Agarose Gel Electrophoresis Unit

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Agarose Gel Electrophoresis Unit
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  • …submarine unit is ideal for any molecular biology lab Run as many as 60 samples at once Multichannel pipettor-compatible combs available The HE99X Max Submarine Unit offers a variety of gel lengths and comb sizes so that you can run exactly the gel you need. Cast gels 15 cm wide…

  • …samples simultaneously on one agarose gel and still produce clear, tight banding patterns with no “smiling”. The unit’s end gate casting design provides a leakproof seal without tape. Built-in leveling ensures the casting of flat, uniformly thick gels. Sample loading is enhanced…

  • Gator Wide Gel Electrophoresis System

    Owl Separation Systems

    …to 600 samples on a single gel Multiple comb slots The Gator horizontal A3-1 wide system can run from 25 to 600 samples on one gel. The gel can be cast in varying lengths to help conserve agarose when fewer samples need to be run utilizing a wall comb. This unit comes with built in buffer…

  • …agarobiose units. During agarose gel formation, the polymers aggregate to form a network with varying pore sizes. This property is used in agarose gel electrophoresis to separate DNA. Other Notes: Agarose MP is particularly well suited for pulsed-field gel electrophoresis, because it allows…

  • Buffer Puffer Electrophoresis System

    Owl Separation Systems

    …from the heat generated during electrophoresis are collected at the cathode end of the unit and then shunted through a conduit tube to the anode end of the unit passively creating effective recirculation within the chamber. A gasketed, UV Transmissable (UVT) gel tray allows for leak-free casting…

  • Easycast Mini Electrophoresis Systems

    Owl Separation Systems

    …EasyCast gel casting system allows the gel to be cast and run in the same unit. No tapes, casting dams or other accessories are required. UV Transmissable (UVT) gel tray allows user to view bands on a transilluminator without removing the gel from the tray. The tray can withstand hot agarose (as…

  • …repeats General description: Agarose is obtained from seaweed and contains repeated agarobiose units. During agarose gel formation, the polymers aggregate to form a network with varying pore sizes. This property is used in agarose gel electrophoresis to separate DNA. Other Notes: …

  • …a high resolution system ideal for separation of nucleic acids in agarose gels. It is also designed for rapid screening of PCR fragments, RFLP analysis or plasmid screening, field inversion, genomic DNA separations and electrophoresis procedures requiring recirculation. Constructed of 3/8" cast…

  • …with the use of Agarose LE. General description: Agarose is obtained from seaweed and contains repeated agarobiose units. During agarose gel formation, the polymers aggregate to form a network with varying pore sizes. This property is used in agarose gel electrophoresis to separate DNA.…

  • …commonly used buffer for DNA agarose gel electrophoresis but is also used for non-denaturing RNA agarose gel electrophoresis. 1 Double-stranded DNA tends to run faster in TAE than in other buffers but can also become exhausted during extended electrophoresis. Buffer circulation or buffer…

  • Gel Box Science Kit

    G-Biosciences

    …a gel box, specifically horizontal agarose gel electrophoresis. The kit is supplied with all the reagents necessary to conduct 4 gel box science experiments, each using a gel box (not supplied). The multifaceted kit will introduce students to the equipment used in horizontal electrophoresis and…

  • …Labnet molecular biology line. The 96-well format horizontal gel electrophoresis unit is compatible with 8-channel multichannel pipettes and matches up with the standard 96-well plate configuration. The average run time for this 10 x 12 cm gel is 15 - 30 minutes. The layout of wells is designed to…

  • …vertical unit, complete Run denaturing and native polyacrylamide, 2-D, electrophoresis, agarose, and nucleic acid gel electrophoresis Maintain temperature between 1 and 45°C with built-in heat exchanger for faster runs with no sacrifice in quality Run two gels simultaneously-or run four gels

  • …the agarose through a small orifice in the gel nebulizer and the resultant gel slurry is sprayed into the sample filter cup.Prepared DNA requires no further purification for most applications, including cloning and radioisotopic or fluorescent DNA sequencing. Since agarose gel electrophoresis has…

  • …commonly used buffer for DNA agarose gel electrophoresis but is also used for non-denaturing RNA agarose gel electrophoresis. Double-stranded DNA tends to run faster in TAE than in other buffers but can also become exhausted during extended electrophoresis. Buffer circulation or buffer replacement…

  • …submarine unit. Convenient, leak-proof casting trays mean fast gel casting without tape. Coolant-insulated buffer chamber runs 7 x 10 cm agarose gels in less than 20 min. Convenient, leak-proof casting trays mean fast gel casting without tape. UV-transparent gel tray offers convenient gel

  • …3,6-anhydro-L-galactose units. Agarose is a purified linear galactan hydrocolloid isolated from agar or agar-bearing marinealgae. As a gelling agent, agarose is used: 1.) to separate nucleic acids electrophoretically because its gels have larger pore sizes than polyacrylamide gels at low…

  • Panther Semi-Dry Electroblotters

    Owl Separation Systems

    …or agarose gels to membranes Traditional Southern, Northern and Western blotting methods Buffer contained within the blotting filter paper is sufficient for transfers High purity, 100% cotton fiber filter papers Solid plate electrodes provide even transfer over entire gel area…

  • …commonly used buffer for DNA agarose gel electrophoresis but is also used for non-denaturing RNA agarose gel electrophoresis. 1 Double-stranded DNA tends to run faster in TAE than in other buffers but can also become exhausted during extended electrophoresis. Buffer circulation or buffer…

  • …the samples (5-10 mul) can then be loaded directly onto an agarose gel for electrophoresis following PCR. The red dye migrates slightly faster than bromophenol blue at about the same rate as a 125 base pair fragment in a 1% agarose gel. Since no additional loading buffers are added to the reaction…

  • …can be directly used on an agarose gel for electrophoresis General description: REDAccuTaq LA DNA polymerase allows for quick recognition in high throughput applications as well as direct loading of amplification products onto agarose gels for electrophoresis. The inert red dye has no effect…

  • …the enzyme has been added and that proper component mixing of the reaction has occurred. Samples can be loaded directly onto an agarose gel for electrophoresis with no loading dye additions General description: JumpStart REDTaq DNA Polymerase is Sigma's high performance Taq DNA Polymerase…

  • Tris-Borate-EDTA Buffer

    MP Biomedicals

    …buffer for polyacrylamide and agarose gel electrophoresis. When diluted to a 1X concentration, it yields a TBE buffer solution that contains 100 mM Tris, 90 mM boric acid and 1mM EDTA. Applied voltages of less than 5 V/cm (distance between the electrodes of the unit) are recommended for maximum…

  • …C to denature the double stranded DNA, 55 C to anneal the DNA segments and 72 C to extend the DNA segments. Following electrophoresis of the reaction products in 1.5% agarose gel, a single band of approximately 500 base pairs was visualized for PCRs containing 1-1.5mM MgCl2. Application: 10x PCR…

  • …non-denaturing agarose gel electrophoresis; In non-denaturing and urea-denaturing polyacrylamide gel electrophoresis; DNA digest analysis with capillary electrophoresis. The pH values of all buffers are temperature- and concentration-dependent. For Tris buffers, pH increases about 0.03 unit per…

  • …Incubation temperature +25°C PFGE tested Sma I has been tested in Pulsed-Field Gel Electrophoresis (on bacterial chromosomes). For cleavage of genomic DNA ( E. coli C 600) embedded in agarose for PFGE analysis, we recommend 10 U of enzyme/μg DNA and 4 hour incubation time. …

  • …has been tested in Pulsed- Field Gel Electrophoresis (on bacterial chromosomes). For cleavage of genomic DNA (E. coli C600) embedded in agarose for PFGE analysis, we recommend using 10U of enzyme/mug DNA and 4 hour incubation time. Unit Definition: One unit is the enzyme activity that completely…

  • …for DNA and RNA polyacrylamide gel electrophoresis. 1, TBE is used with non-denaturing or denaturing (7 M urea) gels. It is also routinely used for DNA automated sequencing gel. 2 TBE can also be used for agarose gels but is not recommended for preparative gels for recovery of nucleic acids. …

  • …for DNA and RNA polyacrylamide gel electrophoresis. 1, TBE is used with non-denaturing or denaturing (7 M urea) gels. It is also routinely used for DNA automated sequencing gel. 2 TBE can also be used for agarose gels but is not recommended for preparative gels for recovery of nucleic acids. …

  • …sequence. PFGE tested Dra I has been tested in Pulsed- Field Gel Electrophoresis (on bacterial chromosomes). For cleavage of genomic DNA (E.coli C600) embedded in agarose for PFGE analysis, we recommend using 10 units of enzyme/μg DNA and 4 hour incubation time. Ligation and recutting…

  • … Incubation temperature +37°C PFGE tested Mlu I has been tested in Pulsed-Field Gel Electrophoresis (on bacterial chromosomes). For cleavage of genomic DNA ( E.coli C 600) embedded in agarose for PFGE analysis, we recommend using 10 U of enzyme/μg DNA and 4 hour incubation time.…

  • … Incubation temperature +37°C PFGE tested Spe I has been tested in Pulsed-Field Gel Electrophoresis (on bacterial chromosomes). For cleavage of genomic DNA ( E. coli C 600) embedded in agarose for PFGE analysis, we recommend using 10U of enzyme/μg DNA and 4 hour incubation time. …

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