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Misc. Molecular Biology Supplies |
Super-Agarose®
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Size-select and concentrate your DNA or RNA right in your Gel! Recovering intact nucleic acids from a gel is simplified with our special Super-Agarose® formulation. Once you have run your gel, cut a small trough in front of your band(s) of interest, fill it in with our ready made Super-Agarose, and electrophorese in the nucleic acid.
The Super-Agarose formulation decreases the DNA's electrophoretic mobility to near zero; thus messy broad bands, and even multiple bands, pile-up and are compressed into a minimum volume of agarose (fig. 1). That means you get all of your nucleic acid in a few microliters of high-quality, low-melting temperature gel, rather than in a few hundred microliters. Plus there is no loss or shearing of high molecular weight molecules since they remain in the gel.
Use Super-Agarose to obtain preparative amounts of DNA or RNA from minor bands, or of size-selected genomic DNA (fig. 2). Run your gel as usual, loading several adjacent lanes with the same sample of interest; cut out the appropriate band across those lanes; cut another perpendicular hole, slightly longer than your band slice, elsewhere in the gel (or in a new gel). Place your band slice in the new hole and fill the extra space (toward the anode) with Super-Agarose (fig.2). Your nucleic acid will run until it becomes highly concentrated within our formulation: ready for your demanding application! (fig.2) Virtually all enzymatic reactions can be performed in gelo or you can extract if you wish.
Every batch of Super-Agarose® is tested and guaranteed to be free of nuclease, protease, and enzyme inhibitors.
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†
These are our list prices. If you are paying with an Institutional
Purchase Order or by check, you qualify for a 7.5% discount. Click
here
to change your payment method and see the lower prices.
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Super-Agarose®
|
Size-select and concentrate your DNA or RNA right in your Gel! Recovering intact nucleic acids from a gel is simplified with our special Super-Agarose® formulation. Once you have run your gel, cut a small trough in front of your band(s) of interest, fill it in with our ready made Super-Agarose, and electrophorese in the nucleic acid.
The Super-Agarose formulation decreases the DNA's electrophoretic mobility to near zero; thus messy broad bands, and even multiple bands, pile-up and are compressed into a minimum volume of agarose (fig. 1). That means you get all of your nucleic acid in a few microliters of high-quality, low-melting temperature gel, rather than in a few hundred microliters. Plus there is no loss or shearing of high molecular weight molecules since they remain in the gel.
Use Super-Agarose to obtain preparative amounts of DNA or RNA from minor bands, or of size-selected genomic DNA (fig. 2). Run your gel as usual, loading several adjacent lanes with the same sample of interest; cut out the appropriate band across those lanes; cut another perpendicular hole, slightly longer than your band slice, elsewhere in the gel (or in a new gel). Place your band slice in the new hole and fill the extra space (toward the anode) with Super-Agarose (fig.2). Your nucleic acid will run until it becomes highly concentrated within our formulation: ready for your demanding application! (fig.2) Virtually all enzymatic reactions can be performed in gelo or you can extract if you wish.
Every batch of Super-Agarose® is tested and guaranteed to be free of nuclease, protease, and enzyme inhibitors.
|
†
These are our list prices. If you are paying with an Institutional
Purchase Order or by check, you qualify for a 7.5% discount. Click
here
to change your payment method and see the lower prices.
|
|
|
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Super-Agarose®
|
Size-select and concentrate your DNA or RNA right in your Gel! Recovering intact nucleic acids from a gel is simplified with our special Super-Agarose® formulation. Once you have run your gel, cut a small trough in front of your band(s) of interest, fill it in with our ready made Super-Agarose, and electrophorese in the nucleic acid.
The Super-Agarose formulation decreases the DNA's electrophoretic mobility to near zero; thus messy broad bands, and even multiple bands, pile-up and are compressed into a minimum volume of agarose (fig. 1). That means you get all of your nucleic acid in a few microliters of high-quality, low-melting temperature gel, rather than in a few hundred microliters. Plus there is no loss or shearing of high molecular weight molecules since they remain in the gel.
Use Super-Agarose to obtain preparative amounts of DNA or RNA from minor bands, or of size-selected genomic DNA (fig. 2). Run your gel as usual, loading several adjacent lanes with the same sample of interest; cut out the appropriate band across those lanes; cut another perpendicular hole, slightly longer than your band slice, elsewhere in the gel (or in a new gel). Place your band slice in the new hole and fill the extra space (toward the anode) with Super-Agarose (fig.2). Your nucleic acid will run until it becomes highly concentrated within our formulation: ready for your demanding application! (fig.2) Virtually all enzymatic reactions can be performed in gelo or you can extract if you wish.
Every batch of Super-Agarose® is tested and guaranteed to be free of nuclease, protease, and enzyme inhibitors.
|
†
These are our list prices. If you are paying with an Institutional
Purchase Order or by check, you qualify for a 7.5% discount. Click
here
to change your payment method and see the lower prices.
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Oligo-Designer® 1.0
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OS-1:
$32.43
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- Ships in 1-5 days
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Design Oligo-Nucleotide Probes in about 1 minute!
Oligo-Designer 1.0 maximizes your chances of cloning genes by protein sequence homology by helping you choose probes with the lowest degeneracy. It takes your protein sequence (which you can type in, or cut and paste from anywhere) and Reverse-Translates it for you. The key is in the graphic form of the output: the degenerate nucleotide code "hangs down" from the amino-acid sequence. This makes finding the least ambiguous sequences quick and easy - just look for indentations (contiguous areas where the least is hanging down) and you have your probe sequences, ready to synthesize and clone your gene!!! It's an almost instantaneous process.
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†
These are our list prices. If you are paying with an Institutional
Purchase Order or by check, you qualify for a 7.5% discount. Click
here
to change your payment method and see the lower prices.
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Handheld UV Lamp
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UV-1:
$46.49
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- In Stock
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Our little Hand-held UV Lamp Is Big on Illumination
Not a new concept, but an AMAZING price! These hand-held UV lights illuminate ethidium bromide stained DNA superbly (as good or better than the common models costing over 5 times as much). - Bright long-wavelength UV keeps DNA damage to a minimum
- Light-weight design is easy to hold
 | Our little hand-held UV | Traditional hand-held UV |
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†
These are our list prices. If you are paying with an Institutional
Purchase Order or by check, you qualify for a 7.5% discount. Click
here
to change your payment method and see the lower prices.
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