Attune™ NxT Flow Cytometer, blue/red/yellow
Attune™ NxT Flow Cytometer, blue/red/yellow
Invitrogen™

Attune™ NxT Flow Cytometer, blue/red/yellow

Green features
The 2020 Attune NxT Flow Cytometer has expanded functionalities to drive your research forward. Designed and developed to remove commonRead more
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A289931 each
Catalog number A28993
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The 2020 Attune NxT Flow Cytometer has expanded functionalities to drive your research forward. Designed and developed to remove common barriers associated with flow cytometry, the evolutionary capabilities of the Attune NxT Flow Cytometer offer adaptable optical configuration options so you can get the most out of your multicolor analysis.

  • New CytKick and CytKick Max autosampler—more efficiency for high-throughput assays
  • New 21 CFR part 11 compliant software for regulated laboratories on Windows 10 operating system
  • Improved workflow for run protocol and instrument settings management

Fast flow

The innovative combination of acoustic focusing technology coupled with traditional hydrodynamic focusing results in acquisition speeds up to 10X faster than other flow cytometers. This technology reduces the time needed to obtain results.

  • True 35,000 event/sec (+10% coincidence rates)
  • Maximum electronic speed of 65,000 events/sec
  • Analyze small or limited samples faster than ever
  • Efficiently run traditionally long assays

The Attune NxT Flow Cytometer is ideal for immunophenotyping and signaling studies, cell cycle analysis, detection of rare events, stem cell analysis, cancer and apoptosis studies, microbiological assays, and more.

Fit for your lab today and in the future

The instrument's modular design provides the flexibility to meet future capability needs with a variety of upgrade options. Purchase what you need now and easily upgrade later. The small footprint of the instrument requires minimal bench space, even allowing use in a cell culture hood.

  • Flexibility—1 to 4 lasers, 14 colors, and 16 parameters
  • Field upgradeable—choose to add additional lasers when you decide
  • Customizable band pass filters for expanded fluorochrome choices

Tune into your data

The Attune NxT Flow Cytometer easily runs most samples including cardiomyocytes. The system is designed with a clog-resistant syringe-driven system to push the sample with a force of up to 75 psi.

  • Flexibility in sample concentrations and sample types
  • Elimination of time-consuming concentration steps with No-Wash, No-Lyse Filter Kit
  • Analysis of dilute samples, including CSF, stem cells, mouse bone marrow, mouse blood, and thin needle aspirates
  • Acquisition of a high volume of samples in minimal time
For Research Use Only. Not for use in diagnostic procedures.
Specifications
For Use With (Equipment)Attune™ Acoustic Focusing Cytometer
FormatTube, 384-well plate, 96-well plate
Frequency50/60 Hz
Green FeaturesLess hazardous
Laser FeaturesBlue Excitation Laser (488 nm), Red Excitation Laser (638 nm), Yellow Excitation Laser (561 nm)
Product LineAttune™
Quantity1 each
Shipping ConditionRoom Temperature
Unit SizeEach
Contents & Storage
• Attune NxT Flow Cytometer
• Minitower Windows 10 64-bit computer with Attune Cytometric Software
• Power cord with adapters
• USB cable
• Attune Shutdown Solution
• Attune Wash Solution
• Attune Focusing Fluid
• Attune NxT Flow Cell Cleaning Solution
• Attune Performance Tracking Beads
• Quick reference card

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Frequently asked questions (FAQs)

My Attune NxT Flow Cytometer performance test keeps failing. What steps can I take to minimize the number of failed performance tests?

To minimize the number of failed performance tests on your Attune NxT Flow Cytometer, we suggest the following:

•   Make sure to carry out daily, weekly, and monthly maintenance procedures (pages 8-14 of the Maintenance and Troubleshooting Guide, linked below).
•   Always run 3 startup cycles and 2 Rinse procedures (pages 46-47 of the Maintenance and Troubleshooting Guide linked below).
•   If the performance test fails, carry out the following priming sequence: run 3 startup cycles, 2 de-bubble cycles, and 5 rinse procedures, followed by running the SIP sanitize function.

Please review the Attune Flow Cytometry Maintenance and Troubleshooting Guide for more information about performing routine maintenance procedures and troubleshooting.

Find additional tips, troubleshooting help, and resources within our Flow Cytometry Support Center.

Can I use the Attune Nxt Flow Cytometer to detect bacteria?

Yes. The Attune Nxt Flow Cytometer can detect down to 0.2 µm and using a special configuration, down to 0.1 µm. Optimize your settings using Flow Cytometry Sub-micron Particle Size Reference Kit, Cat. No. F13839.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

Of all the Attune NxT filters you offer, I don't see one that matches our application. Can I use a filter other than what you offer?

Yes. You would need to purchase Attune NxT Custom Filter Holder Kit, Cat. No. A27784 to make your own custom emission or dichroic filters in order to customize the optical configuration of the instrument. Each kit contains sufficient parts to make 2 emission filters and 2 dichroic filters. The kit includes instructions for attaching the filter to the filter blade, but does not include the glass filter. Other accessories to optimize for special applications include Cat No. 100083194 Attune NxT Small Particle Side-Scatter Filter, Cat. No. 100083194 and Attune NxT Blocker Bar Conversion Kit, Cat No. A35966.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

With the Attune Nxt Flow Cytometer, if I wish to only start with a single laser, can I expand to more lasers and channels?

Yes. There are 6 lasers to choose from (blue, green, yellow, red, violet, and violet 6). You can start with one laser and at any time upgrade the same instrument with up to 4 lasers to utilize a maximum of 14 detection channels. Using the Violet 6 laser along with the blue, red, and yellow lasers, one can detect up to 16 channels.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

What makes the Attune Nxt Flow Cytometer better than standard flow cytometers?

Because of the acoustic-assisted hydrodynamic technology, the Attune NxT Flow Cytometer uses only 1/10th the amount of fluids, and is 10X faster and less sensitive to clogging compared to standard flow cytometers. You can set the flow rate from 12.5-1,000 µL/min and collect up to 65,000 events/sec using from 20 µL to 4 mL of sample volume. These unique properties allow for rare event analysis, as well standard flow analysis.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

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Citations & References (19)

Citations & References
Abstract
BRCA1 Directs the Repair Pathway to Homologous Recombination by Promoting 53BP1 Dephosphorylation.
Authors:Isono M, Niimi A, Oike T, Hagiwara Y, Sato H, Sekine R, Yoshida Y, Isobe SY, Obuse C, Nishi R, Petricci E, Nakada S, Nakano T, Shibata A
Journal:Cell Rep
PubMed ID:28076794
'BRCA1 promotes homologous recombination (HR) by activating DNA-end resection. By contrast, 53BP1 forms a barrier that inhibits DNA-end resection. Here, we show that BRCA1 promotes DNA-end resection by relieving the 53BP1-dependent barrier. We show that 53BP1 is phosphorylated by ATM in S/G2 phase, promoting RIF1 recruitment, which inhibits resection. 53BP1 ... More
DRP-1 is required for BH3 mimetic-mediated mitochondrial fragmentation and apoptosis.
Authors:Milani M, Byrne DP, Greaves G, Butterworth M, Cohen GM, Eyers PA, Varadarajan S
Journal:Cell Death Dis
PubMed ID:28079887
'The concept of using BH3 mimetics as anticancer agents has been substantiated by the efficacy of selective drugs, such as Navitoclax and Venetoclax, in treating BCL-2-dependent haematological malignancies. However, most solid tumours depend on MCL-1 for survival, which is highly amplified in multiple cancers and a major factor determining chemoresistance. ... More
Enhanced CRISPR/Cas9-mediated precise genome editing by improved design and delivery of gRNA, Cas9 nuclease, and donor DNA.
Authors:Liang X, Potter J, Kumar S, Ravinder N, Chesnut JD
Journal:J Biotechnol
PubMed ID:27845164
'While CRISPR-based gene knock out in mammalian cells has proven to be very efficient, precise insertion of genetic elements via the cellular homology directed repair (HDR) pathway remains a rate-limiting step to seamless genome editing. Under the conditions described here, we achieved up to 56% targeted integration efficiency with up ... More
Development of a Bacillus subtilis cell-free transcription-translation system for prototyping regulatory elements.
Authors:Kelwick R, Webb AJ, MacDonald JT, Freemont PS
Journal:Metab Eng
PubMed ID:27697563
'Cell-free transcription-translation systems were originally applied towards in vitro protein production. More recently, synthetic biology is enabling these systems to be used within a systematic design context for prototyping DNA regulatory elements, genetic logic circuits and biosynthetic pathways. The Gram-positive soil bacterium, Bacillus subtilis, is an established model organism of ... More
Evaluation of Receptor-Ligand Mechanisms of Dual-Targeted Particles to an Inflamed Endothelium.
Authors:Fromen CA, Fish MB, Zimmerman A, Adili R, Holinstat M, Eniola-Adefeso O
Journal:Bioeng Transl Med
PubMed ID:28066821
'Vascular-targeted carriers (VTCs) are designed as leukocyte mimics, decorated with ligands that target leukocyte adhesion molecules (LAMs) and facilitate adhesion to diseased endothelium. VTCs require different design considerations than other targeted particle therapies; adhesion of VTCs in regions with dynamic blood flow requires multiple ligand-receptor (LR) pairs that provide particle ... More
19 total citations

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