Reagents P

Inactive at room temperature Increased specificity This is the Hot-Start version of Choice-Taq&trade DNA Polymerase that requires a pre-activation step at 95&degC for 5 minutes in order to achieve a fully functional polymerase enzyme. The

Inactive at room temperature Increased specificity This is the Hot-Start version of Choice-Taq&trade DNA Polymerase that requires a pre-activation step at 95&degC for 5 minutes in order to achieve a fully functional polymerase enzyme. The

Hot-Start Taq Mastermix&trade is the heat activated version of Denville&#39s 2X, ready to go reaction mixture. It is inactive at room temperature and only requires addition of template, primers, and water.

Hot-Start Taq Mastermix™ is the heat activated version of Denville's 2X, ready to go reaction mixture. It is inactive at room temperature and only requires addition of template, primers, and water.

Hybridase&trade Thermostable RNase H specifically degrades the RNA in a DNA:RNA hybrid, without affecting DNA or unhybridized RNA.

Hydrochloric Acid, 37% w/w, Trace Metal grade, also meets ACS specifications

Hydrochloric Acid, 37% w/w, Trace Metal grade, also meets ACS specifications

Hydrochloric Acid, 37% w/w, Trace Metal grade, also meets ACS specifications

CAS: 12304-65-3 MDL No: MFCD01746913 Powder Molecular Formula: CH₁₆Al₂Mg₆O₁₉&middot4H₂O MW: 603.98 Flash Point: &gt110&degC (&gt230&degF) Density (g/mL): 2.0

IMMOLASE&trade is a heat-activated, thermostable DNA polymerase. IMMOLASE provides high yield and improved specificity when compared to standard polymerases and can eliminate the presence of non-specific binding, such as primer-dimers and

IMMOLASE&trade is a heat-activated, thermostable DNA polymerase. IMMOLASE provides high yield and improved specificity when compared to standard polymerases and can eliminate the presence of non-specific binding, such as primer-dimers and

IMMOLASE&trade is a heat-activated, thermostable DNA polymerase. IMMOLASE provides high yield and improved specificity when compared to standard polymerases and can eliminate the presence of non-specific binding, such as primer-dimers and