site in any vector system
-100% Sequence Accuracy: Guaranteed with Sanger sequencing and NGS
-Unlimited Sites: Introduce your mutations at any site
-Cost-effective: All mutations found within a 30-base region will be defined as one whole mutation
Related Resource
Does Tsingke provide codon optimization? Does optimization have an impact on gene expression?
Tsingke offers free codon optimization.
For the same amino acid in different hosts, the corresponding codons may exhibit varying degrees of preference. Codon optimization involves utilizing preferred codons and avoiding rare codons to optimize the expression of a sequence in a specified host. There is a strong correlation between gene expression levels and codon preference. Tsingke's unique GeneOptimizer software utilizes a codon optimization algorithm that supports optimization for tens of thousands of hosts and provides customized services. The main parameters for optimization include codon preference, GC content, restriction enzyme sites (deletion), poly structure, sequence repeats, etc.
Which termination codon is preferred in the E. coli expression system? What about in mammalian systems?
In E. coli, TAG is rarely used; TAA is frequently used; TGA is also available.
In mammals, TGA is used more frequently than TAA and TAG.
Relative to the differences between mammals and E. coli, codon usage tables do not differ very much between different mammalian organisms.
How does Tsingke solve high-difficulty genes, such as those with high or low GC content, highly repetitive sequences, very long sequences, and special
High and low GC content, repetitive sequence:
Solution: Divide the sequence into small segments to reduce the impact of structure on synthesis, and choose the optimal connection solution, such as enzyme digestion and ligation and multi-segment recombination.
Very long sequences:
Solution: use multi-segment recombination to construct divided small segments, and combine them with vitro and vivo assembly.
Special parts of vectors (e.g. ccdB, LTR):
Solution: Use different competent cells corresponding to different parts of vectors, such as DB3.1, which renders the strain resistant to the toxic effects of the ccdB gene, the recombination-deficient Stbl series, etc.
Other unpredictable difficulties, such as genetic instability and toxicity, and the introduction of random mutations and deletions
Solution: Try different competent cells.
Can you keep my sequence information confidential?
Yes, all customer information will be kept confidential.
Which sites in the pUC57 vector will the synthesized gene be cloned?
Generally, the default clone is between EcoRⅠ and Hind Ⅲ. If you have particular needs, please note and we can select other suitable cloning sites according to the experimental needs based on your sequence.
Are there any requirements for my provided-vector?
We need you to ship at least 2 μg plasmid.
What vector does Tsingke use by default? Can I send my vectors to you?What vector does Tsingke use by default? Can I send my vectors to you?
We provide pUC57 vectors containing Amp (ampicillin) for free by default, and we also have a vector library for 160+ options that you could use for free.
Alternatively, you may use your own vector. Simply provide the vector sequence and a vector sample. It is recommended to ship your vector in advance, otherwise, the Turnaround Time (TAT)  may need to be extended by 3 business days to verify the vector.
What information do you need to prepare a quote?
We require information on the insert DNA sequence or amino acid sequence, and the host species if codon optimization is needed. Please ensure that the restriction sites are specified at the 5'/3' end or indicate if any internal modifications need to be avoided. Additionally, let us know if you wish to include other elements in the sequence, such as the Kozak sequence, stop codon, etc. 
Feel free to complete the evaluation form and send it via email to For any inquiries or project requirements, you can contact our account managers or sales managers through email. Our technical support team will promptly assess the price and turnaround time (TAT) and provide you with a detailed quotation as soon as possible."
*For Research Use Only. Not for use in diagnostic procedures.
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