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fodog414 fodog414
wrote...
Posts: 279
11 years ago
Thalassemia is a recessive blood disease caused by reduced synthesis of one of the globin genes. While SCD is a mutation in the structure of hemoglobin, thalassemias can also be caused by mutations in the regulatory elements, causing too little globin to be produced and resulting in anemia. You've designed a DNA probe that you want to use to screen a family for a rare mutation in the β-globin gene that causes thalassemia. First you will use the probe for northern blotting. What information will the northern blot tell you?

   
whether the mRNA for β-globin is being translated into functional proteins in a given cell population
   
the size of the mRNA being transcribed
   
whether the amount of the β-globin gene transcript is within normal range, and the size of the mRNA gene product
   
whether the amount of the β-globin gene being transcribed (mRNA levels) is within normal range
   
the presence of a particular mutation by restriction fragment analysis
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2 Replies
Replies
wrote...
11 years ago
something that will help is using the "snow drop"  Typically you wont really get any questions that will require much more info on this topic.

S dNA
N rNA
O
W pROTEINS
Answer accepted by topic starter
fodog414 Authorfodog414
wrote...
Posts: 279
11 years ago
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