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experimental principle
< "72" > < " > center" >1 < p"center" > < p-align> 2. Shake the tubes well and keep warm for 15 minutes in a 40C water bath.
3. In tubes 3 and 4 each iodized solution 2 drops, observe the experimental phenomenon, do a good job of recording.
4. Add 3.0mL 0.4M triclosan acetic acid solution to the control tube and tube 1 and 2 respectively, shake well, filter separately, each absorb 1.0 ml of filter fluid, plus 0.4M sodium carbonate solution 5.0 ml, forin reagent 1.0 ml, shake well, keep warm for 15 minutes in a 40c water bath. Observe the phenomenon of the three tubes after removal and record them.
contrast
2
3
4
1% casein Solution (ml)
1.0
1.0
1.0
pH10 buffer (ml)
1.0
distilled water (ml)
2.0
1.0
1.0
1.0
1% starch solution (ml)
1.0
1.0
1/2000 alkaline protein enzyme solution (ml)
1.0
1.0
1/2000 amylase solution (ml)
1 .0
1.0
3. In tubes 3 and 4 each iodized solution 2 drops, observe the experimental phenomenon, do a good job of recording.
4. Add 3.0mL 0.4M triclosan acetic acid solution to the control tube and tube 1 and 2 respectively, shake well, filter separately, each absorb 1.0 ml of filter fluid, plus 0.4M sodium carbonate solution 5.0 ml, forin reagent 1.0 ml, shake well, keep warm for 15 minutes in a 40c water bath. Observe the phenomenon of the three tubes after removal and record them.
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