research use only
Cat.No.S3028
| Related Targets | Integrase Bacterial Anti-infection Fungal Antiviral COVID-19 Parasite Reverse Transcriptase HIV HCV Protease |
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| Other Antibiotics Inhibitors | Puromycin Nanchangmycin Sitafloxacin Hydrate Fusidine Gamithromycin Thiamphenicol Tildipirosin Spiramycin Nadifloxacin 6-Aminopenicillanic acid |
| Cell Lines | Assay Type | Concentration | Incubation Time | Formulation | Activity Description | PMID |
|---|---|---|---|---|---|---|
| GES-1 cells | Function assay | be used to select and expand the G418-resistant colonies | 29963172 | |||
| A549 cells | Cell viability assay | 100-1200 μg/ml | IC50=494.1 μg/ml | 30594785 | ||
| Sf21 cells | Function assay | 60 mins | Inhibition of ribosomal activity in Spodoptera frugiperda Sf21 cells assessed as inhibition of translation after 60 mins by fluorescence assay, IC50 = 2 μM. | 20409719 | ||
| Click to View More Cell Line Experimental Data | ||||||
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In vitro |
Water : 100 mg/mL
DMSO
: Insoluble
Ethanol : Insoluble |
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In vivo |
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Step 2: Enter the in vivo formulation (This is only the calculator, not formulation. Please contact us first if there is no in vivo formulation at the solubility Section.)
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Working concentration: mg/ml;
Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )
Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.
Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.
Note: 1. Please make sure the liquid is clear before adding the next solvent.
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| Molecular Weight | 692.71 | Formula | C20H40N4O10.2H2SO4 |
Storage (From the date of receipt) | |
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| CAS No. | 108321-42-2 | Download SDF | Storage of Stock Solutions |
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| Synonyms | N/A | Smiles | CC(C1C(C(C(C(O1)OC2C(CC(C(C2O)OC3C(C(C(CO3)(C)O)NC)O)N)N)N)O)O)O.OS(=O)(=O)O.OS(=O)(=O)O | ||
| In vitro |
G418 is an inhibitor of many pro- and eukaryotes at concentrations from 1-300 microgram/ml. Resistance to G418 conferring by the neo gene from Tn5 encoding an aminoglycoside 3'-phosphotransferase, APT 3' II is commonly used in laboratory research to select genetically engineered cells. In general for bacteria and algae concentrations of 5 mg/L or less are used, for mammalian cells concentrations of approximately 400 mg/L are used for selection and 200 mg/L for maintenance. Resistant clones selection could require from 1 to up to 3 weeks. |
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| In vivo |
Doses of G418 of between 40 and 80 mg/kg for three consecutive days are sufficient to eliminate all nontransfected T. brucei brucei parasites from infected mice. |
References |
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