ABclonal Technology

Gloria Nova HS DNA polymerase is an ideal enzyme for high fidelity PCR with excellent processivity. It is a novel engineered enzyme with comparable performance to Pyrococcus furiosus DNA polymerase.
With unique structure Gloria Nova HS DNA polymerase contains a recombinant synthesis enhancement domain to increase fidelity and extension speed. The antibody-mediated hot-start feature significantly inhibits non-specific amplifications at room temperature.
Gloria Nova is one of the thermostable DNA polymerases with strong 3’-5’ exonuclease activity (proofreading activity), which results in its extreme high fidelity, 10-15 times higher than Taq DNA polymerase and 6 times higher than Pyrococcus furiosus DNA polymerase.
The Gloria Nova HS PCR Kit is supplied with a 5X Gloria Nova HF Buffer and a 2.5X Gloria Nova GC Buffer. The 5X Gloria Nova HF Buffer is an optimized buffer for general high fidelity amplifications while the 2.5X Gloria Nova GC Buffer is used in the amplifications of problematic or GC-rich templates.

Gloria U Hot-Start DNA Polymerase is a DNA polymerase obtained through molecular modification, which can effectively amplify templates containing uracil. The uracil-binding ability of Gloria U polymerase is inactivated, allowing it to efficiently amplify DNA that has been treated with bisulfite. Moreover, this enzyme exhibits the same high yield and low GC bias as Gloria Nova Hot-Start DNA Polymerase.
Gloria U Hot-Start High-Fidelity DNA Polymerase possesses 5′-3′ polymerase and 3′→5′ exonuclease (proofreading) activities, but lacks 5′-3′ exonuclease activity.
The Gloria U 2X HS Master Mix contains Gloria U DNA Polymerase, dNTPs, 5X Gloria U Reaction Buffer, and other components. Only template and primers need to be added.

Gloria U Hot-Start DNA Polymerase is a DNA polymerase obtained through molecular modification, which can effectively amplify templates containing uracil. The uracil-binding ability of Gloria U polymerase is inactivated, allowing it to efficiently amplify DNA that has been treated with bisulfite. Moreover, this enzyme exhibits the same high yield and low GC bias as Gloria Nova Hot-Start DNA Polymerase.
Gloria U Hot-Start High-Fidelity DNA Polymerase possesses 5′-3′ polymerase and 3′→5′ exonuclease (proofreading) activities, but lacks 5′-3′ exonuclease activity.
The Gloria U 2X HS Master Mix contains Gloria U DNA Polymerase, dNTPs, 5X Gloria U Reaction Buffer, and other components. Only template and primers need to be added.

Gloria U Hot-Start DNA Polymerase is a typical Family B polymerase with unique characteristics. Through molecular modification of the Gloria polymerase, the binding capability of uracil has been inactivated. As a result, Gloria U can efficiently amplify bisulfite-treated DNA or libraries containing uracil. The enzyme exhibits the same high yield, low GC bias, and uniform coverage as the Gloria Nova Hot-Start DNA Polymerase. The Gloria U 2X Mix for NGS has 5′-3′ polymerase activity and 3′→5′ exonuclease (proofreading) activity, making it suitable for amplifying templates containing uracil or amplifying libraries containing uracil.

Gloria U Hot-Start DNA Polymerase is a typical Family B polymerase with unique characteristics. Through molecular modification of the Gloria polymerase, the binding capability of uracil has been inactivated. As a result, Gloria U can efficiently amplify bisulfite-treated DNA or libraries containing uracil. The enzyme exhibits the same high yield, low GC bias, and uniform coverage as the Gloria Nova Hot-Start DNA Polymerase. The Gloria U 2X Mix for NGS has 5′-3′ polymerase activity and 3′→5′ exonuclease (proofreading) activity, making it suitable for amplifying templates containing uracil or amplifying libraries containing uracil.

Gloria U Hot-Start DNA Polymerase is a DNA polymerase obtained through Gloria modification, which can effectively amplify templates containing uracil. The uracil-binding ability of Gloria U polymerase is inactivated, allowing it to efficiently amplify bisulfite-treated DNA. Moreover, this enzyme exhibits the same high yield as Gloria Nova Hot-Start DNA Polymerase. Gloria U Hot-Start High-Fidelity DNA Polymerase possesses 5′-3′ polymerase and 3′→5′ exonuclease (proofreading) activities but lacks 5′-3′ exonuclease activity. This polymerase can effectively incorporate dUTP and efficiently amplify template DNA containing dUTP. It also has the ability to recognize primers containing dUTP and complete the amplification process.

Gloria U Hot-Start DNA Polymerase is a DNA polymerase obtained through Gloria modification, which can effectively amplify templates containing uracil. The uracil-binding ability of Gloria U polymerase is inactivated, allowing it to efficiently amplify bisulfite-treated DNA. Moreover, this enzyme exhibits the same high yield as Gloria Nova Hot-Start DNA Polymerase. Gloria U Hot-Start High-Fidelity DNA Polymerase possesses 5′-3′ polymerase and 3′→5′ exonuclease (proofreading) activities but lacks 5′-3′ exonuclease activity. This polymerase can effectively incorporate dUTP and efficiently amplify template DNA containing dUTP. It also has the ability to recognize primers containing dUTP and complete the amplification process.

application (IF-P, IHC-P, ELISA) & cross reactivity (Mouse, Rat)

application (IF-P, IHC-P, ELISA) & cross reactivity (Mouse, Rat)

application (IF-P, IHC-P, ELISA) & cross reactivity (Mouse, Rat)

application (IF-P, IHC-P, ELISA) & cross reactivity (Mouse, Rat)

application (WB, ELISA) & cross reactivity (Human, Rat)

application (WB, ELISA) & cross reactivity (Human, Rat)

application (WB, IF/ICC, ELISA) & cross reactivity (Mouse, Rat)

application (WB, IF/ICC, ELISA) & cross reactivity (Mouse, Rat)

application (WB, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, IHC-P, ELISA) & cross reactivity (Human, Mouse)

application (WB, IHC-P, ELISA) & cross reactivity (Human, Mouse)

application (WB, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, IHC-P, IF/ICC, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, IHC-P, IF/ICC, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, IP, ELISA) & cross reactivity (Human)

application (WB, IP, ELISA) & cross reactivity (Human)

application (WB, IHC-P, ELISA) & cross reactivity (Human, Mouse)

application (WB, IHC-P, ELISA) & cross reactivity (Human, Mouse)

application (WB, IF/ICC, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, IF/ICC, ELISA) & cross reactivity (Human, Mouse, Rat)

application (IF-P, IHC-P, ELISA) & cross reactivity (Mouse, Rat)

application (IF-P, IHC-P, ELISA) & cross reactivity (Mouse, Rat)

application (IF-P, IHC-P, ELISA) & cross reactivity (Human, Mouse, Rat)

application (IF-P, IHC-P, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, IF-P, IHC-P, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, IF-P, IHC-P, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, IP, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, IP, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, IHC-P, IF/ICC, ELISA) & cross reactivity (Human, Mouse)

application (WB, IHC-P, IF/ICC, ELISA) & cross reactivity (Human, Mouse)

application (WB, IHC-P, IF/ICC, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, IHC-P, IF/ICC, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, IHC-P, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, IHC-P, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, IHC-P, ELISA) & cross reactivity (Human, Rat)

application (WB, IHC-P, ELISA) & cross reactivity (Human, Rat)

application (WB, ELISA) & cross reactivity (Human, Rat)

application (WB, ELISA) & cross reactivity (Human, Rat)

application (WB, ELISA) & cross reactivity (Human)