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Depositing Lab
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Publication
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Sequence Information
Full plasmid sequence is not available for this item.
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 17363 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepBR322
- Backbone size w/o insert (bp) 2100
Growth in Bacteria
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Bacterial Resistance(s)Ampicillin, 100 μg/mL
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Growth Temperature37°C
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Growth Strain(s)DH5alpha
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Copy numberUnknown
Gene/Insert
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Gene/Insert nameMMLV proviral DNA
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SpeciesMoloney murine leukemia virus
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Insert Size (bp)8000
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site ClaI (unknown if destroyed)
- 3′ cloning site NdeI (unknown if destroyed)
- 5′ sequencing primer n/a (Common Sequencing Primers)
Resource Information
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Articles Citing this Plasmid
Terms and Licenses
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Academic/Nonprofit Terms
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Industry Terms
- Not Available to Industry
Trademarks:
- Zeocin® is an InvivoGen trademark.
Depositor Comments
The plasmid pA8.2 is a full-length permuted copy of
the M-MuLV genome in the vector pACYC177 (Lobel &
Goff, 1984). The full-length, non-permuted M-MuLV
clone pNCA was constructed from the 5.5 kb ClaI-
HindIII fragment of pA8.2, the 2.5 kb HindIII-NdeI
fragment of pNDE (Colicelli & Goff. 1985) and the 2.1 kb
ClaI-NdeI fragment of pBR322. It is, in effect, an 11kb
non-permuted wild-type clone reconstructed from a
permuted clone and with no flanking cellular sequences.
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.
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For your Materials & Methods section:
pNCA was a gift from Stephen Goff (Addgene plasmid # 17363 ; http://n2t.net/addgene:17363 ; RRID:Addgene_17363) -
For your References section:
Sequence and spacing requirements of a retrovirus integration site. Colicelli J, Goff SP. J Mol Biol. 1988 Jan 5. 199(1):47-59. 10.1016/0022-2836(88)90378-6 PubMed 3351923