pZY102
(Plasmid
#73933)
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PurposeThis plasmid was derived from pZY101 by inserting a GUS-intron reporter gene cassette into multiple cloning sites. This plasmid is recommended for use as empty control for service event request.
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 73933 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepPZP201
- Backbone size w/o insert (bp) 7132
- Total vector size (bp) 11605
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Modifications to backbonebar gene cassette was inserted into multiple cloning site adjacent to T-DNA left border.
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Vector typePlant Expression
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Selectable markersBasta ; bar
Growth in Bacteria
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Bacterial Resistance(s)Spectinomycin, 50 μg/mL
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Growth Temperature37°C
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Growth Strain(s)DH5alpha
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Growth instructionsFor growing Agrobacterium, 28 C is needed and the same antibiotics selection are needed for selecting the vector. SmR gene confers resistance to spectinomycin and streptomycin in bacteria
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Copy numberHigh Copy
Gene/Insert 1
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Gene/Insert namebar
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Alt namePAT
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SpeciesSynthetic
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Insert Size (bp)567
- Promoter 35S
Cloning Information for Gene/Insert 1
- Cloning method Restriction Enzyme
- 5′ cloning site Xho I (not destroyed)
- 3′ cloning site Hind III (not destroyed)
- 5′ sequencing primer GAAACCTCCTCGGATTCCAT
- 3′ sequencing primer CAGCAGGTGGGTGTAGAGCGT (Common Sequencing Primers)
Gene/Insert 2
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Gene/Insert nameGUS
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Alt namebeta-glucuronidase
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SpeciesSynthetic
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Insert Size (bp)3000
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Mutationintron is inserted into the GUS coding region
- Promoter 35S
Cloning Information for Gene/Insert 2
- Cloning method Restriction Enzyme
- 5′ cloning site Hind III (not destroyed)
- 3′ cloning site Hind III (not destroyed)
- 5′ sequencing primer CGTCCTGTAGAAAACCCAACC
- 3′ sequencing primer TCATTGTTTGCCTCCCTGCTG (Common Sequencing Primers)
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
This vector is suitable for plant transformation and has been used as standard service empty vector control.
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:
pZY102 was a gift from Zhanyuan Zhang (Addgene plasmid # 73933 ; http://n2t.net/addgene:73933 ; RRID:Addgene_73933) -
For your References section:
Refined glufosinate selection in Agrobacterium-mediated transformation of soybean [Glycine max (L.) Merrill]. Zeng P, Vadnais DA, Zhang Z, Polacco JC. Plant Cell Rep. 2004 Feb;22(7):478-82. Epub 2003 Sep 30. 10.1007/s00299-003-0712-8 PubMed 15034747