ABclonal Technology

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)

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

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

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