2002
DOI: 10.1002/gene.10127
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PPTGAL, a convenient Gal4 P‐element vector for testing expression of enhancer fragments in drosophila

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Cited by 117 publications
(110 citation statements)
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References 12 publications
(16 reference statements)
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“…DNA immediately 5′ of the DmCCAP coding region and extending from -516 to +39 bp was obtained by PCR using wild-type genomic DNA as a template. The PCR products were inserted into the pPTGAL transformation vector (Sharma et al, 2002). The recombinant DmCCAP promoter-GAL4 fusion (CCAP-GAL4) construct was introduced into the germline using standard methods.…”
Section: Generation Of Ccap-gal4 Drivermentioning
confidence: 99%
“…DNA immediately 5′ of the DmCCAP coding region and extending from -516 to +39 bp was obtained by PCR using wild-type genomic DNA as a template. The PCR products were inserted into the pPTGAL transformation vector (Sharma et al, 2002). The recombinant DmCCAP promoter-GAL4 fusion (CCAP-GAL4) construct was introduced into the germline using standard methods.…”
Section: Generation Of Ccap-gal4 Drivermentioning
confidence: 99%
“…We also cloned the same cis-regulatory region into a new, highly versatile GAL4 transformation vector (pPT-GAL4; Sharma et al, 2002). For this cloning, a KpnI to NotI fragment was excised from P[w ϩ ; dpp85.8MX.lacZ] and inserted into these sites in pPTGAL4 to create P[w ϩ ; PS.GAL4].…”
mentioning
confidence: 99%
“…tslGAL4 constructs. To generate the tsl(G)GAL4 construct, an EcoRI/BamHI fragment from C4PLZ-tsl(G) was subcloned into the pPTGAL vector (35). To generate the tsl(F)GAL4 construct, an EcoRI/BamHI fragment from C4PLZ-tsl(F) was subcloned into the pChs-Gal4 vector (36).…”
Section: Methodsmentioning
confidence: 99%