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ProductsPlasmid kits Gel Extraction PCR Cleanup Our Technology Free Samples Orders Contact AdBiotec | . |
![]() . Gel extraction kits are available in one size: . GEK-1 will process 100 agarose gel samples. . Buy 2 or more kits and save. Yes, get two or more kits at the bulk purchase price of A$195 per kit (that's just $1.95/sample). . Each kit is supplied with spin columns fitted into 2ml receiver tubes, an equal number of 1.7 ml receiver/storage tubes, chemistry and instructions. . Experienced users: AdBiotec gel extraction kits work with either TAE or TBE agarose gels, recover virtually all the DNA from the agarose, yet this remarkable product is significantly cheaper than our major competitors kits. . . ![]() . A 1 kb ladder was run on a 1% TAE agarose gel. Four single bands of 10, 6, 4 and 3 kb were extracted using the AdBiotec Gel Extraction Kit. Lanes 1-4 represent the purified DNA fragments. The Agarose Gel DNA Extraction spin kit provides a quick and reliable method for the isolation of DNA from all types of agarose gels and buffer systems. The resulting DNA is free of unwanted DNA fragments, primers, nucleotides, enzymes and salts. The agarose is solubilized using a strong chaotropic solution containing a proprietary mixture of additives which enables the rapid extraction of DNA from both TAE and TBE agarose gels with equal efficiency. Our unique multi-layer silica membranes can adsorb up to 20ug of double stranded DNA per column. This kit can be used for the isolation of DNA sizes ranging from 100 bp up to 10 kbp, with recovery efficiencies ranging from 85 - 95% on average. ![]() DNA fragments were extracted from a 1% TBE gel using the AdBiotec Gel Extraction Kit. Lane 1 represents the cloning vector pUC21 containing a 150 bp insert. Lanes 2 and 3 are the gel-purified DNA bands of the insert (150 bp) and the pUC21 (3.2 kbp). Lane 4 is a pUC21 clone containing a 9.6 kbp insert. Lanes 5 and 6 are the gel-purified DNA products. . Downstream applications include: sequencing, cloning, restriction analysis and preparation of DNA probes. . . ![]() ![]() ![]() | . |