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Nano Spectrophotometers for DNA, RNA, and Protein Analysis

 

Nano spectrophotometers (microvolume UV-Vis spectrophotometers) quantify the concentration and purity of DNA, RNA, and protein samples from 1 to 2 microliters of sample placed directly on the measurement surface without cuvettes or dilution, measuring absorbance from 190 to 850 nm and calculating concentration, A260/A280 purity ratio, and A260/A230 purity ratio automatically. They are a standard instrument in any molecular biology laboratory performing PCR, RT-qPCR, sequencing library preparation, cloning, and protein expression, and are used daily to verify sample quality before downstream applications.

MBP provides purchase order procurement for nano spectrophotometers for research institutions across the USA and Canada. Request a quote for nano spectrophotometers for DNA, RNA, and protein quantification and purity analysis by contacting customerservice@mbpinc.net.

Nano Spectrophotometer

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Accuris™ Smart-Q Fluorometer Series
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USD100.80 - USD9,615.67
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USD72.00 - USD6,868.33
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Accuris™ SmartDrop Nano Spectrophotometers
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Additional Standard-Size Cuvettes, pack of 2
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USD72.43
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Extra paper roll for SmartDrop internal printer, Pk 3
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SmartDrop pedestal reconditioning solution, 1.0 ml
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USD149.35
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USD106.68
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What Are Nano Spectrophotometers?

 

A nano spectrophotometer (microvolume UV-Vis spectrophotometer) measures the absorbance of ultraviolet and visible light through a small volume (1 to 2 microliters) of sample held by surface tension between two optical-quality fiber pedestals or on a measurement arm surface, without a cuvette. The Beer-Lambert law relates absorbance to concentration: at 260 nm, 1 absorbance unit (AU) corresponds to 50 micrograms/mL of double-stranded DNA (dsDNA), 40 micrograms/mL of RNA, and 33 micrograms/mL of single-stranded DNA (ssDNA). At 280 nm, protein absorption from aromatic amino acids (tyrosine, tryptophan, phenylalanine) allows concentration estimation using the A280 method or extinction coefficients. Purity ratios A260/A280 and A260/A230 indicate contamination: A260/A280 of 1.8 (DNA) or 2.0 (RNA) indicates high purity; ratios below these values indicate protein or other UV-absorbing contaminant carryover. A260/A230 above 2.0 indicates the absence of carryover from EDTA, guanidinium, or carbohydrate contaminants common from silica-column purification kits. The full spectrum from 190 to 850 nm allows additional analysis: OD600 for bacterial culture density; custom wavelength measurements; and detection of heme, chlorophyll, and other chromophores. A nano spectrophotometer is the fastest way to verify DNA or RNA concentration and purity before PCR, sequencing, or cloning; it uses 1 to 2 microliters, takes 5 to 10 seconds per read, and requires no cuvette or dilution for concentrations above approximately 2 ng/microliter.

 

What you will find:

  • Nano spectrophotometers for rapid microvolume nucleic acid and protein quantification using pedestal and cuvette measurement modes.
  • Fluorometer systems for highly sensitive DNA, RNA, and protein quantification using fluorescence-based assays.
  • Nano Spectrophotometer Accessories for SmartDrop instruments, including replacement printer paper rolls, pedestal reconditioning solution, and standard-size cuvettes.

 

How to Choose a Nano Spectrophotometer

 

Single-sample vs. multi-sample throughput

Single-pedestal nano spectrophotometers (most models) measure one sample at a time, with read times of 5 to 10 seconds per sample. For labs measuring fewer than 20 samples per session, a single-sample model is adequate. High-throughput eight-pedestal models (such as the NanoDrop Eight) accept a row of 8 samples simultaneously from a 96-well plate strip, processing 96 samples in approximately 2 minutes, which is essential for next-generation sequencing library prep workflows, automated sample QC, and high-throughput screening.

Measurement range and sensitivity

The upper concentration limit of nano spectrophotometers is set by the path length: standard 1 mm path length accommodates dsDNA from 2 to 3,700 ng/microliter without dilution (NanoDrop-type instruments auto-select 0.2 mm or 1.0 mm path length based on absorbance). The lower detection limit is approximately 2 ng/microliter for dsDNA in UV mode; samples more dilute than this require fluorometric quantification (Qubit-type instruments with fluorescent dyes specific to DNA, RNA, or protein).

Contaminant detection algorithms

Basic nano spectrophotometers report A260, A280, A260/A280, A260/A230, and calculated concentration. Advanced models (NanoDrop Ultra type) include software algorithms (Acclaro-type intelligence) that use full-spectrum data to identify and correct for specific contaminants: dsDNA contamination in RNA samples; RNA contamination in dsDNA; guanidinium from RNA extraction kits; and EDTA carryover. Specify these advanced features for workflows where sample purity assessment matters for downstream application success (RT-qPCR, long-read sequencing, CRISPR libraries).

Touchscreen vs. PC-connected operation

Standalone touchscreen nano spectrophotometers allow operation without a connected PC, storing results internally or exporting via USB. PC-connected models require a laptop or PC with the instrument software installed for operation and data export, but provide more flexibility in data management, LIMS integration, and custom method programming. For shared lab equipment where multiple users access the instrument, touchscreen standalone models are operationally simpler.

Protein measurement modes

All nano spectrophotometers measure protein at A280 using a user-specified extinction coefficient. Advanced models add preprogrammed protein types (BSA, IgG, lysozyme, human serum albumin), A205 direct measurement for proteins with low or no A280 signal, and colorimetric assay support (BCA, Bradford, Lowry, Pierce 660 nm) for protein quantification using plate-reader-style microvolume cuvette adapters.

 

Specifications Context

 

Measurement accuracy at 260 nm is typically stated as plus or minus 1 to 2% coefficient of variation for repeat measurements of the same sample. Wavelength accuracy is specified as plus or minus 1 nm. Confirm the dynamic range covers the sample concentrations typically encountered in your workflow; highly concentrated DNA libraries from solid-phase extraction (above 500 ng/microliter) are accurately measured at 0.2 mm path; dilute RNA samples from small cell numbers or rare tissues may fall below the UV detection limit and require fluorometric quantification. Calibrate the blank (blanking solution) using the same buffer or elution solution as the sample; blanking with water when the sample is in TE buffer introduces a measurement error at A230 from EDTA absorption.

 

To discuss product availability or get selection guidance, contact the MBP team.

FAQ

A nano spectrophotometer (microvolume UV-Vis spectrophotometer) measures the absorbance of ultraviolet and visible light through 1 to 2 microliters of sample placed directly on a measurement surface without a cuvette. It calculates DNA, RNA, or protein concentration using Beer-Lambert law and reports purity ratios (A260/A280 and A260/A230) that indicate sample contamination. It is used in molecular biology laboratories to verify nucleic acid quality before PCR, RT-qPCR, sequencing, cloning, and other downstream applications.
Standard nano spectrophotometers require 1 to 2 microliters of sample placed directly on the fiber pedestal or measurement arm surface. Surface tension holds the sample in the light path without a cuvette; no dilution is required for most nucleic acid samples in the concentration range of 2 to 3,700 ng/microliter (dsDNA). After measurement, the sample is recovered by wiping the pedestal with lint-free lens tissue, allowing the valuable sample to be used for downstream applications.
The A260/A280 ratio indicates nucleic acid purity relative to protein contamination. Values of 1.8 (DNA) or 2.0 (RNA) indicate high purity; values below 1.8 suggest protein or phenol contamination absorbing at 280 nm. The A260/A230 ratio indicates contamination from EDTA, guanidinium (from RNA extraction kits), carbohydrates, or other compounds that absorb at 230 nm. Values above 2.0 indicate high purity; values below 1.5 to 1.8 suggest significant carryover of extraction reagents that can inhibit downstream enzymatic reactions.
Standard nano spectrophotometers detect dsDNA from approximately 2 ng/microliter to 3,700 ng/microliter using UV absorbance at 260 nm. RNA detection is similar: approximately 2 ng/microliter lower limit. Samples below 2 ng/microliter (dilute RNA from rare cells, small tissue biopsies, or highly diluted library preparations) require fluorometric quantification using dye-based instruments (Qubit-type) that provide much lower detection limits (0.2 pg/microliter to 0.1 ng/microliter, depending on the assay).
Blank the nano spectrophotometer using the exact buffer or elution solution the sample was collected in -- not deionized water unless the sample is in deionized water. Blanking with water when samples are in TE buffer (10 mM Tris, 1 mM EDTA) causes a measurement error at A230 from EDTA absorption, which artificially lowers the A260/A230 ratio and overestimates contamination. For RNA samples eluted in RNase-free water, blank with RNase-free water. For DNA eluted in TE buffer, blank with TE buffer. Re-blank between different sample buffers and after extended idle periods.
Use a nano spectrophotometer when speed, simplicity, and purity information (A260/A280, A260/A230 ratios) are required, and sample concentration is above 2 ng/microliter. Nano spectrophotometers are fast (5 to 10 seconds per sample), require no reagents, and are sufficient for routine QC of DNA or RNA from standard extractions. Use a fluorometer (Qubit-type) when samples are more dilute than 2 ng/microliter, when specificity is critical (fluorescent dyes are specific for dsDNA, ssDNA, or RNA separately), or when downstream sensitivity to contamination is high (such as long-read sequencing or single-cell applications). Many labs use both instruments for complementary information.
Yes. Nano spectrophotometers measure protein at A280 using aromatic amino acid absorbance. Users enter the protein's extinction coefficient (in L mol^-1 cm^-1) or select from preprogrammed protein types (BSA, IgG, lysozyme). Advanced models support A205 measurement for proteins with low or no A280 signal. For proteins in buffers with high UV absorbance (guanidinium, detergents, imidazole from his-tag purification), accurate A280 measurement requires dialysis or buffer exchange first, as these reagents absorb at 280 nm and interfere with the protein signal.
Yes. MBP provides purchase order procurement for nano spectrophotometers for research institutions across the USA and Canada. MBP is a registered vendor for Howard Hughes Medical Institute, Vanderbilt University, and MD Anderson Cancer Center. Contact MBP via the contact page or Quick Order portal with your throughput requirements, required concentration range, and desired features (contaminant detection, fluorometry, or multi-sample capability) for a prompt quote.
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