Catalase degrades easily at room temperature b. Glucose oxidase is inactivated at low pH c. Glucose oxidase is only active at low pH d. Glucose oxidase has a higher molecular weight than catalase .
B
chloroform
The Time-Taken the sample Or elute in the column is called the retention time in hplc.
Run the mixture on the TLC plate. Find the different colored pigments. Scrape each spot and elute the pigments.
Total volume of mobile phase in a fully wet packed column- the space between the particles of the stationary phase plus the volume within the particles
You can do a tedious phenol-chloroform extraction, or do it the easy way: QIAquick PCR purification kit where you bind the DNA to a column and elute it off in water or TE. You will lose some of your DNA though so keep this in mind.
They can actually elute in either order. It depends on your mobile phase. In a weakly basic solution, the phosphate ions are found more as HPO4 (2-) rather than PO4 (3-) and thus will elute before sulfate which is larger and has the same charge. In a strongly basic mobile phase, the PO4 (3-) ion will dominate, and will elute after the sulfate ion
Usually, but not always. Depends on the bond position and polarity of the column. Alkenes are less likely to elute first on polar columns.
chloroform
The Time-Taken the sample Or elute in the column is called the retention time in hplc.
Elute, Ettle, Tutee, Lute, Teel, Telt, Tutu, Eel, Ut, Te, Et
Run the mixture on the TLC plate. Find the different colored pigments. Scrape each spot and elute the pigments.
Total volume of mobile phase in a fully wet packed column- the space between the particles of the stationary phase plus the volume within the particles
You can do a tedious phenol-chloroform extraction, or do it the easy way: QIAquick PCR purification kit where you bind the DNA to a column and elute it off in water or TE. You will lose some of your DNA though so keep this in mind.
I assume you are talking about thin-layer chromatography. If the spots are submerged in the solvent, they will dissolve into it and become so diluted that they will most likely be undetectable. Plus, they will elute as a band, not as a spot. Your solvent will also be contaminated.
The suppressor reduces the background conductivity of the chemicals used to elute samples from the ion-exchange column. This improves the conductivity measurement of the ions being tested. check it http://www.dionex.com/en-us/products/accessories/suppressors/lp-73569.html
The dead volume in HPLC is 137.45. The dead volume in science is used in retention measurements and also in thermodynamic studies and the abbreviation HPLC stands for High Pressure Liquid Chromatography.
because in normal phase HPLC mobile phase is non polar and stationary phase is polar. Most of the compound of interest are polar, if you increase the polarity of mobile phase compound of analyte will stay in mobile phase and will elute faster and retention time will be shorter.