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The fusion protein hH 2 R-G sαL ensures a defi ned 1:1 stoichiometry of the receptor and G sαL subunit. hH 2 R-G sαL and hH 2 R-G sαS (cat.# PR-619) exhibit similar constitutive activity as assessed by the effi cacies of inverse agonists and partial agonists in the steadystate GTPase assay. The fusion protein contains a N-terminal FLAG-Tag ® for immunological detection. Protein concentration: 3.9 mg/ml Store: -80 °C Selected references: Kelley et al. (2001) Distinct interaction of human and guinea pig histamine H 2 -receptor with guanidine type agonists. Mol. Pharmacol. 60:1210. Wenzel-Seifert et al. (2001) Similar apparent constitutive activity of human histamine H 2 -receptor fused to long and short splice variants of G sα . J. Pharmacol. Exp. Ther. 299:1013. Gantz et al. (1991) Molecular cloning of the human histamine H 2 receptor. Biochem. Biophys. Res. Commun. 178:1386. Histamine H 2 -Receptor-G sαS (H 2 R-G sαS ) human, Recombinant, Sf9 insect cells Cat. No. Amount Price (€) PR-619 1 ml 300,-- Membrane suspension. Supplied in 75 mM Tris-HCl, pH 7.4, 12.5 mM MgCl 2, and 1 mM EDTA. hH 2 R-G sαS is a fusion protein in wich the G sαS N-terminus is linked to the C-terminus of human H 2-receptor (hH 2R) via a hexahistidine (His 6)-Tag. The H 2R couples to G s-proteins to activate adenylate cyclase (AC). Among the many responses mediated by the H 2 R are gastric acid secretion, smooth muscle relaxation, inotropic and chronotropic effects on heart muscle, and inhibition of leukocyte function. G sαS is the short splice variant of the α-subunit of the heterotrimeric G-protein G s. G s activates the effector AC. G sαS differs from the long splice variant (G sαL ) by the absence of a 15-amino acid insert between the ras-like domain and the α-helical domain. G sαS (cat.# PR-505) possesses a higher GDP-affi nity than G sαL (cat.# PR-501). The fusion protein hH 2 R-G sαS ensures a defi ned 1:1 stoichiometry of the receptor and G sαS subunit. hH 2R-G sαS and hH 2R-G sαL (cat.# PR-618) exhibit similar constitutive activity as assessed by the effi cacies of inverse agonists and partial agonists in the steadystate GTPase assay. The fusion protein contains a N-terminal FLAG-Tag ® for immunological detection. Protein concentration: 0.7 – 4.5 mg/ml Store: -80 °C Selected references: Kelley et al. (2001) Distinct interaction of human and guinea pig histamine H 2 -receptor with guanidine type agonists. Mol. Pharmacol. 60:1210. Wenzel-Seifert et al. (2001) Similar apparent constitutive activity of human histamine H 2 -receptor fused to long and short splice variants of G s α. J. Pharmacol. Exp. Ther. 299:1013. Gantz et al. (1991) Molecular cloning of the human histamine H 2 receptor. Biochem. Biophys. Res. Commun. 178:1386. Histamine H 2 -Receptor(H 2 R) rat, Recombinant, Sf9 insect cells Cat. No. Amount Price (€) PR-620 1 ml 300,-- Membrane suspension. Supplied in 75 mM Tris-HCl, pH 7.4, 12.5 mM MgCl 2, and 1 mM EDTA. The histamine H 2 -receptor (H 2 R) belongs to the superfamily of seven transmembrane domain (7TM), G-protein-coupled receptors (GPCRs). The endogenous agonist for the H 2 R is histamine which is both neurotransmitter and autacoid. The H 2 R couples to G s -proteins to mediate adenylate cyclase (AC) activation. In some systems, the H 2 R also couples to G q -proteins and phospholipase C. Among the many responses mediated by the H 2 R are gastric acid secretion, smooth muscle relaxation, positive ionotropic and chronotropic effects on heart muscle, and inhibition of leukocyte function. The rat H 2 R was prepared from Sf9 cells infected with rat H 2R-encoding baculovirus. In this system, the rat H 2 R couples to the G sα -like G-proteins of the insect cells to mediate AC activation. Protein concentration: 1 – 1.5 mg/ml Store: -80 °C Selected references: Houston et al. (2002) The human histamine H 2 -receptor couples more effi ciently to Sf9 insect cell G s -proteins than to insect cell G q -proteins: limitations of Sf9 cells for the analysis of receptor/G q -protein coupling. J. Neurochem. 80:678. Harteneck et al. (1995) The Drosophila cation channel trpl expressed in insect Sf9 cells is stimulated by agonists of Gprotein-coupled receptors. FEBS Lett. 358:297. Leopoldt et al. (1997) G Proteins endogenously expressed in Sf9 cells: interaction with mammalian histamine receptors. Naunyn-Schmiedeberg’s Arch. Pharmacol. 356:216. Histamine H 2 -Receptor + G sαS (H 2 R + G sαS ) human, Recombinant, Sf9 insect cells Cat. No. Amount Price (€) PR-621 1 ml 300,-- Membrane suspension. Supplied in 75 mM Tris-HCl, pH 7.4, 12.5 mM MgCl 2, and 1 mM EDTA. The histamine H 2-receptor (H 2R) belongs to the superfamily of seven transmembrane domain (7TM), G-protein-coupled receptors (GPCRs). The endogenous agonist for the H 2R is histamine which is both neurotransmitter and autacoid. The H 2R couples to G s-proteins to mediate adenylate cyclase (AC) activation. In some systems, the H 2 R also couples to G q -proteins and phospholipase C. Among the many responses mediated by the H 2R are gastric acid secretion, smooth muscle relaxation, positive ionotropic and chronotropic effects on heart muscle, and inhibition of leukocyte function. hH 2R reconstituted with G sαS was prepared from Sf9 cells coinfected with hH 2R- and G sαS-encoding baculoviruses. hH 2R contains a N-terminal FLAG-Tag ® and a C-terminal hexahistidine (His 6 )-Tag for immunological detection, to allow purifi cation, and to provide additional protection against proteolysis. Protein concentration: 0.8 mg/ml Store: -80 °C Selected references: Houston et al. (2002) The human histamine H 2 -receptor couples more effi ciently to Sf9 insect cell G s -proteins than to insect cell G q -proteins: limitations of Sf9 cells for the analysis of receptor/G q -protein coupling. J. Neurochem. 80:678. Gantz et al. (1991) Molecular cloning of the human histamine H 2 receptor. Biochem. Biophys. Res. Commun. 178:1386. Leopoldt et al. (1997) G Proteins endogenously expressed in Sf9 cells: interaction with mammalian histamine receptors. Naunyn-Schmiedeberg’s Arch. Pharmacol. 356:216. Dopamine Receptor GTP Signal Transduction Dopamine D 1 -Receptor (D 1 R) human, Recombinant, Sf9 insect cells Cat. No. Amount Price (€) PR-581 1 ml 300,-- Membrane suspension. Supplied in 75 mM Tris-HCl, pH 7.4, 12.5 mM MgCl 2 , and 1 mM EDTA. The dopamine D 1 -receptor (D 1 R) belongs to the superfamily of seven transmembrane-domain (7TM), G-protein-coupled receptors (GPCRs). The D 1R couples to the G-protein G s to mediate adenylyl cyclase (AC) activation. The endogenous catecholamine dopamine infl uences many cellular activities including behavior, hormone synthesis, blood pressure control and intracellular ion transport. The human D 1 R was prepared from Sf9 cells infected with D 1 R-encoding baculovirus. In this system the D 1 R couples to the G sα -like G-proteins of the insect cells to mediate AC activation. The D 1 R contains a N-terminal c-myc-Tag for immunochemical detection. Protein concentration: 1.2 mg/ml Receptor expression level: 3.5 pmol/mg Store: -80 °C Selected references: Drago et al. (1998) Dopamine receptors and dopamine transporter in brain function and addictive behaviors: Insight from targeted mouse mutants. Dev. Neurosci. 20:188. Dumartin et al. (2000) Dopamine tone regulates D 1 receptor traffi cking and delivery in striatal neurons in dopamine transporter-defi cient mice. Proc. Natl. Acad. Sci. USA 97:1879. Gille, A. and Seifert, R. (2003) Co-expression of the β 2 - adrenoceptor and dopamine D 1 -receptor with G sα proteins in Sf9 insect cells: limitations in comparison with fusion proteins. Biochim. Biophys. Acta 1613:101. Complement Component 5a Receptors Complement C5a-Receptor (C5aR) + co-expressed Gprotein G i α 1 β 1 γ 2 complex human, Recombinant, Sf9 insect cells Cat. No. Amount Price (€) PR-571 1 ml 300,-- Membrane suspension. Supplied in 75 mM Tris-HCl, pH 7.4, 12.5 mM MgCl 2 , and 1 mM EDTA. The anaphylatoxin C5a-receptor (C5aR, CD88) belongs to the superfamily of seven transmembranedomain (7TM), G protein-coupled receptors (GPCRs). In monocytes and granulocytes, activation of C5aR causes chemotaxis, degranulation, and superoxide anion production. C5aR is also involved in the formation of adhesion molecules as well as in the production of so-called “acute-phase” proteins. C5aR reconstituted with the G-protein G i α 1 β 1 γ 2 was prepared from Sf9 cells triple-infected with C5aR-, G i α 1 -, and Gβ 1 γ 2 -encoding baculoviruses. C5aR contains a N-terminal FLAG-Tag ® and a C-terminal hexahistidine (His6)-Tag for immunochemical detection and protection against proteolysis. Recombinant Proteins 145
Recombinant Proteins 146 Protein concentration: 0.9 mg/ml Store: -80 °C Selected references: Seifert, R. and Wenzel-Seifert, K. (2001) Unmasking different constitutive activity of four chemoattractant receptors using Na + as universal stabilizer of the inactive (R) state. Receptors Channels 7:357. Taylor et al. (2001) Development of response-selective agonists of human C5a anaphylatoxin: Conformational, biological, and therapeutic considerations. Curr. Med. Chem. 8:675. Schlaf et al. (2003) Expression and induction of anaphylatoxin C5a receptors in rat liver. Histol. Histopathol. 18:299. Complement C5a-Receptor (C5aR) + co-expressed G-protein G i α 2 β 1 γ 2 complex human, Recombinant, Sf9 insect cells Cat. No. Amount Price (€) PR-572 1 ml 300,-- Membrane suspension. Supplied in 75 mM Tris-HCl, pH 7.4, 12.5 mM MgCl 2 , and 1 mM EDTA. The anaphylatoxin C5a-receptor (C5aR, CD88) belongs to the superfamily of seven transmembranedomain (7TM), G protein-coupled receptors (GPCRs). In monocytes and granulocytes, activation of C5aR causes chemotaxis, degranulation and superoxide anion production. C5aR is also involved in the formation of adhesion molecules as well as in the production of so-called “acute-phase” proteins. C5aR reconstituted with the G-protein G iα 2β 1γ 2 was prepared from Sf9 cells triple-infected with C5aR-, G iα 2-, and Gβ 1γ 2-encoding baculoviruses. C5aR contains a N-terminal FLAG-Tag ® and a C-terminal hexahistidine (His6)-Tag for immunochemical detection and protection against proteolysis. Protein concentration: 0.5 mg/ml Store: -80 °C Selected references: Seifert, R. and Wenzel-Seifert, K. (2001) Unmasking different constitutive activity of four chemoattractant receptors using Na + as universal stabilizer of the inactive (R) state. Receptors Channels 7:357. Taylor et al. (2001) Development of response-selective agonists of human C5a anaphylatoxin: Conformational, biological, and therapeutic considerations. Curr. Med. Chem. 8:675. Schlaf et al. (2003) Expression and induction of anaphylatoxin C5a receptors in rat liver. Histol. Histopathol. 18:299. Complement C5a-Receptor (C5aR) + co-expressed G-protein G i α 3 β 1 γ 2 complex human, Recombinant, Sf9 insect cells Cat. No. Amount Price (€) PR-573 1 ml 300,-- Membrane suspension. Supplied in 75 mM Tris-HCl, pH 7.4, 12.5 mM MgCl 2 , and 1 mM EDTA. The anaphylatoxin C5a-receptor (C5aR, CD88) belongs to the superfamily of seven transmembranedomain (7TM), G protein-coupled receptors (GPCRs). In monocytes and granulocytes, activation of C5aR causes chemotaxis, degranulation and superoxide anion production. C5aR is also involved in the formation of adhesion molecules as well as in the production of so-called “acute-phase” proteins. C5aR reconstituted with the G-protein G iα 3β 1γ 2 was prepared from Sf9 cells triple-infected with C5aR-, G i α 3 -, and Gβ 1 γ 2 -encoding baculoviruses. C5aR contains a N-terminal FLAG-Tag ® and a C-terminal hexahistidine (His6)-Tag for immunochemical detection and protection against proteolysis. Protein concentration: 0.5 – 1.5 mg/ml Store: -80 °C Selected references: Seifert, R. and Wenzel-Seifert, K. (2001) Unmasking different constitutive activity of four chemoattractant receptors using Na + as universal stabilizer of the inactive (R) state. Receptors Channels 7:357. Taylor et al. (2001) Development of response-selective agonists of human C5a anaphylatoxin: Conformational, biological, and therapeutic considerations. Curr. Med. Chem. 8:675. Schlaf et al. (2003) Expression and induction of anaphylatoxin C5a receptors in rat liver. Histol. Histopathol. 18:299. Formyl Peptide Receptors Formyl Peptide Receptor (FPR-26) + co-expressed G-protein G i α 2 β 1 γ 2 complex, human, Recombinant, Sf9 insect cells Cat. No. Amount Price (€) PR-591 1 ml 300,-- Membrane suspension. Supplied in 75 mM Tris-HCl, pH 7.4, 12.5 mM MgCl 2, and 1 mM EDTA. The formyl peptide receptor (FPR) is expressed in neutrophils, couples to pertussis toxin (PTX)sensitive G i-proteins and activates phospholipase C, chemotaxis and cytotoxic cell functions. The FPR, like most GPCRs, is a type IIIb membrane protein with an extracellular N-terminus without a signal sequence. Adding a signal sequence to the N-terminus serves to direct the membrane insertion of proteins cotranslationally and enhances the production of functional GPCR protein in insect cells. The human FPR exists in various isoforms, FPR-26, FPR-98 (cat.# PR-592) and FPR-G6 (cat.# PR-593), respectively. These FPR isoforms differ from each other in amino acid positions 101 (localized at the top of the third transmembrane domain), 192 (localized in the center of the second extracellular loop) and 346 (localized at the extreme C-terminus). (FPR-26: V101, N192, E346; FPR-98: L101, N192, A346; FPR-G6: V101, K192, A346). E346 critically determines constitutive activity, G i-protein coupling and physical state of FPR-26. FPR-26 reconstituted with the G-protein G i α 2 β 1 γ 2 is constitutively active and was prepared from Sf9 cells triple-infected with FPR-, G i α 2 -, and Gβ 1 γ 2 -encoding baculoviruses. FPR-26 was constructed with a N-terminal FLAG- Tag ® and a C-terminal hexahistidine (His6)-Tag for immunological detection and protection against proteolysis and migrates as a monomer in SDS polyacrylamide electrophoresis. Protein concentration: 1.3 – 1.9 mg/ml Store: -80 °C Selected references: Wenzel-Seifert et al. (1998) High constitutive activity of the human formyl peptide receptor. J. Biol. Chem. 273:24181. Wenzel-Seifert K and Seifert R. (2003) Functional differences between human formyl peptide rceptor isoforms 26, 98 and G6. Naunyn-Schmiedeberg’s Arch. Pharmacol. 367:509. Seifert R and Wenzel-Seifert K (2001) Defective G i -protein coupling in two formyl peptide receptor mutants associated with localized juvenile periodontitis. J. Biol. Chem. 276:42043. Boulay et al. (1990) The human N-formylpeptide receptor. Characterization of two cDNA isolates and evidence for a new subfamily of G-protein-coupled receptors. Biochemistry 29:11123. http://www.jenabioscience.com Formyl Peptide Receptor (FPR-98) + co-expressed G-protein G i α 2 β 1 γ 2 complex human, Recombinant, Sf9 insect cells Cat. No. Amount Price (€) PR-592 1 ml 300,-- Membrane suspension. Supplied in 75 mM Tris-HCl, pH 7.4, 12.5 mM MgCl 2 , and 1 mM EDTA. The formyl peptide receptor (FPR) is expressed in neutrophils, couples to pertussis toxin (PTX)sensitive G i -proteins and activates phospholipase C, chemotaxis and cytotoxic cell functions. The FPR, like most GPCRs, is a type IIIb membrane protein with an extracellular N-terminus without a signal sequence. Adding a signal sequence to the N-terminus serves to direct the membrane insertion of proteins cotranslationally and enhances the production of functional GPCR protein in insect cells. The human FPR exists in various isoforms, FPR-26 (cat.# PR-591), FPR-98 and FPR-G6 (cat.# PR-593), respectively. These FPR isoforms differ from each other in amino acid positions 101 (localized at the top of the third transmembrane domain), 192 (localized in the center of the second extracellular loop) and 346 (localized at the extreme C-terminus). (FPR-26: V101, N192, E346; FPR-98: L101, N192, A346; FPR-G6: V101, K192, A346) FPR-98 reconstituted with the G-protein G i α 2 β 1 γ 2 was prepared from Sf9 cells triple-infected with FPR-, G i α 2 -, and Gβ 1 γ 2 -encoding baculoviruses. It exhibits a partial G i -protein coupling defect relative to FPR-26. FPR-98 was constructed with a N-terminal FLAG- Tag ® and a C-terminal hexahistidine (His6)-Tag for immunological detection and protection against proteolysis and migrates as dimers and tetramers in SDS polyacrylamide electrophoresis. Protein concentration: 1.3 – 4.3 mg/ml Store: -80 °C Selected references: Wenzel-Seifert, K. and Seifert, R. (2003) Functional differences between human formyl peptide rceptor isoforms 26, 98 and G6. Naunyn-Schmiedeberg’s Arch. Pharmacol. 367:509. Seifert, R. and Wenzel-Seifert, K. (2001) Defective G i -protein coupling in two formyl peptide receptor mutants associated with localized juvenile periodontitis. J. Biol. Chem. 276:42043. Gwinn et al. (1999) Single nucleotide polymorphisms of the N-formyl peptide receptor in localized juvenile periodontitis. J. Periodontol.70:1194. Wenzel-Seifert et al. (1998) High constitutive activity of the human formyl peptide receptor. J. Biol. Chem. 273:24181. Boulay et al. (1990) The human N-formylpeptide receptor. Characterization of two cDNA isolates and evidence for a new subfamily of G-protein-coupled receptors. Biochemistry 29:11123. Formyl Peptide Receptor (FPR-G6) + co-expressed G-protein G iα 2β 1γ 2 complex human, Recombinant, Sf9 insect cells Cat. No. Amount Price (€) PR-593 1 ml 300,-- Membrane suspension. Supplied in 75 mM Tris-HCl, pH 7.4, 12.5 mM MgCl 2 , and 1 mM EDTA. The formyl peptide receptor (FPR) is expressed in neutrophils, couples to pertussis toxin (PTX)sensitive G i-proteins and activates phospholipase C, chemotaxis and cytotoxic cell functions. The FPR, like most GPCRs, is a type IIIb membrane protein with an extracellular N-terminus without a signal sequence. Adding a signal sequence to the N-terminus
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JENA BIOSCIENCE Nucleotides and the
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2 Imprint: Design and Layout by: Gr
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Fax Order Form 4 Jena Bioscience Fa
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Terms/Conditions 6 General Business
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8 http://www.jenabioscience.com
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Nucleotide Analogs 10 General Infor
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Nucleotide Analogs 12 Fluorescent C
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Nucleotide Analogs 14 Labeled Amino
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Nucleotide Analogs 16 Labeled Cytid
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Nucleotide Analogs 18 Labeled γ-Am
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Nucleotide Analogs 20 Labeled with
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Nucleotide Analogs 26 Intrinsically
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Nucleotide Analogs 28 Selected refe
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Nucleotide Analogs 30 mant-GTPγS 2
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Nucleotide Analogs 32 http://www.je
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Nucleotide Analogs 34 Labeled Cytid
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Nucleotide Analogs 36 Labeled 8-[(4
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Nucleotide Analogs 38 Non-hydrolyza
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Nucleotide Analogs 40 dATPαS 2‘-
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Nucleotide Analogs 42 Selected refe
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Nucleotide Analogs 44 XTPγS Xantho
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Nucleotide Analogs 46 Bisubstrate I
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Nucleotide Analogs 48 Halogen conta
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Nucleotide Analogs 50 Hei et al. (1
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Nucleotide Analogs 52 Amine-labeled
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Nucleotide Analogs 54 Other Bases
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Nucleotide Analogs 56 dATPαS 2‘-
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Nucleotide Analogs 58 γ-Aminohexyl
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Nucleotide Analogs 60 Adenosine Nuc
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Nucleotide Analogs 62 d4TTP 2’,3
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Nucleotide Analogs 64 6-Thio-GTP 6-
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Nucleotide Analogs 66 Cyclic Nucleo
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Nucleotide Analogs 68 m 7 GTP 7-Met
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Nucleotide Analogs 70 XTP Xanthosin
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Nucleotide Analogs 72 Vial et al. (
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Nucleotide Analogs 74 Non-modifi ed
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Macromolecular Crystallography 78 C
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Macromolecular Crystallography 80 J
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Recombinant Proteins 196 CK2 substr
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Recombinant Proteins 198 PTP 1B is
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Recombinant Proteins 200 Prion Prot
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Recombinant Proteins 202 Ovine (She
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Recombinant Proteins 204 bovPrPc cD
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Recombinant Proteins 206 HIV-1 Nef
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Recombinant Proteins 208 Antioxidan
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Recombinant Proteins 210 Interleuki
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Enzymes 212 Restriction Enzymes Res
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Enzymes 214 http://www.jenabioscien
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Enzymes 216 Restriction Enzymes Buf
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Enzymes 218 Relative Activity of Re
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Enzymes 220 Acc I 5’...GTMKAC...3
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Enzymes 222 EcoR V 5’...GATATC...
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Enzymes 224 Sca I 5’...AGTACT...3
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Enzymes 226 Selected references: Br
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Enzymes 228 GST-RPB9 (RNA Polymeras
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Enzymes 230 T4 dNMP kinase Bacterio
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Enzymes 232 Topo I Core (Human DNA
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Antibodies 236 Transcription Factor
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Antibodies 238 anti-Dr1 rabbit poly
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Antibodies 240 PI3 Kinase Antibodie
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PCR related Products 244 Standard P
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PCR related Products 246 DNA Mutage
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PCR related Products 248 Polymerase
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PCR related Products 250 Primers an
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PCR related Products 252 DNA Sequen
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PCR related Products 254 50 bp DNA
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Affi nity Chromatography 256 Immobi
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Affi nity Chromatography 260 γ-Ami
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Affi nity Chromatography 264 γ-Ami
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Affi nity Chromatography 268 2’/3
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Index 270 Product Catalog number Pa
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Index 272 Labeled 5-Propargylamino-
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Index 274 Labeled EDA-ATP + 5-FAM..
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Index 276 Labeled γ-Aminooctyl-dUT
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Index 278 Constitutive LEXSY Starte
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Index 280 PrPc (full length, residu
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Index 282 dPTP, L pack ............
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Index 284 Catalog number Product Pa
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Index 286 CC-105 JBScreen Cryo 3 ..
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Index 288 NU-1014L NTP bundle (larg
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Index 290 NU-407S AppNHp (AMPPNP) .
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Index 292 NU-810-540Q Labeled EDA-A
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Index 294 NU-819L γ-Aminoethyl-App
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Index 296 PR-306 RCC1 (RanGEF) ....
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Nucleotide Analogs - Jena Bioscience

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