Hot Taq DNA Polymerase Kit
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Hot Taq DNA Polymerase Kit´Â Chemically modified Hot Taq DNA polymerase¿Í PCR buffer, dNTP mixture, Gel loading dye°¡ °¢°¢ÀÇ component·Î Á¦°øµÇ¸ç, ±ú²ýÇϰí, ³·Àº ¿Âµµ¿¡¼ÀÇ ºñƯÀÌ ¹ÝÀÀÀ» ¹æÁöÇÏ¿©, Á¤È®ÇÑ band¸¦ Á¦°øÇÕ´Ï´Ù. |
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- Hot Taq DNA Polymerase, PCR buffer, dNTPs, Gel loading dye°¡ kit component·Î Á¦°øµË´Ï´Ù.
- Modified Taq DNA Polymerase´Â ³·Àº ¿Âµµ¿¡¼ Çü¼ºµÈ primer-dimer¿Í nonspecifically annealed primersÀÇ extensionÀ» ¸·¾ÆÁÝ´Ï´Ù.
- background ¾øÀÌ ±ú²ýÇϰí nonspecific amplificationÀÌ °¨¼ÒµÈ Á¤È®ÇÑ °á°ú¸¦ ¾òÀ» ¼ö ÀÖ½À´Ï´Ù.
- ³ôÀº GC content¸¦ °¡Áø targetÀÇ ÁõÆøÀ» ÃËÁø½ÃŰ´Â Magic buffer°¡ ÇÔ²² Á¦°øµË´Ï´Ù.
- Hot Taq concentration : 5U/ul
- Extension reate : 2-4kb/min at 72¡ÆC
- Amplification efficiency : ¡Ã105 fold
- 5'¡æ3' exonuclease activity : Yes
- 3'¡æ5' exonuclease activity : No
- Extra A addition : Yes

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- Hot Taq DNA polymerase
- 10X Hot Taq PCR buffer
- dNTP Mixture
- Loading Buffer
- Magic Buffer (for high GC)
- Highly Specific PCR
- Low Copy Number Target PCR. (e.g. Viral Detection in Blood)
- RT-PCR of rare transcripts
- Differential Display
- Multiplex PCR, PCR-based DNA fingerprinting (VNTR, STR, and RAPD)etc
- Degenerate PCR

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Figure 1. Human TNF gene amplification by serial dilution Hot Taq DNA polymerase and HotStarTaq DNA polymerase.
Lane 1 : 2.5 unit
Lane 2 : 1.2 unit
Lane 3 : 0.6 unit
Lane 4 : 0.3 unit
Lane 5 : 0.15 unit
Lane 6 : 0.08 unit
Figure 2. Low Copy Template DNA (HIV detection in human genomic DNA)
Lane 1 : 0 copy of HIV DNA in 50ng human gDNA
Lane 2 : 2 copies of HIV DNA in 50ng human gDNA
Lane 3 : 5 copies of HIV DNA in 50ng human gDNA
Lane 4 : 10 copies of HIV DNA in 50ng human gDNA
Lane M : 100bp ladder