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Topic :: Enzyme
What happen to a denaturated enzyme regarding its functionality? How that result can be explained with the help of the lock and key model?
1156What is the name of the dna duplication process? What is the main enzyme that participates in it?
1 1985What is the activation center of an enzyme? Is it the key or the lock of the lock and key model?
1094How does the formation of the enzyme-substrate complex? Explain the reduction of the activation energy of chemical reactions?
1035
Which vitamins participate, in coenzyme form, in reactions of the tricarboxylic acid cycle?
A blastomere was removed from an 8-cell human embryo, and its beta-globin gene was amplified by PCR. The beta-globin DNA was treated with an enzyme that cuts on either side of and within the normal allele (producing a small fragment), but not within the sickle cell allele (producing a large fragment). Electrophoresis of the treated DNA from the blastomere demonstrated the presence of both a large and small fragment derived from the beta-globin genes. How should you interpret this test?
Can angiotensin-converting enzyme (ACE) inhibitors and angiotensin receptor blockers cause urticarial skin eruptions?
Compare and contrast feedback inhibition and enzyme repression?
What are the enzymes produced by streptococci?
The elution volume of an enzyme on a gel filtration column can be predicted from a) its enzyme activity b) its protein absorbance at 280 nm c) subunit composition and monomer molecular mass(es) d) Choices a) and b) are both correct.
What is enzyme-ligand interaction?
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 Two ml of above reaction mixture was withdrawn and mixed with 3 ml of Tris–HCl buffer, 5 ml of 125 mM Na2CO3, and 0.5 ml of phenolphthalein (25 mg phenolphthalein/100 ml absolute alcohol).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 to analyse serum cardiac marker, cardiac enzymes, troonin and myoglobin?
What are some biological examples in which lysosomic enzymes play fundamental role?
What are the enzymes used for labeling of antibodies?
Name two enzymes that have been employed for elisa?
What happen to a denaturated enzyme regarding its functionality? How that result can be explained with the help of the lock and key model?
What are allosteric enzymes?
What is the importance of enzymes for the living beings?
