Microscope Fluorescent
![]() |
![]() MICROSCOPE Accessories Zeiss Insert for Fluorescent US $89.00
|
![]() DIN 4X Fluor Objective for Fluorescent Microscopes US $69.99
|
![]() 4X Fluor Objective Lens for EPI Fluorescent Microscopes US $59.99
|
![]() Microscope Back light Fluorescent Illuminator US $40.00
|
![]() New FLUORESCENT RING LIGHT For STEREO MICROSCOPE US $39.90
|
![]() Microscope Fluorescent Circular Light Tube 220 240V 8W US $36.34
|
![]() NEW 12W FLUORESCENT RING LIGHT MICROSCOPE ADAPTER US $34.98
|
![]() Fluorescent Ring Light for Stereo Microscopes w 2 Bulbs US $37.38
|
![]() 8W STEREO MICROSCOPE FLUORESCENT RING LIGHT ADAPTER US $35.19
|
![]() NEW FLUORESCENT RING LIGHT FOR MICROSCOPE 60mm Dia US $29.99
|
![]() NEW FLUORESCENT RING LIGHT FOR MICROSCOPE 63mm Dia US $29.99
|
![]() NEW 8W FLUORESCENT RING LIGHT FOR MICROSCOPE Illuminator 63mm Dia US $29.99
|
![]() New FLUORESCENT RING LIGHT FOR MICROSCOPE US $29.99
|
![]() NEW FLUORESCENT RING LIGHT FOR MICROSCOPE WITH ADATER US $29.99
|
![]() STOCKER YALE MICROSCOPE ILLUMINATOR BLACKLIGHT BLUE FLUORESCENT LAMP US $29.95
|
![]() 8W Ring Bulb For Microscope Fluorescent Ring Light US $14.99
|
![]() 8W RING BULB FOR MICROSCOPE FLUORESCENT RING LIGHT US $14.98
|
![]() 12W RING BULB MICROSCOPE FLUORESCENT RING LIGHT US $14.98
|
![]() Fluorescent Tube 110V 220V 5W 4 Microscope Illuminator US $7.99
|
![]() 6500K Ring Tube for 8W Microscope Fluorescent Light US $7.99
|
![]() 5000K Ring Tube for 8W Microscope Fluorescent Light US $7.99
|
Simple Crystal Experiments You Are Able To Share Using Your Kids
Simply by Aurora Lipper, Supercharged Technology
This short article teaches kids about the Crystal Farming and gives a handful of totally exciting activities to experiment with for their homeschool technology learning (such as rock candy and homemade geodes). Its also good for boy scouts focusing on a logo, or for almost any kids that love science experiments. These kinds of experiments are part of a homeschool science program that i teach, and I promise your children will love it.
Deposits are produced with atoms make in patterns if the substance solidifies (or maybe the water evaporates and leaves the remainder behind). You can find crystals everywhere by means of salt, sugar, crushed lime stone, expensive diamonds, quartz, and many, additional. But just how do the atoms understand how and when to fall into line (in a crystalline composition)? Lets have a closer look at atoms while teaching homeschool science:
Suppose we've a decrease of h2o. If we consider it very carefully, well view a drop regarding water, nice and smooth. If you grab your microscope and magnify that roughly some, 000 occasions (the drop is now 40 foot across, the size of a large classroom) and appearance very tightly, well still see relatively sleek water, but there are wiggly things boating (paramecia). We could stop here and study these types of interesting little critters, however, get married to side-track ourselves into biology. Therefore lets target more on the water.
Let us magnify the water 2, 000 periods again, thus its roughly 15 mls across. Once we consider it very closely now, all of us see what seems like a teeming mob involving Super Bowl fans making their way to the nearest exit lots and lots of movement, yet its still fuzzy and hard to produce out. Today well magnify it another 250 instances (for a total magnifying of about 1 billion dollars times), and well observe two forms of blobs hydrogen atoms and oxygen atoms arranged in a little class like Mickey Mouse. Every little group of these atoms is called a molecule.
This particular picture on the right is actually idealized in a few approaches, but above all, the idea doesnt move on the site, whereas the actual molecule wiggles and jiggles as we watch it magnified one particular billion periods. Another way this specific picture is not quite proper is that the atoms are actually stuck together like glue, very similar way magnets attract each other. Yet unlike magnets, if you squeeze these kinds of atoms together too hard, these people repel.
The actual jiggling action is what we call heat. When we boost the temperature (say, water over a hot stove), the actual jiggles increase and the volume involving the atoms increase.
Imagine now we reduce the temperature of our own drop involving water, and we discover the jiggling movement decreases, and the attractive forces between your atoms gets control of and at suprisingly low temperatures, the particular atoms freeze together into a new style called glaciers. The interesting factor is that there's a spot for each and every atom throughout its reliable form (crystalline variety). Water is among the only molecules that expands whenever solidified. The crystal design of glaciers is proven (correct) they have many holes in it. This specific open structure collapses when the atoms jiggle tough enough to shake by themselves loose (reduction) and rush to complete the gaps because the temperature (and jiggling) boosts.
How big is an atom? If an tangerine is magnified to how big the earth, how big the atoms in the orange are usually approximately how big is the original orange.
Crystals are manufactured by both solidifying (take into account the ice crystals in your freezer), or maybe by expanding them (as in the homschool science activities were going to start). Lets learn more about how to grow (or maybe farm) your personal crystals.
When coming up with crystals, there exists a very special kind of solution to make. It's called a "super soaked solid solution". What does which means that? Here is an illustration: If you constantly add salt by the spoonful to a cup of water, you'll reach a spot where the salt doesn't disappear (reduce) anymore and forms any lump at the end of the glass.
The point at which it begins to make a lump is just past the point to be a over loaded solution. If you heat up the saltwater, the particular lump disappears. It's simple to add increasingly more salt, till it can't take anymore salt (you'll see another lump beginning to form at the bottom). This is now a super saturated reliable solution. Mix in a little bit of water to make the lump go away. Your solution is ready in making crystals. Yet how?
If you add something for the crystals to cling to, such as a rock or even a stick, crystals is now able to grow. If you "seed" the item (coating it with the stuff you formed the solution with, just like salt or even sugar), they will start developing faster.
SUGGESTION for Fast Crystals: If you keep the solution in a warm location, crystals may grow quicker. Use the highest place within your house, any heating pad, or even enclosed box with a lit lamp (such as an overnight ride in the oven).
When you have an excessive amount of salt (or even other sturdy) mixed in, the solution may crystallize all at the same time and you should obtain a huge rock that you can't pull out of the jar. When you have too little salt, then you'll definitely wait forever for crystals to grow. Choosing the best total mix in takes time and patience.
Geodes Any geode is really a crystallized vitamin deposit, and are usually very dull and ordinary-looking externally, before you crack all of them open! A eggshell is going to be used to simulate a gas bubble within flowing lava. Simply by dissolving alum within water (actual life uses mineral deposits dissolved in ground drinking water) and placing it into your eggshell (in real life, its a gas bubble bank account), you'll be left with a geode. (Notice: these types of crystals are not for having, merely looking.)
Generating the Geode Make sure your eggshells tend to be clean. Fill a small cup with hot water and dissolve just as much alum in the water as you can to make a saturated option (meaning that if you add anymore alum, it'll only fall to the bottom rather than dissolve). Fill up the eggshells with the solution and put aside. Observe as the solution evaporates within the next few days. When the solution offers completely evaporated, you will have a homemade geode. If no crystals formed, you then had too much water and not enough alum in your solution.
Gemstones Fill a clean a glass jar along with saturated solution made above and leave it for 2 days. Strain it and save yourself the water for afterwards. Keep the crystals!
Thread Crystals Fill another glass jar with spare saturated solution, and suspend any crystal (from experiment over) with string from the jar cover. Reduce it into the solution and wait several days. (Seeds the thread for more rapidly growth.)
Rock and roll Candy Were likely to take advantage of the process of crystallization to produce candy. You are likely to create a super soaked solution regarding sugar and put it to use to grow your own personal homemade sugars candy uric acid. An excellent saturated option would be one which has the maximum amount of sugar dissolved in the water that you can. (If we didnt heat the water, wed wind up with just a saturated solution.)
Producing Rock Candies Boil three glasses of water in a large pot on the stove. Add eight glasses of sugar, a single cup at a time, slowly stirring as you go. The actual liquid should be thick and yellowish. Switch off the warmth and let it sit for four hours (or until the temperature is actually below 120 degrees F). Put the sugars nsa water filters into clean glass jars and put in a couple drops of meals coloring (intended for colored deposits). Connect a string to a skewer, regenerating the skewer horizontally over the jar jaws.
Jello Crystals This kind of water jello crystal (within the gardening portion of your hardware store, usually called "Soil Moist") will certainly grow above 300 times its own size whenever hydrated (adding water). Fill each glass half high in water. Put in a few falls of foodstuff coloring and stir. Add a small number of crystals and let stand 20 mins. Squish them together with your hands! Combine a number of different colors (within layers) in a empty water bottle watching the shades melt into each other (try layering glowing blue, yellow, and red and watch orange and green appear out of nowhere!) Make a huge offers a wand utilizing a plastic neon tube casing (from the hardware retail outlet they come in 4 to 8' areas!) along with stoppers glued to the ends. To reuse crystals, lay on a paper towel and let dried (they might stain underneath the towel, so put in a layer regarding foil) over several days.
Salt Stalactites Produce a saturated solution from tepid to warm water and Epsom salts. (Add enough salt so that if you add a lot more, you won't dissolve additional.) Fill two empty glass jars with the salt option. Space the containers a ft . apart on a layer involving foil or on a cookie sheet. Suspend a piece of yarn or even string from jar to the other. Hold out impatiently for approximately three days. The stalactite need to form from the midst of the line!
_____________________________________________________________
Which motor proteins are of most probability to be involved in mitosis:Kinesins,dyneins or myosins?Why?
2.In order to find the exact answer of this question, design an experiment. Your experiment should have controls. To design this experiment pay attention to these points:
a.How can you show that a factor (here, the protein that you are working on) has a specific effect in an environment (here, the cell)? And that effect is not the result of other factors?
b.How can you measure the results of absence of that effect and compare it to when that effect is present, in the cell?
You will need many types of equipment to do this experiment: microscopes, fluorescent dyes, many proteins, etc.
Since the spindle complex is know to be heavily involved with mitosis, you assume that myosin (an actin-based motor) isn't the one you're looking for.
For this experiment, I would remove the activity of each motor protein from cultured cells and see how that affected mitosis...ostensibly, if you "turn off" one of the motors and mitosis stops (or doesn't even begin) you can assume that protein is involved.
You can use RNAi (this is a system that uses small pieces of RNA to destabilize mRNA for a specific gene), but there are multiple kinds of each motor, so I wouldn't suggest it.
I would use small molecule inhibitors, so:
Butanedione-monoxime (BDM) for myosin,
Taxanes inhibit microtubules, so that would take care of kinesins and dyneins.
erythro-9-[3-(2-hydroxynonyl)] (EHNA) adenine is an inhibitor of dyneins.
So you culture cells, add DAPI or Hoechst dyes (this will make the chromosomes fluoresce). Have four plates of cells. Treat one with BDM, one with EHNA, and one with a taxane.
Culture them for an hour or so, and then observe under a fluorescent microscope.
Count the number of cells in the untreated plate that are in mitosis as a percentage of all cells.
Then count the number of cells in the treated plates.
If the BDM plate has fewer percent of cells in mitosis, then you can assume that myosins are important for mitosis.
If the taxane plate has fewer in mitosis, but the dynein-specific inhibitor EHNA has a normal amount of mitotic cells, then you know that another microtubule-based motor is important - kinesins. You would need to comfirm this with RNAi, because I am not aware of any kinesin specific inhibitor.
If the taxane plate has fewer mitotic cells and EHNA plate also has fewer mitotic cells, then you know that dyneins are important in mitosis.
There are lots of labs working on this very topic...I suggest you Google search this...this is a pretty blunt experiment on my part...you might find more elegant ones using recombinant proteins and frog egg extracts, which cell cycle people love to use for these experiments.
A Touch of Understanding: Gene Tweak Opens Sensory Black Box (Wired - Wired Science)
For nearly 250 years, the intricate detail and complexity of skin's nervous-
system wiring has thwarted attempts at understanding. But if researchers
studying skin could be imagined as technicians reverse-engineering a
supercomputer's peripherals, they'd have just traced about four lines back to
the motherboard.
Intro to Fluorescence Microscopy
You can follow any responses to this entry through the RSS 2.0 feed. Both comments and pings are currently closed.


US $7,700.00

























































































Comments are closed.