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PurposeHigh copy number plasmid 2 to prepare Penn State DNA molecular weight ladders
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 89566 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepUC9
- Backbone size w/o insert (bp) 2635
- Total vector size (bp) 7750
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Vector typeBacterial Expression
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 numberHigh Copy
Gene/Insert 1
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Gene/Insert name750 bp EcoRV fragment
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Alt namelambda DNA position 650-1399
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Speciesphage lambda
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Insert Size (bp)750
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GenBank IDNC_001416.1
Cloning Information for Gene/Insert 1
- Cloning method Restriction Enzyme
- 5′ cloning site HindIII (not destroyed)
- 3′ cloning site EcoRI (not destroyed)
- 5′ sequencing primer N/A
- 3′ sequencing primer N/A (Common Sequencing Primers)
Gene/Insert 2
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Gene/Insert name3000 bp EcoRV fragment
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Alt namelambda DNA position 25345-26210
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Speciesphage lambda
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Insert Size (bp)3000
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GenBank IDNC_001416.1
Gene/Insert 3
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Gene/Insert name4000 bp EcoRV fragment
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Alt namelambda DNA position 22948-24306
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Speciesphage lambda
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Insert Size (bp)4000
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GenBank IDNC_001416.1
Gene/Insert 4
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Gene/Insert name50 bp PstI fragment
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Alt namelambda DNA position 26172-26210
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Speciesphage lambda
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Insert Size (bp)50
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GenBank IDNC_001416.1
Gene/Insert 5
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Gene/Insert name100 bp PstI fragment
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Alt namelambda DNA position 2554-2656
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Speciesphage lambda
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Insert Size (bp)100
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GenBank IDNC_001416.1
Cloning Information for Gene/Insert 5
- Cloning method Restriction Enzyme
- 5′ cloning site NgoMIV (not destroyed)
- 3′ cloning site None (not destroyed)
- 5′ sequencing primer N/A
- 3′ sequencing primer N/A (Common Sequencing Primers)
Gene/Insert 6
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Gene/Insert name200 bp PstI fragment
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Alt namelambda DNA 37262-37455
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Speciesphage lambda
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Insert Size (bp)200
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GenBank IDNC_001416.1
Gene/Insert 7
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Gene/Insert name300 bp PstI fragment
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Alt namelambda DNA postion 3856-4149
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Speciesphage lambda
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Insert Size (bp)300
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GenBank IDNC_001416.1
Cloning Information for Gene/Insert 7
- Cloning method Restriction Enzyme
- 5′ cloning site None (not destroyed)
- 3′ cloning site BsrGi (not destroyed)
- 5′ sequencing primer N/A
- 3′ sequencing primer N/A (Common Sequencing Primers)
Gene/Insert 8
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Gene/Insert name400 bp PstI fragment
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Alt namelambda DNA position 19833-20232
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Speciesphage lambda
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Insert Size (bp)400
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GenBank IDNC_001416.1
Cloning Information for Gene/Insert 8
- Cloning method Restriction Enzyme
- 5′ cloning site BglII (not destroyed)
- 3′ cloning site None (not destroyed)
- 5′ sequencing primer N/A
- 3′ sequencing primer N/A (Common Sequencing Primers)
Gene/Insert 9
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Gene/Insert name500 bp PstI fragment
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Alt namelambda DNA position 11835-12334
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Speciesphage lambda
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Insert Size (bp)500
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GenBank IDNC_001416.1
Cloning Information for Gene/Insert 9
- Cloning method Unknown
- 5′ sequencing primer N/A
- 3′ sequencing primer N/A (Common Sequencing Primers)
Gene/Insert 10
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Gene/Insert name600 bp PstI fragment
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Alt namelambda DNA position 2858-3447
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Speciesphage lambda
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Insert Size (bp)600
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GenBank IDNC_001416.1
Cloning Information for Gene/Insert 10
- Cloning method Restriction Enzyme
- 5′ cloning site None (not destroyed)
- 3′ cloning site BsrGi (not destroyed)
- 5′ sequencing primer N/A
- 3′ sequencing primer N/A (Common Sequencing Primers)
Gene/Insert 11
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Gene/Insert name1500 bp Psti fragment
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Alt namelambda DNA position 25340-26170 and 743-1399
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Speciesphage lambda
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Insert Size (bp)1500
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GenBank IDNC_001416.1
Gene/Insert 12
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Gene/Insert name4100 bp PstI fragment
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Alt namelambda DNA position 22948-24306
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Speciesphage lambda
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Insert Size (bp)4100
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GenBank IDNC_001416.1
Resource Information
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Supplemental Documents
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Article 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.
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:
pPSU2 was a gift from Song Tan (Addgene plasmid # 89566 ; http://n2t.net/addgene:89566 ; RRID:Addgene_89566) -
For your References section:
The pPSU Plasmids for Generating DNA Molecular Weight Markers. Henrici RC, Pecen TJ, Johnston JL, Tan S. Sci Rep. 2017 May 26;7(1):2438. doi: 10.1038/s41598-017-02693-1. 10.1038/s41598-017-02693-1 [pii] PubMed 28550309