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Cvt6883

Manufactured by Merck Group
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Sourced in United States

The CVT6883 is a laboratory instrument designed for analytical applications. It is capable of performing various measurements and analyses within a controlled laboratory environment. The core function of the CVT6883 is to provide accurate and reliable data to support scientific research and product development.

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Lab products found in correlation

Trypsin inhibitor, by Thermo Fisher Scientific (2 mentions) Mrs1754, by Merck Group (2 mentions) Sch58261, by Merck Group (2 mentions) Hank s balanced salt solution, by Thermo Fisher Scientific (2 mentions) Substance p, by Merck Group (2 mentions) Ppads, by Merck Group (2 mentions) Adenosine deaminase ada u46619 9 11 dideoxy 11α 9α epoxymethanoprostaglandin f2α, by Merck Group (2 mentions) Fetal bovine serum (fbs), by Thermo Fisher Scientific (2 mentions) Antibiotic antimycotic, by Thermo Fisher Scientific (2 mentions) Collagenase type 1, by Thermo Fisher Scientific (2 mentions) Dmem medium, by Thermo Fisher Scientific (2 mentions)

2 protocols using cvt6883

1

Pharmacological Modulation of Purinergic Signaling

Check if the same lab product or an alternative is used in the 5 most similar protocols
SCH58261, PPADS (pyridoxalphosphate-6-azophenyl-2′,4′-disulfonic acid), MRS1754, CVT6883, catalase-polyethylene glycol (Catalase), Glibenclamide, adenosine deaminase (ADA), U46619 (9,11-dideoxy-11α,9α epoxymethanoprostaglandin F2α), and substance P were all purchased from Sigma–Aldrich (Ann Arbor, MI, USA). Up4A was obtained from Biolog Life Science (Bremen, Germany). SCH58261, MRS1754 and CVT6883 were firstly dissolved in DMSO. All subsequent dilutions (at least 1000 fold) and other drugs were obtained with distilled water. PPADS was protected from light. For the cell culture, Hanks’ balanced salt solution, DMEM medium, fetal bovine serum (FBS), antibiotic-antimycotic, collagenase type I, and trypsin inhibitor were purchased from GIBCO (Carlsbad, CA, USA).
Sun C., Jiao T., Merkus D., Duncker D.J., Mustafa S.J, & Zhou Z. (2019). Activation of adenosine A2A but not A2B receptors is involved in uridine adenosine tetraphosphate-induced porcine coronary smooth muscle relaxation. Journal of pharmacological sciences, 141(1), 64-69.
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2

Pharmacological Modulation of Purinergic Signaling

Check if the same lab product or an alternative is used in the 5 most similar protocols
SCH58261, PPADS (pyridoxalphosphate-6-azophenyl-2′,4′-disulfonic acid), MRS1754, CVT6883, catalase-polyethylene glycol (Catalase), Glibenclamide, adenosine deaminase (ADA), U46619 (9,11-dideoxy-11α,9α epoxymethanoprostaglandin F2α), and substance P were all purchased from Sigma–Aldrich (Ann Arbor, MI, USA). Up4A was obtained from Biolog Life Science (Bremen, Germany). SCH58261, MRS1754 and CVT6883 were firstly dissolved in DMSO. All subsequent dilutions (at least 1000 fold) and other drugs were obtained with distilled water. PPADS was protected from light. For the cell culture, Hanks’ balanced salt solution, DMEM medium, fetal bovine serum (FBS), antibiotic-antimycotic, collagenase type I, and trypsin inhibitor were purchased from GIBCO (Carlsbad, CA, USA).
Sun C., Jiao T., Merkus D., Duncker D.J., Mustafa S.J, & Zhou Z. (2019). Activation of adenosine A2A but not A2B receptors is involved in uridine adenosine tetraphosphate-induced porcine coronary smooth muscle relaxation. Journal of pharmacological sciences, 141(1), 64-69.
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