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Addgene

AAV-CAGGS-mNAGA
(Plasmid #196448)

Ordering

This material is available to academics and nonprofits only.
Item Catalog # Description Quantity Price (USD)
Plasmid 196448 Standard format: Plasmid sent in bacteria as agar stab 1 $85

Backbone

  • Vector backbone
    AAV-CAGGS-EGFP
  • Backbone manufacturer
    Rudolf Jaenisch Lab
  • Backbone size w/o insert (bp) 9102
  • Total vector size (bp) 10380
  • Modifications to backbone
    Replaced the EGFP cDNA of AAV-CAGGS-EGFP (Addgene #22212) with mNAGA cDNA.
  • Vector type
    Mammalian Expression
  • Selectable markers
    Puromycin

Growth in Bacteria

  • Bacterial Resistance(s)
    Ampicillin, 100 μg/mL
  • Growth Temperature
    37°C
  • Growth Strain(s)
    DH5alpha
  • Copy number
    Unknown

Gene/Insert

  • Gene/Insert name
    modified alpha-N-acetylgalactosaminidase
  • Alt name
    modified NAGA
  • Alt name
    Mod NAGA
  • Alt name
    mNAGA
  • Species
    H. sapiens (human)
  • Insert Size (bp)
    1278
  • Entrez Gene
    NAGA (a.k.a. D22S674, GALB)
  • Promoter CAG

Cloning Information

  • Cloning method Restriction Enzyme
  • 5′ cloning site SalI (not destroyed)
  • 3′ cloning site MluI (not destroyed)
  • 5′ sequencing primer 5'-TTCGGCTTCTGGCGTGTGAC-3'
  • 3′ sequencing primer 5'-CAGGAAACAGCTATGACCATG-3'
  • (Common Sequencing Primers)

Terms and Licenses

  • Academic/Nonprofit Terms
  • Industry Terms
    • Not Available to Industry
Trademarks:
  • Zeocin® is an InvivoGen trademark.

Depositor Comments

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:

    AAV-CAGGS-mNAGA was a gift from Yuichiro Miyaoka (Addgene plasmid # 196448 ; http://n2t.net/addgene:196448 ; RRID:Addgene_196448)
  • For your References section:

    In Vivo Delivery of Therapeutic Molecules by Transplantation of Genome-Edited Induced Pluripotent Stem Cells. Nakajima I, Tsukimura T, Ono T, Shiga T, Shitara H, Togawa T, Sakuraba H, Miyaoka Y. Cell Transplant. 2023 Jan-Dec;32:9636897231173734. doi: 10.1177/09636897231173734. 10.1177/09636897231173734 PubMed 37183961