in pcr technique we take original dna first heat it to separate to strands in thermocycler then add rna primer after the formation of about 10 sequences on both parental strands add dna polymerase to construct further
- as a support to weigh samples of solid reagents- to cover a Berzelius beaker
Yes only some... It depends
IT act as a buffering agent to maintain the PH of a PCR
Grignard reagents are stable in ether medium. Ether generally forms an adduct with Grignard reagents. In addition, if solvents containing acidic hydrogens are present, Grignard reagents are decomposed to the corresponding hydrocarbon.
The substances you have at the beginning of a chemical reaction are the reactants or the reagents.
The use of dNTP is PCR and multiplex PCR
to check is there any contamination in pcr products
enzyme cofactor
types of pcr: AFLP -PCR. Allele-specific PCR. Alu-PCR. Assembly -PCR. Assemetric -PCR. Colony -PCR. Helicase dependent amplification. Hot start pCR. Inverse -PCR. Insitu -pCR. ISSR-PCR. RT-PCR(REVERSE TARNSCRIPTASE). REAL TIME -PCR
There are several advantages of using real-time PCR over other methods. Real-time PCR assays are thousand folds more sensitive than RNase protection assays or dot blot hybridization. It allows you to quite precisely calculate and compare of the amount of template in each cycle, instead of determining the amount of product at the end of the reaction. Quantitative RT-PCR is commonly used for clinical applications. For example, you could use this method to quantify the amount of HIV RNA particles per ml of blood plasma in a patient who is undergoing treatment with antiviral drugs to see if it's working or not. The main problem with real-time PCR is that it requires specialised thermal cyclers (PCR machine) with fluorescence monitors and its reagents are quite expensive.
One can use a PCR to amplify and quantify a certain DNA molecule. A TaqMan real-time PCR is a certain type of PCR which uses the TaqMan method to increase its specificity.
PCR is an enzymatically guided process. In optimum pH the enzyme will work best.
PCR
Polymerase chain reaction
PCR
PCR is a biotechnological method to amplify your gene (DNA) of your interest. It produce millions of your DNA fragments hence used in cloning. There are variants of this method using the same thermocycling principle such as touch down PCR, gradient PCR, RFLP, multiplex PCR, Q PCR, RT PCR and so on.
The enzyme DNA polymerase ( Taq polymerase) used in the PCR requires Mg 2+ ions for its functioning.These Ions act as cofactors for the enzyme . Hence the requirement for the use of Mg Cl2 in PCR reactions.