Difference between revisions of "Sequencing Analysis using Serial Cloner 2-6-1"

From Real Vegan Cheese
Jump to navigation Jump to search
 
Line 2: Line 2:


1. Using Serial Cloner Freeware (2-6-1) open the forward sequencing reaction from the TEF primer.
1. Using Serial Cloner Freeware (2-6-1) open the forward sequencing reaction from the TEF primer.
[[File:Open forward.png | 400px]]
     a. Search for ATG (and translate the protein by selection sequence from ATG onward). This provides you with a preliminary idea of  
     a. Search for ATG (and translate the protein by selection sequence from ATG onward). This provides you with a preliminary idea of  
         whether or not your sequencing worked. You should see (at the very least) the FAKS signal peptide. Also, in the forward reaction,  
         whether or not your sequencing worked. You should see (at the very least) the FAKS signal peptide. Also, in the  
        make sure you are using ATG on the + or 'sense' strand.
        forward reaction, make sure you are using ATG on the + or 'sense' strand.
[[File:Search for ATG.png | 400px]]
[[File:Search for ATG.png | 400px]]


Line 10: Line 11:
         reaction with the original file. I.e. Human Kappa Kex + hypothetical sequence :: Human Kappa Kex + clone 1A TEF reaction results.
         reaction with the original file. I.e. Human Kappa Kex + hypothetical sequence :: Human Kappa Kex + clone 1A TEF reaction results.


 
[[File:Function Align two seqs.png |400px]]




2. Open the reverse sequence, reverse complement it using Sequence>Antiparallel function.
2. Open the reverse sequence, reverse complement it using Sequence>Antiparallel function.
     a. Align this sequence to both the forward and hypothetical sequences as detailed in 1b.
     a. Save the sequence as "Name Reverse Complement"
    b. Align this sequence to both the forward and hypothetical sequences as detailed in 1b.

Latest revision as of 21:21, 16 October 2014

Sequencing Analysis

1. Using Serial Cloner Freeware (2-6-1) open the forward sequencing reaction from the TEF primer. Open forward.png

   a. Search for ATG (and translate the protein by selection sequence from ATG onward). This provides you with a preliminary idea of 
       whether or not your sequencing worked. You should see (at the very least) the FAKS signal peptide. Also, in the 
       forward reaction, make sure you are using ATG on the + or 'sense' strand.

Search for ATG.png

   b. Align the DNA to the original file using the Function>Align Two Sequences function. You will be aligning the forward sequencing 
       reaction with the original file. I.e. Human Kappa Kex + hypothetical sequence :: Human Kappa Kex + clone 1A TEF reaction results.

Function Align two seqs.png


2. Open the reverse sequence, reverse complement it using Sequence>Antiparallel function.

   a. Save the sequence as "Name Reverse Complement"
   b. Align this sequence to both the forward and hypothetical sequences as detailed in 1b.