MIC220_Modern techniques for taxonomy

MIC220_Modern techniques for taxonomy

University

14 Qs

quiz-placeholder

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MIC220_Modern techniques for taxonomy

MIC220_Modern techniques for taxonomy

Assessment

Quiz

Biology

University

Medium

Created by

DR ABIDIN

Used 156+ times

FREE Resource

14 questions

Show all answers

1.

MULTIPLE CHOICE QUESTION

1 min • 1 pt

Which of the following is a correct step for hybridisation?


1- add DNA probe that labelled with detector

2 - bind DNA to a membrane

3 - probes hybridise to the target DNA region

4- wash off the excess probes

5 - develop film

1, 2, 3, 4, 5

2, 1, 3, 4, 5

2, 1, 3, 5, 4

1, 2, 4, 3, 5

2.

MULTIPLE CHOICE QUESTION

20 sec • 1 pt

Which of the following statement is NOT true about radioactive probe?

the nucleic acid is labelled with isotope

the most common is biotin-streptavidin complex

the probes can be observed by autoradiography

the probes can be observed by scintillation

3.

MULTIPLE CHOICE QUESTION

20 sec • 1 pt

Which blotting technique is to detect RNA?

Southern blot

Northern blot

Western blot

Eastern blot

4.

MULTIPLE CHOICE QUESTION

20 sec • 1 pt

Which blotting technique is to detect protein?

Southern blot

Northern Blot

Western Blot

eastern blot

5.

MULTIPLE CHOICE QUESTION

20 sec • 1 pt

Which is the primary purpose of using restriction enzymes in gel electrophoresis?

It allows the strands of DNA to be cut into various lengths for testing

It makes the testing simpler by moving the strands into the gel faster

It restricts the number of base pairs that can be tested in a sample

It charges the DNA strands

6.

MULTIPLE CHOICE QUESTION

20 sec • 1 pt

In gel electrophoresis, the largest DNA fragment will appear

closest to the starting wells

three quarters away from the starting wells

farthest from the starting wells

it depends on how many fragments there are

7.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Why do the fragments of DNA in gel electrophoresis travel away from the negative electrode?

DNA is negatively charged so attracted to the positive end of the unit

the agarose gel in negatively charged

DNA is positively charged to attracted to the negative end of the unit

the agarose gel is positively charged

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