

Integrated ELISA Reader and Washer System
酶标仪洗板机一体机
- SKU ELS-0003
- ELISA Systems
- CE (to be confirmed)
- ISO 13485 manufacturing (to be confirmed)
- NMPA class II registration (to be confirmed)
Price on request — FOB / CIF quoted per order
Prices depend on configuration, quantity and destination port.
Key specifications
| Wavelength range | 400–750 nm, 4–6 filters |
|---|---|
| Photometric range | 0–3.5 absorbance units |
| Wash channels | 8 or 12 channel manifold for 96-well plates |
| Residual volume | < 3 µL per well |
| Plate capacity | 1–2 plates per run |
| Incubation | Ambient to 45 °C with timer |
By Lab Manufacturers China Technical TeamLast reviewed Standards: ISO 15189, CLSI EP05, CLSI I/LA20
What is the Integrated ELISA Reader and Washer System?
This system combines the reader and washer in one instrument with shared software, so plate washing and reading are performed in a single sequence with one protocol. It suits laboratories that want consistent ELISA processing without the footprint and alignment issues of two separate devices.
What is the Integrated ELISA Reader and Washer System?
This system combines the reader and washer in one instrument with shared software, so plate washing and reading are performed in a single sequence with one protocol. It suits laboratories that want consistent ELISA processing without the footprint and alignment issues of two separate devices.
Overview
The plate is loaded once and moved internally between the wash station and the optical measuring position, so the delay between the final wash and the reading is fixed by the instrument rather than by the operator. Protocols combine wash cycles, substrate incubation timing and reading wavelengths, and the software links results to the plate layout defined in the assay template. Because the two functions share a single mechanical platform, calibration and verification procedures cover optical accuracy and washing performance in one qualification document. Capacity is usually one or two plates at a time, which suits small to medium volumes. Maintenance is simpler than with two devices, but a fault in either function stops the whole instrument, so a backup plan matters.
How does it work?
Enzyme-linked immunosorbent assay uses a plastic microplate whose wells carry a bound capture antibody or antigen. Sample is added, and any target present binds to the solid phase during incubation. After washing, a detection antibody conjugated to an enzyme such as horseradish peroxidase or alkaline phosphatase is added and binds to the captured target. A further wash removes unbound conjugate, then a substrate is added and the enzyme converts it into a coloured product. The reaction is stopped with acid or base and the absorbance is read at a defined wavelength, usually 450 nanometers with a reference wavelength between 600 and 650 nanometers. Absorbance is proportional to the amount of bound analyte, and a calibration curve, often four-parameter logistic, converts readings into concentrations or index values. Strict washing, incubation timing and temperature control determine the reliability of the result.
What are the key features?
- Internal transport between wash station and optical reader
- Single protocol controlling washing and reading in sequence
- Fixed delay between last wash and measurement
- Template-based plate layout with result mapping
- One qualification covering optics and washing performance
- Compact footprint compared with two separate instruments
What are the technical specifications?
A typical integrated elisa reader and washer system configuration offers wavelength range of 400–750 nm, 4–6 filters, photometric range of 0–3.5 absorbance units, wash channels of 8 or 12 channel manifold for 96-well plates, residual volume of < 3 µL per well, plate capacity of 1–2 plates per run and incubation of Ambient to 45 °C with timer. 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 Integrated ELISA Reader and Washer System is used in low to medium volume ELISA testing, clinics with limited bench space, veterinary serology laboratories and research laboratories standardising protocols. Across the wider ELISA Systems class, laboratories also deploy it for infectious disease serology, allergy specific IgE testing and autoimmune antibody screening.
Which standards and certifications apply?
Relevant standards and methods include ISO 15189, CLSI EP05, CLSI I/LA20, CLSI M29, IEC 61010-1 and IEC 61010-2-101. Certification candidates for this model are CE, ISO 13485 manufacturing and NMPA class II registration; each is to be confirmed for the specific configuration before shipment, and certificates are supplied only where they have been issued.
Place the reader and washer on a level bench away from vibration and direct light, and keep the plate carrier and optical window free of dust. Verify performance at installation with a reference dye plate for optical accuracy and with controls for each assay. Daily tasks include checking the washer manifold for blockage, priming the wash lines and running controls at two or three levels. Plates should be read immediately after stopping the reaction, since colour continues to develop and delays bias results, and consistent timing across the plate matters more than absolute speed. Replace tubing and manifold pins when flow becomes uneven, and dispose of wash waste and plates as biohazardous material.
How do I select the right Integrated ELISA Reader and Washer System?
Choose this variant when bench space is limited, when consistent timing between washing and reading matters, or when a single qualification document simplifies accreditation. In the RFQ confirm plate capacity, residual volume, whether incubation is integrated, and the supplier's backup support, since one instrument failure removes both functions.
How does it compare with other ELISA Systems variants?
Define the assays first, then decide how much automation is appropriate. Laboratories running fewer than one hundred wells per day can work with a reader and washer plus manual pipetting, while larger volumes justify an automated processor with plate handling, incubation and reporting. Compare readers by wavelength range, filter set, linearity, and whether they support kinetic and dual-wavelength measurement. For washers, check residual volume, the number of wash cycles programmable, and the manifolds for 96-well and strip formats. For automated systems, check plate capacity, walkaway time, whether the software handles assay protocols centrally, and the traceability of each step with lot numbers and operator identification. Confirm the assay registration status in your market, since ELISA kits are regulated separately from the instruments.
Full specifications
| Wavelength range | 400–750 nm, 4–6 filters |
|---|---|
| Photometric range | 0–3.5 absorbance units |
| Wash channels | 8 or 12 channel manifold for 96-well plates |
| Residual volume | < 3 µL per well |
| Plate capacity | 1–2 plates per run |
| Incubation | Ambient to 45 °C with timer |
| Data output | PC software with curve storage and CSV export |
| Interfaces | USB, LAN with LIS option |
| Power supply | AC 100–240 V, 50/60 Hz |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Low to medium volume ELISA testing
- Clinics with limited bench space
- Veterinary serology laboratories
- Research laboratories standardising protocols
Key features
- Internal transport between wash station and optical reader
- Single protocol controlling washing and reading in sequence
- Fixed delay between last wash and measurement
- Template-based plate layout with result mapping
- One qualification covering optics and washing performance
- Compact footprint compared with two separate instruments
Frequently asked questions about Integrated ELISA Reader and Washer System
Accuracy is comparable when both are correctly calibrated, but integration removes operator-dependent delays between washing and reading, which improves reproducibility. Separate devices allow independent replacement and maintenance, while integration reduces handling and footprint.
The reader also stops, because the instrument shares one platform. Laboratories should keep a documented contingency, such as a standalone reader for optical measurement or an arrangement with a nearby laboratory, and ensure spare parts for the manifold and tubing are available locally.
The software stores multiple protocols, but the plate capacity and single transport path mean plates are processed sequentially rather than in parallel. For mixed menus with different incubation times, plan the run order so that timing-critical assays are not delayed by longer protocols.
Models with an integrated incubator hold the plate at a set temperature, typically up to 45 degrees Celsius, while timing is controlled by the protocol. Temperature uniformity across the plate should be verified during qualification, because edge wells can react differently if heating is uneven.
A reader only measures absorbance after the assay has been performed manually, while an automated system also handles sample and reagent pipetting, incubation, washing, substrate addition and timing. Readers suit low volumes and flexible menus; automated systems reduce variability and labour at higher volumes.
Reading at the assay wavelength and subtracting a reference wavelength between 600 and 650 nanometers corrects for scratches, dust and bubbles on the plate. It reduces well-to-well variation and is standard practice for quantitative ELISA, especially at low absorbance values where optical artefacts have more influence.
Check the manifold for blocked or misaligned pins before each run, and verify residual volume weekly with a gravimetric or dye test. Uneven aspiration leaves wash solution that carries over unbound conjugate, which raises background and reduces precision, so any change in background should prompt a washer check.




