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scoundrel [369]
3 years ago
9

How does the process of gel electrophoresis produce DNA fingerprints? An electric current sorts DNA nucleotides according to the

ir bases. O An electric current cuts a DNA strand into segments of various lengths O An electric current causes segments of DNA to move at different rates O An electric current supplies a charge to uncharged segments of DNA ​
Biology
1 answer:
solong [7]3 years ago
6 0

Answer:

Gel electrophoresis

Explanation:

Gel electrophoresis is a technique used to separate DNA fragments according to their size. DNA samples are loaded into wells (indentations) at one end of a gel, and an electric current is applied to pull them through the gel. DNA fragments are negatively charged, so they move towards the positive electrode.

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Which of the following distinguishes the outer limits of a standard growing season?
Elis [28]

Answer:

frost dates

Explanation:

edge 2021

4 0
3 years ago
CAN ANYONE HELP THANK YOU VERY MUCH. Btw another Question is : How are low pressure and high pressure systems different?
Mashutka [201]

"A low pressure system has lower pressure at its center than the areas around it. Winds blow towards the low pressure, and the air rises in the atmosphere where they meet. As the air rises, the water vapor within it condenses forming clouds and often precipitation too. ... Wind blows away from high pressure."

4 0
3 years ago
is a protein found in blood that is represented by a + or – sign, which affects the compatibility of blood with other blood type
Tema [17]

Answer:

Yes, the protein is found on the surface of the red blood cell which is represented by a positive or negative sign.

It is termed as Rh factor.

Rh factor refers to the class of antigen or protein found on the red blood cell.

If the protein is present, then the person is said to be Rh positive and when the protein is absent the person is said to be Rh negative.

4 0
3 years ago
Read 2 more answers
in the box below, please illustrate any enzymes and substrate. label the following key words in your illustration: enzymes, subs
iogann1982 [59]

Explanation:

  • Enzymes are biological catalysts that speed up biochemical reactions.
  • A substrate is the molecule that the enzyme acts upon and converts to product.
  • An active site is the part of the enzyme where the substrate binds to it. Active sites contain a specific amino acid sequence and conformation which make it easy for the substrate to bind.
  • Enzymes are stringently substrate specific i.e. only a certain substrate can fit in and bind to the active site of a specific enzyme, just like only one key can fit into a specific lock.

3 0
3 years ago
You spread 0.1 mL volume of a 10^(-5) dilution onto a nutrient agar plate. After 24 hours of incubation at 37°C, there were 223
Sidana [21]

Answer:

The correct answers are 2.23 * 10^8 CFU/ml and 2 colonies.

Explanation:

Based on the given information, 0.1 ml is the amount of bacterial culture plated, 10^-5 is the dilution factor and the number of bacterial colonies produced is 223.  

A) 223 is the number of colonies produced when 0.1 ml of the culture is plated. Therefore, the number of colonies produced when 1 milliliter of bacterial culture plated us (223/0.1)*1 = 2230

The calculation of the CFU/ml is done by using the formula,  

CFU/ml = Number of colonies per ml plated / dilution factor

Thus, 2230/10^-5

= 2230 * 10^5 or 2.23 * 10^8 CFU/ml

B) The number of colonies, which would grow on a plate, which is inoculated with 0.1 ml volume of 10^-7 dilution from the similar bacterial stock will be calculated as,  

CFU/ml = Number of colonies per ml plated/ dilution * volume plated.  

2.23 * 10^8 CFU/ml = Number of colonies per ml plated / 10^-7 * 0.1

Number of colonies per ml plated = 2.23 * 10^8 * 0.1 / 10^7 = 2.23 or 2 colonies.  

8 0
3 years ago
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