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AAVS1 CAG rtTA3 TauP301L 2N4R-EGFP
(Plasmid #132393)

Ordering

Item Catalog # Description Quantity Price (USD)
Plasmid 132393 Standard format: Plasmid sent in bacteria as agar stab 1 $75

This material is available to academics and nonprofits only.

Backbone

  • Vector backbone
    AAVS1-T2A-Puro-Cas9-TREtight
  • Backbone manufacturer
    Addgene
  • Total vector size (bp) 8048
  • Vector type
    Mammalian Expression, Cre/Lox, CRISPR
  • Selectable markers
    Puromycin

Growth in Bacteria

  • Bacterial Resistance(s)
    Ampicillin
  • Growth Temperature
    37°C
  • Growth Strain(s)
    DH5alpha
  • Growth instructions
    Bacteria may truncate DNA, please select multiple clones and perform restriction digest after purification to confirm.
  • Copy number
    High Copy

Gene/Insert

  • Gene/Insert name
    human TauP301L 2N4R-EGFP
  • Species
    H. sapiens (human), Synthetic
  • Mutation
    Proline 301 to Leucine (P301L)
  • Entrez Gene
    MAPT (a.k.a. DDPAC, FTDP-17, MAPTL, MSTD, MTBT1, MTBT2, PPND, PPP1R103, TAU, tau-40)
  • Promoter TREtight
  • Tag / Fusion Protein
    • EGFP (C terminal on insert)

Cloning Information

  • Cloning method Restriction Enzyme
  • 5′ cloning site BbvCI (not destroyed)
  • 3′ cloning site KpnI (not destroyed)
  • 5′ sequencing primer TTCAGGTTGGACCGGTCCTCA
  • (Common Sequencing Primers)

Resource Information

How to cite this plasmid ( Back to top)

These plasmids were created by your colleagues. Please acknowledge the Principal Investigator, cite the article in which the plasmids were described, and include Addgene in the Materials and Methods of your future publications.

  • For your Materials & Methods section:

    AAVS1 CAG rtTA3 TauP301L 2N4R-EGFP was a gift from Gerold Schmitt-Ulms (Addgene plasmid # 132393 ; http://n2t.net/addgene:132393 ; RRID:Addgene_132393)
  • For your References section:

    Rapid Generation of Human Neuronal Cell Models Enabling Inducible Expression of Proteins-of-interest for Functional Studies. Wang X, Friesen E, Müller I, Lemieux M, Dukart R, Maia IB, Kalia S, and Schmitt-Ulms G. Bio-protocol. 2020; 10(9): e3615 10.21769/BioProtoc.3615