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PrimeScript III Reverse Transcriptase (3,000 U/µl, 5% Glycerol)

• 10 μl x 3,000 U/μl, 5% glycerol
• 1 ml x 5X PrimeScript Buffer
• 1 ml x Storage Buffer, low glycerol

• Optimal reaction temperature of 52–55°C
• Fast reaction speed
• Tolerant to typical inhibitors in biological fluids, prevents template degradation (RNase H minus)
• Specific for complex secondary RNA structures (strong strand displacement activity starting at 42°C)

SMART MMLV Reverse Transcriptase (25 U/µl, Glycerol-Free)

• 10 μl x 25 U/μl, glycerol-free
• 1 ml x 5X First-Strand Buffer

• Optimal reaction temperature of 42°C
• Wild type
• RNase H plus
• Ideal for low template copy number and isothermal amplification protocols

Recombinant RNase Inhibitor (300 U/µl, 5% Glycerol)

• 20 μl x 300 U/μl, 5% glycerol

• Recombinant protein
• Reversible, competitive, broad-spectrum RNase A/B/C inhibitor not affecting RNase H activity of RT
• Can be irreversibly inactivated to restore ribonuclease activity
• Works across a wide pH range and with low-DTT formulations

50X Titanium Taq DNA Polymerase (Glycerol-Free)

• 50 μl x 50X, glycerol-free enzyme mix
• 0.3 ml x 10X Titanium Taq PCR Buffer

• Extremely high yield, hot‑start enzyme
• T/A overhangs
• Ample Mg²⁺ concentration tolerance
• No 5’–3’ or 3’–5’ exonuclease activity
• Ideal for high-level multiplexed reactions, multitarget and sensitive PCR applications, microarrays, and forensics

TaKaRa Taq HS (25 U/µl, Glycerol-Free)

• 50 μl x 25 U/μl, glycerol-free
• 1 ml x 10X PCR Buffer, Mg²⁺ plus
• 1 ml x rTaq Storage Buffer, glycerol-free

• Hot-start enzyme
• <4 kb amplicons (T/A overhangs)
• 5’–3’ exonuclease activity and no 3’–5’ exonuclease activity
• Ideal for routine qPCR and RT-qPCR assays
• dUTP/UNG- and multiplex-compatible

TaKaRa Ex Taq HS (30 U/µl, Glycerol-Free)

• 20 μl x 30 U/μl, glycerol-free
• 1 ml x 10X Ex Taq Buffer, Mg²⁺ plus
• 1 ml x rTaq Storage Buffer, glycerol-free

• High yield, hot‑start enzyme with inhibitor tolerance
• <20 kb amplicons (T/A overhangs)
• 5’–3’ and 3’–5’ exonuclease activity
• A proofreading polymerase for large amplicons and high-sensitivity qPCR assays

PrimeSTAR GXL DNA Polymerase (25 U/µl, Glycerol-Free)

• 20 μl x 25 U/μl, glycerol-free
• 1 ml x 5X PrimeSTAR GXL Buffer, Mg²⁺ plus
• 1 ml x Storage Buffer, glycerol-free

• Highest-fidelity and fastest hot‑start enzyme for long amplicons (<30 kb, blunt ends), high GC content (up to 74%), repetitive sequence templates, and excess template
• Suitable for NGS applications

SpeedSTAR HS DNA Polymerase (25 U/µl, Glycerol-Free)

• 20 µl x 25 U/µl, glycerol-free
• 1 ml x 10X Fast Buffer I, Mg²⁺ plus
• 1 ml x 10X Fast Buffer II, Mg²⁺ plus
• 1 ml x Storage Buffer, glycerol-free

• High yield, hot‑start enzyme with fastest speed
• <20 kb amplicons (T/A overhangs)
• 5’–3’ and 3’–5’ exonuclease activity
• Suitable for fast qPCR and long amplicons

• Lyophilization-ready one-step qPCR mix for RNA and DNA targets

• Lyophilized one-step qPCR mix for RNA and DNA targets

• Lyophilization-ready qPCR mix for DNA targets only

• Lyophilized qPCR mix for DNA targets only

200 Rxns

• High-concentration (5X) mix for DNA target detection; with or without ROX

• 2X mix for routine RT-qPCR applications

• 2X mix with UNG to prevent carryover contamination

• High-concentration (5X) mix for RNA target detection; with or without ROX

• High fidelity
• Wide template input range (12.5–1,250 ng)
• Fast processing (~5 sec/kb)

• Handles GC-rich targets, excess template, and long products (up to 30 kb)

• Hot-start enzyme
• Handles GC-rich targets with minimal PCR bias