Qubit™ 3 Fluorometer
Qubit™ 3 Fluorometer
Invitrogen™

Qubit™ 3 Fluorometer

The Qubit 3 Fluorometer is the next generation of the popular benchtop fluorometer that accurately measures DNA, RNA, and proteinRead more
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Catalog NumberQuantity
Q332161 each
Catalog number Q33216
Price (BRL)
-
Quantity:
1 each
The Qubit 3 Fluorometer is the next generation of the popular benchtop fluorometer that accurately measures DNA, RNA, and protein using the highly sensitive fluorescence-based Qubit quantitation assays. The fluorescent dyes used in these assays emit signals only when bound to specific target molecules, even at low concentrations, thus minimizing the effects of contaminants, including degraded DNA or RNA. The integrated design of the instrument and assays results in quantitation that is far more sensitive than UV absorbance, making this system essential for quantitation of precious samples (samples that are rare, difficult to purify, or expensive to either obtain or prepare) or samples for 'delicate' applications (samples for downstream assays that are extremely sensitive to sample conditions).

Key features of the Qubit 3 Fluorometer include:
• Powerful dual-core processor quickly and accurately quantifies DNA, RNA, and protein in less than 5 seconds per sample
• Uses as little as 1 μL of sample
• Stores up to 1000 sample results
• Large, 5.7-inch, state-of-the-art color touch screen for easy workflow navigation
• Ability to personalize your Qubit fluorometer with the assays you run most, add new assays, or even create your own with the MyQubit software and web tool
• Small footprint saves space on your bench
• Language of your choice including English, French, Spanish, German, simplified Chinese and Japanese
• Android-based operating system

The Qubit 3 Fluorometer can also be used to directly measure the fluorescence of samples. Additionally, Ion Sphere Particle quality can be evaluated on the Qubit 3 Fluorometer using the Ion Sphere Quality Control Kit prior to performing a sequencing run on the Ion PGM Sequencer.

Enables more accurate results than with UV absorbance at low concentrations
The Qubit 3 Fluorometer is far more sensitive than UV absorbance, which measures anything absorbing at 260 nm, including DNA, RNA, protein, free nucleotides, or excess salts. Moreover, UV spectrophotometry is often not sensitive enough to accurately measure low concentrations of DNA and RNA. With the Qubit fluorometer, your research is enhanced by more accurate measurements because the dyes in the Qubit assay kits fluoresce only when bound to the selected molecule—DNA, RNA, or protein—in your sample. This allows you to avoid repeating work due to inaccurate measurements.

Save samples—and bench space
The thoughtfully designed Qubit 3 Fluorometer requires samples of only 1–20 μL. It is intended for use at room temperature and occupies only a small amount of bench space. The Qubit 3 Fluorometer features advanced optics and data analysis algorithms, and comes equipped with a USB thumb drive and cable for data transfer to Excel™ software and for software downloads, a universal power supply, four plug adapters, and electromagnetic CE certification.

Single sample measurements are a breeze
This user-friendly fluorometer is combined with quick, simple assay procedures. Calculations and settings are automatically performed by the instrument. The Qubit assays for use with the Qubit 3 Fluorometer are all performed using the same general protocol, which uses a simple mix-and-read format with incubation times of only 2 minutes for DNA and RNA assays. 500- μL thin-walled PCR tubes (Cat. No. Q32856) are required.

System specifications include:
Instrument dimensions: 5.4'(w) x 10'(l) X 2.2' (h) (13.6 cm X 25 cm X 5.5 cm)
Weight: 743 g
Dynamic range: 5 orders of magnitude
Processing time: ≤5 seconds/sample
Light sources: blue LED (max ∼470 nm), red LED (max ∼635 nm)
Excitation filters: blue 430-495 nm, red 600-645 nm
Emission filters: green 510-580 nm, red 665-720 nm
Detectors: photodiodes, measurement capability from 300-1,000 nm
Warm-up time: <35 seconds
USB thumb drive: 4 GB
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Dimensions (L x W x H)10 x 5.4 x 2.2 in. (25 x 13.6 x 5.5 cm)
Display Type5.7 in. Capacitive Touchscreen
For Use With (Application)DNA Quantification, RNA Quantification, Protein Quantification
Holds1 Assay Tube per Read
Memory1000 Samples
Quantity1 each
Sample Volume1 to 20 μL
Shipping ConditionRoom Temperature
Voltage100/240 VAC
Weight (Metric)743.0 g
Excitation Wavelength430 to 495 nm Blue LED, 600 to 645 nm Red LED
For Use With (Equipment)Qubit Fluorometer
Product LineQubit
TypeFluorometer
Unit SizeEach

Frequently asked questions (FAQs)

How does the accuracy and sensitivity of the Qubit quantitation assays using the Qubit fluorometer compare to a microplate reader?

The accuracy and sensitivity of the Qubit quantitation assays are the same as that of a microplate reader. This was a requirement during product development. The detection limits for each Qubit kit can be found on the corresponding product manual, which can be found by searching our website by keyword or catalog number.

Find additional tips, troubleshooting help, and resources within our Nucleic Acid Quantification Support Center.

Can the Qubit kits give an indication of sample quality in nucleic acid samples?

No. The Qubit DNA and RNA kits only quantify the amount of either DNA or RNA in the sample. The Qubit fluorometer cannot take absorbance readings to provide a A260/A280 ratio or detect protein in nucleic acid samples. This can be done with the NanoDrop instrument. If your sample contains protein or other contaminants that can affect the assay, it should be further purified.

If your sample may contain both DNA and RNA, one may use either (or both) the DNA and RNA Qubit kits and compare with samples treated with either RNase or DNase to get an accurate determination of DNA or RNA, respectively.

Can I use the Quant-iT and Qubit Kits with other fluorometers?

All Quant-iT and Qubit kits are compatible with all fluorometers and microplate readers that have the appropriate light sources and filters. You won't have access to the algorithm in the Qubit fluorometer for generating the standard curve provided by the instrument, instead, you must make a few dilutions of the highest standard DNA or RNA (Standard #2) in the Qubit kits to generate a standard curve with multiple data points.

Can I use other kits besides the Ion Library Equalizer Kit for library normalization?

If you are not using the Ion Library Equalizer Kit for library normalization, one of the following can be used (but the library should be at 100 pM):

- Ion Library TaqMan Quantitation Kit
- Qubit 3.0 Fluorometer or Qubit 2.0 Fluorometer
- Qubit dsDNA HS Assay Kit
- Agilent 2100 Bioanalyzer Instrument
- Agilent High Sensitivity DNA Kit

Find additional tips, troubleshooting help, and resources within our Next-Generation Sequencing Support Center.

With the Oncomine BRCA Research Assay, which method do you recommend for quantifying gDNA?

We recommend two methods for gDNA quantification:

- Qubit 3.0 Fluorometer (Cat. No. Q33216) with Qubit dsDNA HS Assay Kit (Cat. Nos. Q32851, Q32854)
- qPCR using TaqMan RNase P Detection Reagents Kit (Cat. No. 4316831)

Citations & References (11)

Citations & References
Abstract
Let-7e modulates the inflammatory response in vascular endothelial cells through ceRNA crosstalk.
Authors:Lin Z, Ge J, Wang Z, Ren J, Wang X, Xiong H, Gao J, Zhang Y, Zhang Q
Journal:Sci Rep
PubMed ID:28195197
'The inflammatory responses of vascular endothelial cells (VECs) are critical in the development of many cardio-cerebrovascular diseases. Let-7e is an important regulator of endothelial function and inflammation. However, the effects and mechanisms of let-7e on VECs inflammation have not been studied until recently. Thus, we investigated these issues and found ... More
Fibroblast activation protein is dispensable in the anti-influenza immune response in mice.
Authors:Tan SY, Chowdhury S, Polak N, Gorrell MD, Weninger W
Journal:PLoS One
PubMed ID:28158223
'Fibroblast activation protein alpha (FAP) is a unique dual peptidase of the S9B serine protease family, being capable of both dipeptidyl peptidase and endopeptidase activities. FAP is expressed at low level in healthy adult organs including the pancreas, cervix, uterus, submaxillary gland and the skin, and highly upregulated in embryogenesis, ... More
RNF40 regulates gene expression in an epigenetic context-dependent manner.
Authors:Xie W, Nagarajan S, Baumgart SJ, Kosinsky RL, Najafova Z, Kari V, Hennion M, Indenbirken D, Bonn S, Grundhoff A, Wegwitz F, Mansouri A, Johnsen SA
Journal:Genome Biol
PubMed ID:28209164
'Monoubiquitination of H2B (H2Bub1) is a largely enigmatic histone modification that has been linked to transcriptional elongation. Because of this association, it has been commonly assumed that H2Bub1 is an exclusively positively acting histone modification and that increased H2Bub1 occupancy correlates with increased gene expression. In contrast, depletion of the ... More
Rapid Metagenomic Next-Generation Sequencing during an Investigation of Hospital-Acquired Human Parainfluenza Virus 3 Infections.
Authors:Greninger AL, Zerr DM, Qin X, Adler AL, Sampoleo R, Kuypers JM, Englund JA, Jerome KR
Journal:J Clin Microbiol
PubMed ID:27795347
'Metagenomic next-generation sequencing (mNGS) is increasingly used for the unbiased detection of viruses, bacteria, fungi, and eukaryotic parasites in clinical samples. Whole-genome sequencing (WGS) of clinical bacterial isolates has been shown to inform hospital infection prevention practices, but this technology has not been utilized during potential respiratory virus outbreaks. Here, ... More
High diversity of airborne fungi in the hospital environment as revealed by meta-sequencing-based microbiome analysis.
Authors:Tong X, Xu H, Zou L, Cai M, Xu X, Zhao Z, Xiao F, Li Y
Journal:Sci Rep
PubMed ID:28045065
'Invasive fungal infections acquired in the hospital have progressively emerged as an important cause of life-threatening infection. In particular, airborne fungi in hospitals are considered critical pathogens of hospital-associated infections. To identify the causative airborne microorganisms, high-volume air samplers were utilized for collection, and species identification was performed using a ... More