Mitosis root tip squash Flashcards
What equipment do we need?
= hydrochloric acid- soften and loosen root tissues
= acetin orcein stain- turns chromosomes a purple-red colour
= mounted needle- to lower cover slip and prevent air bubbles under the slip
root tip; this is where mitosis should be occuring
What is the method?
= grow garlic ontop of a beaker of water for 3 days- new roots in the dark
= cut of the tip of the root 5mm from the end this is where mitosis is occurinb
What is the next step?
= place root tip in a tets tube of hcl and leave in water bath for 60 degrees
= leave for 10 mins so acid can soften the cells
= pour acid out of test tube and place root tip on a watch glass rinse with distilled water
= place root tip on microscopic slide then use filter paper to excess water
What is the next step?
=add two drops of indiacator
= use mounted needle to lower cover slip and leave for 10 mins- stains chromosomes
= place filter paper on top and push down make sure it does not slip or move the coverslip spreads the cell into a single layer so light can pass through
How do we calculate the mitotic index?
= the number of cells in mitosis/ total number of cells x 100
What is the hazard of a scalpel?
= risk of cutting yourself
= control: keep away from fingers
What is the hazard of hcl?
= causes irritation to eyes and previous injuries
= wear eye protection, tie up long hair, avoid contact with skin
What is the risk of the stain?
= causes irritation
= wear eye protection, tie up long hair, avoid skin
What is the risk of broken glass?
= risk of cutting yourself
= take care when handling
When counting the cells to calculate the mitotic index what should you do to make sure this is accurate?
= examine large field of cells/large number of cells
= ensure a represenative sample
What does the eye peice graticule do?
= used to measure the size of the object,
= each time you change the ibjective lense, and magnification, you have ti calibrate
What does a stage micrometer do?
= used to calibrate the eye peice graticule
= glass slide with a scale with it, this is usually 2mm apart and and the sub divisions are 10 micrometrees apart
How do we calibrate this?
= lie up the stage micrometer and eye peice graticule whulst lookimg through the eye peice
= count how many divsions, on the eye peice graticule fit in one divisiom, on the micrometer scale
= each divison on the micrometer is 10um so this can be used to calulate what one divison is at the current magnification