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Showing Results For: Nylon membranes

Nylon membranes


260P.1, Carl Roth

MF Part: 260P.1
MOQ: 1 - 5
£ 411.21
In Stock
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260L.1, Carl Roth

MF Part: 260L.1
MOQ: 1 - 5
£ 411.21
In Stock
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260T.1, Carl Roth

MF Part: 260T.1
MOQ: 1 - 5
£ 212.85
In Stock
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261A.1, Carl Roth

MF Part: 261A.1
MOQ: 1 - 5
£ 411.21
In Stock
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260N.1, Carl Roth

MF Part: 260N.1
MOQ: 1 - 5
£ 149.99
In Stock
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260Y.1, Carl Roth

MF Part: 260Y.1
MOQ: 1 - 5
£ 106.43
In Stock
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261C.1, Carl Roth

MF Part: 261C.1
MOQ: 1 - 5
£ 212.85
In Stock
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261H.1, Carl Roth

MF Part: 261H.1
MOQ: 1 - 5
£ 149.99
In Stock
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261E.1, Carl Roth

MF Part: 261E.1
MOQ: 1 - 5
£ 198.36
In Stock
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260X.1, Carl Roth

MF Part: 260X.1
MOQ: 1 - 5
£ 149.99
In Stock
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New Items
New
260P.1, Carl Roth

260P.1, Carl Roth

Material: nylon 6.6. Autoclavable: yes. . Transfer membrane ROTI ® Nylon 0.45 The optimal membrane for DNA/RNA transfer, especially colony and plaque lifting and all multiple rehybridisations. R OTI ® Nylon 0.45 is a neutral, reinforced nylon membrane. Like all R OTI ® Nylon membranes, it has a very high tensile strength and is highly resistant to alcohols, acetone and many other organic solvents. R OTI ® Nylon 0.45 is not charged at buffer pH 6.5 and has excellent hydrophilic properties due to the amino and carboxy groups on the surface. The membrane charge (ζ-potential) can be adjusted by the pH value of the buffer system (positive membrane charge at pH<6.5; negative membrane charge at pH>6.5). Steam sterilisation is possible. The covalent binding of transferred nucleic acid is achieved by crosslinking (UV crosslinking for 20 s at 260 nm). The excellent signal/background ratio of the membrane then enables highly sensitive detections (single copy gene detection) and multiple rehybridisations without loss of signal quality. Detection by radioactivity, chemiluminescence, fluorescence Application: Southern and Northern blotting Western blotting Microarrays and Macroarrays Dot/Slot blotting Not a medical device / Not an IVD product

Product Detail
New
260L.1, Carl Roth

260L.1, Carl Roth

Material: nylon 6.6. Autoclavable: yes. . Transfer membrane ROTI ® Nylon 0.2 The optimal membrane for DNA/RNA transfer, especially colony and plaque lifting and all multiple rehybridisations. R OTI ® Nylon 0.2 is a neutral, reinforced nylon membrane. Like all R OTI ® ylon membranes, it has a very high tensile strength and is highly resistant to alcohols, acetone and many other organic solvents. R OTI ® Nylon 0.2 is not charged at buffer pH 6.5 and has excellent hydrophilic properties due to the amino and carboxy groups on the surface. The membrane charge (ζ-potential) can be adjusted by the pH value of the buffer system (positive membrane charge at pH<6.5; negative membrane charge at pH>6.5). Steam sterilisation is possible. The covalent binding of transferred nucleic acid is achieved by crosslinking (UV crosslinking for 20 s at 260 nm). The excellent signal/background ratio of the membrane then enables highly sensitive detections (single copy gene detection) and multiple rehybridisations without loss of signal quality. Detection by radioactivity, chemiluminescence, fluorescence Application: Southern and Northern blotting Western blotting Microarrays and Macroarrays Dot/Slot blotting Not a medical device / Not an IVD product

Product Detail
New
260T.1, Carl Roth

260T.1, Carl Roth

Material: nylon 6.6. Autoclavable: yes. . Transfer membrane ROTI ® Nylon 0.45 The optimal membrane for DNA/RNA transfer, especially colony and plaque lifting and all multiple rehybridisations. R OTI ® Nylon 0.45 is a neutral, reinforced nylon membrane. Like all R OTI ® Nylon membranes, it has a very high tensile strength and is highly resistant to alcohols, acetone and many other organic solvents. R OTI ® Nylon 0.45 is not charged at buffer pH 6.5 and has excellent hydrophilic properties due to the amino and carboxy groups on the surface. The membrane charge (ζ-potential) can be adjusted by the pH value of the buffer system (positive membrane charge at pH<6.5; negative membrane charge at pH>6.5). Steam sterilisation is possible. The covalent binding of transferred nucleic acid is achieved by crosslinking (UV crosslinking for 20 s at 260 nm). The excellent signal/background ratio of the membrane then enables highly sensitive detections (single copy gene detection) and multiple rehybridisations without loss of signal quality. Detection by radioactivity, chemiluminescence, fluorescence Application: Southern and Northern blotting Western blotting Microarrays and Macroarrays Dot/Slot blotting Not a medical device / Not an IVD product

Product Detail
New
261A.1, Carl Roth

261A.1, Carl Roth

Material: nylon 6.6. Autoclavable: yes. . Transfer membrane ROTI ® Nylon Plus Reprobe The optimal membrane for DNA/RNA transfer. ROTI ® Nylon Plus Reprobe is a cationic, supported nylon 6.6 membrane specially developed for multiple reprobings. The membrane has an extremely high tensile strength. The inherent positively charged membrane surface guarantees fast and efficient binding of DNA and RNA. After 12 rounds of reprobing, ROTI ® Nylon Plus Reprobe has a lower background and a higher signal. Steam sterilisation is possible. Also available as practical pre-cuts in common gel sizes! Fixation of the nucleic acids on the membrane can be achieved by UV irradiation. No fixation is required for alkaline transfer conditions. Under these conditions, the negatively charged DNA forms a very stable complex with the positively charged ROTI ® Nylon Plus Reprobe membrane. Detection by radioactivity, chemiluminescence, fluorescence Application: Southern and Northern blotting Alkaline blotting Multiple reprobings Not a medical device / Not an IVD product

Product Detail
New
260N.1, Carl Roth

260N.1, Carl Roth

Material: nylon 6.6. Autoclavable: yes. . Transfer membrane ROTI ® Nylon 0.2 The optimal membrane for DNA/RNA transfer, especially colony and plaque lifting and all multiple rehybridisations. R OTI ® Nylon 0.2 is a neutral, reinforced nylon membrane. Like all R OTI ® ylon membranes, it has a very high tensile strength and is highly resistant to alcohols, acetone and many other organic solvents. R OTI ® Nylon 0.2 is not charged at buffer pH 6.5 and has excellent hydrophilic properties due to the amino and carboxy groups on the surface. The membrane charge (ζ-potential) can be adjusted by the pH value of the buffer system (positive membrane charge at pH<6.5; negative membrane charge at pH>6.5). Steam sterilisation is possible. The covalent binding of transferred nucleic acid is achieved by crosslinking (UV crosslinking for 20 s at 260 nm). The excellent signal/background ratio of the membrane then enables highly sensitive detections (single copy gene detection) and multiple rehybridisations without loss of signal quality. Detection by radioactivity, chemiluminescence, fluorescence Application: Southern and Northern blotting Western blotting Microarrays and Macroarrays Dot/Slot blotting Not a medical device / Not an IVD product

Product Detail
New
260Y.1, Carl Roth

260Y.1, Carl Roth

Material: nylon 6.6. Autoclavable: yes. . Transfer membrane ROTI ® Nylon 0.45 The optimal membrane for DNA/RNA transfer, especially colony and plaque lifting and all multiple rehybridisations. R OTI ® Nylon 0.45 is a neutral, reinforced nylon membrane. Like all R OTI ® Nylon membranes, it has a very high tensile strength and is highly resistant to alcohols, acetone and many other organic solvents. R OTI ® Nylon 0.45 is not charged at buffer pH 6.5 and has excellent hydrophilic properties due to the amino and carboxy groups on the surface. The membrane charge (ζ-potential) can be adjusted by the pH value of the buffer system (positive membrane charge at pH<6.5; negative membrane charge at pH>6.5). Steam sterilisation is possible. The covalent binding of transferred nucleic acid is achieved by crosslinking (UV crosslinking for 20 s at 260 nm). The excellent signal/background ratio of the membrane then enables highly sensitive detections (single copy gene detection) and multiple rehybridisations without loss of signal quality. Detection by radioactivity, chemiluminescence, fluorescence Application: Southern and Northern blotting Western blotting Microarrays and Macroarrays Dot/Slot blotting Not a medical device / Not an IVD product

Product Detail
New
261C.1, Carl Roth

261C.1, Carl Roth

Material: nylon 6.6. Autoclavable: yes. . Transfer membrane ROTI ® Nylon Plus Reprobe The optimal membrane for DNA/RNA transfer. ROTI ® Nylon Plus Reprobe is a cationic, supported nylon 6.6 membrane specially developed for multiple reprobings. The membrane has an extremely high tensile strength. The inherent positively charged membrane surface guarantees fast and efficient binding of DNA and RNA. After 12 rounds of reprobing, ROTI ® Nylon Plus Reprobe has a lower background and a higher signal. Steam sterilisation is possible. Also available as practical pre-cuts in common gel sizes! Fixation of the nucleic acids on the membrane can be achieved by UV irradiation. No fixation is required for alkaline transfer conditions. Under these conditions, the negatively charged DNA forms a very stable complex with the positively charged ROTI ® Nylon Plus Reprobe membrane. Detection by radioactivity, chemiluminescence, fluorescence Application: Southern and Northern blotting Alkaline blotting Multiple reprobings Not a medical device / Not an IVD product

Product Detail
New
261H.1, Carl Roth

261H.1, Carl Roth

Material: nylon 6.6. Autoclavable: yes. . Transfer membrane ROTI ® Nylon Plus Reprobe The optimal membrane for DNA/RNA transfer. ROTI ® Nylon Plus Reprobe is a cationic, supported nylon 6.6 membrane specially developed for multiple reprobings. The membrane has an extremely high tensile strength. The inherent positively charged membrane surface guarantees fast and efficient binding of DNA and RNA. After 12 rounds of reprobing, ROTI ® Nylon Plus Reprobe has a lower background and a higher signal. Steam sterilisation is possible. Also available as practical pre-cuts in common gel sizes! Fixation of the nucleic acids on the membrane can be achieved by UV irradiation. No fixation is required for alkaline transfer conditions. Under these conditions, the negatively charged DNA forms a very stable complex with the positively charged ROTI ® Nylon Plus Reprobe membrane. Detection by radioactivity, chemiluminescence, fluorescence Application: Southern and Northern blotting Alkaline blotting Multiple reprobings Not a medical device / Not an IVD product

Product Detail
New
261E.1, Carl Roth

261E.1, Carl Roth

Material: nylon 6.6. Autoclavable: yes. . Transfer membrane ROTI ® Nylon Plus Reprobe The optimal membrane for DNA/RNA transfer. ROTI ® Nylon Plus Reprobe is a cationic, supported nylon 6.6 membrane specially developed for multiple reprobings. The membrane has an extremely high tensile strength. The inherent positively charged membrane surface guarantees fast and efficient binding of DNA and RNA. After 12 rounds of reprobing, ROTI ® Nylon Plus Reprobe has a lower background and a higher signal. Steam sterilisation is possible. Also available as practical pre-cuts in common gel sizes! Fixation of the nucleic acids on the membrane can be achieved by UV irradiation. No fixation is required for alkaline transfer conditions. Under these conditions, the negatively charged DNA forms a very stable complex with the positively charged ROTI ® Nylon Plus Reprobe membrane. Detection by radioactivity, chemiluminescence, fluorescence Application: Southern and Northern blotting Alkaline blotting Multiple reprobings Not a medical device / Not an IVD product

Product Detail
New
260X.1, Carl Roth

260X.1, Carl Roth

Material: nylon 6.6. Autoclavable: yes. . Transfer membrane ROTI ® Nylon 0.45 The optimal membrane for DNA/RNA transfer, especially colony and plaque lifting and all multiple rehybridisations. R OTI ® Nylon 0.45 is a neutral, reinforced nylon membrane. Like all R OTI ® Nylon membranes, it has a very high tensile strength and is highly resistant to alcohols, acetone and many other organic solvents. R OTI ® Nylon 0.45 is not charged at buffer pH 6.5 and has excellent hydrophilic properties due to the amino and carboxy groups on the surface. The membrane charge (ζ-potential) can be adjusted by the pH value of the buffer system (positive membrane charge at pH<6.5; negative membrane charge at pH>6.5). Steam sterilisation is possible. The covalent binding of transferred nucleic acid is achieved by crosslinking (UV crosslinking for 20 s at 260 nm). The excellent signal/background ratio of the membrane then enables highly sensitive detections (single copy gene detection) and multiple rehybridisations without loss of signal quality. Detection by radioactivity, chemiluminescence, fluorescence Application: Southern and Northern blotting Western blotting Microarrays and Macroarrays Dot/Slot blotting Not a medical device / Not an IVD product

Product Detail
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