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Pd145305

Manufactured by Peptide Institute
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PD145305 is an analytical laboratory instrument used for the analysis and characterization of peptides and proteins. It is designed to provide precise and accurate measurements of molecular properties such as mass, purity, and composition. The core function of PD145305 is to support researchers and scientists in the field of peptide and protein research, enabling them to gather critical data for their studies.

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Lab products found in correlation

Ruthenium red, by Merck Group (2 mentions) Gsmtx 4, by Peptide Institute (2 mentions) Pd150606, by Merck Group (2 mentions) Pd151746, by Santa Cruz Biotechnology (2 mentions) L nmma n methyl l arginine, by Merck Group (2 mentions) Cn585, by Merck Group (2 mentions)

2 protocols using pd145305

1

Inhibition of Cell Activity

Check if the same lab product or an alternative is used in the 5 most similar protocols
GsMTx4, a toxin from the tarantula Grammostola spatulata, was from Peptide Institute Inc. PD145305 (3-phenyl-2-sulfanylpropanoic acid) and PD151746 (3-(5-fluoro-3-indolyl)-2-mercapto-(Z)-2-propenoic acid) were from Santa Cruz Biotechnology. PD150606 (3-(4-iodophenyl)-2-mercapto-(Z)-2-propenoic acid), CK59 (2-(2-hydroxyethylamino)-6-aminohexylcarbamic acid tert-butyl ester-9-isopropylpurine) and CN585 (6-(3,4-dichlorophenyl)-4-(N,N-dimethylaminoethylthio)-2-phenyl-pyrimidine) were from EMD Millipore. L-NMMA (N-methyl-L-arginine) and ruthenium red were from Sigma-Aldrich. The solvent for each stock solution was dimethylsulphoxide except in the cases of GsMTx4, ruthenium red and L-NMMA when it was water. Inhibitors were pre-incubated with cells for 1 h prior to evoking cell activity.
Li J., Hou B., Tumova S., Muraki K., Bruns A., Ludlow M.J., Sedo A., Hyman A.J., McKeown L., Young R.S., Yuldasheva N.Y., Majeed Y., Wilson L.A., Rode B., Bailey M.A., Kim H.R., Fu Z., Carter D.A., Bilton J., Imrie H., Ajuh P., Dear T.N., Cubbon R.M., Kearney M.T., Prasad R.K., Evans P.C., Ainscough J.F, & Beech D.J. (2014). Piezo1 integration of vascular architecture with physiological force. Nature, 515(7526), 279-282.
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2

Inhibition of Cell Activity

Check if the same lab product or an alternative is used in the 5 most similar protocols
GsMTx4, a toxin from the tarantula Grammostola spatulata, was from Peptide Institute Inc. PD145305 (3-phenyl-2-sulfanylpropanoic acid) and PD151746 (3-(5-fluoro-3-indolyl)-2-mercapto-(Z)-2-propenoic acid) were from Santa Cruz Biotechnology. PD150606 (3-(4-iodophenyl)-2-mercapto-(Z)-2-propenoic acid), CK59 (2-(2-hydroxyethylamino)-6-aminohexylcarbamic acid tert-butyl ester-9-isopropylpurine) and CN585 (6-(3,4-dichlorophenyl)-4-(N,N-dimethylaminoethylthio)-2-phenyl-pyrimidine) were from EMD Millipore. L-NMMA (N-methyl-L-arginine) and ruthenium red were from Sigma-Aldrich. The solvent for each stock solution was dimethylsulphoxide except in the cases of GsMTx4, ruthenium red and L-NMMA when it was water. Inhibitors were pre-incubated with cells for 1 h prior to evoking cell activity.
Li J., Hou B., Tumova S., Muraki K., Bruns A., Ludlow M.J., Sedo A., Hyman A.J., McKeown L., Young R.S., Yuldasheva N.Y., Majeed Y., Wilson L.A., Rode B., Bailey M.A., Kim H.R., Fu Z., Carter D.A., Bilton J., Imrie H., Ajuh P., Dear T.N., Cubbon R.M., Kearney M.T., Prasad R.K., Evans P.C., Ainscough J.F, & Beech D.J. (2014). Piezo1 integration of vascular architecture with physiological force. Nature, 515(7526), 279-282.
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