Brands

<h2 dir="ltr">What Are miRNA Lentiviral Negative Controls?</h2>
 MicroRNAs (miRNAs) are approximately 22-nucleotide non-coding RNAs that regulate gene expression post-transcriptionally by binding to the 3&prime; UTR of target mRNAs, triggering mRNA degradation or translational repression via the RNA-induced silencing complex (RISC). Lentiviral delivery of miRNA expression constructs enables stable, long-term modulation of miRNA activity &mdash; essential where transient transfection approaches are insufficient.
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<h2 dir="ltr">What you will find:</h2>
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<ul>
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Control Viruses models used in miRNA overexpression studies, for negative control normalization
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Validation of 3'UTR target utilizing bioluminescent-based reporter assays.
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miRNA-Off Control Lentiviruses used to baseline microRNA knockdown effects.
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Blank 5&rsquo; UTR reporter vector optimized for gene expression normalization and translational regulation studies&nbsp;
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Reporter Stable Cell Lines models with Luciferase or GFP markers for reliable assay standardization.
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</ul>
<h2 dir="ltr"> How to Choose a miRNA Negative Control</h2>
 Experiment Type Matching miRNA mimic (gain-of-function) experiments require a non-targeting miRNA mimic control. miRNA inhibitor/antagomiR (loss-of-function) experiments require a non-targeting inhibitor control. Lentiviral miRNA expression requires an empty vector or scrambled miRNA sequence. Mimic Control Design A non-targeting miRNA mimic control is a double-stranded RNA molecule resembling a mature miRNA duplex but with no significant homology to any known miRNA target in human, mouse, or rat transcriptomes &mdash; entering RISC the same way as a functional mimic. Inhibitor Control Design Non-targeting miRNA inhibitor (antagomiR) controls are single-stranded antisense sequences that enter the relevant cellular compartment without blocking any known miRNA, establishing the baseline for inhibitor-treated versus non-inhibitor comparisons. Vector Backbone for Lentiviral Delivery Stable lentiviral expression of miRNAs is used for long-term gain-of-function studies; the matched non-targeting lentiviral control must use the same promoter and vector backbone as the experimental construct to isolate sequence-specific effects. Inducible Format Availability Tet-On (doxycycline-responsive) non-targeting miRNA lentiviral controls are available for experiments requiring temporal control, used alongside inducible experimental constructs to control for doxycycline treatment itself. 
<h2 dir="ltr"> Specifications Context</h2>
 miRNA controls are designed to reflect the endogenous processing pathway of microRNAs, including Drosha and Dicer-mediated maturation before RISC loading. Because siRNA and miRNA constructs enter the RNA interference pathway differently, pathway-matched controls are important for accurate experimental interpretation. Non-targeting miRNA controls help distinguish sequence-specific effects from background effects associated with vector delivery and miRNA pathway activation. Available formats include lentiviral vectors, packaged viruses, reporter constructs, and stable cell line controls for miRNA and UTR-based studies. Product availability reflects MBP's catalogue as of mid-2026. 
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<a href="https://mbpinc.net/contact-us">Contact the expert team at MBP</a> and request a quote for efficient miRNA control requirements.

miRNA Control

Blank 5’ UTR Reporter Lentiviral Vector (Luc)

Unit Quantity

Species

Vector Map

Shipping Condition

<h2 dir="ltr">What Are Lentiviral Control &amp; Reporter Constructs?</h2>
 Rigorous experimental design requires matched controls that enter the same delivery workflow as the test construct. Lentiviral control and reporter constructs use the same vector backbones, promoters, and packaging systems as experimental vectors &mdash; ensuring observed differences between treated and control cells reflect genuine biological effects rather than artefacts of the delivery process.
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<h2 dir="ltr">What you will find:</h2>
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<ul>
<li dir="ltr" aria-level="1"><a href="https://mbpinc.net/reagents/dna/cloning-services-products/lentivirus/over-expression/control/reporter/luciferase-reporter">Luciferase Reporters: </a>for reliable assay validation using selective promoter-specific vectors, fluorescent reporters, dual-reporter systems, and background control</li>
<li data-section-id="644n3l" data-start="108" data-end="253">Fluorescent Reporter Controls: GFP and RFP lentiviral vectors and viruses for monitoring transduction efficiency and transgene expression.</li>
<li data-section-id="19809zr" data-start="255" data-end="399">Blank Control Vectors &amp; Viruses: Empty lentiviral backbones for negative controls, promoter evaluation, and custom construct development.</li>
<li data-section-id="112pumm" data-start="401" data-end="569">Promoter &amp; UTR Reporter Systems:&nbsp; Reporter vectors designed for promoter activity and regulatory element analysis, including promoter and 5&prime; UTR reporter formats.</li>
<li data-section-id="1j5a9h3" data-start="571" data-end="736">Selectable Marker Controls: Control constructs with puromycin, neomycin, hygromycin, and blasticidin resistance markers for selection and workflow validation.</li>
</ul>
<h2 dir="ltr"> How to Choose Control &amp; Reporter Constructs</h2>
 Control Type Needed Empty vector controls carry only the selection marker (puromycin, blasticidin, or hygromycin resistance) without a gene of interest, providing the baseline reference for overexpression or knockdown experiments. Fluorescent Reporter Channel GFP and RFP lentiviral reporters allow real-time monitoring of transduction efficiency by flow cytometry or fluorescence microscopy, matching the experimental construct's promoter for an accurate expected-expression reference. Luciferase Reporter Pairing Firefly luciferase (P. pyralis) and Renilla luciferase (R. reniformis) are the two most commonly paired reporters; because they use different substrates (D-luciferin and coelenterazine, respectively), both signals can be measured sequentially from the same sample. Promoter-less Baseline A promoter-less dual luciferase control vector provides a no-promoter baseline against which promoter-driven reporter constructs are normalised &mdash; useful for establishing background signal levels. Vector Backbone Matching Using a matched vector backbone ensures observed differences between experimental and control cells are due to the transgene, not differences in vector, promoter strength, integration preference, or selection marker. 
<h2 dir="ltr"> Specifications Context</h2>
 Because lentiviral integration is heritable, transduced cells maintain stable reporter gene expression across cell divisions &mdash; stable luciferase or GFP reporter cell lines generated this way are widely used in drug screening, pathway activation assays, and long-term in vivo imaging. Through ABM, MBP can supply promoter-reporter lentiviral constructs covering human and mouse promoters, driving firefly luciferase or GFP expression, as plasmid DNA or pre-packaged particles. Both plasmid and pre-packaged formats are available for immediate dispatch, with institutional account pricing available for core facilities. Core facilities managing reporter constructs across multiple research groups often standardise on a small set of validated control vectors to simplify inventory and ensure consistency across projects.&nbsp; 
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<a href="https://mbpinc.net/contact-us">Contact the expert team</a> at MBP today to get high-quality lentiviral control/reporters for your lab.

Control/Reporter

AAV Infection Guideline

Lentivirus Infection Protocol

Lentiviral Vector Amplification Protocol

AAV Packaging Protocol

Selection-Drug Killing Curve

Lentivector Packaging Protocol

Blank Promoter Reporter Lentiviral Vector (GFP)

Note

Blank Promoter Reporter Lentiviral Vector (Luc)

<h2 dir="ltr">What Are Protein Vector Control &amp; Reporter Constructs?</h2>
 Successful protein over-expression depends on knowing your starting point. Control and reporter vectors provide the experimental baseline against which the performance of experimental protein expression constructs is measured &mdash; confirming transfection efficiency, assessing promoter strength, or validating a new expression system.
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<h2 dir="ltr">What you will find:</h2>
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<ul>
<li data-section-id="jtohhd" data-start="2388" data-end="2536">Blank-Control Protein Vector (PV001): Empty protein expression control vector for use as a baseline control in protein expression experiments.</li>
<li data-section-id="ker4sd" data-start="2537" data-end="2674">Blank-Control Protein Vector (PV002): Blank-control expression vector for comparative studies and expression workflow optimisation.</li>
<li data-section-id="dmrpow" data-start="2675" data-end="2807">GFP-Control Protein Vector (PV003): GFP-expressing control vector for monitoring transfection performance and gene expression.</li>
</ul>
<h2 dir="ltr"> How to Choose Control &amp; Reporter Constructs</h2>
 Reporter Signal Type GFP/copGFP (fluorescence) suits transfection efficiency monitoring via FACS or microscopy. Firefly luciferase, Renilla luciferase, and NanoLuc (bioluminescence) suit promoter activity and pathway assays via plate reader. &beta;-galactosidase (LacZ) provides a colorimetric readout. Empty Vector Matching An empty vector control uses the same backbone, promoter, and selection marker as the experimental construct, with no gene of interest inserted &mdash; establishing the baseline effect of transfection, selection pressure, and promoter activity on cell physiology. Sensitivity Requirements NanoLuc (~19 kDa, furimazine substrate) is approximately 150-fold brighter than firefly or Renilla luciferase, useful for low-expression promoter studies and sensitive detection in small cell numbers; its small size also minimises steric interference as a fusion tag. Dual-Reporter Normalisation Paired firefly + Renilla luciferase systems allow internal normalisation per well &mdash; the Renilla reporter under a constitutive promoter corrects for differences in cell number, transfection efficiency, and lysis variability. 
<h2 dir="ltr"> Specifications Context</h2>
 A matched promoter between reporter and experimental construct ensures the reporter responds to the same transcriptional environment &mdash; differences in promoter strength between control and experimental vectors can generate misleading apparent expression differences attributable to the promoter rather than the protein of interest. NanoLuc and firefly luciferase use different substrates (furimazine vs. D-luciferin) and can be measured independently from the same sample, enabling dual-reporter assays even when the Renilla channel is occupied elsewhere. Reporter vectors can be stably integrated by antibiotic selection or lentiviral transduction to generate stable reporter cell lines for monitoring expression systems over time. Promoterless reporter backbone vectors are also available as empty cloning vehicles for inserting custom regulatory sequences. Product availability may vary. Browse the MBP control/reporter catalogue for current product information and availability. 
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<a href="https://mbpinc.net/contact-us">Contact the expert team </a>at MBP today and get high-quality control/reporter vectors for your lab.

Blank-Control Protein Vector

Accession Number

<h2 dir="ltr">What Is a Hot Start Taq Master Mix?</h2>
 Hot start 2x master mixes combine the convenience of the ready-to-use master mix format with the improved specificity of hot-start technology. These products are the standard reagent format for high-throughput genotyping, clinical diagnostic PCR, and multiplex reactions where non-specific amplification would compromise results. The right hot-start master mix supports cleaner amplification and streamlined setup. Select a formulation designed for reliable PCR performance.
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<h2 dir="ltr">What you will find:</h2>
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<li>Hot-start formulations from Azura, Accuris, BlasTaq, and Zymo Research for reduced non-specific amplification and primer-dimer formation.</li>
<li>Antibody-mediated hot-start activation in selected products, including ZymoTaq PreMix and Accuris Hot Start Taq Master Mix.</li>
<li>2X master mix and premix formats containing hot-start Taq polymerase, MgCl₂, dNTPs, and optimized PCR buffers.</li>
<li>Red-dye formulations for direct gel loading, including Azura 2X HS Taq Red Mix and Accuris Hot Start Taq Master Mix Red Dye.</li>
<li>Buffer systems optimized for endpoint PCR, multiplex PCR, and challenging template amplification.</li>
</ul>
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<h2 dir="ltr">How to Choose a Hot Start Taq Master Mix</h2>
 Activation Mechanism Format Antibody-mediated hot-start master mixes activate during the standard initial denaturation step; chemically modified formats may require a longer or dedicated activation incubation &mdash; confirm cycling protocol compatibility before adopting a new product. Component Pre-Optimisation A 2x hot-start Taq master mix is a pre-formulated, double-concentrated solution containing hot-start Taq DNA polymerase, dNTPs, MgCl2, and PCR buffer &mdash; the hot-start polymerase remains inactive at room temperature until the activation step is reached during cycling. Multiplex Compatibility For multiplex PCR (multiple primer pairs in a single reaction), hot-start master mixes substantially reduce primer-primer cross-reactivity compared to standard Taq master mixes, improving reliable detection of all intended targets. Diagnostic and Clinical Applications High-specificity master mixes are the standard reagent format for clinical diagnostic PCR, where false-positive bands from non-specific amplification could affect result interpretation. Throughput and Format 2x hot-start master mixes are designed for high-throughput genotyping pipelines, requiring only template and primer addition &mdash; minimising pipetting steps across large sample sets. 
<h2 dir="ltr"> Specifications Context</h2>
 Hot-start 2x master mixes are set up like standard master mixes&mdash;combined with template and primers at the manufacturer-specified ratio to achieve a 1x working concentration&mdash;but the polymerase remains inactive until the activation step, typically during initial denaturation for antibody-mediated formats. This combination of convenience and specificity has made hot-start master mixes a widely used choice for high-throughput genotyping, multiplex PCR, and other applications requiring reliable target-specific amplification. Product availability reflects MBP's catalogue as of mid-2026. Labs validating a new hot-start master mix should evaluate performance using known positive and negative samples and document results by lot number to support quality assurance, audits, and troubleshooting. 
<a href="https://mbpinc.net/contact-us">Contact the expert team</a> at MBP and get premium-quality Hot Start Taq Master Mix formulations for your lab today.

Hot Start Taq Master Mix

DataSheet

MSDS

Flyer

PCR Product Guide

BlasTaq 2X PCR MasterMix

Application

Concentration

Storage Condition

<h2 dir="ltr"> What Is a Primer-Probe Master Mix?</h2>
 A primer-probe master mix is a 2x concentrated formulation built around a hot-start Taq DNA polymerase, dNTPs, MgCl2, and optimised buffer, designed for use with hydrolysis-probe detection chemistries such as TaqMan. Unlike SYBR Green dye-based mixes, primer-probe formulations rely on a separately added, fluorescently labelled, sequence-specific probe combined with target-specific primers to generate the detection signal, with specificity coming from both primer and probe sequence matching. Choose a primer-probe master mix when assay specificity is critical, when multiplexing several targets in one well is needed, or when working with an established probe-based assay design.
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<h2 dir="ltr">What you will find:</h2>
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<ul>
<li data-section-id="qhwnhl" data-start="279" data-end="413">Probe-based qPCR master mixes with HiROX, LoROX, and ROX-free options for compatibility across a range of real-time PCR instruments.</li>
<li data-section-id="1cnihmh" data-start="414" data-end="543">Hot-start polymerase formulations designed to support specific target detection in hydrolysis probe (TaqMan-style) qPCR assays.</li>
<li data-section-id="51tf3n" data-start="544" data-end="643">Blue tracking dye probe master mixes for easier reaction setup and visual pipetting confirmation.</li>
<li data-section-id="cjeacg" data-start="644" data-end="749">2X ready-to-use probe qPCR master mixes containing optimized buffers, dNTPs, and polymerase components.</li>
<li data-section-id="xfwfro" data-start="750" data-end="884">One-step probe RT-qPCR formats that combine reverse transcription and real-time PCR amplification in a single tube for RNA analysis.</li>
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<h2 dir="ltr"> How to Choose a Primer-Probe Master Mix</h2>
 Reference Dye Inclusion Primer-probe master mixes commonly include ROX as a passive reference dye for signal normalisation across wells on instruments that require it -- confirm whether your real-time PCR instrument needs ROX and whether the chosen master mix includes it or requires separate addition. Multiplexing Capability A core advantage of probe-based chemistry is multiplexing -- detecting multiple targets in a single well using probes labelled with spectrally distinct fluorophores. Confirm the master mix is validated for the number of multiplexed targets your assay requires. Probe Chemistry Compatibility While TaqMan-style hydrolysis probes are the most common, other probe chemistries such as Scorpion primers, exist; confirm the master mix is formulated for compatibility with your specific probe chemistry. Primer and Probe Concentration Guidelines Standard setups commonly use primer pairs at a final concentration around 0.5 &micro;M and probes at 0.25-0.5 &micro;M -- confirm the master mix manufacturer's recommended ranges, since probe concentration affects both signal intensity and background. One-Step vs. Two-Step Application Primer-probe master mixes are used in both two-step workflows (with a separately generated cDNA template) and as the chemistry component within one-step RT-qPCR kits -- confirm which configuration matches your workflow when selecting a product. 
<h2 dir="ltr"> Specifications Context</h2>
 In probe-based qPCR, the 5'-3' exonuclease activity of the Taq DNA polymerase cleaves the dual-labelled probe annealed to the target sequence during amplification, separating a fluorescent reporter from its quencher and generating signal proportional to target abundance -- the mechanism underlying the widely used TaqMan probe system. Because both primer and probe sequence must match the target for signal generation, probe-based assays generally offer higher specificity than dye-based detection, and because probes can be labelled with spectrally distinct fluorophores, multiple targets can be detected in a single well. Standard reaction setup adds primer pairs at approximately 0.5 &micro;M and probes at 0.25-0.5 &micro;M to the 2x master mix. Primer-probe master mixes are typically stored at &minus;20 &deg;C to &minus;30 &deg;C and protected from light; lot-specific CoAs are available on request. 
<a href="https://mbpinc.net/contact-us">Contact the expert team</a> at MBP today and get optimized Primer-Probe real-time master mixes for your lab.

Primer-Probe

ROX Machine Compatibility

BlasTaq™ 2X qPCR MasterMix Product Testing Report

Blastaq™ 2X qPCR MasterMix Product Stability Report

BlasTaq 2X qPCR MasterMix

<h2 dir="ltr">What Is Hot Start Taq DNA Polymerase?</h2>
 Hot-start Taq DNA polymerase is the enzyme of choice for PCR applications where non-specific amplification or primer dimer formation has been problematic with standard Taq. By keeping the polymerase inactive until a high-temperature activation step, hot-start formulations prevent the room-temperature primer extension that drives non-specific products in standard Taq reactions. Choose a polymerase suited to your assay requirements.
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<h2 dir="ltr">What you will find:</h2>
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<ul>
<li data-section-id="1hsv5i3" data-start="233" data-end="391">Hot-start Taq DNA polymerases are designed to support multiplex PCR by reducing non-specific amplification and primer-primer interactions during reaction setup.</li>
<li data-section-id="bhgh5r" data-start="392" data-end="516">Formulations suitable for high-throughput PCR workflows requiring a stable room-temperature setup before thermal activation.</li>
<li data-section-id="1h2z623" data-start="517" data-end="640">Improved specificity for amplification of low-abundance targets compared with conventional non-hot-start Taq polymerases.</li>
<li data-section-id="1nifv8r" data-start="641" data-end="743">Cleaner amplicon generation for downstream applications such as cloning, sequencing, and genotyping.</li>
<li data-section-id="bof93a" data-start="744" data-end="892">Enzyme and buffer systems formulated to support amplification of challenging templates, including GC-rich regions and complex genomic DNA samples.</li>
</ul>
<h2 dir="ltr"> How to Choose Hot Start Taq DNA Polymerase</h2>
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Inactivation Mechanism Antibody-mediated formulations use a heat-sensitive antibody that reversibly binds and inhibits the enzyme until denatured during the initial high-temperature step. Chemically modified formulations use covalent modifications to active-site residues that are reversed by heat during cycling. Standard vs. Hot-Start Comparison Standard Taq DNA polymerase is a formulation of recombinant Taq that remains active at ambient temperatures, permitting non-specific primer extension during reaction setup &mdash; hot-start formulations are reversibly inactivated at ambient temperature specifically to prevent this. Buffer Compatibility As with standard Taq, optimised 10x PCR buffer formulations are designed to complement the specific hot-start enzyme's activation and activity profile. Activation Time Considerations Confirm whether your chosen hot-start formulation activates within a standard initial denaturation step or requires an extended/dedicated activation incubation, as this affects total cycling protocol time. Application Fit Hot-start Taq is recommended wherever specificity is a concern: multiplex PCR, low-template-abundance amplification, diagnostic PCR, and any workflow where primer dimer formation has been observed with standard Taq. 
<h2 dir="ltr"> Specifications Context</h2>
 Hot-start Taq DNA polymerase is a recombinant Taq formulation that remains inactive during reaction setup, preventing the non-specific primer extension that standard Taq can permit before thermal cycling begins. This improved specificity is particularly valuable for multiplex PCR, low-abundance templates, and applications where non-specific products could affect result interpretation. Hot-start enzymes are typically stored at &minus;20 &deg;C and commonly supplied with matched PCR buffer. Because antibody-mediated and chemically modified formats can require different activation conditions, initial denaturation parameters should be verified when introducing a new enzyme. Product availability reflects MBP's catalogue as of mid-2026. 
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<a href="https://mbpinc.net/contact-us">Contact the expert team </a>at MBP today to request a quote and identify the most suitable hot start Taq DNA polymerase for your workflow.