true blue bac ii plasmid (Genomics One Corporation)
90
Structured Review
Genomics One Corporation
true blue bac ii plasmid
True Blue Bac Ii Plasmid, supplied by Genomics One Corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/true+blue+bac+ii+plasmid/true+blue+bac+ii+plasmid/10__1128_slash_jvi__79__6__3797___3806__2005-150-27-32
Average 90 stars, based on 1 article reviews
True Blue Bac Ii Plasmid, supplied by Genomics One Corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/true+blue+bac+ii+plasmid/true+blue+bac+ii+plasmid/10__1128_slash_jvi__79__6__3797___3806__2005-150-27-32
Average 90 stars, based on 1 article reviews
true blue bac ii plasmid - by Bioz Stars,
2026-10
90/100 stars
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Derivative Assay:Article Title: Identification of an Essential Domain in the Herpes Simplex Virus 1 U L 34 Protein That Is Necessary and Sufficient To Interact with U L 31 Protein Article Snippet: The viral DNA digests were then separated in 1% agarose gels, transferred to nitrocellulose membranes, probed with [α- 32 P]dCTP (Amersham)-labeled DNA, and exposed to radiographic film as described previously ( 20 ). .. The DNA probes used for the experiments were derived from the purified full-length U L 34 PCR product, a fragment bearing the Kan r gene generated by PCR, and the Article Title: Identification of an Essential Domain in the Herpes Simplex Virus 1 U L 34 Protein That Is Necessary and Sufficient To Interact with U L 31 Protein Article Snippet: The viral DNA digests were then separated in 1% agarose gels, transferred to nitrocellulose membranes, probed with [ -32P]dCTP (Amersham)-labeled DNA, and exposed to radiographic film as described previously (20). .. The DNA probes used for the experiments were derived from the purified full-length UL34 PCR product, a fragment bearing the Kanr gene generated by PCR, and the Purification:Article Title: Identification of an Essential Domain in the Herpes Simplex Virus 1 U L 34 Protein That Is Necessary and Sufficient To Interact with U L 31 Protein Article Snippet: The viral DNA digests were then separated in 1% agarose gels, transferred to nitrocellulose membranes, probed with [α- 32 P]dCTP (Amersham)-labeled DNA, and exposed to radiographic film as described previously ( 20 ). .. The DNA probes used for the experiments were derived from the purified full-length U L 34 PCR product, a fragment bearing the Kan r gene generated by PCR, and the Article Title: Identification of an Essential Domain in the Herpes Simplex Virus 1 U L 34 Protein That Is Necessary and Sufficient To Interact with U L 31 Protein Article Snippet: The viral DNA digests were then separated in 1% agarose gels, transferred to nitrocellulose membranes, probed with [ -32P]dCTP (Amersham)-labeled DNA, and exposed to radiographic film as described previously (20). .. The DNA probes used for the experiments were derived from the purified full-length UL34 PCR product, a fragment bearing the Kanr gene generated by PCR, and the Polymerase Chain Reaction:Article Title: Identification of an Essential Domain in the Herpes Simplex Virus 1 U L 34 Protein That Is Necessary and Sufficient To Interact with U L 31 Protein Article Snippet: The viral DNA digests were then separated in 1% agarose gels, transferred to nitrocellulose membranes, probed with [α- 32 P]dCTP (Amersham)-labeled DNA, and exposed to radiographic film as described previously ( 20 ). .. The DNA probes used for the experiments were derived from the purified full-length U L 34 PCR product, a fragment bearing the Kan r gene generated by PCR, and the Article Title: Identification of an Essential Domain in the Herpes Simplex Virus 1 U L 34 Protein That Is Necessary and Sufficient To Interact with U L 31 Protein Article Snippet: The viral DNA digests were then separated in 1% agarose gels, transferred to nitrocellulose membranes, probed with [ -32P]dCTP (Amersham)-labeled DNA, and exposed to radiographic film as described previously (20). .. The DNA probes used for the experiments were derived from the purified full-length UL34 PCR product, a fragment bearing the Kanr gene generated by PCR, and the Generated:Article Title: Identification of an Essential Domain in the Herpes Simplex Virus 1 U L 34 Protein That Is Necessary and Sufficient To Interact with U L 31 Protein Article Snippet: The viral DNA digests were then separated in 1% agarose gels, transferred to nitrocellulose membranes, probed with [α- 32 P]dCTP (Amersham)-labeled DNA, and exposed to radiographic film as described previously ( 20 ). .. The DNA probes used for the experiments were derived from the purified full-length U L 34 PCR product, a fragment bearing the Kan r gene generated by PCR, and the Article Title: Identification of an Essential Domain in the Herpes Simplex Virus 1 U L 34 Protein That Is Necessary and Sufficient To Interact with U L 31 Protein Article Snippet: The viral DNA digests were then separated in 1% agarose gels, transferred to nitrocellulose membranes, probed with [ -32P]dCTP (Amersham)-labeled DNA, and exposed to radiographic film as described previously (20). .. The DNA probes used for the experiments were derived from the purified full-length UL34 PCR product, a fragment bearing the Kanr gene generated by PCR, and the BAC Assay:Article Title: Identification of an Essential Domain in the Herpes Simplex Virus 1 U L 34 Protein That Is Necessary and Sufficient To Interact with U L 31 Protein Article Snippet: The viral DNA digests were then separated in 1% agarose gels, transferred to nitrocellulose membranes, probed with [α- 32 P]dCTP (Amersham)-labeled DNA, and exposed to radiographic film as described previously ( 20 ). .. The DNA probes used for the experiments were derived from the purified full-length U L 34 PCR product, a fragment bearing the Kan r gene generated by PCR, and the Article Title: Identification of an Essential Domain in the Herpes Simplex Virus 1 U L 34 Protein That Is Necessary and Sufficient To Interact with U L 31 Protein Article Snippet: The viral DNA digests were then separated in 1% agarose gels, transferred to nitrocellulose membranes, probed with [ -32P]dCTP (Amersham)-labeled DNA, and exposed to radiographic film as described previously (20). .. The DNA probes used for the experiments were derived from the purified full-length UL34 PCR product, a fragment bearing the Kanr gene generated by PCR, and the Plasmid Preparation:Article Title: Identification of an Essential Domain in the Herpes Simplex Virus 1 U L 34 Protein That Is Necessary and Sufficient To Interact with U L 31 Protein Article Snippet: The viral DNA digests were then separated in 1% agarose gels, transferred to nitrocellulose membranes, probed with [α- 32 P]dCTP (Amersham)-labeled DNA, and exposed to radiographic film as described previously ( 20 ). .. The DNA probes used for the experiments were derived from the purified full-length U L 34 PCR product, a fragment bearing the Kan r gene generated by PCR, and the Article Title: Cell lines that support replication of a novel herpes simplex virus 1 UL31 deletion mutant can properly target UL34 protein to the nuclear rim in the absence of UL31. Article Snippet: .. The Article Title: Identification of an Essential Domain in the Herpes Simplex Virus 1 U L 34 Protein That Is Necessary and Sufficient To Interact with U L 31 Protein Article Snippet: The viral DNA digests were then separated in 1% agarose gels, transferred to nitrocellulose membranes, probed with [ -32P]dCTP (Amersham)-labeled DNA, and exposed to radiographic film as described previously (20). .. The DNA probes used for the experiments were derived from the purified full-length UL34 PCR product, a fragment bearing the Kanr gene generated by PCR, and the |