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 Á¦Ç°¾È³»  ºÐÀÚ»ý¹°ÇР PCR Amplification  PCR Enzymes

Hot Taq DNA Polymerase Kit

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)
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  • 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
    »ç¿ë¿¹
    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
ÁÖ¹®Á¤º¸(Ordering Information)
Cat.NOProductSizeAdd.
K0567100Hot Taq DNA Polymerase Kit250U¹Ù±¸´Ï