MBP Inc. supplies a complete portfolio of PCR reagents and kits — standard Taq DNA polymerase, hot-start formulations, 2x master mixes, high-fidelity enzymes, and qPCR kits — for routine amplification, genotyping, cloning, and quantitative gene expression analysis.
All products are sourced from verified manufacturers for research labs across the USA and Canada. Request a quote today by contacting customerservice@mbpinc.net
PCR reagents are the enzymes, buffers, and master mix formulations that drive DNA amplification — the polymerase chain reaction first described by Kary Mullis in 1985 and recognised with the Nobel Prize in Chemistry in 1993. Reagent selection directly affects amplification specificity, sensitivity, and the suitability of products for downstream applications such as cloning or sequencing.
dNTPs (Deoxynucleotide Triphosphates): High-purity, functionally validated nucleotides offered in sets or premixes for smooth polymerization.
Hot Start PCR: Sophisticated "Hot Start" methods aimed at isolating polymerase function and enhancing specificity in intricate assays.
Standard PCR: Reliable and adaptable reagents fine-tuned for consistent outcomes in regular lab screening and amplification.
RT-PCR & cDNA Synthesis Products: Expert enzymes for accurate reverse transcription, guaranteeing dependable transformation of RNA to cDNA.
High-Fidelity PCR: Advanced proofreading polymerases designed for enhanced accuracy to reduce mutation rates in cloning processes.
Specialized PCR: Customized approaches for challenging protocols, incorporating GC-rich templates and bisulfite-treated DNA research.
qPCR/Real-Time PCR: Highly sensitive master mixes for accurate measurement and real-time observation of gene expression.
Miscellaneous Items: Crucial accessories such as loading dyes, stabilizers, and inhibitors for optimizing your PCR setup.
LAMP and Additional Isothermal Amplification: Quick, stable-temperature instruments aimed at effective diagnostics and on-site molecular testing.
Polymerase Type
Standard Taq DNA polymerase, isolated from Thermus aquaticus, provides reliable amplification for genotyping and screening without proofreading activity. Hot-start variants remain inactive until a high-temperature activation step. High-fidelity proofreading enzymes (Phusion, Q5, KOD, Pfu equivalents) minimise misincorporation for cloning and sequencing applications.
Format
Individual enzymes with optimised buffers and optional MgCl2 solutions suit custom protocol development. 2x master mixes pre-combine all components except template and primers, simplifying high-throughput setups and improving reproducibility.
Specificity vs. Speed Trade-off
Standard Taq is active immediately, which can lead to non-specific amplification at room temperature during setup. Hot-start formulations trade a brief activation step for substantially improved specificity, particularly valuable in multiplex or low-template-abundance reactions.
Downstream Application
Genotyping and colony screening tolerate standard Taq's error rate; cloning into expression vectors, site-directed mutagenesis, and sequencing-bound amplicons require high-fidelity polymerases with proofreading activity.
Dye-Containing vs. Standard Master Mixes
Dye-containing master mixes allow direct loading onto agarose gels without a separate loading dye addition step, streamlining workflows for routine band-confirmation PCR.
The choice between standard, hot-start, and high-fidelity formats should be made based on the specific application — standard Taq for routine genotyping and colony screening; hot-start for specificity-sensitive multiplex or low-abundance targets; high-fidelity for any application where the amplicon will be cloned, sequenced, or otherwise used in a context where occasional misincorporation could be costly. PCR reagents typically require −20 °C frozen storage with documented multiple freeze-thaw tolerance; lot-specific CoAs are available on request. When switching between reagent tiers for the same project -- for example, screening colonies with standard Taq before confirming a positive clone with high-fidelity PCR ahead of sequencing -- using consistent primer designs across both steps simplifies interpretation, since amplicon size and specificity should match between the two reactions. Product availability reflects MBP's catalogue as of mid-2026.
Ensure the precision of your experiments—reach out to the MBP team now for a quote on our expert PCR reagents and kits.