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SNPase

SNPase was recognized as one of the best Polymerases in SNP detection by allele-specific PCR and micro sequencing.

Catalog #Pack sizePrice, EURSHOP
108205500 units120,00Add to cart
1082252500 units510,00Add to cart
108210 "HoT Start"500 units135,00Add to cart
108250 "HoT Start"2500 units560,00Add to cart


Download Datasheet: SNPase

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Applications:

-SNP- genotyping  , allele specific PCR, allele specific primer extension, mini
 sequencing
-Highly specific PCR
-Multiplex PCR
-Highest fidelity PCR
-Real Time PCR with intercalating dyes (SYBR Green, Eva Green)

Description: SNPase is Taq DNA Polymerase  with N-terminal deletion and prioprietary amino acids substitutions introduced into the active center of the enzyme. This modification causes dramatic increase of sensitivity of the enzyme to mismatches at 3’-end of the primer. Consequently , non-perfect annealing of the primers does not result in unspecific amplicons formation.

Features:

-High sensitivity to mismatches at 3’end of primers
-high fidelity of dNTPs and ddNTPs  incorporation
-Lack of 5’- and 3’- exonuclease activity
-High specificity, low level of background PCR

Concentration: 20-25 µl
Storage conditions :  -20°C

Supplied with : 5x Buffer without Mg 2+; MgCl2 solution ( 100mM);

Magnesium concentration: SNPase DNA polymerase provides successful PCR in range of Mg 2+ concentration from 2,5 mM to 4mM in the 1xreaction mixture. Increase of Mg 2+ concentration from 2,5 mMupto 4 mM can provide higher yield of PCR products . On the other hand  low magnesium concentration favors specific  PCR.

Associated activities: Endonuclease and exonuclease activities were not detected.

 

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