I don't know why I can't figure this out..I know I am over thinking thisany help?
Danewith 8 Sufix Siege. All the major rod companies are making rods that will suit what you are looking for, so try going to a store near you and try a couple out and see how they feeltry it with a reel on it as well ( as close to what you are going to be using or one you are going to buy) to check the balance. You will want a rod a min. of 7 ft with 7'-6 preferable, to make long casts so you can get the bait down and keep it in the strike zone longer (max. running depth). With a good quality low geared reel. Remember the smaller the line diameter, the less water resistance and the deeper your crankbait will dive, would also suggest using nothing but mono line, because it stretches and has some give, which is important when using crankbaits.
Gas chromatography (GC) and spectrophotometry are mainly used to determine the concentration of one substance in another, or the results can be used to identify a certain unknown compound. For GC a small sample is heated and boiled. Once in the gas phase it flows through the instrument and the detector analyzes it and makes a graph. The graph will tell you how much of the substance there was and at what point it boiled. Different compounds have different boiling points so you can determine an unknown this way. Specs are usually used for the same purpose as the GC. A small sample is subject to a ray of light and the spec measures how much of the light that sample absorbed. Different samples usually absorb different amounts of light at different wavelengths so you can use this to determine an unknown substance. You can also construct an absorption graph to determine the concentration of a substance. Higher concentrations will absorb more light, thereby having lower absorption values. These are the most common forms of chromatography and spectrophotometry. Gel electrophoresis is usually used to determine size or charge or both of a sample. The gel is porous and when a current is passed through the buffer the sample migrates across the gel. Small samples will travel more easily through the gel and migrate further than large samples. Similar with charge, samples with greater opposite charge will be more attracted to the opposite side of the gel and travel further than neutrally charged samples.
