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Can you please help me to make this table profesional, I need two table the other which will be table 2 with trend line equation and R2 value please and thank you

Can you please help me to make this table profesional, I need two table the other which will be table 2 with trend line equation and R2 value please and thank you

Biochemistry
Biochemistry
9th Edition
ISBN:9781319114671
Author:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.
Publisher:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.
Chapter1: Biochemistry: An Evolving Science
Section: Chapter Questions
Problem 1P
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Can you please help me to make this table profesional, I need two table the other which will be table 2 with trend line equation and R2 value please and thank you
(mm) 4 Din solution. F. Analyzing the Gel 1. Pour destain into waste container. Add approximately 200mL of water to gel box. Gel may curl up for a few minutes but will eventually become flat again. 2. Place plastic wrap on the surface of the light box. Carefully transfer your gel to the plastic wrap. Take a photograph of your gel for your records and lab report. Completely cover your gel with a layer of plastic wrap. 3. Measure the distance travelled by the dye front. DYE FRONT = 54 mm 4. Measure in mm (not cm) the distance travelled (or "migration distance") for each protein in your ladder. Measure from the bottom of the well to each band. 5. Use the Excel Tutorial Video on graphing and solving for the KD sizes of the unknowns. Protein Ladder (for trendline graph): Migration Rf= Distance Band Migration Dye Front Migration 0-074 17 22. Gently rock gel for one or two hours. 1010 Pemove excess stain. 28 31 Fi 0-111 0-166 0.203 0.314 0-407 esis 2.stup 0.759, Molecular Weight (in kD) 260 250. 75 站 20 15 Results Disclusion Analys Conclussion or Reface. 10 kDa --260 --140- --100- -70- -50. -40. -35- -25- -15- --10 Log of Molecular Weight 2.415 217 2 1.87 +7 1.57 1.4 1.3 1.17
Transcribed Image Text:(mm) 4 Din solution. F. Analyzing the Gel 1. Pour destain into waste container. Add approximately 200mL of water to gel box. Gel may curl up for a few minutes but will eventually become flat again. 2. Place plastic wrap on the surface of the light box. Carefully transfer your gel to the plastic wrap. Take a photograph of your gel for your records and lab report. Completely cover your gel with a layer of plastic wrap. 3. Measure the distance travelled by the dye front. DYE FRONT = 54 mm 4. Measure in mm (not cm) the distance travelled (or "migration distance") for each protein in your ladder. Measure from the bottom of the well to each band. 5. Use the Excel Tutorial Video on graphing and solving for the KD sizes of the unknowns. Protein Ladder (for trendline graph): Migration Rf= Distance Band Migration Dye Front Migration 0-074 17 22. Gently rock gel for one or two hours. 1010 Pemove excess stain. 28 31 Fi 0-111 0-166 0.203 0.314 0-407 esis 2.stup 0.759, Molecular Weight (in kD) 260 250. 75 站 20 15 Results Disclusion Analys Conclussion or Reface. 10 kDa --260 --140- --100- -70- -50. -40. -35- -25- -15- --10 Log of Molecular Weight 2.415 217 2 1.87 +7 1.57 1.4 1.3 1.17
2 Table 2 INCLUDE YOUR TRENDLINE, EQUATION, and R2 VALUE Label Y-axis Body* 72 W #3 E Graph here Label x-axis A $ 4 R B % 5 I MacBoc T U 6
Transcribed Image Text:2 Table 2 INCLUDE YOUR TRENDLINE, EQUATION, and R2 VALUE Label Y-axis Body* 72 W #3 E Graph here Label x-axis A $ 4 R B % 5 I MacBoc T U 6
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