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Services

Subcloning Services and Vector Cloning for Research

Custom cloning services for shRNA, sgRNA, and siRNA constructs, pooled libraries, and complex vector projects

Synthesis and cloning services in this category come from several suppliers. Describing what your construct has to do lets the scientific team in Heidelberg match you to the supplier whose service fits your budget and your quality control requirements.

Standard cloning and expression plasmids such as pET, pUC, and pcDNA are handled through the gene synthesis service. Custom cloning covers the more involved work: AAV constructs, minicircles, PiggyBac systems, and custom backbones, together with shRNA, sgRNA, and siRNA constructs and pooled shRNA and sgRNA libraries. Knowing which of the two routes your project belongs to shortens the conversation considerably.

Custom lentiviral and AAV cloning can be combined with a viral packaging service, so your construct is designed, built, and delivered as ready-to-transduce particles within one project. If you have found a plasmid on the site and want it combined with a synthesis and cloning service, the scientific team can tell you whether that combination is workable for your project and which supplier would handle it.

Named offerings in this category include the SYN2CLONE custom cDNA cloning service from System Biosciences; custom lentiviral shRNA and dual-shRNA expression constructs, and custom shRNA and sgRNA libraries from Cellecta; as well as cloning services covering highly customised lentiviral and AAV constructs from our partner Applied Biological Materials (abm). Formats, pack sizes, and quality control differ between them, and those details are confirmed for you with your quote.

How to choose a cloning route

  1. Standard cloning and expression plasmids. Work built on pET, pUC, or pcDNA backbones belongs with the gene synthesis service, which covers routine expression constructs of the kind your standard workflows rely on.
  2. Complex vector projects. AAV constructs, minicircles, PiggyBac systems, and custom backbones sit with custom cloning, where your design and assembly are scoped and quoted together.
  3. Custom sgRNA cloning. For CRISPR knockout, CRISPRi, or CRISPRa work, sgRNA cloning spans sgRNA-only, all-in-one sgRNA-Cas9, dual-sgRNA, and inducible vectors. Two-vector and single-vector CRISPR-Cas9 systems are both available, with non-targeting and non-specific control guides in any backbone. Deliverables reach you as lentiviral plasmids or pre-packaged lentiviral particles.
  4. Custom shRNA and siRNA cloning. Custom lentiviral constructs can express shRNA against any transcript, with a constitutive or tet-inducible H1 or U6 promoter and a choice of GFP, RFP, PuroR, BleoR, NeoR, or Hygro-HK markers. Three to five shRNA constructs against a given human or mouse gene can be supplied, designed on the parameters Cellecta uses for its own libraries. Custom cloning is offered for siRNA constructs as well, with formats for your targets confirmed by supplier at quotation.
  5. Custom shRNA and sgRNA libraries. Pooled library work runs through Cellecta, which has more than fifteen years of experience building pooled shRNA, barcode, and sgRNA lentiviral libraries targeting any defined gene set. Libraries arrive in plasmid and pre-packaged, ready-to-transduce formats, in the constitutive or inducible vectors your screen calls for.

Applications

CRISPR knockout screens

Custom sgRNA libraries from Cellecta target any defined gene set and reach you as plasmid or pre-packaged, ready-to-transduce lentiviral preparations.

CRISPRi and CRISPRa studies

sgRNA vectors for interference and activation are built as sgRNA-only or all-in-one designs, with matched control guides in the backbone your work already uses.

Gene knockdown panels

Three to five shRNA constructs against one human or mouse gene give you a small panel to test, designed on the parameters Cellecta applies to its own libraries.

Genome-wide RNAi screens

Custom shRNA libraries from Cellecta cover any gene set, carrying a barcode in each construct so your enrichment readout avoids sequencing hairpin structures.

AAV construct work

Custom AAV cloning follows the complex projects route and pairs with viral packaging where your experiment needs particles as well as plasmid.

Lineage tracing

Cellecta builds barcode libraries at 1,000, 5,000, or 20,000 distinct barcodes, in specialised vectors carrying markers such as Thy1.1 or luciferase for your tracing work.

Frequently asked questions

Can a plasmid listed on the site be combined with a synthesis and cloning service?

Yes. Where you have found a plasmid in the catalogue and want it modified, extended, or rebuilt as part of a cloning project, getting in touch with the scientific team is the way to check. Suppliers differ in what they will take on, so feasibility is confirmed before a quote is issued.

What quality control is applied to custom pooled libraries?

Quality control varies by supplier. For custom sgRNA libraries, Cellecta isolates a few dozen constructs for full-insert Sanger sequencing to confirm the sgRNA expression cassette configuration and correct insertion, then deep-sequences all guide sequences by NGS to confirm representation of the oligo pool and assess distribution. Libraries that do not meet those standards are remade.

Can I supply my own proprietary expression vector?

In many cases yes. Most of BioCat's partners can clone into a customer-provided vector including AAV and retroviral formats. Feasibility is confirmed with the supplier before your project is quoted.

Parent category: Contract research services

Product catalogs

Not sure which catalog to start with? We will help you find the right products.

Tell us what you are looking for — antibodies, kits, proteins, or supplies — and our team will point you to the best catalog filters, suppliers, and product matches for your workflow.

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