«ALMASS Bench» for HPLC-MS

Недавно просмотренные товары

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  ALZYME

  Real-Time PCR master mix «ALZYME SYBR Mix»

  Ready-to-use 2X mix for PCR reactions with SYBR Green I dye.

  Ready-to-use mix for PCR with SYBR Green I.

  • DNA polymerase resistant to PCR inhibitors.
  • Increased stability and specificity.
  • Protection against contamination (ALZYME SYBR Mix variant with UDG).
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  ALZYME

  PCR master mix «ALZYME Mix»

  Ready-to-use 2X mix for PCR reactions.

  Ready-to-use mix for PCR.

  • DNA polymerase resistant to PCR inhibitors.
  • Increased stability and specificity.
  • Protection against contamination (ALZYME Mix with UDG).
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  ALZYME

  «ALZYME Elaine HSTaq» DNA polymerase

  Thermostable Hot-start Taq-polymerase.

  Thermostable hot-start DNA polymerase for direct PCR.

  • «Hot Start» technology avoids nonspecific amplification and enables room temperature reaction setup.
  • 5′ → 3′ exonuclease activity.
  • Resistance to PCR inhibitors.
  • Increased amplification rate.
  • Amplification of fragments for TA cloning.
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  ALZYME

  «ALZYME Elaine Taq» DNA polymerase

  Thermostable Taq-polymerase.

  Thermostable DNA polymerase for direct PCR.

  • 5′ → 3′ exonuclease activity.
  • Resistance to PCR inhibitors.
  • Increased amplification rate.
  • Amplification of fragments for TA cloning.
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  ALZYME

  «ALZYME HSPfu» DNA polymerase

  Highly processive thermostable Hot-start Pfu-polymerase.

  A highly processive thermostable hot-start DNA polymerase.

  • «Hot Start» technology avoids nonspecific amplification and enables room temperature reaction setup.
  • 3’→5′ proofreading activity.
  • Devoid of 5’→3′ exonuclease activity.
  • Allows efficient amplification of DNA fragments up to 20000 bp.
  • Amplification of GC-rich sequences.
  • Resistance to PCR inhibitors.
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  CLEANCHECK

  «CleanCheck Remover» Decontamination solution

  Removal of trace amounts of DNA, RNA, DNases, and RNases from work surfaces and equipment.

  Designed for the removal of trace amounts of DNA, RNA, DNases, and RNases from work surfaces, equipment, and instruments.

  • Efficiently degrades DNA/RNA fragments regardless of their size.
  • Decontaminates surfaces without inhibiting PCR.
  • Achieves surface decontamination within 15 minutes.
  • Suitable for both remediation of existing contamination and its prevention.
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  ALZYME

  «ALZYME K» Proteinase

  Purification of enzyme mixtures and cell lysates from unwanted proteins.

  Used for purification of enzyme mixtures and cell lysates from proteins during RNA/DNA isolation.

  • Effectively lyses matrices during nucleic acid isolation.
  • Stable in urea, SDS, EDTA.
  • Inactivates RNases and DNases.
  • It retains activity in the pH range of 6.5-9.5 & at high temperatures (optimally 50-65 °C), functions in the presence of chaotropic salts and detergents.
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  ALZYME

  «ALZYME HSTaq» DNA polymerase

  Hot-start Taq-poly­merase.

  A thermostable hot start DNA polymerase.

  • «Hot Start» technology avoids nonspecific amplification and enables room temperature reaction setup.
  • 5′ → 3′ exonuclease activity.
  • Does not exhibit proofreading activity.
  • Allows efficient amplification of DNA fragments up to 5000 bp.
  • Amplification of fragments for TA cloning.
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  ALZYME

  «ALZYME Pfu» DNA polymerase

  Highly processive thermostable DNA polymerase.

  A highly processive thermostable DNA polymerase.

  • 3′ → 5′ proofreading activity.
  • Devoid of 5′ → 3′ exonuclease activity.
  • Allows efficient amplification of DNA fragments up to 20000 bp.
  • Amplification of GC-rich sequences.
  • Resistance to PCR inhibitors.
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  ALZYME

  «ALZYME Taq» DNA polymerase

  Taq-poly­merase.

  A thermostable DNA polymerase.

  • 5′ → 3′ exonuclease activity.
  • Does not exhibit proofreading activity.
  • Allows efficient amplification of DNA fragments up to 5000 bp.
  • Amplification of fragments for TA cloning.