Tube made of polypropylene Cap made of polyethylene The SnapTwist&trade Micrewtube® provides all the advantages of a modern microcentrifuge tube with screw cap but the closure is a true time saver. The SnapTwist&trade Micrewtube® has a
Tube made of polypropylene Cap made of polyethylene The SnapTwist&trade Micrewtube® provides all the advantages of a modern microcentrifuge tube with screw cap but the closure is a true time saver. The SnapTwist&trade Micrewtube® has a
4ml External Thread, Freestanding Cryovial, Sterile, Silicone Seal 100/Bag, PP, Certified DNase, RNase, Pyrogen and DNA Free. Autoclavable, Temp as Low as -196 Degree C.
4ml External Thread, Freestanding Cryovial, Sterile, Silicone Seal 100/Bag, PP, Certified DNase, RNase, Pyrogen and DNA Free. Autoclavable, Temp as Low as -196 Degree C.
9(R)-HODE is one of several monohydroxylated products of linoleic acid. All known mammalian lipoxygenases appear to catalyze the oxygenation of arachidonic and linoleic acid to give products having strictly the (S) configuration at the site of
9(R)-HODE is one of several monohydroxylated products of linoleic acid. All known mammalian lipoxygenases appear to catalyze the oxygenation of arachidonic and linoleic acid to give products having strictly the (S) configuration at the site of
13(S)-HODE-d4 contains four deuterium atoms at the 9, 10, 12, and 13 positions. It is intended for use as an internal standard for the quantification of 13(S)-HODE by GC- or LC-MS.
13(S)-HODE-d4 contains four deuterium atoms at the 9, 10, 12, and 13 positions. It is intended for use as an internal standard for the quantification of 13(S)-HODE by GC- or LC-MS.
13(R)-HODE is the opposite enantiomer of the 13(S)-HODE produced when linoleic acid is incubated with soybean LO. The presence of 13(R)-HODE in the supernatants and membranes of cultured bovine endothelial cells has been attributed to COX metabolism.
13(R)-HODE is the opposite enantiomer of the 13(S)-HODE produced when linoleic acid is incubated with soybean LO. The presence of 13(R)-HODE in the supernatants and membranes of cultured bovine endothelial cells has been attributed to COX metabolism.
9(R)-HODE is one of several monohydroxylated products of linoleic acid. All known mammalian lipoxygenases appear to catalyze the oxygenation of arachidonic and linoleic acid to give products having strictly the (S) configuration at the site of
9(R)-HODE is one of several monohydroxylated products of linoleic acid. All known mammalian lipoxygenases appear to catalyze the oxygenation of arachidonic and linoleic acid to give products having strictly the (S) configuration at the site of
13(R)-HODE is the opposite enantiomer of the 13(S)-HODE produced when linoleic acid is incubated with soybean LO. The presence of 13(R)-HODE in the supernatants and membranes of cultured bovine endothelial cells has been attributed to COX metabolism.
13(R)-HODE is the opposite enantiomer of the 13(S)-HODE produced when linoleic acid is incubated with soybean LO. The presence of 13(R)-HODE in the supernatants and membranes of cultured bovine endothelial cells has been attributed to COX metabolism.
A staurosporine analog that potently inhibits JAK2 kinase (IC<sub>50</sub> = 1 nM) and downstream targets STAT5 (IC<sub>50</sub> = 10-30 nM) and STAT3 in a human erythroleukemic cell line expressing the JAK2V617F mutation potently inhibits the
A staurosporine analog that potently inhibits JAK2 kinase (IC<sub>50</sub> = 1 nM) and downstream targets STAT5 (IC<sub>50</sub> = 10-30 nM) and STAT3 in a human erythroleukemic cell line expressing the JAK2V617F mutation potently inhibits the
9(R)-HODE is one of several monohydroxylated products of linoleic acid. All known mammalian lipoxygenases appear to catalyze the oxygenation of arachidonic and linoleic acid to give products having strictly the (S) configuration at the site of
9(R)-HODE is one of several monohydroxylated products of linoleic acid. All known mammalian lipoxygenases appear to catalyze the oxygenation of arachidonic and linoleic acid to give products having strictly the (S) configuration at the site of
A labeled analog of AEA that is non-fluorescent when outside the cell but upon transport into the cell, is cleaved by esterases to give a bright fluorescence at 530 nm used as an alternative substrate to study AEA transport via the AEA transporter.
A labeled analog of AEA that is non-fluorescent when outside the cell but upon transport into the cell, is cleaved by esterases to give a bright fluorescence at 530 nm used as an alternative substrate to study AEA transport via the AEA transporter.