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Create a schemetic diagram of the experimental procedures down below (Also, attached below is a copy of an example of a schematic diagram)

Create a schemetic diagram of the experimental procedures down below (Also, attached below is a copy of an example of a schematic diagram)

Cardiopulmonary Anatomy & Physiology
Cardiopulmonary Anatomy & Physiology
7th Edition
ISBN:9781337794909
Author:Des Jardins, Terry.
Publisher:Des Jardins, Terry.
Chapter6: Oxygen And Carbon Dioxide Transport
Section: Chapter Questions
Problem 7RQ: 7. If a patient normally has a 12 g/dL Hb, cyanosis will likely appear when A. 10 g/dL Hb is...
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Create a schemetic diagram of the experimental procedures down below

(Also, attached below is a copy of an example of a schematic diagram)

A. Isolation of Chloroplasts 1. Devein 10g of fresh papaya leaves and wash with distilled water. 2. Place the leaves and 50 mL cold phosphate buffered saline (PBS, 0.2 M phosphate buffer, pH 7.0 and 0.35 M NaCl solution), in an ice-cold blender. 3. Blend at high speed for 30 sec, then cool the jar in an ice bucket for 30 sec. Do this three times. 4. Strain the extract through two layers of cheesecloth into an ice-cold beaker. 5. Transfer the suspension into two cold 50-mL centrifuge tubes ensuring that they are of equal weight. 6. Centrifuge at 200 xg for 5 min. 7. Decant the supernate into two clean 50-mL centrifuge tubes and discard the pellet. 8. Centrifuge at 1400 xg for 15 min. Discard the supernatant and resuspend the pellet by adding 5_mL PBS to each tube. Collect all suspensions in a small beaker immersed in an ice bath. (Note: Compute for rpm value of the angular speeds given in g using r = 8 cm.)
Transcribed Image Text:A. Isolation of Chloroplasts 1. Devein 10g of fresh papaya leaves and wash with distilled water. 2. Place the leaves and 50 mL cold phosphate buffered saline (PBS, 0.2 M phosphate buffer, pH 7.0 and 0.35 M NaCl solution), in an ice-cold blender. 3. Blend at high speed for 30 sec, then cool the jar in an ice bucket for 30 sec. Do this three times. 4. Strain the extract through two layers of cheesecloth into an ice-cold beaker. 5. Transfer the suspension into two cold 50-mL centrifuge tubes ensuring that they are of equal weight. 6. Centrifuge at 200 xg for 5 min. 7. Decant the supernate into two clean 50-mL centrifuge tubes and discard the pellet. 8. Centrifuge at 1400 xg for 15 min. Discard the supernatant and resuspend the pellet by adding 5_mL PBS to each tube. Collect all suspensions in a small beaker immersed in an ice bath. (Note: Compute for rpm value of the angular speeds given in g using r = 8 cm.)
Group I (n=10) Aluminium chloride (AC) Prepared 40 specimens of teeth with flattened dentin surface embedded in cold cure acrylic ↓ Group II (n=10) Ferric sulphate (FS) Group III (n=10) Tannic acid (TA) The hemostatic agent applied for 5 minutes ។ Group IV (n=10) Control group Rinsed with distilled water and gently air dried for 3-5 seconds Self-adhesive resin cement placed into a 2X2 mm dimension matrix attached to the dentinal surface Polymerized with visible light curing unit for 30 seconds Shear bond strength tested using an Instron universal testing machine
Transcribed Image Text:Group I (n=10) Aluminium chloride (AC) Prepared 40 specimens of teeth with flattened dentin surface embedded in cold cure acrylic ↓ Group II (n=10) Ferric sulphate (FS) Group III (n=10) Tannic acid (TA) The hemostatic agent applied for 5 minutes ។ Group IV (n=10) Control group Rinsed with distilled water and gently air dried for 3-5 seconds Self-adhesive resin cement placed into a 2X2 mm dimension matrix attached to the dentinal surface Polymerized with visible light curing unit for 30 seconds Shear bond strength tested using an Instron universal testing machine
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