Lactate can be denatured by subjecting it to high heat, extreme pH levels, or strong chemicals. The denaturation process disrupts the structure of lactate, causing it to lose its biological activity or function.
Yes, sodium lactate is the conjugate base of lactic acid. When lactic acid (a weak acid) donates a proton (H⁺), it forms lactate, which is the conjugate base. Sodium lactate is the sodium salt of lactate, meaning it contains the lactate ion paired with sodium. Thus, it can act as a source of lactate in solution.
Yes, L-lactate is a chiral molecule as it has a stereocenter at the carbon atom bound to the carboxyl group. It exists in two enantiomeric forms, L-lactate and D-lactate, which are non-superimposable mirror images of each other.
Lactic acid dissociates into lactate and hydrogen ions.
Temperature, pH, organic solvent, mechanical forces
Acids, high temperatures, organic solvents, and heavy metals can denature proteins.
Lactate threshold is caused when lactate production exceeds lactate clearance during exercise or increasing intensity.
lactate dehydrogenase
Yes, sodium lactate is the conjugate base of lactic acid. When lactic acid (a weak acid) donates a proton (H⁺), it forms lactate, which is the conjugate base. Sodium lactate is the sodium salt of lactate, meaning it contains the lactate ion paired with sodium. Thus, it can act as a source of lactate in solution.
Correct answer: I, II, III and IV
To convert millimoles per liter (mmol/L) of lactate to milliequivalents per liter (mEq/L), you need to consider the charge of the lactate ion. Lactate (C3H5O3^-) has one negative charge, so 1 mmol/L of lactate is equivalent to 1 mEq/L. Therefore, the conversion is straightforward: 1 mmol/L of lactate equals 1 mEq/L of lactate.
Yes, L-lactate is a chiral molecule as it has a stereocenter at the carbon atom bound to the carboxyl group. It exists in two enantiomeric forms, L-lactate and D-lactate, which are non-superimposable mirror images of each other.
Not quite; they have to give birth to a calf in order to lactate.
yap it looks possible to dilute with ringer lactate
The high concentration of ammonium lactate in the lotion surprised me.
I am doing a paper and need to know the difference between ringer's lactate and lactate ringers
After the completion of oxidation of lactate, 2 ATP molecules are produced. Lactate is then sent to the liver to be turned back into glycolysis.
Yes, lactate can be utilized as an energy source in the body through a process called lactate metabolism, where it is converted into energy in the form of ATP.