pSpark® II
For highly Efficient, Accurate & Easy general Cloning with classical MCS, without the use of Toxic Genes
pSpark® II is a highly efficient, accurate and easy-to-use DNA Cloning system based on a breakthrough technology for cloning blunt ended DNA generated by PCR with a proofreading or high fidelity DNA polymerases.
The vector is prepared by digestion of pSpark® II at the EcoRV site before treating both ends to prevent vector self-ligation. The end treatment is supported by a proprietary know-how that guarantees a higher cloning efficiency than with simply a desphorylated vector.
Price: 175.00 €
Detailed information:
Advantages & Features
- Unprecedented high cloning efficiency: more than 2,500 positive colonies expected under optimal conditions.
- Great efficiency: over hundreds positive colonies with few nanograms of insert.
- High stability: eliminates cloning bias or pitfalls.
- Time-saving protocol: no hidden steps such as phosphorylation, just ligation after PCR and transformation.
- Powerful: clone from less than 1 ng/kb to up to 14 kb; obtain 4-fold more positive colonies using 3-fold less DNA insert.
- Easy-to-use: eliminate recombinant screening due to its minumum background (lower than 1%), avoiding “suicide” strategies from toxic genes.
- Great versatility: compatible with any protocol, proofreading Polymerase, Competent Cells, ligation time or primers.
- Flexible: ligation time from 10 minutes to overnight.
- Robust for every DNA size: just 6.7 ng per kb of insert needed for optimal ligation.
- High cost-saving: reduces your cloning costs as no expensive phosphorylated primers are needed.
- Eliminates positive selection vector.
Specifications
Includes
– 20 rxn pSpark® II (20 ng/µL)
– 20 µL T4 DNA Ligase (5 Weiss U/µL)
– 100 µL T4 DNA Ligase Buffer (10x)
– 150 µL PEG 6000 (10x)
– 5 µL Insert Control 1 kb (20 ng/µL)
Applications
- General cloning.
- Clone PCR fragments included in a low amount.
- Cloning of PCR products amplified with High Fidelity polymerases.
- Cloning of PCR fragments generated with a blend of polymerases.
- Production of ssDNA.
- Blue/white screening for recombinants.
- In vitro transcription from T7/SP6 dual-opposed promoters.
Tables & Figures
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Quality Control
- Functional test using a 1.0 kb PCR fragment.
Advice
- Recommendations: All pSpark® DNA cloning vectors are stable for at least 1 month at 4 °C and even at 20 – 25 °C for up to 2 days although storage temperatures above -20 °C are not recommended. In case of incident, such as a power failure, stored vectors should be tested with the supplied control insert before considering discarding it. However, please note that T4 DNA Ligase is extremely temperature-sensitive and storage temperatures above -20 °C inactivates the enzyme.
Storage, Shipping & Guarantee
- Shipped in: Gel pack.
- Storage: -20 ºC (NON Frost-Free Freezer).
Citations
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- Badosa, E., Montesinos, L., Camó, C., Ruz, L., Cabrefiga, J., Francés, J., … & Feliu, L. (2017). CONTROL OF FIRE BLIGHT INFECTIONS WITH SYNTHETIC PEPTIDES THAT ELICIT PLANT DEFENSE RESPONSES. Journal of Plant Pathology, 99.
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- Burnat, M., & Flores, E. (2014). Inactivation of agmatinase expressed in vegetative cells alters arginine catabolism and prevents diazotrophic growth in the heterocyst‐forming cyanobacterium Anabaena. MicrobiologyOpen, 3(5), 777-792.
- Ejarque-Ortiz, A., Solà, C., Martínez-Barriocanal, Á., Schwartz Jr, S., Martín, M., Peluffo, H., & Sayós, J. (2015). The receptor CMRF35-like molecule-1 (CLM-1) enhances the production of LPS-induced pro-inflammatory mediators during microglial activation. PloS one, 10(4), e0123928.
- Munoz-Jimenez, C. M., Ayuso, C., Dobrzynska, A., Torres, A., de la Cruz-Ruiz, P., & Askjaer, P. (2017). An efficient FLP-based toolkit for spatiotemporal control of gene expression in Caenorhabditis elegans. bioRxiv, 107029.
- Gómez-Marín, C., Tena, J. J., Acemel, R. D., López-Mayorga, M., Naranjo, S., de la Calle-Mustienes, E., … & Bovolenta, P. (2015). Evolutionary comparison reveals that diverging CTCF sites are signatures of ancestral topological associating domains borders. Proceedings of the National Academy of Sciences, 112(24), 7542-7547.
- Rojas, M. (2014). Papel de los reguladores moleculares Fbp1 y Bmh2 en la virulencia de Fusarium oxysporum.
- VIDAL, A. G. (2016). Potencial de los tratamientos por termoterapia con agua caliente para el control de hongos de la madera de la vid y su efecto sobre la micoflora total, después de un año de cultivo.
- Corral Ramos, C. (2016). Metabolismo del glucógeno y procesos celulares implicados en dinámica nuclear y fusión de hifas en Fusarium oxysporum.
- Navarro Velasco, G. Y. (2013). Identificación de nuevos componentes de la ruta TOR de Fusarium oxysporum y determinación de su papel en la patogénesis.
- Ruiz-Roldán, C., Pareja-Jaime, Y., González-Reyes, J. A., & G. Roncero, M. I. (2015). The transcription factor Con7-1 is a master regulator of morphogenesis and virulence in Fusarium oxysporum. Molecular Plant-Microbe Interactions, 28(1), 55-68.
- Jiménez Munguía, I. (2015). Multi-omic approach applied to the selection of vaccine antigens and molecules for diagnosis and treatment agianst caused by Streptococcus pneumoniae and Staphylococcus aureus.
- Nürnberg, D. J. (2015). Intercellular communication in filamentous cyanobacteria
- Lambert Rodríguez, R. (2016). Actividad nucleasa en judía y su relación con la síntesis de ureidos durante la germinación y senescencia.
- Ocaña Calahorro, F. J. (2013). El óxido nítrico y la asmilación de nitrógeno en Chlamydomonas.
- Domínguez Martín, M. A. (2015). Diversity of regulatory mechanisms in the C/N metabolism of the marine cyanobacteria Prochlorococcus and synechococcus.
- Sein-Echaluce, V. C., Castejón, M. F. F., & Rodríguez, A. G. (2012). Estudios funcionales de la proteína FurB en Anabaena sp. PCC 7120.
- Bravo Ruiz, G. A. (2013). Sistemas hidrolíticos de componentes vegetales en el patógeno de tomate Fusarium oxysporum f. sp. lycopersici: lipasas y poligalaturonasas.
- Chamizo-Ampudia, A., Galvan, A., Fernandez, E., & Llamas, A. (2011). The Chlamydomonas reinhardtii molybdenum cofactor enzyme crARC has a Zn-dependent activity and protein partners similar to those of its human homologue. Eukaryotic cell, 10(10), 1270-1282.
Safety Statements
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.
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