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Showing Results For: Agarose and Gelling Reagents

Agarose and Gelling Reagents


9012-36-6, Carl Roth

MF Part: 9012-36-6
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£ 676.31
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9012-36-6, Carl Roth

MF Part: 9012-36-6
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£ 444.11
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9012-36-6, Carl Roth

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£ 39.60
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39346-81-1, Carl Roth

MF Part: 39346-81-1
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£ 51.80
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9012-36-6, Carl Roth

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£ 37.67
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9012-36-6, Carl Roth

MF Part: 9012-36-6
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£ 333.81
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39346-81-1, Carl Roth

MF Part: 39346-81-1
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£ 695.66
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9012-36-6, Carl Roth

MF Part: 9012-36-6
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£ 865.94
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9012-36-6, Carl Roth

MF Part: 9012-36-6
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£ 1059.44
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9012-36-6, Carl Roth

MF Part: 9012-36-6
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£ 21.78
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39346-81-1, Carl Roth

MF Part: 39346-81-1
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£ 2704.19
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9012-36-6, Carl Roth

MF Part: 9012-36-6
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£ 991.71
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9012-36-6, Carl Roth

9012-36-6, Carl Roth

Our agarose ROTI ® Garose is a neutral polysaccharide which is obtained in many purification steps from the cell wall of certain algae, called Rhodophyceae. ROTI ® Garose forms very clear gels with all standard running buffers and will result in a sharp and clear separation of your biomolecules. Extremely pure agarose with very low interference binding to staining reagents. ROTI ® Garose produces a low background and high contrast appearance after staining. For clear and sharp bands Gels with high transparency Low background Suitable for all standard running buffers and high-speed buffer systems Compatible with all nucleic acid staining systems Non-toxic in cell immobilisation assays Of course DNase and RNase free Agarose as Gelling Reagent Chemically, agarose is a galactan which is capable of forming extremely solid gels, even at a low concentration. The pore size of the gels is determined by the concentration of the agarose used. Because there are no ionic groups in the gel, hydrophilic materials without any interaction with the gel matrix will also be separated according to their size. The high hysteresis of the agarose, that is the thermal stability after solidifi cation, ensures that the gels remain reliably stable even during heatproducing running conditions. Agarose Broad Range ROTI ® Garose BioScience Grade High-molcular linear polymer of particularly high DNA mobility in electrophoresis The ideal choice for Pulse Field gel electrophoresis Excellent for resolving DNAfragments between 200 bp and 40 kb in conventional gel electrophoresis Low EEO allows speedy and efficient resolution of very large DNA-molecules Extremely high gel strength guarantees good handling even at low concentrations of 0,3 % agarose Also suitable for separation of particles like ribosomes, virions or chromosomes

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9012-36-6, Carl Roth

9012-36-6, Carl Roth

Our agarose ROTI ® Garose is a neutral polysaccharide which is obtained in many purification steps from the cell wall of certain algae, called Rhodophyceae. ROTI ® Garose forms very clear gels with all standard running buffers and will result in a sharp and clear separation of your biomolecules. Extremely pure agarose with very low interference binding to staining reagents. ROTI ® Garose produces a low background and high contrast appearance after staining. For clear and sharp bands Gels with high transparency Low background Suitable for all standard running buffers and high-speed buffer systems Compatible with all nucleic acid staining systems Non-toxic in cell immobilisation assays Of course DNase and RNase free Agarose as Gelling Reagent Chemically, agarose is a galactan which is capable of forming extremely solid gels, even at a low concentration. The pore size of the gels is determined by the concentration of the agarose used. Because there are no ionic groups in the gel, hydrophilic materials without any interaction with the gel matrix will also be separated according to their size. The high hysteresis of the agarose, that is the thermal stability after solidifi cation, ensures that the gels remain reliably stable even during heatproducing running conditions. Agarose High Resolution ROTI ® Garose for small fragments High resolution of PCR-products and DNA fragments in the 50-1000 bp range Low gel background after staining, even for highly concentrated gels Can be used in concentrations of up to 5 % agarose Low DNA binding and low EEO for efficient separation of very small fragments Tip: cool the gel for 30 mins. at 4-8 °C before use for superior separation Separation range in 1 x TAE: 1,8 % proof agarose gel: 500-1000 bp 3,0 % proof agarose gel: 150-600 bp 4,5 % proof agarose gel: 50-350 bp

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9012-36-6, Carl Roth

9012-36-6, Carl Roth

Our agarose ROTI ® Garose is a neutral polysaccharide which is obtained in many purification steps from the cell wall of certain algae, called Rhodophyceae. ROTI ® Garose forms very clear gels with all standard running buffers and will result in a sharp and clear separation of your biomolecules. Extremely pure agarose with very low interference binding to staining reagents. ROTI ® Garose produces a low background and high contrast appearance after staining. For clear and sharp bands Gels with high transparency Low background Suitable for all standard running buffers and high-speed buffer systems Compatible with all nucleic acid staining systems Non-toxic in cell immobilisation assays Of course DNase and RNase free Agarose as Gelling Reagent Chemically, agarose is a galactan which is capable of forming extremely solid gels, even at a low concentration. The pore size of the gels is determined by the concentration of the agarose used. Because there are no ionic groups in the gel, hydrophilic materials without any interaction with the gel matrix will also be separated according to their size. The high hysteresis of the agarose, that is the thermal stability after solidifi cation, ensures that the gels remain reliably stable even during heatproducing running conditions. Agarose-Tablets ROTI ® Garose 0,5 g agarose/tablet Easy-to-use and safe tablets for constant gel strength and well reproducible gels Reliable agarose for routine analyses for detection of inserts or PCR amplificates of over 300 bps Agarose with high gel strength, applicable from 0,5 to 2,5 % Compatible with all standard running buffers and nucleic acid-staining methods

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39346-81-1, Carl Roth

39346-81-1, Carl Roth

Our agarose Roti ® garose is a neutral polysaccharide which is obtained in many purification steps from the cell wall of certain algae, called Rhodophyceae. Roti ® garose forms very clear gels with all standard running buffers and will result in a sharp and clear separation of your biomolecules. Extremely pure agarose with very low interference binding to staining reagents. Roti ® garose produces a low background and high contrast appearance after staining. For clear and sharp bands Gels with high transparency Low background Suitable for all standard running buffers and high-speed buffer systems Compatible with all nucleic acid staining systems Non-toxic in cell immobilisation assays Of course DNase and RNase free Agarose LM/PCR ROTI ® Garose Genetic engineering quality, with low melting and gelling temperature High resolution low melting agarose in genetic engineering quality. For optimal fragment separation, DNA recovery and cloning of PCR amplificates. Low melting point and low gelling temperature Fine resolution of fragments from 50 to 1500 bp Very well suited for analysis and recovery of PCR amplificates and fragments derived from restriction digests Also well suitable for in-gel-applications Low gel background, compatible with all standard nucleic acid-staining methods Low viscosity agarose, recommended for use in concentrations of 3 to 6 % agarose.

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New
9012-36-6, Carl Roth

9012-36-6, Carl Roth

Our agarose ROTI ® Garose is a neutral polysaccharide which is obtained in many purification steps from the cell wall of certain algae, called Rhodophyceae. ROTI ® Garose forms very clear gels with all standard running buffers and will result in a sharp and clear separation of your biomolecules. Extremely pure agarose with very low interference binding to staining reagents. ROTI ® Garose produces a low background and high contrast appearance after staining. For clear and sharp bands Gels with high transparency Low background Suitable for all standard running buffers and high-speed buffer systems Compatible with all nucleic acid staining systems Non-toxic in cell immobilisation assays Of course DNase and RNase free Agarose as Gelling Reagent Chemically, agarose is a galactan which is capable of forming extremely solid gels, even at a low concentration. The pore size of the gels is determined by the concentration of the agarose used. Because there are no ionic groups in the gel, hydrophilic materials without any interaction with the gel matrix will also be separated according to their size. The high hysteresis of the agarose, that is the thermal stability after solidifi cation, ensures that the gels remain reliably stable even during heatproducing running conditions. Agarose Pulsed-Field ROTI ® Garose Genetic engineering quality, for pulsed field electrophoresis Optimised for separation of fragments of 20 to 50 kb or for Pulsed Field Gel Electrophoresis (PFGE) High gel-strength agarose for tearproof gels that are easy to handle High DNA mobility for fast and efficient gel electrophoresis Low background fluorescence after ethidium bromide staining In general, suitable for separation of fragments larger than 1000 bp Tested for absence of DNAses, RNAses and DNA binding Figure (left to right): 0,3 % Agarose Pulsed-Field, extended 1kbp Ladder (1 µg) and High Molecular Weight Marker (0,3 µg, heated for 10 mins. at 65 °C); then same markers on 0,5 % Agarose Pulsed-Field.

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New
9012-36-6, Carl Roth

9012-36-6, Carl Roth

Our agarose ROTI ® Garose is a neutral polysaccharide which is obtained in many purification steps from the cell wall of certain algae, called Rhodophyceae. ROTI ® Garose forms very clear gels with all standard running buffers and will result in a sharp and clear separation of your biomolecules. Extremely pure agarose with very low interference binding to staining reagents. ROTI ® Garose produces a low background and high contrast appearance after staining. For clear and sharp bands Gels with high transparency Low background Suitable for all standard running buffers and high-speed buffer systems Compatible with all nucleic acid staining systems Non-toxic in cell immobilisation assays Of course DNase and RNase free Agarose as Gelling Reagent Chemically, agarose is a galactan which is capable of forming extremely solid gels, even at a low concentration. The pore size of the gels is determined by the concentration of the agarose used. Because there are no ionic groups in the gel, hydrophilic materials without any interaction with the gel matrix will also be separated according to their size. The high hysteresis of the agarose, that is the thermal stability after solidifi cation, ensures that the gels remain reliably stable even during heatproducing running conditions. Agarose Standard ROTI ® Garose for DNA/RNA electrophoresis Inexpensive agarose for routine gels and standard analyses Good separation efficiency for nucleic acids of 1 to 20 kb length Easily melting, non-foaming agarose Low background fluorescence after ethidium bromide staining Very cost-effective Figure (left to right): Roth Lambda Hind lll Marker (Art. No. X910.1) 0,6 µg, 1 kbp DNA Ladder (Art. No. Y014.1) 0,8 µg, DNA-Marker short-run extended (Art. No. CL05.1) 0,4 µg, PCR-Marker DNA score (Art. No. T146.1) 0,5 µg.

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New
39346-81-1, Carl Roth

39346-81-1, Carl Roth

Our agarose Roti ® garose is a neutral polysaccharide which is obtained in many purification steps from the cell wall of certain algae, called Rhodophyceae. Roti ® garose forms very clear gels with all standard running buffers and will result in a sharp and clear separation of your biomolecules. Extremely pure agarose with very low interference binding to staining reagents. Roti ® garose produces a low background and high contrast appearance after staining. For clear and sharp bands Gels with high transparency Low background Suitable for all standard running buffers and high-speed buffer systems Compatible with all nucleic acid staining systems Non-toxic in cell immobilisation assays Of course DNase and RNase free Agarose Super LM ROTI ® Garose with particularly low melting and gelling temperature Fine resolution of fragments over 1000 bp Very well suited for analysis and recovery of longer PCR amplificates or other longer fragments like vectors, rare cutter digestions etc. Recommended for in-gel-applications, virus plaque-assays and tissue/cell culture applications Low gel background, compatible with all standard nucleic acid-staining methods Lower gel strength than Agarose Low Melt. Recommended for use in concentrations of over 1 % agarose

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New
9012-36-6, Carl Roth

9012-36-6, Carl Roth

Our agarose ROTI ® Garose is a neutral polysaccharide which is obtained in many purification steps from the cell wall of certain algae, called Rhodophyceae. ROTI ® Garose forms very clear gels with all standard running buffers and will result in a sharp and clear separation of your biomolecules. Extremely pure agarose with very low interference binding to staining reagents. ROTI ® Garose produces a low background and high contrast appearance after staining. For clear and sharp bands Gels with high transparency Low background Suitable for all standard running buffers and high-speed buffer systems Compatible with all nucleic acid staining systems Non-toxic in cell immobilisation assays Of course DNase and RNase free Agarose as Gelling Reagent Chemically, agarose is a galactan which is capable of forming extremely solid gels, even at a low concentration. The pore size of the gels is determined by the concentration of the agarose used. Because there are no ionic groups in the gel, hydrophilic materials without any interaction with the gel matrix will also be separated according to their size. The high hysteresis of the agarose, that is the thermal stability after solidifi cation, ensures that the gels remain reliably stable even during heatproducing running conditions. Agarose NEEO ultra-quality ROTI ® Garose low electroendosmosis (EEO = 0.05-0.13) Excellent separative power for nucleic acids of 500 bp to 20 kb High gel strength for stable gels and good handling Extremely low EEO allows speedy and efficient separation of nucleic acid molecules Fast melting, non-foaming agarose Figure: (left to right) Roth Lambda Hind III / phiX Hae III marker (Art. No. CP49.1) 1 µg, 1 kbp DNA-ladder (Art. No. Y014.1) 0,8 µg, 100 bp-DNA-ladder extended (Art. No. T835.1) 0,8 µg, pBR328 Mix I (Art. No. T146.1) 0,8 µg.

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New
9012-36-6, Carl Roth

9012-36-6, Carl Roth

Our agarose ROTI ® Garose is a neutral polysaccharide which is obtained in many purification steps from the cell wall of certain algae, called Rhodophyceae. ROTI ® Garose forms very clear gels with all standard running buffers and will result in a sharp and clear separation of your biomolecules. Extremely pure agarose with very low interference binding to staining reagents. ROTI ® Garose produces a low background and high contrast appearance after staining. For clear and sharp bands Gels with high transparency Low background Suitable for all standard running buffers and high-speed buffer systems Compatible with all nucleic acid staining systems Non-toxic in cell immobilisation assays Of course DNase and RNase free Agarose as Gelling Reagent Chemically, agarose is a galactan which is capable of forming extremely solid gels, even at a low concentration. The pore size of the gels is determined by the concentration of the agarose used. Because there are no ionic groups in the gel, hydrophilic materials without any interaction with the gel matrix will also be separated according to their size. The high hysteresis of the agarose, that is the thermal stability after solidifi cation, ensures that the gels remain reliably stable even during heatproducing running conditions. Agarose HEEO ultra-quality ROTI ® Garose high electroendosmosis (EEO = 0,23-0,26) Gels are well-to-handle and have a strong matrix, even when using thin gels of 1-2 mm Very clear and transparent matrix, even for thick gels

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New
9012-36-6, Carl Roth

9012-36-6, Carl Roth

Our agarose ROTI ® Garose is a neutral polysaccharide which is obtained in many purification steps from the cell wall of certain algae, called Rhodophyceae. ROTI ® Garose forms very clear gels with all standard running buffers and will result in a sharp and clear separation of your biomolecules. Extremely pure agarose with very low interference binding to staining reagents. ROTI ® Garose produces a low background and high contrast appearance after staining. For clear and sharp bands Gels with high transparency Low background Suitable for all standard running buffers and high-speed buffer systems Compatible with all nucleic acid staining systems Non-toxic in cell immobilisation assays Of course DNase and RNase free Agarose as Gelling Reagent Chemically, agarose is a galactan which is capable of forming extremely solid gels, even at a low concentration. The pore size of the gels is determined by the concentration of the agarose used. Because there are no ionic groups in the gel, hydrophilic materials without any interaction with the gel matrix will also be separated according to their size. The high hysteresis of the agarose, that is the thermal stability after solidifi cation, ensures that the gels remain reliably stable even during heatproducing running conditions. Agarose Standard ROTI ® Garose for DNA/RNA electrophoresis Inexpensive agarose for routine gels and standard analyses Good separation efficiency for nucleic acids of 1 to 20 kb length Easily melting, non-foaming agarose Low background fluorescence after ethidium bromide staining Very cost-effective Figure (left to right): Roth Lambda Hind lll Marker (Art. No. X910.1) 0,6 µg, 1 kbp DNA Ladder (Art. No. Y014.1) 0,8 µg, DNA-Marker short-run extended (Art. No. CL05.1) 0,4 µg, PCR-Marker DNA score (Art. No. T146.1) 0,5 µg.

Product Detail
New
39346-81-1, Carl Roth

39346-81-1, Carl Roth

Our agarose Roti ® garose is a neutral polysaccharide which is obtained in many purification steps from the cell wall of certain algae, called Rhodophyceae. Roti ® garose forms very clear gels with all standard running buffers and will result in a sharp and clear separation of your biomolecules. Extremely pure agarose with very low interference binding to staining reagents. Roti ® garose produces a low background and high contrast appearance after staining. For clear and sharp bands Gels with high transparency Low background Suitable for all standard running buffers and high-speed buffer systems Compatible with all nucleic acid staining systems Non-toxic in cell immobilisation assays Of course DNase and RNase free Agarose Low Melt ROTI ® Garose with low melting and gelling temperature Low melting point and low gelling temperature High transparency and very low self fluorescence. For particular clear gels. The ideal solution when nucleic acid fragments or proteins are to be recovered after electrophoretic resolution Suitable for enzymatic reactions in liquid agarose (in-gel-applications) Excellent for immobilising microorganisms and virus-plaque-assays Suitable for cell culture applications (animal and plant) Tested for stability after autoclaving

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New
9012-36-6, Carl Roth

9012-36-6, Carl Roth

Our agarose ROTI ® Garose is a neutral polysaccharide which is obtained in many purification steps from the cell wall of certain algae, called Rhodophyceae. ROTI ® Garose forms very clear gels with all standard running buffers and will result in a sharp and clear separation of your biomolecules. Extremely pure agarose with very low interference binding to staining reagents. ROTI ® Garose produces a low background and high contrast appearance after staining. For clear and sharp bands Gels with high transparency Low background Suitable for all standard running buffers and high-speed buffer systems Compatible with all nucleic acid staining systems Non-toxic in cell immobilisation assays Of course DNase and RNase free Agarose as Gelling Reagent Chemically, agarose is a galactan which is capable of forming extremely solid gels, even at a low concentration. The pore size of the gels is determined by the concentration of the agarose used. Because there are no ionic groups in the gel, hydrophilic materials without any interaction with the gel matrix will also be separated according to their size. The high hysteresis of the agarose, that is the thermal stability after solidifi cation, ensures that the gels remain reliably stable even during heatproducing running conditions. Agarose MEEO ultra-quality ROTI ® Garose middle electroendosmosis (EEO = 0,16-0,19) Suitable for separation of nucleic acids between 500 bp and 10 kb Gels are well-to-handle and have a strong matrix, even when using thin gels of 1-2 mm

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