• StarLighter Hot Start Taq Pro DNA Polymerase
  • StarLighter Hot Start Taq Pro DNA Polymerase

StarLighter Hot Start Taq Pro DNA Polymerase

No.FS-P3001/FS-P3002/FS-P3003
StarLighter HotStart PCR Mix It is a ready-to-use PCR Mix configured with ultra-high performance hot-start DNA polymerase. The optimized buffer system can efficiently amplify complex and difficult samples. There are two types of PCR Mix to choose from, one with Loading Dye and the other without Loading Dye. The Mix with Loading Dye can be directly spotted on gel electrophoresis after PCR amplification without adding Loading buffer, which is convenient for electrophoresis operation and does not affect the amplification efficiency.
The polymerase in this PCR Mix is blocked with antibodies, and the enzyme activity can be restored at 90℃ or above for 30 seconds. The enzyme catalyzes the synthesis of DNA in the 5'→3' direction, has 5'→3' exonuclease activity, and has no 3'→5' proofreading exonuclease activity. This product has 3'-dA protruding ends in the amplified product, and the amplification speed is 1-10 s/kb.
Item No./Specification/Price:
FS-P3001/100 U/¥300.00
FS-P3002/500 U/¥1200.00
FS-P3003/2500 U/¥4800.00
  • StarLighter Hot Start Taq Pro DNA Polymerase

Product Description

StarLighter HotStart Tag Pro DNA Polymerase

StarLighter Hot Start Taq Pro DNA Polymerase



Product Advantages

  • High amplification efficiency;
  • Rapid expansion rate;
  • Good anti-inhibition performance.

Application

  • Genotyping;
  • GMO testing;
  • Knockout analysis.

Product composition


Product Performance

The amplification efficiency is good and the specificity is high.

Compared with kits from other suppliers on the market, Qihengxing PCR Mix exhibits superior amplification efficiency and amplification specificity for different amplification product lengths and GC contents.

Fig.1A

Fig.1B

Fig.1 Using 20 ng human gDNA as template, 6 pairs of primers (amplification product 400-950 bp) were amplified for 35 cycles using PCR Mix from Qihengxing and other suppliers, and the electrophoresis results of PCR products are shown in the figure. Amplification product length and GC% As shown in the above figure, the reagents from suppliers VZ, TG, CW, AB, YS, TK1 and TK2 had non-specific amplification or no amplification.

Fig.2 Using 20 ng human gDNA as template, 3 pairs of primers (amplification product 1200-1400 bp) were amplified for 35 cycles using PCR Mix from Qihengxing and other suppliers, and the electrophoresis results of PCR products are shown in the figure. Amplification product length and GC% As shown in the above figure, the reagents from suppliers VZ, TG, CW, AB, YS, TK1 and TK2 had non-specific amplification or no amplification.


Fig.3 Using 20 ng human gDNA as template, PCR Mix from Qihengxing and other suppliers were used to amplify 4 pairs of primers (amplification product 2000-3000 bp) for 35 cycles. The electrophoresis results of PCR products are shown in the figure. Amplification product length and GC% As shown in the above figure, the reagents from suppliers VZ, TG, CW, AB, YS, TK1 and TK2 had non-specific amplification or no amplification.

Related Product Links

Taq enzyme/DNA enzyme/reverse transcriptase/UDG enzyme

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