REQUEST FOR DNA SEQUENCING
MBCL, Room 6004, Eppley Institute, Ph. 559-6075/Fax 559-4651/Campus Zip 6805

Principal Investigator: __________________                                 Date:__________
             Department:__________________                    Sample Name:_____________(7 character limit)
               Account #:
______________             Purification Method:_____________
Contact Person/ph #:__________________                      Concentration:__________ng/ul (via fluorometry)

COMPLETE SECTIONS I, II, & III BELOW.   USE ONE SHEET PER PRIMER/TEMPLATE PAIR
Submit All Samples in Water/Buffer WITHOUT EDTA

I
SAMPLE TYPE: CHECK ONE OF THE FOLLOWING BOXES
Double Stranded Vector Name_____________Vector Size_____bp Insert Size_____bp Total Construct_____bp 
Single Stranded Vector Name____________________  
Is sample G-C rich? Yes___ No___  DMSO for sample?____ Sample returned?_______  (Sample held for 30 days) 

ATTACH A GEL PICTURE OF PURIFIED PCR SAMPLE HERE.
Indicate volume loaded
Include size marker/# ug loaded
PCR rxn annealing temp________(REQUIRED)   
Length of insert or PCR product_______bp
Is sample G-C rich? _____
DMSO for sample?____
Sample returned?______

II
PRIMER TYPE: CHECK ONE OF THE FOLLOWING BOXES
STANDARD PRIMERS (PROVIDED): CIRCLE ONE SELECTION
(use additional sheets as needed)
M13-21 Forward           T3                    puc M13 For            KS                           T7 terminator 
M13 Reverse
                
T7                puc M13 Rev           SK                            T7 eev promotor
M13-40 Forward
           PGEX5'          
GL primer 1               Polyhedrin For         BGHrev
SP6
                               PGEX3'          RV primer 3              Polyhedrin Rev

CUSTOM PRIMERS: PROVIDE AT 1uM                                    NEW PRIMER (in synthesis)
Primer Name:____________(limit of 5 character)                         Primer Name________________
Tm of primer_____________                                                      Core Number______________
( Provide a MINIMUM of 10 ul per reaction)                                  Ext. Coefficient______
_____

III
ANALYSIS/FEES (make selection):
______ General analysis includes: raw data-must be edited by user via computer $20 per sample
______ Custom analysis includes: Editing, Color Electropherogram, Sequence Printouts $30 per sample $35 for non-university customers            
______ Sequence Alignments:$5.00 /2 primers (More than 2 primers, inquire for pricing)
______ Placement into Folder for GCG work, FREE!! Login:____________________
A $7.00 setup fee is charged to cover the cost of chemicals for samples that do not provide data.
A $10.00 setup fee is charged for a sample that is setup twice without results.

DO NOT WRITE BELOW THIS LINE. FOR CORE USE ONLY
Core #___________           Alignment Charge:$________                 
Gel #:_________                              Charge:$________                   Total Charges: $_______                 
Gel #:_________                              Charge:$________         Month/Year Charged:___________
         


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