5 Key Features of DNA Plasmids Explained
Have you heard of DNA plasmids, sometimes called DNA vectors, but you aren’t quite sure what exactly...
pCambia1391Z is a reliable vector plasmid derived from pPZP and is a robust tool for genetic manipulation in plants. Versatile and stable, pCambia1391Z adapts to a wide array of plant species, maintaining the integrity of inserted DNA throughout transformation and regeneration. Designed specifically for promoter testing in plants, this vector harbors a promoterless version of gusA for tracking and visualizing transformed cells. It is additionally coupled with a catalase intron downstream of a truncated lacZ gene, enabling blue/white screening in suitable E. coli host strains.
pCAMBIA1391Z contains the powerful, double-enhancer version of the CaMV35S promoter, ensuring robust expression. pCAMBIA1391Z also features a reporter gene with a hexa-Histidine tag at the C-terminus, offering a purification method by immobilized metal affinity chromatography resins.
pCambia1391Z boasts a multiple cloning site (MCS) flanked by border sequences, facilitating seamless insertion of foreign DNA into plant cells. The vector includes antibiotic resistance genes for kanamycin and hygromycin for quick identification of transformed cells. In conjunction with a helper plasmid, pCambia1391Z facilitates T-DNA transfer into plants, ensuring precise genetic modifications without unwanted elements and, as a binary vector, it features T-DNA borders essential for Agrobacterium-mediated transfer into plant genomes. pCambia1391Z was engineered to remove an unwanted IS4 element from the original clone, pCambia1391.
Concentration: 0.2 μg/μL in TE
Volume: 50 μL
Backbone size: 11,226 bp
Vector type: Cloning vector
Promoter: CAMV 35S / LacZ
Bacterial Resistance(s): Kanamycin
Plant Resistance(s): Hygromycin B
Copy number: High Copy
Genbank Assession Number: AF234312.1
GoldBio Vector Map and Sequence for pCambia1391Z
pCambia1391Z DNA is at 0.2 μg/μL concentration in TE buffer.
Store all plasmids at -20°C.
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