Difference between revisions of "Part:BBa K4195140"
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When constructing this circuit, regular PCR and gene sequencing were used to verify that the plasmids were correct. Target bands (418 bp) can be observed at the position between 250 bp and 500 bp (Fig. 1). | When constructing this circuit, regular PCR and gene sequencing were used to verify that the plasmids were correct. Target bands (418 bp) can be observed at the position between 250 bp and 500 bp (Fig. 1). | ||
| + | [[File:T--XMU-China-BBa K4195140.png|200px]] | ||
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| + | '''Fig. 1 DNA gel electrophoresis of the regular PCR products of BBa_K4195140_pUC57-simple.''' | ||
===Reference=== | ===Reference=== | ||
Revision as of 17:04, 10 October 2022
J23100-B0030-array(targeting pirA/B)-B0015
Biology
This part was designed as an element of typeⅠCRISPR/Cas system, in which the array contains several designed spacers to target pirA/B gene and repeats derived from Vibrio parahaemolyticus FOC_022 (1) that could be recognized and handled by Cas proteins.
Usage and design
The circuit of the basic part BBa_K4195023 was assembled into vector pUC57-simple to construct this composite part.
Characterization
1. Identification
When constructing this circuit, regular PCR and gene sequencing were used to verify that the plasmids were correct. Target bands (418 bp) can be observed at the position between 250 bp and 500 bp (Fig. 1).
Fig. 1 DNA gel electrophoresis of the regular PCR products of BBa_K4195140_pUC57-simple.
Reference
1. P. Baliga, M. Shekar, M. N. Venugopal, Investigation of direct repeats, spacers and proteins associated with clustered regularly interspaced short palindromic repeat (CRISPR) system of Vibrio parahaemolyticus. Mol. Genet. Genomics 294, 253-262 (2019).
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 7
Illegal NheI site found at 30 - 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]