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Séquenceur d'analyse génétique SeqStudio

Constructeur
Thermo Fisher Scientific
Réf. HTTS
HTS-SA-0477
Réf. HTDS
SEQUENCEUR DANALYSE GENETIQUE SEQSTUDIO
Séquenceur d'analyse génétique SeqStudio

Galerie et schémas techniques

Séquenceur d'analyse génétique SeqStudio - Image 1

Description

L’analyseur génétique SeqStudio est facile à utiliser avec un système à cartouche intégré, et vous permet d’accéder et de surveiller votre course ainsi que de visualiser les données à distance.L’analyseur génétique entièrement connecté, ainsi que la conception simple de la cartouche, peuvent être facilement partagés par tous les chercheurs du laboratoire. Le SeqStudio offre les dernières avancées en matière de convivialité de l’écran tactile, vous permettant de rester facilement connecté à vos données. Le système est conçu pour les utilisateurs débutants et expérimentés qui ont besoin d’un séquençage et d’une analyse de fragments Sanger simples et abordables, sans compromettre les performances ou la qualité.

L'analyseur génétique Applied Biosystems™ SeqStudio™ est le seul analyseur génétique qui effectue simultanément le séquençage et l'analyse des fragments s'exécutent sur la même plaque

Obtenez des résultats plus rapidement avec un analyseur génétique multi-applications à cartouche unique

Caractéristiques

  • Logiciel d’instrument simplifié avec écran tactile interactif pour une plus grande facilité d’utilisation
  • Temps de configuration pratique réduit grâce à la cartouche de réactifs intégrée (Cartouche SeqStudio)
  • Flexibilité de l’application pour exécuter le séquençage Sanger et l’analyse des fragments sur la même exécution
  • Connectivité : connexion Wi-Fi ou Ethernet filaire
  • Capacité de surveillance à distance sur le Web
  • Suivi de l’utilisation des consommables grâce à l’identification par radiofréquence (RFID)

Spécifications techniques

Format
Plaque 96 puits, Barrette 8 tubes
Weight
53.6 kg
Hauteur
44.2 cm
Largeur
64.8 cm
Longeur
49.5 cm
Product
Cat. No.
Storage
2–8°C
Warranty
1-year instrument warranty included, extended warranty available
Recycling
For more details, go to thermofisher.com/seqstudiorecycling
Easy to use
Affordable Reliable
Power input
100–240 V
Applications
Sanger sequencing (resequencing for NGS confirmation, indels, heterozygote detection, minor variant detection, microbial
Polymer type
POP-1 (for performing sequencing and fragment analysis)
Configuration
Stand-alone, optional desktop or laptop computer
POP-1 polymer
Polymer delivery system (PDS) assembly
Sample format
96-well standard plate and standard 8-well strip tubes
Software Type
Analyse de fragments
Analysis (MSA)
onboard computer or by using Plate Manager, the
Number of dyes
6
Set up and run
Monitor
is unavailable.
analysis data.
• Easy removal
number of injections (cartridge) and length of time on the
Oncology research
to understand how the genome influences biological
Secondary analysis
• Sequence Analysis Software
electropherograms.
sizing and quality allele calls for all Applied Biosystems
• Share protocols
 Access and share data
AB Maintenance (Plus)
AB Assurance AB Complete
Number of capillaries
4
On-site response time
Target 2 business days* Guaranteed 2 business days* Guaranteed next business day*
SeqStudio Starter Kit
A35000
Dimensions (W x D x H)
49.5 x 64.8 x 44.2 cm
Exigences électriques
100 V à 240 V
On-instrument tracking
RFID
SeqStudio Cartridge v1
A33671
SeqStudio Cartridge v2
A41331
Species identification
(MLPA ) analysis of human copy number variation
following capabilities
multiple datasets in one convenient place, and render them
sample authentication.
calculates the sizes of the fragments. The software allows
Communication interface
Connect platform with cloud-enabled systems, Wi-Fi, and RJ-45 Ethernet ports
Microsatellite Analysis
NGC Next-Generation Confirmation
On-instrument shelf life
4 months (SeqStudio Cartridge v1) or 6 months (SeqStudio Cartridge v2) after opening
Parts, labor, and travel
10% discount (US only)
8 Strip Tube Septa, 24 pk
A35643
De novo Sanger sequencing
Next-generation sequencing (NGS) confirmation
96-Well Plate Septa, 20 pk
A35641
conditions d’expédition
Température ambiante
• Collaborate with peers
 Storage and backup
Internal hard-drive storage
128 GB, approximately 3,500 injections or 14,000 reactions
running quickly in your lab
this covers basic setup, cloud
 Register the instrument
• Monitor run from any device
Cathode Buffer Container, 4 pk
A33401
Integrated Capillary Protector
A31923
package includes the following
fragment length polymorphism (AFLP) analysis, loss
performed with no reconfiguration
• Recycling*
sequence of a particular organism.
your trusted partner for confirming NGS results.
sequencing DNA of fingerprint loci.
copy number of a locus.
consulting services. Benefits include
services
identification, and sequence confirmation
is limited
A comprehensive Applied Biosystems software
in multiapplication functionality, including amplified
DNA sequencing by capillary electrophoresis
 Obtain run protocol • View results
Targeted sequencing using Sanger sequencing
CRISPR-Cas9 genome editing analysis
Analysis of inserts subcloned into plasmids.
Applied Biosystems SNaPshot genotyping
Microsatellite genotyping software that allows
Confirms NGS variants using CE technology.
Automatically checks the quality of traces from
1 2
Cathode Buffer Container Reservoir Septa, 20 pk
A35640
the user to analyze a mixture of DNA fragments,
It allows users to easily visualize the variants
Applied Biosystems SeqStudio Genetic Analyzer is
integrates POP-1 polymer, anode buffer, a polymer
Identification of species in an unknown sample by
Study of inherited human diseases arising from variations in
Sequencing Analysis Software—uses a base-caller
of heterozygosity (LOH), and microsatellite and SNP
The SeqStudio Genetic Analyzer is integrated with
Fast and powerful secondary analysis software to
from Applied Biosystems DNA and genetic analyzers
MVF Software—enables 5% somatic variant detection
technology—providing a high degree of accuracy,
reliable detection and quantitation of markers for cancer
Connect, our cloud-based platform, allowing you to
extract and share results
SAE Administrator Console Software v2.0 (optional)
A46170
for both new and experienced users who need simple
can be configured as a stand-alone system or with a
SeqScape Software—designed for mutation detection
fast, cost-effective, and accurate way to call low-frequency
algorithm for pure- and mixed-base calls; analyzes,
genotyping analysis; includes security and audit features
to set up their plate and samples, and start a run.
based and non-reference–based analysis such as
Analysis (VA), Peak Scanner (PS), and Microsatellite
device, anytime. Runs can be set up using either the
the only genetic analyzer that performs simultaneous
delivery system, and a capillary array; this novel system
Sanger sequencing is the gold standard for sequencing
RNA sequencing and epigenetic analysis, enabling robust,
The SeqStudio Genetic Analyzer is easy to use with an
six months (depending on the cartridge reaction size)
diverse range of applications in many research areas.
of DNA fragments allows for a multitude of applications,
stay connected to your data remotely. Accelerate your
Applied Biosystems Analysis Modules are cloud-based,
From a leader in genetic analysis instrumentation, the
• Universal all-in-one cartridge—unique functionality
integrated and interactive touchscreen. Results can be
sequence confirmation
investment, and optimize performance with professional
Compliance and analytical validation
make adjustments to, or exclude traces from the study.
• Share data and results  Analyze data using cloud apps
species identification and characterization, and human
sizes, provides a profile of the separation, and precisely
Although Sanger sequencing is highly recognized for DNA
from genotyping to bacteria identification and from plant
and affordable Sanger sequencing and fragment analysis,
computer to fit most laboratory needs
and analysis, SNP discovery, pathogen subtyping, allele
somatic variants where the number of relevant targets
export variant calls in standard VCF format. It reports
Connect. By logging into your cloud-based account, remote features are
locate mutations or polymorphisms in diploid organisms,
Human cell line authentication
sample. Microsatellite analysis is commonly used in the
Peak Scanner
triplet repeat expansion in neurodegenerative diseases,
a mixture of DNA fragments according to their
long-read capabilities, and the flexibility to support a
and other genetic disease studies. In addition, analysis
sequencing and fragment analysis runs on the same plate.
design allows for an on-instrument reagent life of four to
Additional run modules can be created or modified via the
mutation detection and analysis, SNP discovery, and
detect genetic rearrangements, and uncover rare variants.
Analysis of specific genetic fingerprint of highly variable
navigate to questionable or borderline data, and analyze,
4 Share 3 Analyze
sequence analysis performed to obtain the primary genetic
sequencing technology, our genetic analyzers serve as
sequencing applications, it also supports applications in
screening to gene expression profiling.
research of microsatellite instability in cancer research,
A DNA fragment sizing software that separates
separated by size. This analysis provides a profile of the
detected by both NGS and CE platforms, and to export
stay connected to your data easily. The system is designed
• Maximize benchtop space—this compact instrument
• Four to six months of on-instrument storage, depending
• Four capillaries
(CE). It provides a summary of results based on the quality
 Push run data to Connect
De novo sequencing is the term used to describe the initial
With superior performance and gold-standard Sanger
Identifying heterozygous base positions or small insertions
Confirmation of CRISPR-Cas9–mediated editing events.
The SeqStudio Genetic Analyzer offers users the flexibility
Variant Reporter Software–designed for reference-
research and boost your laboratory’s productivity with the
innovative data analysis applications that bring together
separation, precisely calculates the sizes of the fragments,
confirmed variants in standard VCF format.
• Web-based applications, including free access to Quality
Anywhere, anytime access
in “plate view” as well as from the sequencing plots or raw
GeneMapper Software—designed to provide DNA

Conformités et normes

REACH

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