

Vacuum Manifold Nucleic Acid Purification System
真空歧管核酸纯化系统
- SKU DRE-0004
- DNA/RNA Extraction
- CE (to be confirmed)
- ISO 9001 manufacturing (to be confirmed)
- IEC 61010-1 test report (to be confirmed)
Price on request — FOB / CIF quoted per order
Prices depend on configuration, quantity and destination port.
Key specifications
| Sample capacity | 12-96 per manifold |
|---|---|
| Working vacuum | -60 to -90 kPa |
| Compatible formats | Spin columns, 96-well filter plates |
| Body material | Polycarbonate or acrylic |
| Fittings | Anodised aluminium or stainless luer |
| Waste collection | Removable tray or bottle |
By Lab Manufacturers China Technical TeamLast reviewed Standards: ISO 13485 manufacturing, ISO 15189, CLSI MM13-A
What is the Vacuum Manifold Nucleic Acid Purification System?
A manifold that pulls samples through silica membrane columns or filter plates under vacuum for parallel purification of plasmid DNA, genomic DNA or RNA. It is an economical option for medium-throughput, column-based workflows.
What is the Vacuum Manifold Nucleic Acid Purification System?
A manifold that pulls samples through silica membrane columns or filter plates under vacuum for parallel purification of plasmid DNA, genomic DNA or RNA. It is an economical option for medium-throughput, column-based workflows.
Overview
The vacuum manifold holds a row of spin columns or a 96-well filter plate above a waste tray, and a vacuum source draws lysate, wash buffer and eluate through the silica membrane in sequence. Lysis, neutralisation and binding are still performed in tubes or plates, while the manifold replaces repeated centrifugation, which shortens hands-on time and lets 12 to 96 samples be processed in parallel. Manifolds are made of polycarbonate or acrylic with anodised aluminium or stainless luer fittings, and a vacuum gauge or regulator maintains 60 to 90 kPa for even flow. Elution is collected in tubes or a collection plate for direct use. The method is widely used for plasmid miniprep and midiprep, gel-extraction cleanup, PCR cleanup and RNA purification, and it needs no dedicated instrument electronics, only a vacuum pump.
How does it work?
Extraction begins with lysis, which uses chaotropic salts, detergents and often proteinase K to break cell membranes and denature nucleases. Nucleic acids then bind to a solid phase, either silica in the presence of high salt or magnetic beads with a silica or carboxyl surface. Washing removes proteins, salts and inhibitors, and elution in a low-salt buffer or nuclease-free water releases purified nucleic acid. Automated instruments move magnetic particles with a magnetic rod, or pipette liquid through a filter plate, following a program that controls lysis time, mixing, bead collection, wash steps and heated elution. Yield and purity are checked by absorbance at 260, 280 and 230 nm or by fluorescent dyes. Carryover between samples and cross-contamination are controlled by tip changes, sealed consumables and controlled airflow.
What are the key features?
- Parallel processing of 12 to 96 samples per manifold.
- Accepts spin columns and 96-well filter plates.
- Vacuum gauge or regulator for even flow across wells.
- Replaces repeated centrifugation to cut hands-on time.
- Chemical-resistant body with luer or barbed fittings.
- Compact bench footprint with only a vacuum pump required.
What are the technical specifications?
A typical vacuum manifold nucleic acid purification system configuration offers sample capacity of 12-96 per manifold, working vacuum of -60 to -90 kPa, compatible formats of Spin columns, 96-well filter plates, body material of Polycarbonate or acrylic, fittings of Anodised aluminium or stainless luer and waste collection of Removable tray or bottle. Values are indicative of the product class; the exact figures for each configuration are confirmed on the quotation and the calibration documents supplied with the instrument.
Which applications is it used for?
The Vacuum Manifold Nucleic Acid Purification System is used in plasmid DNA miniprep and midiprep, PCR product and gel extraction cleanup, genomic DNA purification from cultured cells and total RNA cleanup. Across the wider DNA/RNA Extraction class, laboratories also deploy it for clinical pathogen nucleic acid testing, cancer genomics and mutation analysis and next-generation sequencing library preparation.
Which standards and certifications apply?
Relevant standards and methods include ISO 13485 manufacturing, ISO 15189, CLSI MM13-A, IEC 61010-1 and IVDR (EU) 2017/746. Certification candidates for this model are CE, ISO 9001 manufacturing and IEC 61010-1 test report; each is to be confirmed for the specific configuration before shipment, and certificates are supplied only where they have been issued.
Keep extraction and amplification areas physically separate, use dedicated pipettes and filter tips, and clean surfaces with fresh hypochlorite or a validated decontaminant. Note that guanidine-based lysis waste must not be mixed with bleach, because toxic gas can form; collect and dispose of it separately under local rules. Wear gloves and change them frequently, since skin and breath carry nucleases and amplification products. Run negative controls in every batch and monitor extraction efficiency with a known standard. Calibrate heating blocks, pipetting accuracy and any magnetic rod height at fixed intervals. Validate each new sample matrix for yield, purity and inhibitor carryover before routine use, and keep lot records of reagents.
How do I select the right Vacuum Manifold Nucleic Acid Purification System?
Select the manifold when your workflow is already column-based, throughput is moderate and you want to remove centrifugation without buying a robotic platform. Confirm the column and filter plate formats accepted, the vacuum range and whether a waste bottle and trap are included. Specify the elution format and expected yield, and note that a vacuum pump is usually supplied separately.
How does it compare with other DNA/RNA Extraction variants?
Start with the sample: whole blood, tissue, swabs, plasma, plant material or environmental samples each need a different lysis protocol, and input volume drives consumable and platform choice. Next set throughput, whether a few samples per run or several hundred per day, because this decides between manual manifolds, small benchtop instruments and 96-well platforms. Consider the elution volume and concentration required by the downstream assay, since quantitative PCR and sequencing have different sensitivity to inhibitors and RNA integrity. Check contamination controls such as sealed cartridges, UV decontamination, tip management and negative controls. Confirm that the reagents, plasticware and software are supplied continuously, and ask for validated protocols for each matrix you intend to process.
Full specifications
| Sample capacity | 12-96 per manifold |
|---|---|
| Working vacuum | -60 to -90 kPa |
| Compatible formats | Spin columns, 96-well filter plates |
| Body material | Polycarbonate or acrylic |
| Fittings | Anodised aluminium or stainless luer |
| Waste collection | Removable tray or bottle |
| Elution collection | 1.5-2 mL tubes or 96-well plate |
| Typical binding capacity | 20-50 µg DNA per column |
| Typical yield | 5-30 µg plasmid from 5 mL culture |
| Vacuum source | External pump, oil-free recommended |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Plasmid DNA miniprep and midiprep
- PCR product and gel extraction cleanup
- Genomic DNA purification from cultured cells
- Total RNA cleanup
Key features
- Parallel processing of 12 to 96 samples per manifold.
- Accepts spin columns and 96-well filter plates.
- Vacuum gauge or regulator for even flow across wells.
- Replaces repeated centrifugation to cut hands-on time.
- Chemical-resistant body with luer or barbed fittings.
- Compact bench footprint with only a vacuum pump required.
Frequently asked questions about Vacuum Manifold Nucleic Acid Purification System
Only for the binding, washing and elution steps of column purification. Lysis, neutralisation and pelleting of cells or debris still need a centrifuge, so the manifold reduces but does not remove centrifugation from the workflow.
Most silica membranes flow well at minus 60 to 90 kPa, and higher vacuum can draw liquid past the membrane before binding is complete or damage the plate. Use a regulator and watch for uneven well flow.
Yes, provided the manifold, columns and solutions are nuclease-free and the workspace is treated as an RNA area. Clean gaskets and vacuum ports between runs, since dried nucleic acid residue there can contaminate later preparations.
It lyses cells or tissue, captures nucleic acid on magnetic beads, silica columns or cartridges, washes away protein and inhibitors, and elutes purified DNA or RNA in a defined volume for PCR, sequencing or storage.
Check yield, purity and integrity. DNA with an A260/280 near 1.8 and RNA near 2.0 is generally acceptable, A260/230 shows carryover of salts or phenols, and downstream amplification from a standard template confirms that inhibitors were removed.
Often yes, but each matrix needs its own validated protocol. Blood, tissue, swabs, plasma and plant material differ in lysis resistance, inhibitor content and expected yield, so ask the supplier for matrix-specific protocols and verify performance in your laboratory.




