

Microplate ELISA Reader
酶标仪
- SKU ELS-0001
- 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, 4–8 interference filters |
|---|---|
| Photometric range | 0–4.0 absorbance units |
| Accuracy | ±1 % or ±0.005 absorbance units at 1.0 |
| Plate formats | 96-well and strip plates, 6 to 384 wells optional |
| Reading time | About 6–12 s for a 96-well plate |
| Shaking | Linear shaking with adjustable speed and time |
By Lab Manufacturers China Technical TeamLast reviewed Standards: ISO 15189, CLSI EP05, CLSI I/LA20
What is the Microplate ELISA Reader?
A microplate ELISA reader is a photometer that measures absorbance in 96-well or strip plates at selected wavelengths and converts readings into concentrations or index values. It is the core instrument for laboratories performing enzyme immunoassays in microplate format.
What is the Microplate ELISA Reader?
A microplate ELISA reader is a photometer that measures absorbance in 96-well or strip plates at selected wavelengths and converts readings into concentrations or index values. It is the core instrument for laboratories performing enzyme immunoassays in microplate format.
Overview
The reader contains a lamp, a filter wheel or monochromator, a plate carrier and a photodetector. It can measure single or dual wavelength end-point absorbance, kinetic changes over time and sometimes fluorescence or luminescence if the optics are shared. Typical specifications are a wavelength range of 400 to 750 nanometers for absorbance, four to eight filters, a linear range up to 3.0 or 4.0 absorbance units and a plate read time of a few seconds for the standard mode. Software calculates concentrations from stored curves, flags wells outside the assay range, performs replicate averaging and exports or prints a report. Because microplate kits come from many suppliers, readers are usually open instruments and must support the wavelength sets used by the laboratory's assay menu.
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?
- Absorbance measurement at 400 to 750 nanometers with four to eight filters
- Dual-wavelength reading with reference channel subtraction
- End-point, kinetic and multi-point plate protocols
- Linear range up to 4.0 absorbance units for quantitative assays
- Curve fitting with four-parameter logistic and point-to-point modes
- Plate shaking and incubation temperature control in some models
What are the technical specifications?
A typical microplate elisa reader configuration offers wavelength range of 400–750 nm, 4–8 interference filters, photometric range of 0–4.0 absorbance units, accuracy of ±1 % or ±0.005 absorbance units at 1.0, plate formats of 96-well and strip plates, 6 to 384 wells optional, reading time of About 6–12 s for a 96-well plate and shaking of Linear shaking with adjustable speed and time. 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 Microplate ELISA Reader is used in infectious disease serology in microplate format, allergy and autoimmune antibody assays, research immunoassays and ELISpot support and veterinary and food safety immunoassays. 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 Microplate ELISA Reader?
Specify this variant when the assay menu uses microplate kits and manual or semi-automated processing is acceptable. In the RFQ state the wavelengths required by each kit, whether kinetic measurement is needed, the required linear range and the plate formats used. Confirm that the software can store the curve types your kits specify and that results can be exported to the LIS.
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, 4–8 interference filters |
|---|---|
| Photometric range | 0–4.0 absorbance units |
| Accuracy | ±1 % or ±0.005 absorbance units at 1.0 |
| Plate formats | 96-well and strip plates, 6 to 384 wells optional |
| Reading time | About 6–12 s for a 96-well plate |
| Shaking | Linear shaking with adjustable speed and time |
| Incubation | Ambient to 45 °C in some models |
| Data output | PC software with export to CSV and LIS option |
| Interfaces | USB, LAN, RS-232 |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Infectious disease serology in microplate format
- Allergy and autoimmune antibody assays
- Research immunoassays and ELISpot support
- Veterinary and food safety immunoassays
Key features
- Absorbance measurement at 400 to 750 nanometers with four to eight filters
- Dual-wavelength reading with reference channel subtraction
- End-point, kinetic and multi-point plate protocols
- Linear range up to 4.0 absorbance units for quantitative assays
- Curve fitting with four-parameter logistic and point-to-point modes
- Plate shaking and incubation temperature control in some models
Frequently asked questions about Microplate ELISA Reader
Most assays are read at 450 nanometers with a reference at 620 to 650 nanometers. Some kits use 405, 490, 540 or 570 nanometers for other substrates or for colorimetric protein assays. Specify a reader whose filter set covers every kit in your menu, since filters cannot be substituted by software.
Verify optical accuracy and repeatability with a certified reference plate or dye solutions of known absorbance, and check linearity across the working range. Repeat the check at installation, after lamp replacement and annually, and keep the results with the instrument qualification records.
Only if the optics include the appropriate excitation and emission filters and a compatible light source, which is typical of multi-mode readers. Absorbance-only readers cannot measure fluorescence, so laboratories planning to add fluorescent assays later should specify a multi-mode instrument at purchase.
Incomplete washing, over-incubation, reagent deterioration, plate sealing problems or pipetting errors are the usual causes. Background should be monitored with each run, and a sudden rise usually points to the washer or to a reagent lot, so both should be checked before results are reported.
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.




