2007
DOI: 10.5483/bmbrep.2007.40.5.656
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Engineering lacZ Reporter Gene into an ephA8 Bacterial Artificial Chromosome Using a Highly Efficient Bacterial Recombination System

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Cited by 10 publications
(21 citation statements)
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“…The targeting vectors for the EphB2-EphB2 (a full-length mouse Ephb2 cDNA clone) BAC, the EphB2-EphB2-dC (a mouse Ephb2 cDNA clone lacking the coding sequence for amino acids 589-986) BAC, and the EphB2-XIAP (a full-length human XIAP cDNA clone) BAC were constructed as described for EphB2-GFP, except that the GFP reporter and FRT-Kana-FRT cassette were replaced by the indicated cDNA and an IRES-lacZ-FRT-Kana-FRT cassette. The modified recombinant BACs were injected into fertilized C57BL/6 mouse eggs as previously described (Kim et al, 2007b). (005992) (Feldheim et al, 2000), Mapk8 tm1Flv/J (004319) (Dong et al, 1998) and Mapk9 tm1Flv/J (004321) mouse lines were purchased from The Jackson Laboratory.…”
Section: Bac Modification Transgenic and Knockout Micementioning
confidence: 99%
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“…The targeting vectors for the EphB2-EphB2 (a full-length mouse Ephb2 cDNA clone) BAC, the EphB2-EphB2-dC (a mouse Ephb2 cDNA clone lacking the coding sequence for amino acids 589-986) BAC, and the EphB2-XIAP (a full-length human XIAP cDNA clone) BAC were constructed as described for EphB2-GFP, except that the GFP reporter and FRT-Kana-FRT cassette were replaced by the indicated cDNA and an IRES-lacZ-FRT-Kana-FRT cassette. The modified recombinant BACs were injected into fertilized C57BL/6 mouse eggs as previously described (Kim et al, 2007b). (005992) (Feldheim et al, 2000), Mapk8 tm1Flv/J (004319) (Dong et al, 1998) and Mapk9 tm1Flv/J (004321) mouse lines were purchased from The Jackson Laboratory.…”
Section: Bac Modification Transgenic and Knockout Micementioning
confidence: 99%
“…We then inserted homologous arms A and B into pGEM11z, a vector containing a GFP reporter with the SV40 polyadenylation site and a FRT-Kana-FRT cassette. The resulting vector was digested with SfiI and inserted into the Ephb2 BAC genomic DNA (RP23-237B18) using a published bacterial homologous recombination method (Kim et al, 2007b). The targeting vectors for the EphB2-EphB2 (a full-length mouse Ephb2 cDNA clone) BAC, the EphB2-EphB2-dC (a mouse Ephb2 cDNA clone lacking the coding sequence for amino acids 589-986) BAC, and the EphB2-XIAP (a full-length human XIAP cDNA clone) BAC were constructed as described for EphB2-GFP, except that the GFP reporter and FRT-Kana-FRT cassette were replaced by the indicated cDNA and an IRES-lacZ-FRT-Kana-FRT cassette.…”
Section: Bac Modification Transgenic and Knockout Micementioning
confidence: 99%
“…Homologous BAC recombination was performed as described previously (7). For the enhancer trap assay, a transposable vector carrying a β-globin promoter, LacZ gene containing SV40 poly(A) site, and a kanamycin resistance gene was introduced into each BAC clone according to the method of Spitz et al (8,9).…”
Section: Homologous Bac Recombination and Enhancer Trap Assaymentioning
confidence: 99%
“…BAC DNA for microinjection was confirmed on a gel and diluted with injection buffer as described previously (7). The BAC DNA was injected into 200 pronuclei of fertilized oocytes from C57BL/6 mice as described previously (7,10).…”
Section: Generation Bac Transgenic Micementioning
confidence: 99%
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