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  •  Purchase BACE2 plasmid (http://dnasu.org/DNASU/GetCloneDetail.do?cloneid=76140)
  •  Design primers for BACE2 and EYFP
  •  Run PCR on BACE2 and EYFP
  •  Perform golden gate on PCR products and GGDonr
  •  Perform LR reaction with products from previous step, TRE-t, and backbone
  •  Transfect with expression vector from previous step and rtta vector
  •  Digest portion with Bal1, run gel and compare to virtual gel
  •  

    Observe for fluorescence in presence of Dox (more work needed on details of actual experiment) 

     

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Possible ResultsPossible ExplanationControlsProtocolsPartsDone?

YFP visible on surface

success
  • TET-r/BACE2 with Dox
  • TET-r/BACE2 without Dox
  • Hef1a/BACE2
  • No BACE2
PCRPrimers (AL1-4), BACE2 plasmid, eYFP plasmid 
YFP visible in the cellYFP not bound to BACE, YFP disrupts BACE signal sequenceGoldenGate (digest and run on gel to confirm proper assembly)PCR products, GGDonr 
YFP visible out of cellYFP bound to incorrect terminal of BACELR (Gateway) (digest and run on gel to confirm proper assembly)GG product, TRE-t, backbone 
No YFP visibleno Dox, cloning mistakeTransfectLR product, rTTA vector  
no mkate visibletransfection errorAssay Bace2 activity  
  Image  

 

Options for Directly Assaying BACE2 Expression

 

LinkCostComments
https://www.anaspec.com/products/product.asp?id=57836$435This is a kit to directly measure BACE2 expression. Call tech support.
http://www.researchgate.net/post/Which_are_the_dye_suitable_for_visualization_of_neuron_with_beta-amyloid_protein_and_plaque10  
atomic force microscopy, Pittsburgh compound B  

Data

6/17:

Nanodrop from YFP PCR products with original primers : 

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299 ng/uL