We're trying to determine a more efficient method to extract Agarose from Agar powder and unable to determine how much Agarose vs Agaropectin are present in a given sample of Agar. Any procedure/method would be much appreciated.
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Is there any reason for decrease in fluorescence emission intensity of HSA,BSA when increase the concentration ?
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How effective and helpful is it, really.
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I need a procedure to extract the ciprofloxacin hydrochloride from aqueous solution by using dichloromethane in detail,. I thank you very much.
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Can someone please give me some possible things that could go wrong? Here is my recipe: 0.5g Agarose 50 mL of TAE 1x 1 uL ethyl bromide. Gel was run at 100V for 1 hour. The buffer used is also TAE.
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The resultant solid was partitioned three times with 250 ml of petroleum ether (40-60/c) to remove any fatty material and evaporated to dryness.
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