gBlocks Gene Fragments and gBlocks HiFi Gene Fragments are double-stranded DNA fragments up to 3000 bp in length, designed for affordable and easy gene construction or modification. Suited for applications such as antibody research and CRISPR-mediated genome editing, qPCR and NGS controls, and more. Drive your projects to completion faster with these high-fidelity fragments.
1BD, business days. Shipping time is dependent on length and complexity of the dsDNA fragment(s) ordered. In a few cases, shipping time may exceed the estimated time.
gBlocks Gene Fragments are double-stranded DNA fragments 125–3000 bp in length with a median error rate of less than 1:5000. They are manufactured with the same industry-leading, high-fidelity synthesis chemistries that were developed for our Ultramer™ DNA Oligos.
Each gBlocks Gene Fragment goes through a quality control process, which includes size verification by capillary electrophoresis and sequence identification by mass spectrometry. This rigorous testing that most recombinant colonies obtained from cloning each gBlocks Gene Fragment will contain the desired insert. More complex sequences may need the end user to sequence additional clones.
gBlocks HiFi Gene Fragments are double-stranded DNA fragments between 1000–3000 bp that are sequence-verified via NGS with a median error rate of less than 1:12,000. These high-quality, high-fidelity fragments facilitate the assembly of large and complex sequences, matching both the length and accuracy needed to minimize the introduction of unwanted substitution or deletion errors.
With either gBlocks or gBlocks HiFi Gene Fragments, you can easily assemble and clone your DNA fragment into the vector of your choice using a variety of cloning methods. For added flexibility, you can order gBlocks Gene Fragments with or without a 5′‑phosphate group.
gBlocks Gene Fragment Libraries are pooled gBlocks fragments of 251–500 bp in total length. gBlocks Gene Fragment Libraries are ideal for generating recombinant antibodies or for protein engineering, allowing researchers to generate hundreds of thousands of constructs within a reasonable budget. The variable regions can be up to 18 consecutive N (any base) or K (G or T) bases long and must be at least 125 bp from either end of the gene fragment (Figure 1).
Figure 1. Ordering format for gBlocks Gene Fragment Libraries. Placing a K mixed base in the third position of codons eliminates the TAA and TGA stop codons from being included in the gene fragments libraries, leaving only TAG as the possible stop codon.
For gBlocks Gene Fragment Libraries, each constant region is verified similarly to standard gBlocks Gene Fragments. The final library product is size-verified by capillary electrophoresis.
Both gBlocks and gBlocks HiFi Gene Fragments demonstrate consistent high sequence fidelity and purity across various lengths.
Figure 2. IDT gBlocks and gBlocks HiFi Gene Fragments demonstrate high probability of cloning success. With a median error rate of 1:12,000 for gBlocks HiFi Gene Fragments, IDT Gene Fragments demonstrate a high probability of first-time cloning success. Based on data derived from NGS sequencing of gene fragments, gBlocks Gene Fragments and gBlocks HiFi Gene Fragments are up to 45% more likely to give a correct clone the first time when cloning fragments up to 3000 bps compared to an alternate supplier.
In a head-to-head comparison study against two other DNA synthesis suppliers, IDT’s proprietary synthesis and error correction processes resulted in gene fragments with lower error rates. Low error rates ensure more correct clones, allowing researchers to reduce the number of colonies needed to screen by as much as 50%.
Figure 3. IDT gBlocks and gBlocks HiFi Gene Fragments produce a higher percentage of correct colonies when compared to two other suppliers. Based on screening and sequencing of 24 colonies per sequence, IDT’s fragments were the only fragments to have greater than 75% correct colonies with the desired full-length sequence, and the only gene fragments to achieve greater than 90% correct colonies for fragments that were 1 kb or more in length.
Using IDT gene fragments can reduce the time and expense of screening colonies compared to fragments from other suppliers. Cloning efficiency is affected by many factors, including the cloning method used, the stability of the cell line and plasmid, vector preparation, and toxicity or stress from expression of coding sequences. The values in Table 1 represent typical screening numbers needed when using a seamless cloning method.
Table 1. gBlocks and gBlocks HiFi Gene Fragments reduce the time and expense of screening colonies. The approximate number of colonies to screen for a 90% chance of getting a correct clone.
|Length (bp)||gBlocks Gene Fragments||gBlocks HiFi Gene Fragments|
IDT gene fragments are compatible with many cloning and assembly kits and automation platforms, allowing easy assembly of your desired construct sequence into your preferred cloning method. Methods include traditional cloning, Gibson Assembly® (New England Biolabs), Golden Gate, Gateway® (Invitrogen), TOPO™/TA cloning (Thermo Fisher), blunt-end cloning, and others.
The most common source of this issue is an incomplete resuspension of your gBlocks Gene Fragment. The pellets can stick to the side or cap of the tube, and unless you vortex vigorously and incubate the tube at 50°C for 20 minutes, you might not have the DNA concentration you expect. We recommend the following:
In most cases, our system has found a region with either very high G/C content or several small repeats that would prevent us from synthesizing your sequence.
If your sequence contains a coding region, you can use codon optimization to reduce the complexity. Codon optimization uses synonymous codons to retain the final amino acid sequence that is expressed while generating a sequence that we can synthesize.
If your sequence is not a coding region, we might be able to synthesize the sequence as a custom gene, which is delivered in a basic pUC vector, rather than just a linear, dsDNA fragment. For assistance, send your sequences and any questions to email@example.com.
We do not recommend using PCR to add the overhangs, because PCR can preferentially amplify smaller byproducts in the prep, leading to issues with the cloning reaction and increasing the number of colonies you need to screen to find the correct full-length insert. Instead, build the overhangs into the gBlocks Gene Fragment itself. The amount of material you will receive is enough for a couple of assembly reactions.
The additional PCR step is not required to generate additional material and adds an additional enzymatic step to the protocol that can introduce errors.
IDT ships gBlocks HiFi Gene Fragments (IDT) dry unless otherwise requested. While dry, they should be stable almost indefinitely.
After resuspending in a high-quality, molecular-grade water or buffer, pH 7.5–8.0, you should store the DNA at –20°C and if necessary, aliquot to avoid more than 2 or 3 freeze-thaw cycles. Adding a carrier to your resuspension and dilution buffers can help prevent any potential decrease in product concentration.
gBlocks HiFi Gene Fragments are clonal products and can be amplified if necessary. However, most applications such as restriction-digest, blunt-end, and Gibson cloning can be performed with the material provided by IDT, and PCR amplification should not be necessary.
If the purpose of the amplification is to add flanking bases to complete a cloning reaction, we strongly recommend ordering the gBlocks HiFi Gene Fragment (IDT) with the required bases rather than adding them afterwards using PCR.
If you choose to amplify your gBlocks HiFi Gene Fragment, use the minimum amount of starting template required by your PCR kit protocol, limit the cycle number to 10–12, and use a high-fidelity polymerase.
Cloning of gBlocks HiFi Gene Fragments is similar to cloning a very pure PCR product. For restriction cloning, it is important to add 6–8 nt at the ends of the fragment, beyond the restriction recognition sequence.
Most restriction enzymes will not cut efficiently, or at all, if the fragment terminates precisely at the restriction site.
We currently only offer gBlocks™ HiFi Gene Fragments between 1000–3000 bp.
The combination of speed, cost, and purity make gBlocks™ Gene Fragments an ideal solution for most applications, but in some applications, such as the assembly of larger constructs, starting with a fragment with a lower error rate may significantly reduce costs.
gBlocks HiFi Gene Fragments use a proprietary manufacturing technique that can generate double-stranded DNA fragments with average error rates of 1:12,000, which is approximately 2.5–4x fewer errors than other commercially available gene fragments.
IDT can synthesize gBlocks Gene Fragments between 125 bp and 3 kb in length.
However, if you require a double-stranded DNA construct outside of this size range, we offer 2 options:
If you are interested in a custom gene quote or assistance in splitting your sequence into sub-fragments, please email your sequences to firstname.lastname@example.org.
We do not recommend amplifying gBlocks Gene Fragments >1 kb in length.
gBlocks Gene Fragments are synthesized from several smaller overlapping fragments. The final prep may contain some of these smaller byproducts. During PCR, smaller products are more efficiently amplified than longer ones, and at the exponential phase of PCR, smaller products in the reaction will overwhelm the generation of the full-length correct product. When run on the gel, these amplification products appear as a smear or smaller bands than expected.
Most applications such as restriction digest, blunt end, and seamless cloning can be performed with the material provided by IDT, and PCR amplification should not be necessary. If the purpose of the amplification is to add flanking bases to complete a cloning reaction, we strongly recommend ordering the gBlocks Gene Fragment with the required bases rather than adding them afterwards using PCR.
If you must amplify your gBlocks Gene Fragment, use the minimum amount of starting template required by your PCR kit protocol, limit the cycle number to 10–12, and use a high-fidelity polymerase.
Synthesis time depends on the length of the gBlocks fragment.
|Length of gBlocks Gene Fragment||Time to ship after order confirmation (business days)|
|Up to 750 bp||2–4|
|More than 1000 bp||5–8|
Here is a comparison of gBlocks and eBlocks Gene Fragments:
|gBlocks Gene Fragments||eBlocks Gene Fragments|
|Stringent QC process
• Median error rate
• Synthesis & assembly
May rework to meet QC standards
|Format||Plates or tubes||Plate|
|Length||125–3000 bp||300–1500 bp|
† Any eBlocks Gene Fragment that does not meet QC standards after the first attempt will be cancelled and refunded.
IDT ships gBlocks Gene Fragments dry unless otherwise requested. While dry, they should be stable up to two years.
After resuspending in a high-quality, molecular-grade water or buffer, pH 7.5–8.0, you should store the DNA at –20°C and if necessary, aliquot to avoid more than 2 or 3 freeze-thaw cycles.
For gBlocks Gene Fragments at concentrations lower than 1 ng/µL, we recommend resuspending in water or buffer containing 0.1–1.0 mg/mL tRNA (Sigma) or poly A (Sigma). Use this same buffer + carrier solution for subsequent dilutions. Without the carrier, we have observed a steady decrease in measured concentrations of these dilute solutions, even in low-bind tubes. This may be caused by the very high purity of the gBlocks Gene Fragment prep. Because gBlocks Gene fragments are completely synthetic, they lack the normal cellular debris found in DNA isolated from natural sources.
Without these natural carriers, the gBlocks Gene Fragments bind irreversibly to the tube plastic over time, leading to the observed decrease in concentration. Adding a carrier to your resuspension and dilution buffers can help prevent this loss of product.
The constant regions are gBlocks Gene Fragments and undergo size verification by capillary electrophoresis and sequence verification by mass spectrometry.
The variable regions cannot currently receive complete analysis (using NGS, which would be needed for this analysis, would be cost prohibitive). We rely on a validated process that we have experimentally confirmed by NGS that ensures >80% of DNA species are present in the final material shipped.
We are working hard at offering more complex libraries in the future.
Help us prioritize by sharing what you need from us in as much detail as possible (i.e., show us sequences including mixed bases, annotations, drawings, etc.).
You can send your requests to email@example.com.
Sequence Information is secure and confidential at IDT. Please see our Confidentiality Statement for more information. All online ordering steps, including sequence entry and your choice of parameters, are also secure and protected.
We screen the sequence of every gene, gene fragment, and Megamer™ ssDNA fragment order we receive to (1) identify any regulated and other potentially dangerous pathogen sequences, and (2) verify that IDT’s gene customers are legitimate scientists engaged in beneficial research.
IDT is among the five founding members of the International Gene Synthesis Consortium (IGSC) and helped to create the IGSC’s Harmonized Screening Protocol. The Harmonized Screening Protocol describes the gene sequence and customer screening practices that IGSC member companies employ to prevent the misuse of synthetic genes. IDT takes the steps set out in the Harmonized Screening Protocol to screen the sequences of ordered genes and the prospective customers who submit those orders.
For more information about the IGSC and the Harmonized Screening Protocol, please visit the website at www.genesynthesisconsortium.org.
In October 2010, the United States government issued final Screening Framework Guidance for Providers of Synthetic Double-Stranded DNA, describing how commercial providers of synthetic genes should perform gene sequence and customer screening. IDT and the other IGSC member companies supported the adoption of the Screening Framework Guidance, and IDT follows that Guidance in its application of the Harmonized Screening Protocol. For more information, please see 75 FR 62820 (Oct. 13, 2010), or https://federalregister.gov/a/2010-25728.
*RUO—For research use only. Not for use in diagnostic procedures. Unless otherwise agreed to in writing, IDT does not intend for these products to be used in clinical applications and does not warrant their fitness or suitability for any clinical diagnostic use. Purchaser is solely responsible for all decisions regarding the use of these products and any associated regulatory or legal obligations.