EvaGen Green qPCR Master Mix
EvaGen Green qPCR Master Mix is a ready-to-use 2x soluon opmized for
dye-based quantave polymerase chain reacon (qPCR). The Pre-mix contains
anbody-mediated hot-start DNA polymerase, dNTPs, MgCl₂, EvaGreen dye,
enhancers, and stabilizers for robust fluorescent signals. EvaGreen is a
fluorescent nucleic acid dye with similar spectral properes to SYBR green I and
more stable during PCR condions, storage, and handling. A combinaon of
anbody modified DNA polymerase with the opmized EvaGen Green qPCR
Master Mix eliminates the nonspecific amplificaon of DNA in PCR reacons.
NeoTaq DNA Polymerase
NeoTaq DNA Polymerase is derived from recombinant expression of a
genecally modified form of thermostable DNA polymerase from
thermophilic bacterium Thermus aquacus expressed in E. coli.The 98kDa
enzyme catalyzes 5’ to 3’ polymerase acvity and lacks 3’ to 5’ exonuclease
(proof reading) acvity but has an inherent 5’ to 3’ exonuclease acvity. The
enzyme has been genecally modified to offer high sensivity and
amplificaon efficiency as compared to standard Taq DNA polymerases.
NeoTaqDNA Polymerase is ideal for standard PCR templates up to 6.4 kb.
2X NeoTaq Master Mix
2X NeoTaq master mix is a ready-to-use reacon mix opmized for roune PCR
applicaons. It contains high quality NeoTaq DNA polymerase, dNTPs, MgCl2,
enhancers and stabilizers. All the reagents required for PCR (except template and
primer) is at opmal concentraons without the need of addional opmizaon
step. 2X NeoTaq master mix efficiently amplifies a wide range of DNA templates
for most of the PCR applicaons.
Neo Gold Taq DNA Polymerase
Neo Gold Taq DNA Polymerase is a premixed, ready-to-use 2x soluon containing
anbody-mediated hot-start NeoTaq DNA polymerase, dNTPs, MgCl2,
enhancers and stabilizers for efficient amplificaon. Neo Gold Taq DNA
Polymerase prevents non-specific product formaon and allows polymerase
chain reacons (PCR) to proceed at ambient temperature, which has been
achieved using anbody modified polymerase.
JetStart Taq DNA Polymerase
JetStart Taq DNA Polymerase contains recombinant Taq DNA polymerase
bound to a monoclonal anbody that blocks polymerase acvity at ambient
temperature. The DNA polymerase acvity is restored during the inial
denaturaon step of polymerase chain reacon (PCR) reacon. The enzyme is
supplied with a uniquely formulated assay buffer which provides robust
amplificaon of DNA. A combinaon of anbody modified DNA polymerase with
the opmized hot start buffer eliminates the nonspecific amplificaon of DNA in
PCR reacons.
NesTaq Ab Master Mix
NesTaq Ab Master Mix is a premixed, ready-to-use 2x soluon containing
anbody-mediated hot-start NeoTaq DNA polymerase, dNTPs, MgCl2,
enhancers and stabilizers for efficient amplificaon. NesTaq Ab Master Mix
prevents non-specific product formaon and allows polymerase chain reacons
(PCR) to proceed at ambient temperature, which has been achieved using
anbody modified polymerase.
KOD Xpress DNA Polymerase
KOD Xpress DNA Polymerase is derived from recombinant expression of a
genecally modified form of thermostable DNA polymerase from hyperthermophilic
archaeon Thermococcus kodakaraensis expressed in E. coli. The 94kDa enzyme
catalyzes 5’ to 3’ polymerase acvity, 3’ to 5’ exonuclease (proofreading) acvity and
has no 5’ to 3’ exonuclease acvity. KOD XpressDNA Polymerase is ideal for standard
PCR of templates up to 14Kb.
RoBst DNA Polymerase
RoBst DNA polymerase I (large fragment) from Bacillus stearothermophilus
(Bst), is a robust polymerase used for various isothermal amplificaon reacons.
The recombinant enzyme is prepared from an Escherichia coli (E. coli) strain
containing the gene encoding for RoBstDNA Polymerase. Due to its strand
displacement acvies, the enzyme is used for the implementaon of loopmediated isothermal amplificaon (LAMP). The thermostable enzyme detects
low sensivity nucleic acids with higher efficiency and specificity. The enzyme
with a molecular weight of 72kDa catalyses 5' to 3' Polymerase acvity and lacks
5' to 3' exonuclease acvity.