Biomeme
Go-Plate™ & Go-Vial™ Assay Kits

Bundibugyo virus (BDBV)

Lyophilized, shelf-stable nucleic acid amplification test for rapid detection of Bundibugyo ebolavirus RNA. Available in pre-aliquoted 96-well plates or bulk reaction vials. No extraction required.

$1,249
Go-Plate™ · 96 reactions
$649
Go-Vial™ · 600 µL mix
~10
minutes to result
2
targets (duplex)
96 / 120
reactions (Plate / Vial)
15–30°C
room temp storage
Kit Contents

What's in the Kit

Bundibugyo virus 96-well Go-Plate or Go-Vial

Lyophilized duplex reactions with master mix, enzymes, guides, and probes for all targets.

SampleDirect™ Lysis Buffer

Bulk bottle. Liberates nucleic acids from the sample matrix and inactivates degrading nucleases.

SampleDirect™ Recovery Buffer

Bulk bottle. Renders the lysate compatible with nucleic acid amplification chemistry.

Go-Plates™ — Flexible by Design

$1,249 · 96 rxns

Go-Plates are pre-aliquoted, lyophilized plates for lab use in standard commercial thermocyclers. Run the full 96-well plate or cut away and run as strips in any direction.

Each well contains a 20 µL lyophilized duplex reaction with master mix, guides, and probes for all targets. A multiplexed reaction means both targets are in a single reaction — one well equals one sample or replicate.

Compatible with almost all PCR and qPCR cycler models which accept Regular Profile (RP) products, such as ABI/Life Technologies, Agilent, Bio-Rad, Eppendorf, and others.

Cuttable — Multiples of 8

82432485664728096

Cuttable — Multiples of 12

24364860728496

Go-Vials™ — Ultimate Flexibility

$649 · 600 µL mix

Go-Vials are lyophilized for lab use in standard commercial thermocyclers and your own plastics of choice. Run the full 600 µL reaction volume or freeze for later use.

Each vial contains a 600 µL lyophilized duplex reaction with master mix, guides, and probes for all targets. A multiplexed reaction means both targets are in a single reaction — one well equals one sample or replicate.

Compatible with all PCR and qPCR cycler models which detect Cy5 and Cy5.5 fluorophores.

Reaction Yield by Reaction Volume (600 µL Bulk)

120 5 µL

reactions

Maximum yield for micro-volume protocols

60 10 µL

reactions

Optimized for high-throughput screening

30 20 µL

reactions

Standard reaction volume equivalent to Go-Plate

24 25 µL

reactions

Higher template volume for maximum sensitivity

Aliquot into your own tubes or plates at the reaction volume required by your protocol.

Technical Data

Assay Specifications

Product Name Bundibugyo virus Go-Plate Kit / Go-Vial Kit
Price $1,249 (Go-Plate) / $649 (Go-Vial)
Extraction Required No
Specimen Type EDTA Whole Blood (volume flexible)
Reaction Volume 20 µL (Go-Plate) / Flexible (Go-Vial)
Time-to-Result ~10 minutes
Storage Temperature 15–30°C (room temperature)
Color Channels Cy5, Cy5.5
Target 1 Bundibugyo virus RNA (BDBV)
Target 2 Endogenous Positive Control (PPIB)
Form Factor 96 × 0.1 mL plate (cuttable into strips) / Go-Vial
Compatible Cyclers Bio-Rad CFX96, ABI QuantStudio 5+, Agilent, Eppendorf, and other standard RP-profile cyclers / Any cycler able to detect Cy5 and Cy5.5
4-Step Workflow

Protocol

From raw sample to result in approximately 10 minutes. No extraction, no purification, no complex master mix prep.

1

Lyse

Add EDTA whole blood into SampleDirect™ lysis buffer.

2

Recover

Add SampleDirect™ recovery buffer into the lysate.

3

Transfer

Transfer lysed and recovered sample mixture to the assay reaction well.

4

Amplify

Heat at 58°C for 10 minutes. Read results.

Pathogen Profile

About Bundibugyo virus

Bundibugyo virus (BDBV) is a species of ebolavirus closely related to the Zaire ebolavirus (EBOV). It is one of several species that can cause Ebola virus disease (EVD) in humans, manifesting as viral hemorrhagic fever with high mortality rates.

First identified during a 2007 outbreak in the Bundibugyo District of Uganda, BDBV presents a significant biosecurity and public health concern. Rapid, accurate identification of the specific ebolavirus species is critical for outbreak response, contact tracing, and clinical management — particularly in resource-limited and austere field environments where central laboratory infrastructure may be unavailable.

Available in Go-Plate and Go-Vial formats, this assay enables detection of BDBV RNA directly from EDTA whole blood in approximately 10 minutes, with no nucleic acid extraction step required. An endogenous human RNA control (PPIB) is included to verify sample integrity.

Biosafety Classification

Bundibugyo virus is classified as a Risk Group 4 pathogen. Handle specimens in accordance with applicable biosafety regulations and institutional guidelines.

Assay Targets

Cy5

BDBV

Bundibugyo ebolavirus genomic RNA

Cy5.5

PPIB

Endogenous human RNA positive control

Enabling Technology

About the Chemistry

Biomeme's proprietary isothermal chemistry system was developed out of learnings from the COVID pandemic — when supply chains collapsed, labs faced scaling challenges, and labor shortages crippled testing capacity.

SampleDirect™

Sample Preparation

A 2-component system that prepares nucleic acids for amplification. No purification or additional buffer systems needed.

Step 1: Crude sample is added to the lysis buffer, which liberates nucleic acids from the matrix and inactivates degrading nucleases.

Step 2: The lysed sample is mixed with the recovery buffer, which renders the lysate compatible with nucleic acid amplification chemistry.

Tested Matrices

Whole BloodUrineNasal SwabsBuccal SwabsVaginal SwabsEnvironmental SwabsSoilCollection/Transport Media

Target Flexibility

DNA & RNAHuman/Animal CellsVirusesGram+/Gram− BacteriaSporesProtozoa

DTECT™

Amplification Chemistry

Differential Targeted Endonuclease Cleavage Technology — a strand-displacement method employing a novel guide molecule that introduces an exogenous endonuclease restriction site to the target locus of interest.

The System: 2 enzymes (a polymerase and a site-specific nicking endonuclease) + 2 guide oligonucleotides, paired with a Molecular Beacon probe for detection and multiplexing. RNA amplification requires an additional reverse transcriptase and primer.

The DTECT chemistry is lyophilized — pre-mixed, pre-aliquoted, and shelf-stable — eliminating the need for cold-chain logistics and manual reagent preparation.

Reaction Components

Master mix with polymerase + nicking endonuclease
2 target-specific guide oligonucleotides
Molecular Beacon probes
Reverse transcriptase + primer (for RNA targets)
Why Go-Plates and Go-Vials

Key Advantages

No Cold Chain

Ships and stores at room temperature (15–30°C). No dry ice shipment, no −80°C freezer. Eliminates the risk of degradation from freeze-thaw cycles.

No Mixing (or Aliquoting for Go-Plates)

Each Go-Plate well is pre-mixed, pre-aliquoted, and lyophilized. For Go-Vials, reconstitute the bulk mix and aliquot into your preferred volumes. No molecular biologist required. No complex master mix prep.

Maximum Sensitivity

Because each test is lyophilized, you can add more sample template (20 µL in Go-Plates, or flexible volumes in Go-Vials) to directly increase analytical sensitivity without altering reagent concentrations.

Standard Equipment

Runs on standard cyclers: Go-Plates fit regular profile (RP) cyclers (Bio-Rad, ABI, Agilent, Eppendorf), while Go-Vials work with your own plastics on any cycler detecting Cy5 and Cy5.5.

10-Minute Results

From raw sample to actionable result in approximately 10 minutes. Lightning-fast isothermal amplification with no compromise on sensitivity.

Endogenous Control

Includes a human RNA positive control (PPIB) in every reaction to verify sample integrity and confirm successful nucleic acid recovery.

Order Bundibugyo virus Go-Plate or Go-Vial Kits

Ready to deploy rapid BDBV detection in your laboratory? Contact our sales team to place an order or request additional information.

$1,249 (Go-Plate, 96 rxns) · $649 (Go-Vial, 600 µL mix) · No extraction required · Ships at room temperature

For Research Use Only. Not for use in human or veterinary diagnostics. The performance characteristics of this product have not been established.