| Quantity | 250ml, 25ml, 500ml, 50ml, 1ml, 5ml, 100ml | 1mg | 250mg, 5g, 25g, 1g | 10mg, 5mg, 50mg, 1mg, 25mg | 250mg, 25g, 1g |
| Description | 1、Product attributeShelf life: 36 monthsMarker enzyme: Horseradish peroxidase (HRP)Reaction time：short (up to 20 minutes) at 20-25°CLot-to-lot variation：< 10 %Boiling point : 100℃（Calculated flash point）Flash point:：120 °C （1、Product attributeShelf life: 36 monthsMarker enzyme: Horseradish peroxidase (HRP)Reaction time：short (up to 20 minutes) at 20-25°CLot-to-lot variation：< 10 %Boiling point : 100℃（Calculated flash point）Flash point:：120 °C （Calculated flash point）pH-Value (at 20 °C): 4.5-4.9 （Experimental data）Density (20℃) : 1.0064 g/cm³Water solubility: easily solubleAppearance: colourless liquidOdour: odourlessLight sensitiveHeat sensitive2、Requirements for storage rooms and vessels1.Keep container tightly closed.2.Keep cool. Protect from sunlight.3.Keep/Store only in original container.4.Never return spills in original containers for reuse.5. Keep away from: Food and feedingstuffs.6. The solution can be transported at room temperature, but temperatures exceeding 30 °C have to be avoided. Shipping should be completed within one week.7. The solution will still work beyond the expiry date, but a lower sensitivity has to be taken into account and a precipitate may occur.8. Contaminated or leaked out substrate solution from damaged bottles should not be used and has to be destroyed.3、Effective Components and Principle of FunctionA citrate buffer system (pH 4.5 - 5.0) contains the following effective components:Hydrogen peroxide3,3`,5,5`-Tetramethylbenzidine (TMB)precipitating reagentPeroxidase catalyses the decomposition of hydrogen peroxide, taking electrons from TMB (byoxidation). Oxidation of TMB forms a radical cation that stabilizes by dimerisation and shows the typical blue colour. This blue cation is stabilized by forming an insoluble complex with the precipitating reagent. So at positions with horseradish peroxidase activity a blue precipitate will appear. This precipitate is very fine so that even the smallest dots can be coloured regularly.4、Biosafety informationThis mixture is not classified as hazardous in accordance with Regulation (EC) No 1272/2008；Hazardous components：none (according to Regulation (EC) No 1907/2006 (REACH))5、Advantage1. Rapid precipitation2. Strong adherence to plastic surfaces3. Short reaction time4. Intensive dark blue colour5. Homogeneous staining pattern6、Instruction for usageFor bottling consider the following instructions:•Work in a dust free and darkened room.• Pay attention that the solution has no contact with metal parts (leading to catalysis) of yourinstruments. Closed systems of silicon tubes are favoured.• Clean all instruments and vessels very carefully.• Never touch parts of the instruments that are in contact with the solution with the naked hand. Wear powder free gloves.• Close the bottles immediately to minimize the influence of light and dust.• Use bottles that are not permeable to light, made from HDPE or PP.7. General Instructions for the Use on Microchips• This solution should only be used by qualified laboratory staff familiar with the basics of immunological methods.• Note: The substrate solution is very sensitive to impurities. This is why you should never immerse pipette tips in storage bottles. Unused solution is never returned to the bottle! Don't swap the bottles for the cups!• Substrate Solutions Test systems for instrumental measurements on glass or plastic surfaces (polycarbonate or polystyrene).• Depending on the system, it may be sufficient to wash the microarrays after incubation with the conjugate and then cover them with the substrate solution. Arrays can be developed with a rocking motion until visible color appears (approximately 5 to 10 minutes). Measurements can be performed using wet arrays or after washing with distilled water and drying. Dry microchips can be used for recording purposes. (Note: some glues will destroy colored deposits)... Read More | Inquire | Copper tripeptide (GHK-Cu) is a naturally occurring tripeptide that is first isolated from human plasma but can also be found in saliva and urine. During wound healing, Copper tripeptide can be removed from existing extracellular proteins by protein hydrolysis and used as a chemical lure for Copper tripeptide (GHK-Cu) is a naturally occurring tripeptide that is first isolated from human plasma but can also be found in saliva and urine. During wound healing, Copper tripeptide can be removed from existing extracellular proteins by protein hydrolysis and used as a chemical lure for inflammatory and endothelial cells. Copper tripeptide can increase the production of messenger RNA in collagen, elastin, protein polysaccharides and glycosamine polysaccharides in fibroblasts. Copper tripeptide is a natural regulator of many cellular pathways in skin regeneration... Read More | Proteasome-activating peptide 1 TFA is a peptide and a potent proteasome activator. Proteasome-activating peptide 1 TFA increases the chymotrypsin-like proteasomal catalytic activity and, consequently, proteolytic rates both in vitro and in culture. Proteasome-activating peptide 1 TFA prevents Proteasome-activating peptide 1 TFA is a peptide and a potent proteasome activator. Proteasome-activating peptide 1 TFA increases the chymotrypsin-like proteasomal catalytic activity and, consequently, proteolytic rates both in vitro and in culture. Proteasome-activating peptide 1 TFA prevents protein aggregation in a cellular model of amyotrophic lateral sclerosis... Read More | Tyrosine decarboxylase catalyzes the removal of the carboxyl group from tyrosine to produce tyramine and carbon dioxide. Pyridoxal 5'-phosphate is a necessary cofactor. By using the apoenzyme prepared from cells grown on a vitamin B6 deficient medium pyridoxal phosphate may be determined. The Tyrosine decarboxylase catalyzes the removal of the carboxyl group from tyrosine to produce tyramine and carbon dioxide. Pyridoxal 5'-phosphate is a necessary cofactor. By using the apoenzyme prepared from cells grown on a vitamin B6 deficient medium pyridoxal phosphate may be determined. The HOLOenzyme may be used to determine tyrosine, phenylalanine and dihydroxyphenylalanine either manometrically or colorimetrically.L-Tyrosine decarboxylase apoenzyme from Streptococcus faecalis has been used in a study to purify and characterize tyrosine decarboxylase and aromatic-L-amino-acid decarboxylase.L-Tyrosine decarboxylase apoenzyme from Streptococcus faecalis has also been used in a study to investigate the stereospecificity of sodium borohydride reduction of tyrosine decarboxylase.One Unit yields 1µmole of CO2 per minute from L-tyrosine at 37°C, pH 5.5. The APOenzyme activity is measured in the presence of excess pyridoxal phosphate... Read More |