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Nucleotide Analogs - Jena Bioscience

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Recombinant Proteins<br />

192<br />

p42/ERK2/MAPK2 His , inactive<br />

(Extracellular signal-regulated<br />

Kinase/mitogen-activated<br />

protein kinase2)<br />

Rat, Recombinant, E. coli<br />

Cat. No. Amount Price (€)<br />

PR-320 50 µg 160,--<br />

Liquid. Supplied as 1 mg/ml solution in 10 mM<br />

HEPES, pH 7.5, 150 mM NaCl, 0.1 mM EDTA, 1 mM<br />

DTT, and 0.5% n-Octyl-β-D-Glucopyranoside.<br />

Whole sequence with N-terminal His-Tag, inactive.<br />

Extracellular signal-regulated kinase ERK2 is the<br />

key component of the mitogen-activated protein<br />

(MAP) kinase cascade. It plays an essential role in<br />

mitogenesis, differentiation, and cellular transformation<br />

in response to various stimuli such as growth factors.<br />

Purity: > 95% by SDS-PAGE.<br />

Store: -80 °C<br />

Selected reference:<br />

Boulton et al. (1991) ERK´s: a family of protein-serine/threonine<br />

kinases that are activated and tyrosine phosphorylated in<br />

response to insulin and NGF. Cell 65:663.<br />

p44/ERK1/MAPK1 His , active<br />

(extracellular signal-regulated<br />

kinase1/mitogen-activated<br />

protein kinase1)<br />

human, Recombinant, E. coli<br />

Cat. No. Amount Price (€)<br />

PR-322 2.5 µg 240,--<br />

Supplied in 50 mM Tris-HCl pH 8.5, 150 mM NaCl,<br />

1 mM DTT, 50% glycerol.<br />

N-terminal His-tagged full-length protein.<br />

Members of the MAPK families play an important<br />

role in complex cellular programs like proliferation,<br />

differentiation, development, transformation, and<br />

apoptosis. At least three MAPK families have been<br />

characterized: extracellular signal-regulated kinase<br />

(ERK), Jun kinase (JNK/SAPK) and p38 MAPK.<br />

MAPK pathways relay, amplify and integrate signals<br />

from a diverse range of stimuli and elicit an appropriate<br />

physiological response including cellular proliferation,<br />

differentiation, development, infl ammatory responses<br />

and apoptosis in mammalian cells.<br />

Activated ERK can enter the nucleus and<br />

phosphorylate transcription factors providing the link<br />

between cell surface receptor-mediated events and<br />

nuclear induction of gene expression. In the nucleus<br />

activated ERK promotes the transcription and the<br />

activity of transcription factors c-fos, c-myc, c-jun<br />

and p21.<br />

The recombinant human ERK1 was expressed in<br />

E. coli and purifi ed by Ni-agarose chromatography. It<br />

is suitable for labeling ERK1/MAPK1 substrates. The<br />

highly active form is produced by phosphorylation of<br />

the protein in vitro with MEK1. The sequence based<br />

calculated molecular weight is 43.62 kDa.<br />

Purity: > 95% by SDS-PAGE<br />

Specifi c activity: > 15,000 U/mg (1 Unit is defi ned<br />

as 1 picomole phosphate transferred to myelin basic<br />

protein per min at 30°C)<br />

Store: -80 °C<br />

Selected references:<br />

Zhang W. and Liu H.T. (2002) MAPK signal pathways in the<br />

regulation of cell proliferation in mammalian cells. Cell Res.<br />

12:9.<br />

Ajenjo et al. (2004) Subcellular localization determines<br />

the protective effects of activated ERK2 against distinct<br />

apoptogenic stimuli in myeloid leukemic cells. J. Biol. Chem.<br />

279:32813.<br />

p44/ERK1/MAPK1 His , inactive<br />

(extracellular signal-regulated<br />

kinase/mitogen-activated<br />

protein kinase)<br />

human, Recombinant, E. coli<br />

Cat. No. Amount Price (€)<br />

PR-323 5 µg 160,--<br />

Supplied in 50 mM Tris-HCl pH 8.5, 150 mM NaCl,<br />

1 mM DTT, 50% glycerol.<br />

N-terminal His-tagged full-length protein.<br />

MAPK families play an important role in complex<br />

cellular programs like proliferation, differentiation,<br />

development, transformation, and apoptosis. At<br />

least three MAPK families have been characterized:<br />

extracellular signal-regulated kinase (ERK), Jun<br />

kinase (JNK/SAPK) and p38 MAPK.<br />

MAPK pathways relay, amplify and integrate signals<br />

from a diverse range of stimuli and elicit an appropriate<br />

physiological response including cellular proliferation,<br />

differentiation, development, infl ammatory responses<br />

and apoptosis in mammalian cells.<br />

Activated ERK can enter the nucleus and<br />

phosphorylate transcription factors providing the link<br />

between cell surface receptor-mediated events and<br />

nuclear induction of gene expression. In the nucleus<br />

activated ERK promotes the transcription and the<br />

activity of transcription factors c-fos, c-myc, c-jun<br />

and p21.<br />

The recombinant human ERK1 was expressed in<br />

E. coli. The sequence based calculated molecular<br />

weight is 43.62 kDa.<br />

Purity: > 95% by SDS-PAGE<br />

Store: -80 °C<br />

Selected references:<br />

Zhang W. and Liu H.T. (2002) MAPK signal pathways in the<br />

regulation of cell proliferation in mammalian cells. Cell Res.<br />

12:9.<br />

Ajenjo et al. (2004) Subcellular localization determines<br />

the protective effects of activated ERK2 against distinct<br />

apoptogenic stimuli in myeloid leukemic cells. J. Biol. Chem.<br />

279:32813.<br />

http://www.jenabioscience.com<br />

Calcium/Calmodulin<br />

Dependent Kinases<br />

(CAMK Family)<br />

Free calcium is a major second messenger in<br />

all cell types. One mechanism by which calcium<br />

ions exert their function is by binding to a<br />

17 kDa protein, called calmodulin (CaM). The<br />

binding of four calcium ions to CaM changes its<br />

conformation and thereby activates a number<br />

of other proteins such as various classes of<br />

serine/threonine protein kinases. A practical<br />

way of classifying the calcium/CaM-dependent<br />

protein kinases is based on their substrate specifi<br />

city: some of these enzymes have only one<br />

substrate, and are designated as ‘dedicated’<br />

calcium/CaM-dependent protein kinases, while<br />

others have broad substrate specifi city and are<br />

termed ‘multifunctional’ kinases.<br />

CHK2 His , active<br />

(Checkpoint kinase)<br />

human, Recombinant, Sf9<br />

insect cells<br />

Cat. No. Amount Price (€)<br />

PR-313 20 µg 240,--<br />

Supplied in 50 mM Tris-HCl pH 7.5, 150 mM NaCl,<br />

10 mM DTT, 0.1 mM EGTA, 270 mM sucrose,<br />

protease inhibitor cocktail (Roche).<br />

C-terminal His-tagged full-length protein.<br />

Checkpoint kinase 2 (CHK2) is emerging as a key<br />

mediator of diverse cellular responses to genotoxic<br />

stress, guarding the integrity of the genome<br />

throughout eukaryotic evolution. Recent studies<br />

show the fundamental role of CHK2 in the network of<br />

genome-surveillance pathways that coordinate cellcycle<br />

progression with DNA repair and cell survival or<br />

death. Defects in CHK2 contribute to the development<br />

of both hereditary and sporadic human cancers, and<br />

earmark this kinase as a candidate tumour suppressor<br />

and an attractive target for drug discovery.<br />

The recombinant human CHK2 was expressed in<br />

Sf9 insect cells and purifi ed by Ni-NTA agarose<br />

chromatography. It is suitable for labeling CHK<br />

substrates. The sequence based calculated molecular<br />

weight is 66.06 kDa.<br />

Purity: > 95% by SDS-PAGE<br />

Specifi c activity: > 25,000 U/mg (1 Unit is defi ned as<br />

1 picomole phosphate transferred to synthetic peptide<br />

KKKVSRSGLYRSPSMPENLNRPR (cat.# PE-205)<br />

per min at 30°C)<br />

Store: -80 °C<br />

Selected references:<br />

Bartek et al. (2001) CHK2 kinase--a busy messenger. Nat. Rev.<br />

Mol. Cell Biol. 12:877.<br />

Gire et al. (2004) DNA damage checkpoint kinase Chk2 triggers<br />

replicative senescence. EMBO J. 23:2554.

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