pSpark® Universal

– 20 rxn pSpark® II DNA cloning vector (20ng/µL)
– 20 rxn pSpark® TA DNA cloning vector (50ng/µL)
– 150 µL PEG 6000 solution (10X)
– 5 µL control insert 1kb
– 5 µLcontrol insert (TA) 600kb
– 20 µL T4 DNA ligase (5 Weiss U/µL)
– 100 µLT4 DNA ligase Buffer (10x)

• Universal PCR product cloning (TA or blunt-end).

• Sequencing and mutagenesis workflows.

• DNA fragment subcloning.

• Plasmid construction and expression studies.

• Routine molecular cloning in research and diagnostics.

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• Each lot is validated for ligation efficiency, insert stability, and transformation performance, ensuring reproducibility and high cloning success.

• Use clean PCR products from Taq or proofreading polymerases.

• Keep ligation reagents on ice during setup.

• Always include a negative control to assess background ligation.

• Shipped in: Gel Pack.
• Storage: -20 ºC (NON Frost-Free Freezer).

• Alvarez, J. B., Castellano, L., Recio, R., & Cabrera, A. (2019). Wx Gene in Hordeum chilense: Chromosomal Location and Characterisation of the Allelic Variation in the Two Main Ecotypes of the Species. Agronomy, 9(5), 261.
• Benítez Casanova, L. (2017). Caracterización de las principales enzimas celulolíticas de myceliophthora thermophila implicadas en la degradación de biomasa lignocelulósica y mejora de la hidrólisis de hemicelulosa para la producción de bioetanol de segunda generación.
• Oliveras Rovira, À., Baró, A., Montesinos Barreda, L., Feliu Soley, L., & Planas i Grabuleda, M. (2018). Antimicrobial activity of linear lipopeptides derived from BP100 towards plant pathogens. PLoS ONE, 2018, vol. 13, núm. 7, p. e0201571.
• Folgueira, I., Lamas, J., De Felipe, A. P., Sueiro, R. A., & Leiro, J. M. (2019). Evidence for the role of extrusomes in evading attack by the host immune system in a scuticociliate parasite. BioRxiv, 607622.
• Olmos, G., Martínez‐Miguel, P., Alcalde‐Estevez, E., Medrano, D., Sosa, P., Rodríguez‐Mañas, L., … & López‐Ongil, S. (2017). Hyperphosphatemia induces senescence in human endothelial cells by increasing endothelin‐1 production. Aging cell, 16(6), 1300-1312.
• Laguna, J. I. R. (2017). Proliferative and Positional Instructions Underliying Planarian Regeneration and Tissue Renewal(Doctoral dissertation, Universitat de Barcelona).
• Lindo, L., McCormick, S. P., Cardoza, R. E., Kim, H. S., Brown, D. W., Alexander, N. J., … & Gutierrez, S. (2019). Role of Trichoderma arundinaceum tri10 in regulation of terpene biosynthetic genes and in control of metabolic flux. Fungal Genetics and Biology, 122, 31-46.
• Oliveras, À., Baró, A., Montesinos, L., Badosa, E., Montesinos, E., Feliu, L., & Planas, M. (2018). Antimicrobial activity of linear lipopeptides derived from BP100 towards plant pathogens. PloS one, 13(7), e0201571.
• Álvarez-Cao, M. E., Cerdán, M. E., González-Siso, M. I., & Becerra, M. (2019). Bioconversion of Beet Molasses to Alpha-Galactosidase and Ethanol. Frontiers in microbiology, 10.
• Álvarez-Escribano, I., Vioque, A., & Muro-Pastor, A. M. (2018). NsrR1, a nitrogen stress-repressed sRNA, contributes to the regulation of nblA in Nostoc sp. PCC 7120. Frontiers in microbiology, 9, 2267.
• TC, G. Supplemental Material. González-‐Aguilera C. et al.
• Aliaga‐Guerrero, M., Paullada‐Salmerón, J. A., Piquer, V., Mañanós, E. L., & Muñoz‐Cueto, J. A. (2017). Gonadotropin‐inhibitory hormone in the flatfish, Solea Senegalensis: Molecular cloning, brain localization and physiological effects. Journal of Comparative Neurology.
• Reñé, A., Alacid, E., Figueroa, R. I., Rodríguez, F., & Garcés, E. (2016). Life-cycle, ultrastructure, and phylogeny of Parvilucifera corolla sp. nov.(Alveolata, Perkinsozoa), a parasitoid of dinoflagellates. European Journal of Protistology.
• Paullada‐Salmerón, J. A., Cowan, M., Aliaga‐Guerrero, M., Gómez, A., Zanuy, S., Mañanos, E., & Muñoz‐Cueto, J. A. (2016). LPXRFa peptide system in the European sea bass: a molecular and immunohistochemical approach. Journal of Comparative Neurology, 524(1), 176-198.

This product is developed, designed and sold exclusively for Research purposes and in vitro use only (RUO). The product was not tested for use in diagnostics or for drug development, nor is it suitable for administration to humans or animals. For more info, please check its Material Safety Data Sheet available in this website.

Cloning vector plasmid, Universal cloning vector, DNA cloning plasmid, Plasmid vector for cloning, Expression cloning vector

Also known as:

• Spanish: Vector de clonación universal, Plásmido de clonación, Vector plasmídico
• French: Vecteur de clonage universel, Plasmide de clonage, Vecteur plasmidique
• German: Universeller Klonierungsvektor, Klonierungsplasmid, Plasmidvektor
• Italian: Vettore di clonaggio universale, Plasmide di clonaggio, Vettore plasmidico

Q1: What makes pSpark® Universal different from other pSpark® kits?
It supports both A-tailed and blunt-ended PCR products, offering maximum flexibility in one kit.

Q2: Is enzymatic modification required before ligation?
No. Fragments can be directly ligated regardless of the polymerase used.

Q3: What transformation efficiency can be expected?
Typically higher than 10⁶ cfu/µg DNA using standard E. coli strains.