Hey Rye High School and Dr. Cook,

Well, I finally got access to the server and can post your data. I went ahead and PCRed your samples and ran them on again on a gel. I tried a different digital camera that seemed to work better. Below I included the gels you ran and the newer gels.Because of that I have several images here so it may take sometime to download. The lanes are from right to left and what I can figure out from the images. Hope you had fun and sorry about being so late for the posting of your data. Feel free to stop by if you are around USC.

Dan Caprioglio
Associate Professor of Biology
University of Southern Colorado
Pueblo CO 81001
719-549-2027
719-549-2732 FAX
dan.caprioglio@colostate-pueblo.edu

Gel 1

 

 Lane Sample  Genotype
 1 4 -/-
2 9 -/-
3 8 No amplification
 4 6 -/-
5 2 -/-
6 3 -/-
7 10 No amplification
8 Standard  
 

 
Gel 2
 
 Lane  Sample  Genotype
 1 1 -/-
2 7 No amplification
 3 16 No amplification
4 27 No amplification
5 17 No amplification
6 26 No amplification
7 28 No amplification
8 24 No amplification
9 12 -/-
10 23 No amplification
11 22 -/-
12 5 No amplification
13 20 No amplification
14 11 No amplification
 15 21 No amplification
16 30 -/-
17 15 No amplification
 18 no sample  
19 no sample  
20 standard  
21  18 -/-
22 29 No amplification
23 13 No amplification
24 25  -/-
 
 

Gel 3- Re run PCR and gel
 
 Lane Sample  Genotype
 1 1 -/-
2 5 -/-
3 7 -/-
 4 10 -/-
5 11 +/-
6 12 -/-
7 13 -/-
8 Standard  
 
 
 

Gel 4- Re run PCR and gel
 Lane Sample  Genotype
 1 15 -/-
2 16 -/-
3 17 -/-
 4 18 -/-
5 19 +/-
6 20 -/-
7 21 -/-
8 Standard  
 
 

Gel 5- Re run PCR and gel
 
 Lane Sample  Genotype
 1 Standard  
2 22 -/-
3 23 -/-
4 24 -/-
5 25 -/-
6 26 no amplification
 
 
 

Gel 6- Re run PCR and gel
 
 Lane Sample  Genotype
 1 Standard  
2 27 -/-
3 28 -/-
4 29 -/-
5 30 no amplification