TLS Online TPP Program

#Question id: 8933


At which developmental stage should one be able to first distinguish a diploblastic embryo from a triploblastic embryo?

#SCPH06 I Botany
  1. fertilization
  2. cleavage
  3. gastrulation
  4. coelom formation
More Questions
TLS Online TPP Program

#Question id: 1036

#SCPH06 I Botany

A urine sample with more than 100,000 organisms is considered indicative of infection. A urine sample containing 5,000 bacteria, with a generation time of 30 minutes, sits for 3 hours before finally being assayed. How many bacteria will then be present within the sample?

TLS Online TPP Program

#Question id: 3474

#SCPH28 | Zoology

 Polygynous mate choice is not correlated with

TLS Online TPP Program

#Question id: 15222

#SCPH01 Biochemistry

Which conventional technique can resolve hundred to thousand of protein in single gel electrophoresis

TLS Online TPP Program

#Question id: 3058

#SCPH05 I Biotechnology

A urine sample with more than 100,000 organisms is considered indicative of infection. A urine sample containing 5,000 bacteria, with a generation time of 30 minutes, sits for 3 hours before finally being assayed. How many bacteria will then be present within the sample

TLS Online TPP Program

#Question id: 16136

#SCPH01 Biochemistry

You obtain 6 BACs (of known order, as shown below) and 7 STSs (of unknown order) that derive from a region of mouse chromosome 16 whose genomic sequence has not yet been finished.   
 
By PCR (using 20-bp primers at either end of each STS), you test each of the 6 BACs for the presence (+) or absence (-) of each of the 7 STSs. You obtain the following results:
 
Is there a second STS at which you would like to sequence PCR products obtained using BACs as templates? If so, which BACs would you test in this way, and what sequencing results might you predict for each of the BACs tested?