miniA
BBa_K877000 Version 1 (Component)
Mini CipA coding region

BBa_K1733103
BBa_K1733103 Version 1 (Component)
Crisper/spCas9- with NLS

BBa_K1733099
BBa_K1733099 Version 1 (Component)
Crisper/spCas9- with NLS

BBa_K360041
BBa_K360041 Version 1 (Component)
Minimum Blue Light Receptor Promoter

BBa_K1559010
BBa_K1559010 Version 1 (Component)
RFP-Targeting protospacer for CRISPR/Cas9 system

BBa_K578001
BBa_K578001 Version 1 (Component)
E. coli CRISPR I leader sequence

BBa_K786032
BBa_K786032 Version 1 (Component)
cas3 protein in E.coli's CRISPR system

BBa_K512002
BBa_K512002 Version 1 (Component)
K12 CRISPR with GFP target spacer

BBa_J11031
BBa_J11031 Version 1 (Component)
Bacterial Whiteboard by Hannah (w/ Minimal Available Parts)

BBa_K1773000
BBa_K1773000 Version 1 (Component)
I-F type CRISPR-Cas Cascade complex

BBa_K1559006
BBa_K1559006 Version 1 (Component)
CRISPR/Cas9 system with pBAD inducible promoter

BBa_K1559007
BBa_K1559007 Version 1 (Component)
CRISPR/Cas9 system with pLac inducible promoter

BBa_K1559008
BBa_K1559008 Version 1 (Component)
CRISPR/Cas9 system with pRha inducible promoter

BBa_J100090
BBa_J100090 Version 1 (Component)
CRISPR sequence with GFP and AmpR targets

BBa_K578004
BBa_K578004 Version 1 (Component)
Bacillus halodurans C-125 CRISPR leader sequence

BBa_K1773002
BBa_K1773002 Version 1 (Component)
I-F type CRISPR-Cas Cas3 protein

BBa_J100085
BBa_J100085 Version 1 (Component)
short CRISPR sequence with GFP target spacer

BBa_K1773001
BBa_K1773001 Version 1 (Component)
I-F type CRISPR-Cas Cascade complex

BBa_K2060000
BBa_K2060000 Version 1 (Component)
CRISPR-Cas9 guide RNA targeting to 16S RNA

BBa_K1160000
BBa_K1160000 Version 1 (Component)
coding sequence of Cas9 from CRISPR system type II

BBa_K1559005
BBa_K1559005 Version 1 (Component)
CRISPR/Cas9 system with Anderson low-expression constitutive promoter

BBa_K1559003
BBa_K1559003 Version 1 (Component)
CRISPR/Cas9 system with Anderson high-expression constitutive promoter

BBa_K1559004
BBa_K1559004 Version 1 (Component)
CRISPR/Cas9 system with Anderson medium-expression constitutive promoter

BBa_K1774000
BBa_K1774000 Version 1 (Component)
CRISPR-Cas9 contaiment device repressed by arabinose and tryptophan

BBa_K2082251
BBa_K2082251 Version 1 (Component)
Sequence for rpoZ Knock-Out in E. coli through CRISPR/Cas9

BBa_K2087000
BBa_K2087000 Version 1 (Component)
CRISPR/Cas9 sgRNA Targeting Locus 618 on the DD96 Human Gene

BBa_K2087002
BBa_K2087002 Version 1 (Component)
CRISPR/Cas9 sgRNA Targeting Locus 401 on the DD96 Human Gene

BBa_K2116000
BBa_K2116000 Version 1 (Component)
RBS designed to achieve maximal expression of EsaR

BBa_K582000
BBa_K582000 Version 1 (Component)
500bp of Spacer/Repeat Region of the CRISPR genome present in Strep. thermophilus LMD9 strain

BBa_I714003
BBa_I714003 Version 1 (Component)
minimum oriT of plasmid R64 ( origin of transfer, R64 is IncI-1 )

BBa_K1051900
BBa_K1051900 Version 1 (Component)
G1 phase magic with cell synchronization device and CRISPRi induced alternative splicing device.

SEGA
SEGA_collection Version 1 (Collection)
In the Standardized Genome Architecture (SEGA), genomic integration of DNA fragments is enabled by λ-Red recombineering and so-called landing pads that are a common concept in synthetic biology and typically contain features that i) enable insertion of additional genetic elements and ii) provide well-characterized functional parts such as promoters and genes, and iii) provides insulation against genome context-dependent effects. The SEGA landing pads allow for reusable homology regions and time-efficient construction of parallel genetic designs with a minimal number of reagents and handling steps. SEGA bricks, typically synthetic DNA or PCR fragments, are integrated on the genome simply by combining the two reagents (i.e. competent cells and DNA), followed by incubation steps, and successful recombinants are identified by visual inspection on agar plates. The design of the SEGA standard was heavily influenced by the Standard European Vector Architecture (SEVA). SEGA landing pads typically hosts two major genetic “control elements” that influence gene expression on the transcriptional (C1), and translational (C2) level. Furthermore, landing pads contain gadgets such as selection and counterselection markers.