Living Organisms
PLANT CELL TECHNOLOGY Plant Preservative Mixture (PPM™), Broad-spectrum biocide/fungicide, 0.05% - 0.2% v/v, Heat stable at 121°C, Completely soluble in water, Storage at 4°C
The Plant Preservative Mixture (PPM™) from Plant Cell Technology is a heat-stable biocide and fungicide formulated to control microbial contamination in *in vitro* plant tissue cultures. It effectively prevents the germination and growth of harmful microorganisms while preserving critical plant development processes, making it a cost-effective alternative to traditional antibiotics. PPM™ simplifies integration into media preparation protocols and enhances the success rates of culture experiments by managing various types of contamination.
- Broad-spectrum efficacy against bacteria, fungi, yeasts, and molds
- Heat stable; effective after autoclaving at 121°C for 20 min
- Non-phytotoxic at recommended doses
- Reduces airborne, waterborne, and human-introduced contamination
- Economically priced compared to conventional antibiotics
- Targets key microbial enzymatic pathways to reduce resistance
Cayman Chemical HarmalolhydrochlorIde hydra 1g
A β-carboline alkaloid and an active metabolite of harmaline; an inhibitor of DYRK1A (IC50 = 0.63 µM); an inhibitor of MAO-A (IC50 = 0.66 µM); selective for DYRK1A over Cdk1, Cdk5, CK1α1, Clk4, DYRK2, Pim-1, and GSK3β but also inhibits DYRK1B and Clk1 at 10 µM; inhibits proliferation of H4 human glioblastoma cells (IC50s = 23.7 µM); reduces TCDD-induced increases in CYP1A1 levels in HepG2 cells and prevents TCDD-induced activation of AhR in guinea pig hepatic cytosolic extracts; reduces glutamate-induced cytotoxicity, cytochrome c release, caspase-3 activation, and ROS production in PC12 cells at 25 µM
Cayman Chemical Harmalol hydrochloride hydra
A β-carboline alkaloid and an active metabolite of harmaline; an inhibitor of DYRK1A (IC50 = 0.63 µM); an inhibitor of MAO-A (IC50 = 0.66 µM); selective for DYRK1A over Cdk1, Cdk5, CK1α1, Clk4, DYRK2, Pim-1, and GSK3β but also inhibits DYRK1B and Clk1 at 10 µM; inhibits proliferation of H4 human glioblastoma cells (IC50s = 23.7 µM); reduces TCDD-induced increases in CYP1A1 levels in HepG2 cells and prevents TCDD-induced activation of AhR in guinea pig hepatic cytosolic extracts; reduces glutamate-induced cytotoxicity, cytochrome c release, caspase-3 activation, and ROS production in PC12 cells at 25 µM
Cayman Chemical Harmalol hydrochloride hydra
A β-carboline alkaloid and an active metabolite of harmaline; an inhibitor of DYRK1A (IC50 = 0.63 µM); an inhibitor of MAO-A (IC50 = 0.66 µM); selective for DYRK1A over Cdk1, Cdk5, CK1α1, Clk4, DYRK2, Pim-1, and GSK3β but also inhibits DYRK1B and Clk1 at 10 µM; inhibits proliferation of H4 human glioblastoma cells (IC50s = 23.7 µM); reduces TCDD-induced increases in CYP1A1 levels in HepG2 cells and prevents TCDD-induced activation of AhR in guinea pig hepatic cytosolic extracts; reduces glutamate-induced cytotoxicity, cytochrome c release, caspase-3 activation, and ROS production in PC12 cells at 25 µM
Cayman Chemical Harmalol hydrochloride hydra
A β-carboline alkaloid and an active metabolite of harmaline; an inhibitor of DYRK1A (IC50 = 0.63 µM); an inhibitor of MAO-A (IC50 = 0.66 µM); selective for DYRK1A over Cdk1, Cdk5, CK1α1, Clk4, DYRK2, Pim-1, and GSK3β but also inhibits DYRK1B and Clk1 at 10 µM; inhibits proliferation of H4 human glioblastoma cells (IC50s = 23.7 µM); reduces TCDD-induced increases in CYP1A1 levels in HepG2 cells and prevents TCDD-induced activation of AhR in guinea pig hepatic cytosolic extracts; reduces glutamate-induced cytotoxicity, cytochrome c release, caspase-3 activation, and ROS production in PC12 cells at 25 µM
Cayman Chemical SIvelStatsodIM salt hydra 50mg
An inhibitor of neutrophil elastase (IC50 = 44 nM for the human enzyme); selective for neutrophil elastase over trypsin, thrombin, plasmin, kallikrein, chymotrypsin, and cathepsin G at 100 µM; decreases LPS-induced NF-κB nuclear translocation in isolated rat PMVECs at 50 mM; reduces pulmonary edema, increases in the number of MPO-positive cells in the lung tissue, and the severity of lung injury in a rat model of LPS-induced acute lung injury at 10 mg/kg
Cayman Chemical SIvelStatsodIM salt hydra 25mg
An inhibitor of neutrophil elastase (IC50 = 44 nM for the human enzyme); selective for neutrophil elastase over trypsin, thrombin, plasmin, kallikrein, chymotrypsin, and cathepsin G at 100 µM; decreases LPS-induced NF-κB nuclear translocation in isolated rat PMVECs at 50 mM; reduces pulmonary edema, increases in the number of MPO-positive cells in the lung tissue, and the severity of lung injury in a rat model of LPS-induced acute lung injury at 10 mg/kg
Cayman Chemical SIvelestatsodIM salt hydra 5mg
An inhibitor of neutrophil elastase (IC50 = 44 nM for the human enzyme); selective for neutrophil elastase over trypsin, thrombin, plasmin, kallikrein, chymotrypsin, and cathepsin G at 100 µM; decreases LPS-induced NF-κB nuclear translocation in isolated rat PMVECs at 50 mM; reduces pulmonary edema, increases in the number of MPO-positive cells in the lung tissue, and the severity of lung injury in a rat model of LPS-induced acute lung injury at 10 mg/kg