Gene Fragments
Gene Fragments are double-stranded, linear DNA fragments of 100-3,000 bp, which are a convenient option due to their faster delivery time, lower cost, and greater flexibility. These fragments are synthesized with the same industry-leading proprietary technology that GENEWIZ from Azenta has developed for standard gene synthesis products. We provide Gene Fragments in a dried form that can be easily re-suspended, cloned, and screened to identify the correct clone for downstream applications.
More variants. Faster iteration. Rapid engineering.
How are gene fragments made?
Construction begins with the base-by-base synthesis of oligonucleotides (oligos), followed by assembly into double-stranded DNA (dsDNA) fragments. These custom DNA fragments can be used directly, cloned into vectors, or assembled into larger constructs to serve a variety of research uses.
Gene Fragment Synthesis Features and Benefits
Cloning accuracy: More than 85% of the recombinant colonies from cloning Gene Fragments will contain your desired insert
Industry-leading turnaround time: GENEWIZ Fast Fragments ship to your lab as fast as 1 business day
Affordable: Very cost-effective to meet your strict budget constraints
Quality control: Stringent quality control process to ensure high sequence fidelity
Built for speed, scale, and scientific rigor
GENEWIZ Double-stranded DNA Fragments (100–3,000 bp) are delivered dried and clone-ready. Choose Fast Fragments (ships in as little as 1 business day) or our standard FragmentGENE service. Synthesis and QC are 100% US-based.
Typical workflow:
- Design your fragment(s) or variant set
- Select speed — Fast (1-BD) or Standard, choose delivery format
- Resuspend & assemble — move directly to cloning, screening, or edits
Gene Fragment Turnaround Time
▼Fast Fragments
▼FragmentGENE
Gene Block Quality Control
- Size verification by gel electrophoresis
- Sequence confirmation via Sanger sequencing
Gene Fragment Synthesis Applications
- Assemble multiple gene fragments to make full-length gene constructs for protein expression and purification
- gRNA expression cassettes for CRISPR/Cas9-based gene editing
- Donor constructs for gene editing experiments
- Template for in vitro transcription
- Antibody discovery at scale: CDR mutagenesis, affinity maturation, humanization panels
- High-throughput screening: barcoded fragments, reporter cassettes, assay controls
- Protein engineering: linkers/tags/fusions, alanine/tiling scans, domain swaps
- Alanine/tiling mutagenesis to map function and liability
- CDR shuffling & combinatorial libraries for scFv/Fab/IgG
- Display library inserts: yeast, phage, mammalian
- Reporter & MPRA payloads for promoter/UTR tuning
- Barcoded controls & spike-ins for pooled NGS readouts
- HDR donors & landing pads for targeted integration
Gene Fragment Assembly Deliverables
Standard deliverables include 500-1,000 ng of dried double-stranded DNA, depending on sequence length.