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CLONED (Commentary)
ORGANISM
UNIPROT
LITERATURE
a 6-His N-terminal-tagged human dynamin2, lacking the C-terminal proline-rich domain, is constructed, cloned into the pET28a vector for expression in Escherichia coli BL21DE3 cells
a CHO-K1 cDNA library in the pSPORT vector is screened, the PCR product, derived from a positive clone, is cloned using the vectors pcDNA3.1Zeo+Myc6-, pcDNA3.1Zeo+Flag-, pcDNA3.1Zeo+HA2-, and pGEX6P-2, DLP1 cDNA from ZP121 is subcloned into pGEM-Teasy
Dyn1 expression in bovine adrenal chromaffin cells, coexpression with granule marker VMAT2-pH, the amount of dynamin on the plasma membrane in dynamin-transfected cells was increased 2.5 to 3.5 times compared with endogenous dynamin in nontransfected cells
for identification of the EDR3 gene a cosmid library using BAC F27H5 DNA is constructed, for investigation of the subcellular localization a green fluorescent protein fusion to the N-terminus of DRP1E is used
gene DNM1, recombinant expression of the dynamin 1 GTPase domain GG1 from modified pGEX-4T1 vector containing a TEV protease site. The fragments are connected by a linker composed of eight amino acid residues (KHGTDSRV) in Escherichia coli strain BL21 (DE3)
gene Rnf112, recombinant expression of C-terminally HA-tagged enzyme in transgenic C83S/C103S mutant mice and in HeLa cells, and of GFP-tagged enzyme from pEGFP-N1 vector in transgenic mice
human dynamin is expressed in SF9 insect cells, using the Bac-to-Bac baculovirus expression system a full-length cDNA encoding human dynamin1 containing a 6His-tag is subcloned into pFastBac, a bacmid is generated after transposition in Escherichia coli
into the pFLAG-CMV-2 vector, five functional dynamin domains, GTPase, Middle, pleckstrin homology, GTPase effector and proline rich, are subcloned into pGEX-4T2
into the pT-Adv vector, into pET-15b for expression in Escherichia coli BL21DE3codon-plus cells, a 711 bp fragment corresponding to the GTPase N-terminal domain into pET-22b, and into the pSynXIV VI+X3 vector for recombinat expression in the BEV system
recombinant expression of N-terminally Strep-tagged Drp1 with an HRV3C protease site from pET16b vector in Escherichia coli strain BL21 Star (DE3), stable recombinant expression of GFP-tagged DrpI in U2OS cells with partial shRNA suppression of endogenous Drp1 (gDrp-U2OS), GFP-Drp1 functionally compensates for endogenous Drp1 in these cells
recombinant expression of nucleotide-free GTPase-GTPase effector domain fusion protein of enzyme Drp1, and wild-type and mutant full-length enzymes in Escherichia coli strain BL21(DE3)
recombinant expression of the GST-tagged chimeric fusion protein of AtDRP1A fusion protein in Escherichia coli strain BL21(DE3), subcloning in Escherichia coli strain DH5alpha
recombinant expression of truncated enzyme Sey1p(1-692) in Escherichia coli, recombinant expressioj of Myc-tagged scSey1p in COS-7 cells and immunolocalization study
the full-length mouse dynamin-1 cDNA isolated from retina is subcloned into the pGEX-2TK vector, the construct is used to generate three different dynamin-1 domain constructs, the N-terminal domain, aa 1-520, the proline-rich domain, aa 750-814, and the C-terminal domain, aa 521-814