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IT act as a buffering agent to maintain the PH of a PCR

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Q: What is the function of tris hcl in PCR buffer?
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How do you prepare tris-hcl buffer solution of 0.5M?

6g Tris HCl + 100ml dH2O, pH 6.8


What is the difference between TAE buffer and TE buffer?

The main difference is in composition. In TE common Tris buffer is bring down to pH 8 with HCl and EDTA is involved but in TAE instead of Tris HCl in TE Tris-acetate buffer is used.


What is the buffer capacity of Tris HCl?

7.5-9


What is Tris HCl?

"Tris" is a chemical compound used as a buffer. The full name is tris(hydroxymethyl)aminomethane. Tris has the ability to absorb counter ions (+H and -OH) so as to help keep the solution that they are in at a stable pH level. When the pH of Tris is set using HCl (hydrochloric acid) the buffer is called Tris HCl.


How do you prepare 20 mM tris hcl buffer pH 7.4?

to prepare 100ml of 100mM Trissolution: Mol wt of Tris=121.14121.14g in 1000ml ----> 1M12.11g in 100ml -------->1M1M=1000mM121.1g---->1000mM12.11g ----------->100mM1.211g in 100ml and 100mM Tris


Function of tris HCl in DNA isolation?

Tris is here to maintain pH


What is the difference between tris tris cl and tris hcl?

tris tris cl is 6 cl and tris hcl is 3hcl...........


Why do you use Tris Hcl in plasmid isolation?

The role that tris-HCI plays in plasmid isolation is to maintain the pH of the solution. This prevents degradation of the plasmids. Tris stands for the organic compound, tris(hydroxymethyl)aminomethane, which is a common pH buffer. HCl is a salt acid called hydrochloride. This is added as a buffer as well to add stabilization.


What Volume of 5M HCl to make tris buffer at pH 7.5?

The formula weight is 121.5 --> this is equivalent to 1M with 121.5g tris in 1L dH20. For a 5M stock, use 5x as much tris in the same 1L dh20.607.5 g tris into 800ml dH2O - stirring - then pH to 7.5 with 6M HCl and QS to your final volume of 1L


How do you make up 75mM Tris HCL buffer solution?

CONVERT TO THE MOLE (0.075 m/l) * (157.67mw) =11.82 g/l


Tris buffer as pH by HCl why not for sodium acetate?

The question is in poorly worded. I will assume the question is "why adjust the pH of Tris buffer with HCl and not Sodium Acetate?" I would assume the answer is - because sodium acetate is the conjugate base of a weak acid, and HCl is a strong acid. Also the salts you would be putting into the solution as a result would be different. I think the question is actually, "The pH of Tris is adjusted with HCl, why isn't the pH of sodium acetate adjusted with HCl?". I'm not sure of the answer exactly, but I've always assumed its because if you adjust the pH with glacial acetic acid instead of HCl, you won't introduce chloride ions.


What is STE address or STE buffer?

0.1 M NaCl10 mM Tris-HCl (pH 8.0)1 mM EDTA (pH 8.0)