Bio Technology Interview Questions

 
1.
How to calculate protein percentage in lowry method?
2.
Is GMO food good as the prospective of the ethic values of the society?
3.
Sucrose is commonly used to preserve fruits why not glucose?
4.
What are the five greatest discoveries in the field of r DNA technology?
5.
Who is the father of biotechnology?
6.
Why do you want to do Phd?
7.
Dubai is desert how it is possible it is becoming greenery?
8.
What is the future of bio informatics in India?
9.
What is the difference between defined, characterized and standard serum?
10.
What bacteria should we eat?
11.
What is difference between transfection and transduction?
12.
What is the difference between transfection and transduction?why the word trasfection is prefers for transfer of genetic material through non viral particles in eukaryote not for prokaryote?
13.
DOES EUKARYOTES HAVE RESTRICTION MODIFICATION SYSTEM? IF YES, THAN WHY ARE WE NOT USING FOR THE TREATMENT OF HIV?
14.
What is the main objective of northern blotting?
15.
Why do you use DBM instead of NCF in the northern blotting and what are the pre-treatments required for this paper to be used?
16.
What is the nature of DBM paper in northern blotting?
17.
How does the DBM paper entrap the rna probes?
18.
How to calculate protein percentage in lowry method?
19.
Is GMO food good as the prospective of the ethic values of the society?
20.
Sucrose is commonly used to preserve fruits why not glucose?
21.
What are the five greatest discoveries in the field of r DNA technology?
22.
Who is the father of biotechnology?
23.
Why do you want to do Phd?
24.
Dubai is desert how it is possible it is becoming greenery?
25.
What is the future of bio informatics in India?
26.
What is the difference between defined, characterized and standard serum?
27.
What bacteria should we eat?
28.
What is difference between transfection and transduction?
29.
What is the difference between transfection and transduction?why the word trasfection is prefers for transfer of genetic material through non viral particles in eukaryote not for prokaryote?
30.
DOES EUKARYOTES HAVE RESTRICTION MODIFICATION SYSTEM? IF YES, THAN WHY ARE WE NOT USING FOR THE TREATMENT OF HIV?
31.
What is the main objective of northern blotting?
32.
Why do you use DBM instead of NCF in the northern blotting and what are the pre-treatments required for this paper to be used?
33.
What is the nature of DBM paper in northern blotting?
34.
How does the DBM paper entrap the rna probes?