NIAID-sponsored Pathogen Functional Genomic Resource Center, J. Craig Venter Institute
 

1. PFGRC Gateway® Cloning Survey - July 2008

 
We greatly appreciate feedback from investigators who are using (or plan to use) our Invitrogen Gateway® entry clones and ask that you take a few moments to fill out the survey below. Such valuable feedback will enable us to improve our existing service and extend new services to the pathogen research community. This survey is completely anonymous and requires nothing from you but a little time. If you would like to offer suggestions or feedback beyond this survey please e-mail PFGRC@jcvi.org

If you have not recently visited our website and clone ordering page, you can do so at this address: http://pfgrc.jcvi.org/index.php/gateway_clones

Thank you.
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1. How did you hear about our Gateway® entry clone resource?

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2. What type(s) of entry clones have you ordered from the PFGRC in the past?

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3. What criteria motivated your clone selection?

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4. Did you find the current search feature useful when ordering?

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5. Would you use the following features of an enhanced Gateway® clone ordering website?

 Definitely would notProbably would notDo not knowProbably wouldDefinitely would
Look up a clone by locus name
Upload a file of locus names
Search common name text
Search by nucleotide sequence
Search by GI number
Search by EC number
Search by GO term
Search by gene symbol
Cross-homology search (BLAST)
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6. How would you rate us on the following criteria:

 poorfairgoodexcellentN/A
Website ease of use
Quality of information on website
Communication from production lab
Communication from legal dept.
Turnaround time (6-8 week standard)
Professionalism
Quality of clones
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7. What features are important for downstream applications?

 YesNoNo preference
Absent stop codon for COOH-terminal protein fusions
Native stop codons
Altered stop codons
Standardized start codon (ATG)
Ability to order sub-gene fragments
Ability to order knock-down (antisense expression) clones
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8. Would you order clones if available in protein expression vectors (as opposed to entry vector)?

9. What type of expression vectors would be of greatest interest?

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10. Would you be interested in knock-out/knock-in clones if they were made available?

   


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