BrightMAX™ 100 – 1,500 bp

• Concentration: 0.1 μg/μL

– 50 μg of BrightMAX™ DNA Ladder (100–1,500 bp), ready-to-use with loading dye.

• DNA fragment sizing.

• PCR product verification.

• Cloning analysis.

• Routine agarose gel electrophoresis.

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• Each lot is validated for accurate DNA fragment sizes, uniform band intensity, and long-term stability.

• Mix thoroughly before use to ensure homogeneous loading.

• Follow recommended loading volumes for optimal resolution.

• Store in aliquots to prevent repeated freeze-thaw cycles.

• Shipped at: Ambient temperature.
• Storage: Stable at room temperature. For long term, store at -20 ºC (NON Frost-Free Freezer).

• Medina, A. M., Rivera, F. P., Riveros, M., Ochoa, T. J., Pons, M. J., & Ruiz, J. (2023). RESEARCH ARTICLE Transferable mechanisms of quinolone resistance are more frequent among enterotoxigenic Escherichia coli isolates displaying low-level quinolone resistance. Tropical Biomedicine, 40(2), 183-187.
• Villa Suárez, J. M. (2022). Estudio poblacional de hipofosfatasia en la provincia de Granada y caracterización funcional y estructural de las variantes genéticas identificadas.
• Miranda‐Fuentes, P., García‐Carneros, A. B., Montilla‐Carmona, A. M., & Molinero‐Ruiz, L. Evidence of soil‐located competition as the cause of the reduction of sunflower Verticillium wilt by entomopathogenic fungi. Plant Pathology.
• Ortiz‐Bustos, C. M., López‐Bernal, A., Testi, L., & Molinero‐Ruiz, L. Environmental and irrigation conditions can mask the effect of Magnaporthiopsis maydis on growth and productivity of maize. Plant Pathology.
• Espiñeira, M., Herrero, B., Vieites, J. M., & Santaclara, F. J. (2010). Validation of end-point and real-time PCR methods for the rapid detection of soy allergen in processed products. Food Additives and Contaminants, 27(4), 426-432.
• Espiñeira, M., Atanassova, M., Vieites, J. M., & Santaclara, F. J. (2010). Validation of a method for the detection of five species, serogroups, biotypes and virulence factors of Vibrio by multiplex PCR in fish and seafood. Food microbiology, 27(1), 122-131.
• Espiñeira, M., Vieites, J. M., & Santaclara, F. J. (2009). Development of a genetic method for the identification of salmon, trout, and bream in seafood products by means of PCR–RFLP and FINS methodologies. European Food Research and Technology, 229(5), 785-793.
• Osman, I. H., Gabr, H. R., El-Etreby, S. G., & Mohammed, S. Z. (2014). Morphometric variations and genetic analysis of Lessepsian migrant Octopus aegina (Cephalopoda: Octopodidae). Journal of King Abdulaziz University, 25(2), 23.
• Alaniz, S., León, M., Vicent, A., García-Jiménez, J., Abad-Campos, P., & Armengol, J. (2007). Characterization of Cylindrocarpon species associated with black foot disease of grapevine in Spain. Plant Disease, 91(9), 1187-1193.
• Gramaje, D., Mostert, L., & Fortí, J. A. (2011). Characterization of Cadophora luteo-olivacea and C. melinii isolates obtained from grapevines and environmental samples from grapevine nurseries in Spain. In Phytopathologia Mediterranea (Vol. 50, No. Supplement, pp. 112-126). Firenze University Press.
• López Fernández, L. (2013). Papel de la N-glicosilación de proteinas en la virulencia de Fusarium oxysporum.

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.

Q1: What fragment sizes does this ladder include?
It contains DNA fragments from 100 bp to 1,500 bp.

Q2: Is it premixed with loading dye?
Yes, the ladder is ready-to-use and supplied with loading dye for direct application.

Q3: What are the main applications?
It is widely used for PCR product analysis, cloning verification, and routine DNA sizing.