Cloning and expression of isoform A and of a fragment comprising the catalytic calmodulin binding domain (amino acids 165-462) in Escherichia coli BL21(DE3).
Cloning and expression of isoform A and of an enzyme fragment comprising the catalytic calmodulin binding domain in Escherichia coli BL21(DE3). Creating of a point mutant by using PCR-based site-directed QuikChange mutagenesis and expression in Escherichia coli.
Cloning and expression of isoform B and of a fragment comprising the catalytic calmodulin binding domain (amino acids 165-462) in Escherichia coli BL21(DE3).
cloning and expression of the isoenzymes A, B and C in COS-7 cells, the 3 isoenzymes A, B and C can be distinguished by their localization on transfection in COS-7 cells
cloning of a full-length cDNA encoding IP3K isoform C from tongue epithelium, cloning of an enzymatically active and Ca2+/calmodulin-regulated fragment of isoform C and expression in Escherichia coli BL21(DE3)pRIL
cloning of isozyme IP3K-A from erythrocytes and expression of a fragment comprising the catalytic domain and the CaM binding domain of the wild-type and mutant enzyme, respectively, in Escherichia coli strain BL21(DE3)
Cloning, Expression, and Purification of RnIP3K-C isoform and of two different recombinant fragments IP3K-C, one comprising the catalytic domain and the calmodulin binding domain, the other comprising only the catalytic domain, are expressed in Escherichi coli BL21(DE3) cells.
establishment of A549 or H1299 cells overexpressing the enzyme: the cDNA fragment encoding for ITPKAis cloned into the retroviral vector MigRI, for virus production this construct is co-transfected with SVgp (M57) and pHCMV-VSV-G (M75) into HEK293 phoenix ampho cells, after 48 h of incubation the supernatant containing the viruses is filtered and transferred to A549 or H1299 cells
expression of full length enzyme in Escherichia coli: a cDNA fragment encoding the full length form of ITPKA is inserted into the vector pGEX-4T-3 encoding a N-terminal Glutathione S-transferase-tag
expression of His6-tagged fragment comprising residues 151-461 in Escherichia coli, expression of wild-type and mutant cDNA fragments encoding for residues 187-461 of the catalytic domain of isozyme A as unlabeled or selenomethionine-labeled GST fusion proteins in Escherichia coli strains C41(DE3) and B834(DE3)
expression of mutant cDNA fragment encoding for residues 185-459 of the catalytic domain of isozyme A as unlabeled or selenomethionine-labeled GST fusion proteins in Escherichia coli
generation of knock-out rats and point mutant, IP3K-A is overexpressed in DIV 22 hippocampal neurons by infection with adenovirus containing full-length IP3K-A
isozymes IP3K-A and IP3K-B, expression of a fragment comprising the catalytic domain and the CaM binding domain, residues 165-462 of isozyme A, of the wild-type and mutant isozyme A and isozyme B, respectively, in Escherichia coli strain BL21(DE3)
overexpression of enzyme D-IP3K1 leads to increased resistance of flies to H2O2, but not to paraquat-induced oxidative stress, due to a decreased 1D-myo-inositol 1,4,5-trisphosphate level
stable expression of the C-terminal catalytic domain 3KA-cat30, comprising residues Ser185-Arg459, as N-terminally His-tagged and S-tagged protein in Escherichia coli strain BL21(DE3)
transient expression of isozyme B fragment 108-170 fused to EGFP in NRK 52E and PC12 cells co-localizes with F-actin, overexpression of isozyme B fused to EGFP in Escherichia coli, the enzyme co-localizes in with the cytoskeleton as well as with the endoplasmic reticulum and the plasma membrane, overexpression of inactive isozyme B lacking the F-actin target sequence at the noncatalytical N-terminus
transient expression of isozyme B in NRK 52E and PC12 cells, DNA and amino acid sequence determination and analysis, expression of isoform B comprising residues 555-934 as Strep-Tactin-tagged enzyme in Escherichia coli strain XL1-Blue, expression of isoform B comprising residues 108-170 as GST-fusion protein in Escherichia coli strain BL21(DE3)