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what is the difference between MUFA and PUFA?
What role do disulfide bonds play in protein folding, and in protein stability?
How does temperature affect the action of enzymes upon their substrates?
How does hplc differ from normal column chromatography, and what are its advantages?
What is the difference between Gram positive & Gram negative bacteria based on its cell contents?
which solvent mixture is normally used in paper chromatography?
On what structural level of the enzyme (primary, secondary, tertiary, or quaternary) does the enzyme-substrate interaction depend?
One characteristic of the dna molecule is its replication capability. What are the consequences of failures during dna replication?
What is the anhydride of n2o5?
I have given the protocol for the cyclodextrin glygosyl transferase assay: One ml of appropriately diluted enzyme sample was incubated at 60 °C for 15 min with 5 ml of 1% (w/v) gelatinized soluble starch in 50 mM, 7.0-pH Tris–HCl buffer. Reaction was terminated by boiling the reaction mixture for 3 min and reaction volume was made to 10 ml with distilled water. Two ml of above reaction mixture was withdrawn and mixed with 3 ml of Tris–HCl buffer, 5 ml of 125 mM Na2CO3, and 0.5 ml of phenolphthalein (25 mg phenolphthalein/100 ml absolute alcohol). Absorbance was measured at 550 nm. The percent decrease of sample was calculated with respect to control containing 5 ml of buffer, 5 ml of sodium carbonate and 0.5 ml of phenolphthalein. where Acontrol = absorbance of control and Atest = absorbance of sample. The amount of β-cyclodextrin (β-CD) produced was estimated from the standard graph of 0–500 μg/ml β-CD concentration against % decrease in absorbance. One unit of CGTase was defined as the amount of enzyme required to produce 1 μm of β-CD/min. Please can you suggest me the formula for the defination given in the last line
how bpg acts as a haemoglobin regulator?
how do u differentiate pseudoglobulins and euglobulins on the basis of solubility?