1.Which of the sample dyes are negatively charged at neutral pH? 2.Which of the sample dyes are positively charged at neutral pH? 3.1: Did Orange G, Xylene Cyanol and Safranin O move the same distance in the gel? 3.2 : Why or why not? What compounds do you suspect are in the unknown sample? Explain.
1.Which of the sample dyes are negatively charged at neutral pH? 2.Which of the sample dyes are positively charged at neutral pH? 3.1: Did Orange G, Xylene Cyanol and Safranin O move the same distance in the gel? 3.2 : Why or why not? What compounds do you suspect are in the unknown sample? Explain.
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1.Which of the sample dyes are negatively charged at neutral pH?
2.Which of the sample dyes are positively charged at neutral pH?
3.1: Did Orange G, Xylene Cyanol and Safranin O move the same distance in the gel?
3.2 : Why or why not? What compounds do you suspect are in the unknown sample? Explain.
![**Gel Electrophoresis of Dyes: Per. 1 Sample Results**
Gel electrophoresis is a laboratory method used to separate mixtures of DNA, RNA, or proteins according to molecular size. This method involves the use of a gel matrix and an electric field to separate molecules based on their size and charge. When dyed samples are applied to the gel, they migrate at different rates, allowing for their identification and analysis.
In the provided image, the results of a gel electrophoresis experiment of various dyes are shown. Here are the details of the image:
1. **Orientation and Setup:**
- Gel electrophoresis apparatus is displayed with the negative pole (-) at the bottom left and the positive pole (+) at the bottom right.
2. **Dye Samples:**
- Labeled from top to bottom on the left side of the gel:
- Unknown
- Xylene Cyanol
- Janus Green (replacement)
- Bromophenol Blue
- Labeled from top to bottom on the right side of the gel:
- Unknown
- Safranin O
- Orange G
3. **Results:**
- **Xylene Cyanol:** Visible as a light blue spot near the starting point, indicating it did not travel far and is likely a larger molecule or less negatively charged.
- **Janus Green (replacement):** Visible as a bright red spot, which has moved a moderate distance, suggesting an intermediate size and charge.
- **Bromophenol Blue:** Visible as a dark blue spot, which has traveled farther than Xylene Cyanol, indicating it is smaller or more negatively charged.
- **Unknown (left column):** Appears to have multiple colors, possibly consisting of different components.
- **Safranin O:** Marked by a light reddish spot, which indicates it has traveled a moderate distance.
- **Orange G:** Displayed as an orange spot, having traveled a small distance, indicative of its size and charge characteristics.
- **Unknown (right column):** Consists of multiple colors and patterns, demonstrated similarly to the unknown in the left column.
Each dye moved at different rates based on its size and charge, allowing for comparative analysis. This experiment demonstrates how gel electrophoresis can be utilized to analyze and differentiate various chemical compounds based on their electrophoretic mobility.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F20300a2d-84d5-43d2-b063-defa2dc1c334%2Fff47e43c-6282-4c1e-851f-a3dab1a12f01%2F09mq8m9e_processed.png&w=3840&q=75)
Transcribed Image Text:**Gel Electrophoresis of Dyes: Per. 1 Sample Results**
Gel electrophoresis is a laboratory method used to separate mixtures of DNA, RNA, or proteins according to molecular size. This method involves the use of a gel matrix and an electric field to separate molecules based on their size and charge. When dyed samples are applied to the gel, they migrate at different rates, allowing for their identification and analysis.
In the provided image, the results of a gel electrophoresis experiment of various dyes are shown. Here are the details of the image:
1. **Orientation and Setup:**
- Gel electrophoresis apparatus is displayed with the negative pole (-) at the bottom left and the positive pole (+) at the bottom right.
2. **Dye Samples:**
- Labeled from top to bottom on the left side of the gel:
- Unknown
- Xylene Cyanol
- Janus Green (replacement)
- Bromophenol Blue
- Labeled from top to bottom on the right side of the gel:
- Unknown
- Safranin O
- Orange G
3. **Results:**
- **Xylene Cyanol:** Visible as a light blue spot near the starting point, indicating it did not travel far and is likely a larger molecule or less negatively charged.
- **Janus Green (replacement):** Visible as a bright red spot, which has moved a moderate distance, suggesting an intermediate size and charge.
- **Bromophenol Blue:** Visible as a dark blue spot, which has traveled farther than Xylene Cyanol, indicating it is smaller or more negatively charged.
- **Unknown (left column):** Appears to have multiple colors, possibly consisting of different components.
- **Safranin O:** Marked by a light reddish spot, which indicates it has traveled a moderate distance.
- **Orange G:** Displayed as an orange spot, having traveled a small distance, indicative of its size and charge characteristics.
- **Unknown (right column):** Consists of multiple colors and patterns, demonstrated similarly to the unknown in the left column.
Each dye moved at different rates based on its size and charge, allowing for comparative analysis. This experiment demonstrates how gel electrophoresis can be utilized to analyze and differentiate various chemical compounds based on their electrophoretic mobility.
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