By Dawn B. Marks

ISBN-10: 0683055976

ISBN-13: 9780683055979

Used this publication for the 1st 12 months miniboard in med university. It used to be a good overview. not anything staggering.

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It can bind with proteins weakly and give blue colour. 09). It is a preservative and a weighing agent. Addition of glycerol (20-30 or 50%) is often recommended for the storage of enzymes. Glycerol maintains the protein solution at very low temperature, without freezing. It also helps to weigh down the sample into the wells without being spread while loading. 97). CBB is the most popular protein stain. It is an anionic dye, which binds with proteins non-specifically. The structure of CBB is predominantly non-polar.

09). It is a preservative and a weighing agent. Addition of glycerol (20-30 or 50%) is often recommended for the storage of enzymes. Glycerol maintains the protein solution at very low temperature, without freezing. It also helps to weigh down the sample into the wells without being spread while loading. 97). CBB is the most popular protein stain. It is an anionic dye, which binds with proteins non-specifically. The structure of CBB is predominantly non-polar. 025%) in methanolic solution (40%) and acetic acid (7%).

Isotachophoresis Stadia during an ITP separation of a mix of two analytes. White: leading electrolyte; gray: terminating electrolyte; hatched: the analytes The "self-sharpening effect" in ITP: due to a difference in electrical field, an ion will move faster when it comes in the previous zone, and slower when it comes in the next zone. Therefore it will return to its "own" zone. Below the corresponding electrical field for each zone Isotachophoresis is a technique in analytical chemistry used to separate charged particles.

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Biochemistry (Board Review Series) by Dawn B. Marks


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