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WormBase Tree Display for Transgene: WBTransgene00000317

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Name Class

WBTransgene00000317Public_namecgc6123Is1
Summary[bam-2::gfp]
ConstructionConstructWBCnstr00000317
Construction_summarybam-2 expression clones were made in a pSK vector using a PCR-based approach to fuse the coding region of GFP and the 3'UTR from unc-54, amplified from pPD95.75, in-frame to the C-terminus of a full length bam-2 cDNA (yk593b12) to create bam-2::gfp. bam-2 promoter fragments were PCR amplified from N2 genomic DNA and cloned upstream of bam-2::gfp or into the multiple cloning site of pPD95.75. Promoter derivatives were sometimes obtained by restriction digest, for example using XbaI to generate xbaIp:bam-2::gfp.
Genetic_informationIntegrated
Used_forExpr_patternExpr2767
ReferenceWBPaper00006123
SpeciesCaenorhabditis elegans