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Microbiomics Reagents for Microbial Community Profiling and Sequencing Workflows

 

Microbiomics brings together the reagents used to characterize a microbial community, from microbial DNA and RNA extraction with host DNA depletion through 16S rRNA and shotgun metagenomic library preparation for next-generation sequencing, plus the reference standards needed to validate a microbiome workflow's accuracy. As a top-level branch parallel to Cell Biology, Protein Analysis, and RNA Analysis Reagents, this category organizes microbiome-specific workflows separately from general nucleic acid or protein work. Academic and core laboratories profiling microbial communities can benefit from workflow-stage guidance when selecting extraction methods, library preparation strategies, and validation standards.

Explore available microbiomics reagents or request a quotation by contacting customerservice@mbpinc.net. Our team can help identify the appropriate extraction kits, library prep reagents, and reference standards for your microbiome sequencing workflow.

Microbiomics

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25% Yeast Extract Solution (YEL01)
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Bacterial DNA Standards and No Template Control (#1-8)
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Femto™ Bacterial DNA Quantification Kit (100 Rxns.)
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Femto™ Bacterial qPCR Premix (1.8 ml)
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Femto™ Fungal DNA Quantification Kit (100 Rxns.)
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Femto™ Fungal qPCR Premix (1.8 ml)
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Femto™ Human DNA Quantification Kit (100 Rxns.)
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Femto™ Human qPCR Premix (1.8 ml)
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Fungal DNA Standards and No Template Control (#1-8)
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Human DNA Standards and No Template Control (#1-8)
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LB (Lennox) Agar (LBP04)
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What is Microbiomics as a reagent category?

 

Microbiomics spans the reagents used to characterize a microbial community's composition and function: microbial DNA and RNA extraction kits, often including host DNA depletion for host-associated samples like swabs or stool; 16S rRNA gene amplicon library preparation for cost-effective taxonomic profiling; shotgun metagenomic library preparation for unbiased, deeper community characterization; and microbiome reference standards for validating a sequencing workflow's accuracy. As a top-level branch parallel to Cell Biology, Protein Analysis, and RNA Analysis Reagents, this category organizes microbiome-specific tools separately from general nucleic acid extraction or sequencing reagents.

 

What you will discover:

 

  • RNA Sequencing: Unique reagents designed for the isolation and enhancement of microbial mRNA, tailored to minimize ribosomal RNA interference and preserve transcript stability for precise gene expression assessment.

  • Microbial Regulations & Guidelines: Certified reference standards tested for reproducibility that include exact genomic ratios of bacteria and fungi to ensure sequencing precision and confirm minimal sequence bias.

  • PCR & Molecular Assays: Master mixes and buffers designed for high-sensitivity, facilitating the swift detection of specific pathogens and functional genes while ensuring minimal spectral cross-talk.

  • Kits for Preparing 16S/ITS NGS Libraries: Cohesive processes for the specific amplification of hypervariable regions, employing high-fidelity polymerases to guarantee varied library preparation for taxonomic classification.

 

How to navigate microbiomics reagents

 

Choose an extraction method with host DNA depletion for host-associated samples

In samples like swabs or body fluids, host DNA can vastly outweigh microbial DNA, with one analysis finding up to 99% of sequencing reads in some studies mapping to the host genome rather than microbes, so a dedicated extraction method including host DNA depletion meaningfully increases microbial read coverage.

Decide between 16S rRNA amplicon sequencing and shotgun metagenomic sequencing

16S rRNA sequencing is more cost-effective, requires less input DNA, and is less impacted by host DNA contamination, making it the more accessible choice for routine community composition profiling, while shotgun metagenomic sequencing provides deeper insight into functional content like virulence factors, antibiotic resistance genes, and metabolic networks at higher cost and complexity.

Confirm which 16S hypervariable region coverage matches your resolution needs

16S library prep kits commonly target specific hypervariable regions, such as V3-V4, and using primer sets re-designed against an updated 16S reference database can improve taxonomic coverage and resolution compared with older, less comprehensive primer designs.

Include a microbiome reference standard to validate your workflow

A defined microbial DNA or inactivated bacteria standard provides a specific, customized control for confirming your extraction, library prep, and sequencing workflow is performing as expected, supporting reproducibility and enabling comparison of results across different laboratories.

Plan for PCR chimera formation as a known challenge in amplicon sequencing

PCR chimeric sequences, artificial sequences formed from the recombination of two or more templates during amplification, are a recognized challenge in 16S library preparation, and kits using real-time PCR to control cycle number can help limit chimera formation below problematic levels.

 

Specifications context

 

In a comparison of whole metagenome shotgun sequencing approaches, samples prepared without host DNA removal showed over 90% of sequencing reads mapping to the human genome, while a dedicated host DNA depletion method reduced this to under 5% human reads, dramatically increasing the proportion of reads available for actual microbial analysis. As of 2026, full-length 16S rRNA sequencing using long-read platforms continues to expand alongside traditional short-read amplicon approaches, offering improved species- and strain-level resolution for microbiome community profiling.

Reach out to the specialized team at MBP Inc. now to ask for a quote for the appropriate microbiomics reagents for your laboratory.

FAQ

In samples such as swabs or body fluids, host human or animal DNA can vastly outweigh microbial DNA, with one analysis finding up to 99% of sequencing reads in certain studies mapping to the host genome rather than the microbial community of interest. A dedicated extraction method including host DNA depletion can reduce this to under 5% host reads in some cases, dramatically increasing the proportion of data available for actual microbiome analysis.
16S rRNA sequencing is more cost-effective, requires less input DNA, and is less impacted by host DNA contamination, making it a practical choice for routine community composition profiling, while shotgun metagenomic sequencing provides deeper functional insight, such as virulence factors, antibiotic resistance genes, and metabolic networks, at higher cost and complexity. Many studies start with 16S profiling and reserve shotgun metagenomics for projects specifically needing that functional depth.
A PCR chimera is an artificial sequence formed from the recombination of two or more PCR templates during amplification, which can be misinterpreted as a genuine, novel organism if not properly controlled for during 16S library preparation. Kits using real-time PCR to control amplification cycle number can help limit chimera formation to a low, manageable percentage of total reads.
16S library prep kits commonly target specific hypervariable regions of the 16S rRNA gene, such as V3-V4, because these regions provide sufficient taxonomic resolution while keeping the amplicon a practical size for sequencing, and primer sets redesigned against updated 16S reference databases can improve coverage of previously underrepresented taxa. Checking which hypervariable region a specific kit targets helps confirm it matches your study's taxonomic resolution needs.
A microbiome reference standard, typically a defined microbial DNA or inactivated bacteria preparation with a known composition, provides a specific, customized control for confirming that your extraction, library preparation, and sequencing workflow is performing as expected. Including a reference standard also supports reproducibility and allows more reliable comparison of results generated in different laboratories or at different times.
Many microbial DNA extraction kits, particularly those with host DNA depletion features, can support both 16S amplicon and shotgun metagenomic downstream workflows, since both approaches start from the same extracted, purified microbial DNA. The choice of downstream library preparation kit, rather than the extraction method itself, is what determines whether you proceed with 16S or shotgun metagenomic sequencing.
Long-read sequencing platforms can generate full-length 16S rRNA reads rather than reads covering only a single hypervariable region, providing improved species- and strain-level resolution and reducing some of the classification ambiguity that comes from analyzing just a fragment of the gene. This has made full-length 16S sequencing an increasingly used complement to traditional short-read amplicon approaches for studies needing finer taxonomic resolution.
Yes, MBP offers academic and bulk pricing across microbial DNA and RNA extraction kits, 16S rRNA and metagenomic library preparation kits, and microbiome reference standards. Orders ship from MBP's US office in Houston, Texas, with stock available in both USD and CAD.
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