[Passa al contenuto](https://www.sigmaaldrich.com#main-content) [](https://www.sigmaaldrich.com/IT/it) Prodotti Carrello0 ITIT Prodotti ProdottiApplicazioniServiziRisorseSupporto [Login / Registrati](https://www.sigmaaldrich.com/oidc-sign-in) [Ricerca di ordini](https://www.sigmaaldrich.com/IT/it/order-lookup) [Ordine rapido](https://www.sigmaaldrich.com/IT/it/quick-order) Carrello0 [Home](https://www.sigmaaldrich.com/IT/en)[Cloning & Expression](https://www.sigmaaldrich.com/IT/en/applications/genomics/cloning-and-expression)Cloning & Expression Vectors # Cloning & Expression Vectors ## SnapFast™ Vectors for Cloning & Expression Traditional cloning by restriction enzyme digestion remains the most popular way to insert your gene-of-interest (GOI) into an expression vector for expression in the target cell, whether that is an insect, mammalian, or microbial cell. With good planning, this cloning method is easy, reliable, and cost-conscious. However, choice of vector can dramatically affect your experiment in a number of ways. What is important to your work? - Sequence verification - so you know your vector is perfect when you recieve it - Optimal expression levels - from low to high, we have a promoter for every need - Reporters you can use - you choose the detection method you want - IP-friendly terms - you make a new vector or expressed product & it is yours to keep We are committed to bringing you the most options in vector selection - the SnapFast™ collection engineered by Oxford Genetics. This collection gives you options for: - Insect, Yeast, Bacterial & Mammalian Expression Systems - 26 peptide tags - NEW options with FLAG™ and 3xFLAG™ tags - 9 reporter genes - >20 signal peptides - >40 promoters - 10 selection markers   __Related Articles__ - [Introduction to Cell Transfection](https://www.sigmaaldrich.com/IT/en/technical-documents/technical-article/cell-culture-and-cell-culture-analysis/transfection-and-gene-editing/transfection-reagents) - [Reverse Transfection of Plasmid DNA](https://www.sigmaaldrich.com/IT/en/technical-documents/technical-article/cell-culture-and-cell-culture-analysis/transfection-and-gene-editing/xtg-reverse-transfect-pdna) - [3xFLAG® System Expression Vectors for Ultra-Sens](https://www.sigmaaldrich.com/IT/en/technical-documents/technical-article/genomics/cloning-and-expression/3x-flag) - [Blue-White Screening & Protocols for Colony Selection](https://www.sigmaaldrich.com/IT/en/technical-documents/technical-article/genomics/cloning-and-expression/blue-white-screening) - [Bacterial Transformation Protocols](https://www.sigmaaldrich.com/IT/en/technical-documents/technical-article/genomics/cloning-and-expression/competent-cells) - [Genotypes, Phenotypes and Markers](https://www.sigmaaldrich.com/IT/en/technical-documents/technical-article/genomics/cloning-and-expression/definitions-and-genotypes-of-e-coli) - [Restriction Enzyme Cloning Glossary](https://www.sigmaaldrich.com/IT/en/technical-documents/technical-article/genomics/cloning-and-expression/estriction-enzyme-cloning-manual-glossary) - [How Transfection Works](https://www.sigmaaldrich.com/IT/en/technical-documents/technical-article/genomics/cloning-and-expression/how-transfection-works) - [View More](https://www.sigmaaldrich.com/IT/en/search/facet-search?focus=sitecontent&term=facet-search) Top __Autenticati per continuare__ Per continuare a leggere, autenticati o crea un account. 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