Storage stability this product remains active for at least 2 years when stored properly at 20 c.
Rnase a stability room temperature.
I understand the role of rnase and most of us take the optimum measure to get rid it.
In contrast to rnase b it is not a glycoprotein 2 rnase a can be inhibited by alkylation of his12 4 or his119 which are present in the active site of the enzyme 3 activators of rnase a include potassium and sodium salts.
Both the excitation and emission slit widths were fixed at 5 nm.
The fluorescence experiments were done at room temperature 23 c with a shimadzu rf 5000 spectrofluorimeter.
Storage at room temperature does not affect enzyme performance all our products have been tested for stability at room temperature for an extended time.
For illustration the qpcr performance of a product that was stored at 20 c was compared to the same product stored at room temperature for 4 weeks.
That s why some rna extraction protocols include 2 mercaptoethanol in its.
Rnase a is a single chain polypeptide containing 4 disulfide bridges.
Stranded rna 1 room temperature.
Rnase a premixed solutions retain enzymatic activity at room temperature or 2 8ºc for extended periods.
Rnases in general are rich in disulfide bounds which grant them extra stability in adverse conditions such as heat.
Rnase a at the concentrations indicated was incubated at room temperature for 1 hr with radiolabeled standard rna or rna synthesized by the rt pcr competitor construction kit in 1 transcription buffer.
However 20ºc long term storage is recommended for both l yophilized and pre mixed solutions of rnase a.
Rnase a is a very stable enzyme and solutions have been reported to withstand temperatures up to 100 c.
At 100 c an rnase a solution is most stable between ph 2 0 and 4 5 13 for removal of rna from preparations of plasmid dna.
2 suggests to dissolve 10 mg ml rnase a in 0 01 m sodium acetate ph 5 2 to heat to 100 c for 15 minutes in a water bath and to cool down to room temperature very slowly.
How can i improve rna quality with low 260 230 ratio.
The ph value is equilibrated by adding 0 1 fold the volume of 1 m tris cl ph 7 4.
Nuclease stability of rna synthesized with the rt pcr competitor construction kit.
The rnase a samples were prepared from stock solution by dissolving 1 mg of the enzyme into 1 ml of citrate buffer ph 5 0.