Jumo 4Adi-55
SS grid for size 55 and 75 and HCP50 - EACH |
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| CHA4020 | Scientific Laboratory Supplies | EACH | EUR 159.3 |
4Adi Laboratories manufactures the jumo 4adi-55 reagents distributed by Genprice. The Jumo 4Adi-55 reagent is RUO (Research Use Only) to test human serum or cell culture lab samples. To purchase these products, for the MSDS, Data Sheet, protocol, storage conditions/temperature or for the concentration, please contact 4Adi. Other Jumo products are available in stock. Specificity: Jumo Category: 4Adi-55
True Blue Chloride |
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| Toronto Research Chemicals | 100mg | EUR 11200 |
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Description: 71431-30-6 |
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True Blue Chloride |
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| Toronto Research Chemicals | 100 mg | Ask for price |
True Blue Diaceturate Salt |
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| Toronto Research Chemicals | 100mg | EUR 15000 |
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Description: 108321-12-6 |
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True north Cryobox1.5/2mLNatural |
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| Scientific Laboratory Supplies | PK10 | EUR 129.6 |
True Blue Diaceturate Salt |
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| Toronto Research Chemicals | 100 mg | Ask for price |
SS grid for size 55 and 75 and HCP50 - EACH |
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| Scientific Laboratory Supplies | EACH | EUR 159.3 |
True Blue (TB) Diaceturate Salt |
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| Polysciences Europe GmbH | 1mg | Ask for price |
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Description: 108321-12-6 |
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MBM-55 |
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| HY-101029 | MedChemExpress | 1 mg | EUR 411.26 |
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Description: MBM-55 is a potent NIMA-related kinase 2 (Nek2) inhibitor with an IC50 of 1 nM. MBM-55 shows a 20-fold or greater selectivity in most kinases with the exception of RSK1 (IC50=5.4 nM) and DYRK1a (IC50=6.5 nM). MBM-55 effectively inhibits the proliferation of cancer cells by inducing cell cycle arrest and apoptosis. MBM-55 shows antitumor activities, and no obvious toxicity to mice[1]. |
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JW 55 |
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| HY-13968 | MedChemExpress | 10mg | EUR 270.57 |
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Description: JW 55 is a potent and selective β-catenin signaling pathway inhibitor, which functions via inhibition of the PARP domain of tankyrase 1 and tankyrase 2 (TNKS1/2). JW 55 decreases auto-PARsylation of TNKS1/2 in vitro with IC50s of 1.9 μM and 830 nM respectively. |
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PI-55 |
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| HY-141519 | MedChemExpress | 10 mg | EUR 1969.73 |
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Description: PI-55 is a specific cytokinin receptor inhibitor. PI-55 is structurally related to 6-benzylaminopurine (BAP) and was shown to inhibit competitively BAP binding on Arabidopsis-specific receptors CRE1/AHK4 and AHK3. PI-55 inhibits cytokinins induced haustorium formation and increased parasite aggressiveness[1]. |
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JW 55 |
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| MBS384968-100mg | MyBiosource | 100mg | EUR 655 |
JW 55 |
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| MBS384968-10mg | MyBiosource | 10mg | EUR 180 |
JW 55 |
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| MBS384968-25mg | MyBiosource | 25mg | EUR 245 |
JW 55 |
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| MBS384968-50mg | MyBiosource | 50mg | EUR 405 |
JW 55 |
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| MBS384968-5x100mg | MyBiosource | 5x100mg | EUR 2950 |
MBM-55 |
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| MBS387262-10mg | MyBiosource | 10mg | EUR 1905 |
MBM-55 |
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| MBS387262-1mg | MyBiosource | 1mg | EUR 430 |
MBM-55 |
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| MBS387262-5mg | MyBiosource | 5mg | EUR 1165 |
MBM-55 |
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| MBS387262-5x10mg | MyBiosource | 5x10mg | EUR 8565 |
MZP-55 |
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| MBS3843870-10mg | MyBiosource | 10mg | EUR 985 |
MZP-55 |
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| MBS3843870-1mg | MyBiosource | 1mg | EUR 240 |
MZP-55 |
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| MBS3843870-50mg | MyBiosource | 50mg | EUR 3275 |
MZP-55 |
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| MBS3843870-5mg | MyBiosource | 5mg | EUR 655 |
MZP-55 |
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| MBS3843870-5x50mg | MyBiosource | 5x50mg | EUR 14725 |
