Sucrose standards

General Composition: Each liter of concentrate makes 20 L of 1X SSPE buffer (1X = 0.150 M Sodium Chloride, 0.

Molecular biology grade. Specifications: DNase: None detected Heavy metals (as Pb): 0.

Molecular biology grade. Specifications: DNase: None detected Heavy metals (as Pb): 0.

Molecular biology grade. Specifications: Clarity: To pass test DNase: None detected Protease: None detected RNase: None detected Sterility: To pass test Intended for laboratory and manufacturing use only.

Polysucrose is water-soluble, nontoxic, resistant to intestinal enzymes, spherical and can be produced with a molecular weight distribution that relates to the size of many normal food proteins. It is a nonionic synthetic polymer of sucrose.

Polysucrose is water-soluble, nontoxic, resistant to intestinal enzymes, spherical and can be produced with a molecular weight distribution that relates to the size of many normal food proteins. It is a nonionic synthetic polymer of sucrose.

Polysucrose is water-soluble, nontoxic, resistant to intestinal enzymes, spherical and can be produced with a molecular weight distribution that relates to the size of many normal food proteins. It is a nonionic synthetic polymer of sucrose.

A potent, cell-permeable, reversible, ATP-competitive, and selective protein kinase C inhibitor (IC 50 = 15 nM for rat brain PKC). Exhibits some degree of isozyme specificity (IC 50 = 8 nM for PKC &#945 , 8 nM for PKC &#946I , 14 nM for PKC

A selective cell-permeable protein kinase C inhibitor. Displays about 10-fold greater selectivity for PKC &#945 (IC 50 = 9 nM) and 4-fold greater selectivity for PKC &#946I (IC 50 = 28 nM) over PKC &#949 (IC 50 = 108 nM).

A cell-permeable, selective inhibitor of cAMP-specific phosphodiesterase (PDE IV IC 50 = 800 nM). A rolipram-insensitive PDE IV subtype is also known to exist.

A cell-permeable quinolinecarboxamide compound that is shown to inhibit the mitochondrial SIRT3 in a substrate AceCS2- (Acetyl-CoA synthetase 2) competitive ( K i = 0.56 &#181M K m = 2.

A cell-permeable pyrrole-indolinone compound that acts as a potent, reversible, and ATP-competitive tyrosine kinase receptor and angiogenic inhibitor that exhibits greater selectivity for PDGFR&#946 (IC 50 = 3 nM), VEGFR2 (IC 50 = 27 nM), FGFR1