Electroforesis
En esta sección, puede encontrar todos los reactivos y materiales necesarios para realizar electroforesis, una técnica de laboratorio vital utilizada para separar proteínas según su masa molecular y carga. Esta técnica es esencial para analizar la composición y pureza de muestras de proteínas, así como para estudiar ácidos nucleicos y otras biomoléculas. Nuestra selección incluye tampones de electroforesis, geles, colorantes y marcadores de alta calidad, junto con aparatos y accesorios diseñados para garantizar una separación precisa y eficiente. Estos productos son cruciales para la investigación en biología molecular, bioquímica y genética, proporcionando resultados fiables para la caracterización de proteínas, el análisis de la expresión génica y otras aplicaciones. En CymitQuimica, proporcionamos todo lo necesario para realizar electroforesis, apoyando su investigación con precisión y consistencia.
Subcategorías de "Electroforesis"
Se han encontrado 298 productos de "Electroforesis"
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N,N'-Methylene Bisacrylamide 2% Aq. Solution for molecular biology
CAS:Fórmula:C7H10N2O2Forma y color:Clear, Colourless, liquidPeso molecular:154.171X Phosphate Buffered Saline (PBS) for molecular biology
The pH of the buffer is typically maintained within a range of 7.4 ± 0.1, closely resembling the physiological pH found in many biological systems.Forma y color:Clear, Colourless, Liquid10X Phosphate Buffered Saline Tween-20 (PBST) for molecular biology
Forma y color:Clear, Colourless with yellow tinted, Liquid1M Tris Hydrochloride Buffer (1M Tris HCl) pH-7.2 for molecular biology
Forma y color:Clear, Colourless, LiquidBrilliant Blue R-250 for molecular biology
CAS:Fórmula:C45H44N3NaO7S2Forma y color:Dark blue with reddish tinge, PowderPeso molecular:825.9810X MOPS Buffer for molecular biology
MOPS, or morpholino propanesulfonic acid, is a structural analog of MES, the ethanesulfonic acid. With a pKa value of 6.80-7.20, MOPS serves as an excellent buffer for many biological systems at near-neutral pH. It is extensively used as a buffering agent in molecular biology and biochemistry and has been tested and recommended for use in polyacrylamide gel electrophoresis. Additionally, MOPS is applicable in various bioanalytical methods, including isoelectric focusing, protein assays, and X-ray crystallographic studies. Furthermore, it can be used as an electrophoresis buffer for agarose gel electrophoresis of RNA.Forma y color:Clear, Colourless, Liquid20X SSC Buffer pH 6.9-7.1 for molecular biology
The Saline-Sodium Citrate Hybridization Buffer [20X] is a key component in various nucleic acid techniques, ensuring optimal stringency during washing steps in procedures such as Southern blotting, in situ hybridization, DNA microarrays, and Northern blotting. When utilized as 20X SSC, it effectively prevents agarose gels from drying out during vacuum transfers, preserving sample integrity. This solution is specifically formulated to support the diverse needs of end users in nucleic acid hybridizations and blot transfer applications, making it an invaluable resource in molecular biology workflows.Forma y color:Clear, Colourless, SolutionLithium Lauryl Sulphate extrapure, 99%
CAS:Fórmula:C12H25SO4LiPureza:min. 99%Forma y color:White, Crystalline powder, Clear, ColourlessPeso molecular:272.30Albumin Bovine Solution 10% Diluent Solution in PBS (BSA 10% Diluent/Blocking Solution in PBS)
CAS:Forma y color:Clear, Pale yellow, Liquid1M Tris Hydrochloride Buffer (1M Tris HCl) pH-8.0 for molecular biology
Forma y color:Clear, Colourless, Liquid20X SSPE Buffer pH-7.4 suitable for molecular biology
The 20X SSC Buffer, with a pH between 6.9 and 7.1, is essential for in molecular biology, particularly for Southern and Northern hybridization techniques. This solution is sterilized through a 0.22 µm filter, making it suitable for direct use or for dilution based on experimental requirements. In parallel, 20X SSPE is available as a concentrated buffer intended for nucleic acid hybridizations and blot transfer processes. A significant feature of SSPE is its inclusion of EDTA, which chelates divalent metal ions like Mg²+. This property effectively inhibits DNase activity, helping to preserve the concentrations of probe and target DNA during Southern hybridization, thereby enhancing the accuracy of the results.Forma y color:Clear, Colourless, Liquid10X Tris-Tricine-SDS Buffer for molecular biology
The Tris-Tricine-SDS Gel Running Buffer is specifically designed for separating proteins with molecular weights between 1 and 100 kDa, making it particularly effective for resolving proteins smaller than 30 kDa. This approach differs from traditional SDS-PAGE by substituting glycine (pK 9.6) with tricine (pK 8.15), which enhances the stacking and destacking of low molecular weight proteins and improves the resolution of smaller peptides due to the differing pK values. Incorporating urea into the stacking gel allows for the effective separation of two proteins that share the same molecular weight. Additionally, the lower acrylamide concentrations in Tricine gels facilitate the transfer of hydrophobic proteins during Western blotting. Tricine–SDS-PAGE is therefore commonly employed for the separation of lower molecular weight proteins.Forma y color:Clear, Colourless, Liquid
