YFP(159-238)-gamma-11 in pcDNAI/Amp
(Plasmid #55193)

• Purpose: A carboxyl-terminal YFP fragment was fused to Ggamma-11. When co-expressed with an amino-terminal YFP fragment fused to a Gbeta subunit with which it interacts, a fluorescent signal is produced.
• Depositing Lab: Catherine Berlot
• Publication: Mervine et al Mol Pharmacol. 2006 Jul;70(1):194-205. Epub 2006 Apr 26.

Backbone

• Vector backbone: pcDNAI/Amp
• Backbone manufacturer: Invitrogen
• Backbone size w/o insert (bp): 4800
• Total vector size (bp): 5248
• Modifications to backbone: A BglII site was introduced to into the polylinker of pcDNAI/Amp 3' to the BamHI site.
• Vector type: Mammalian Expression

Growth in Bacteria

• Bacterial Resistance(s): Ampicillin, 100 μg/mL
• Growth Temperature: 37°C
• Growth Strain(s): DH10B
• Copy number: High Copy

Gene/Insert

• Gene/Insert name: YFP(159-238)-gamma-11
• Alt name: GNG11
• Species: B. taurus (bovine); Aequorea victoria
• Insert Size (bp): 448
• Mutation: Ggamma-11 was amplified by PCR, which added a BamHI site and a linker sequence (Arg-Ser) to the 5' end and a 3' BglII site. Cloning into the BglII site of YFP(159-238) destroyed the BamHI site.
• Entrez Gene: GNG11
• Promoter: CMV
• Tag / Fusion Protein:
  • YFP(159-238) was fused to the amino terminus of Ggamma-11. (N terminal on insert)

Cloning Information

• Cloning method: Restriction Enzyme
• 5′ cloning site: BamHI (not destroyed)
• 3′ cloning site: BglII (not destroyed)
• 5′ sequencing primer: T7
• 3′ sequencing primer: SP6

Resource Information

• A portion of this plasmid was derived from a plasmid made by: pEYFP was purchased from Clontech. Gamma-11 cDNA was obtained from Janet Robishaw, Weis Center for Research, Geisinger Clinic, Danville, PA.

Terms and Licenses

• Academic/Nonprofit Terms:
  • UBMTA
• Industry Terms:
  • Not Available to Industry