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Ml239

Manufactured by Merck Group
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The ML239 is a laboratory equipment product manufactured by Merck Group. It is a device designed for use in various scientific applications. The core function of the ML239 is to perform precise measurements and analyses within a laboratory setting. Further details on the intended use or specific applications of this product are not available.

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Lab products found in correlation

Ferrostatin 1, by Merck Group (2 mentions) Nsc23766, by Merck Group (2 mentions) Mk571, by Bio-Techne (2 mentions) Cp100356, by Merck Group (2 mentions) Sc 26196, by Bio-Techne (2 mentions) N acetyl l cysteine, by Merck Group (2 mentions) α tocopherol, by Merck Group (2 mentions) Quercetin, by Bio-Techne (2 mentions) Jzl184, by Cayman Chemical (2 mentions) Obatoclax mesylate, by Selleck Chemicals (2 mentions) Ym155, by Selleck Chemicals (2 mentions) Elacridar, by Merck Group (2 mentions) Ml210, by Merck Group (2 mentions)

2 protocols using ml239

1

Small Molecule Acquisition and Preparation

Check if the same lab product or an alternative is used in the 5 most similar protocols
JZL184 (Cat. no. 13158; ≥97% purity) was purchased from Cayman Chemical. ML239 (SML0442; ≥98%), NSC23766 (SML0952; ≥97%), CP-100356 (PZ0171; ≥98%), elacridar (SML0486; ≥98%), ML210 (SML0521; ≥98%), ferrostatin-1 (SML0583; ≥95%), α-tocopherol (T3251; ≥99%), and N-acetyl-L-cysteine (A7250; ≥99%) were purchased from Sigma. YM-155 (S1130; ≥99%), obatoclax mesylate (S1057; ≥99%), and RITA (S2781; 99%) were purchased from SelleckChem. SC-26196 (4189; 99.2%), quercetin (1125; >98%), and MK-571 (2238; >96.9%) were purchased from Tocris. Austocystin D was purchased from eMolecules. The selective CYP2J2 inhibitor 1-(4-bromophenyl)-4-[4-(hydroxydiphenylmethyl)piperidin-1-yl]butan-1-one was synthesized in-house according to the published methodology (>95% purity)48 (link). All small molecules were dissolved in DMSO, except N-acetylcysteine, which was dissolved in cell culture medium then adjusted to pH 7.5.
Rees M.G., Seashore-Ludlow B., Cheah J.H., Adams D.J., Price E.V., Gill S., Javaid S., Coletti M.E., Jones V.L., Bodycombe N.E., Soule C.K., Alexander B., Li A., Montgomery P., Kotz J.D., Hon C.S., Munoz B., Liefeld T., Dančík V., Haber D.A., Clish C.B., Bittker J.A., Palmer M., Wagner B.K., Clemons P.A., Shamji A.F, & Schreiber S.L. (2015). Correlating chemical sensitivity and basal gene expression reveals mechanism of action. Nature chemical biology, 12(2), 109-116.
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2

Small Molecule Acquisition and Preparation

Check if the same lab product or an alternative is used in the 5 most similar protocols
JZL184 (Cat. no. 13158; ≥97% purity) was purchased from Cayman Chemical. ML239 (SML0442; ≥98%), NSC23766 (SML0952; ≥97%), CP-100356 (PZ0171; ≥98%), elacridar (SML0486; ≥98%), ML210 (SML0521; ≥98%), ferrostatin-1 (SML0583; ≥95%), α-tocopherol (T3251; ≥99%), and N-acetyl-L-cysteine (A7250; ≥99%) were purchased from Sigma. YM-155 (S1130; ≥99%), obatoclax mesylate (S1057; ≥99%), and RITA (S2781; 99%) were purchased from SelleckChem. SC-26196 (4189; 99.2%), quercetin (1125; >98%), and MK-571 (2238; >96.9%) were purchased from Tocris. Austocystin D was purchased from eMolecules. The selective CYP2J2 inhibitor 1-(4-bromophenyl)-4-[4-(hydroxydiphenylmethyl)piperidin-1-yl]butan-1-one was synthesized in-house according to the published methodology (>95% purity)48 (link). All small molecules were dissolved in DMSO, except N-acetylcysteine, which was dissolved in cell culture medium then adjusted to pH 7.5.
Rees M.G., Seashore-Ludlow B., Cheah J.H., Adams D.J., Price E.V., Gill S., Javaid S., Coletti M.E., Jones V.L., Bodycombe N.E., Soule C.K., Alexander B., Li A., Montgomery P., Kotz J.D., Hon C.S., Munoz B., Liefeld T., Dančík V., Haber D.A., Clish C.B., Bittker J.A., Palmer M., Wagner B.K., Clemons P.A., Shamji A.F, & Schreiber S.L. (2015). Correlating chemical sensitivity and basal gene expression reveals mechanism of action. Nature chemical biology, 12(2), 109-116.
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