WebApr 30, 1999 · Construction of Full-length BIG2 cDNA in pAcHLT-C. For insertion of BIG2 into the baculovirus transfer vector pAcHLT-C (Pharmingen), restriction sites for NdeI and NotI were introduced, respectively, before the initiation and after the termination codons of BIG2. WebSep 14, 2010 · into baculovirus vector, pAcHLT-C (Pharmingen) via PCR amplifi-cation at XhoI and NcoI sites. Cell culture. Human embryonic kidney (HEK)293, HEK293T, and ... methanol at 4°C at 40 V overnight, and the membranes were incu-bated in TBST (containing 100 mM Tris-Cl, pH 7.5, 150 mM NaCl,
pAcHLT C Sequence and Map - SnapGene
WebThe 450+ PACT Liftvans currently in use have been done in multiple coast to coast uses. We are pleased with PACT’s responsiveness to be able to fine tune the product to fit our … WebThe BRD4 ΔN (amino acids 699–1,400) was generated as a dropout mutant in the pAcHLT-C baculovirus transfer vector from the Flag- BRD4 WT. The plasmid bearing GST-tagged human BRD4 in the pGEX-6P-1 bacterial expression vector was obtained from Addgene (plasmid 14447). The human Flag-tagged BRD4 WT and FAA-AAA mutant in the pCDNA … chase center section 212
Characterization of the Yeast Amphiphysins Rvs161p and Rvs167p Reveals …
http://pufei.com/static/product/bd/554/195852316a479337a.pdf WebThe two fragments were ligated into pAcHLT-C, which had been digested with NdeI and NotI. DCD570 was amplified from DC plasmid by polymerase chain reaction using forward primer 59-AAA-CATATGTTGTGACTTAAATG (NdeI site underlined) and reverse primer G54. The amplified DNA was first subcloned into pCRscript Webthe two PCR products (1 lI of each) using primers C and B. Primer C and reverse primer B were designed to contain, respectively, sites for NdeI and NotI restriction enzymes. The PCR product was subcloned into vector pAcHLT-C, which had been digested with NdeI and Notl and treated with alkaline phosphatase before it was used to transform DH5cx ... chase center section 121 row 21