BIOREADER® 7000 -V

For non-fluoro applications in 384 well to 6 well plates and Petri dishes.

BIOREADER® 7000 -V
For non-fluoro applications in 384 well to 6 well plates and Petri dishes.

The BIOREADER® 7000 -V is equipped with a fully automatic lens changer for different fix focal lengths.

Providing a resolution of  100 - 2000 µm for FOCI, 100 - 5000 µm for Plaques or 50 - 2000 µm for cell clones.

 

Model types:

Alpha with 2-times lens changer e.g. for 96 + 24/12 well plates.

Beta with 3-times lens changer e.g.for 384/96, 48/24/12 and 6 well plates.

Gamma with 4-times lens changer e.g. for 384/96, 48/24/12 and 6 well plates and Petri dishes.

 

Non-Fluoro substrats and staining

This BIOREADER® 7000 is specially designed for visible CV or immunhistochemical substrates.

The patented dual telecentric illumination suppresses reflection of the sidewall of Microfilter plates.

Elispot with all available substrates like AEC,Silver,TMB or BCIP/NBT

Enzyme conjugates like Alkaline Phosphatase (ALP) or Horseradish Peroxidase (HRP) 

 

Features
  • Patented dual telecentric illumination.
  • Front loader with automatic door.
  • Lens changer for high definition lenses with fix focal length.
  • Automated focus, illumination and lens changer are measure protocol controlled (GxP locked).
  • High resolution camera with 5 MPixel (up to 42 MPixel available).
  • Incl. computer and monitor.
  • Excel/Word/PowerPoint and LIMS export capabilities.
  • Interactive content specific video training program.
  • Suitable for research purpose.
  • For ‘phantom spot suppression’, better spot separation and cytokine quantification.
  • Optional full automation with plate 'feeding system'.
  • DQ/IQ/OQ/PQ documentation possible.
  • 12 month warranty.
Software

biocreader_7000_v_software.png

Eazyreader® software

  • Innovative EazyReader® software combines ‘easy of use’ and versatility and flexibility.
  • Scan, analyze and overlay live time.
  • Creates up to 7 images for each well simultaneously during the scan.
  • ‘Profiling’ app helps to create user independent measure protocols for Elispot beginners and references for experts.
  • Verified in collaborative studies.
  • Export options and reports with all scalable images and results even in one file.
  • Customer specific export and report templates.
  • Video clips and content specific help files.
  • Qualified installation and training with each Bioreader® model.
  • On-site or internet remote services and support.
  • ‘Classified’ measure protocols ‘history’ tracking and comparison tools.
  • User specific plates, Studies/projects, plate layouts/designs and measure protocols prevent from mix-up.
  • More accurate ‘cytokine quantification’ based on the patented ‘photometric’ dual illumination system.
  • Optional software features:
  • 'Routine’ software package: Ooptimized applications for commonly used operations, only presents the icons you require for the specific job, quickly read a plate and quickly review, Q.C. and release the results.
  • 21 CFR part 11 based software module available.

Dimension

width
45 cm
height
60 cm
depth
35 cm

Weight

weight
26 kg
The BIOREADER® 7000 -V can also use with the follow applications:
Plaque assay.Very bright plaques in 24 well plate Icon

Plaque assay.Very bright plaques in 24 well plate

Plaque assay with very bright plaques in 24 well plate

Cells were infected and covered with an overlay. Surviving cells stained with CV. Cells killed by the virus.

Foci assay: total well view Icon

Foci assay: total well view

Foci assay: total well view

"The focus forming assay (FFA) is a variation of the plaque assay, but instead of relying on cell lysis in order to detect plaque formation, the FFA employs immunostaining techniques using fluorescently labeled antibodies specific for a viral antigen to detect infected host cells and infectious virus particles before an actual plaque is formed." [https://en.wikipedia.org/wiki/Virus_quantification]

Elispot in 384 microfilter plates Icon

Elispot in 384 microfilter plates

Small volume, higher throughput.

Elispot - enzymatic single color Icon

Elispot - enzymatic single color

Elispot single encymatic

Blue, red, green or silver substrat Elispot.

Detection antibody, enzyme-conjugate and precipitating substrate.

"The enzyme-linked immune absorbent spot (ELISpot) is a type of assay that focuses on quantitatively measuring the frequency of cytokine secretion for a single cell."

[https://en.wikipedia.org/wiki/ELISpot]

Why to use Elispot

•The cytokine Elispot assay is designed to enumerate cytokine secreting cells in single cell suspensions of lymphoid tissue, CNS tissue, bone marrow or preparations of peripheral blood mononuclear cells (PBMC).

•The assay has the advantage of detecting only activated/memory T cells and the cytokine release can be detected at the single cell level, allowing direct determination of T cell frequencies.

•The assay has the advantage of detecting only activated/memory T cells and the cytokine release can be detected at the single cell level, allowing direct determination of T cell frequencies.

The ELISPOT assay is an effective tool to enumerate antigen-specific T cells in the circulation of immunized humans and animals at much lower frequencies than possible with other currently available methods

The ELISPOT assay has proven to be a sensitive and unique system to follow disease progression in human individuals or animals. Several studies have indicated that alterations in the frequency of cytokine pc in different compartments of the body adequately reflect changes in immune function

The ELISPOT assay may be used to determine effects of drugs, chemicals or other compounds on cytokine secretion in vitro, thereby providing data on their putative modulatory effects on immune function in vivo

Elispot - enzymatic dual color Icon

Elispot - enzymatic dual color

Blue and red Elispot substrate (mixed color violet)

Dual cytokine secretion.

non stained cells Icon

non stained cells

Non stained cells may be counted in a kind of phase contrast mode.

Alveolar epithelial cells (AEC) Icon

Alveolar epithelial cells (AEC)

Alveolar epithelial cells (AEC)

"Typically, type 1 alveolar cells comprise the major gas exchange surface of the alveolus and are integral to the maintenance of the permeability barrier function of the alveolar membrane. Type 2 pneumocytesare the progenitors of type 1 cells and are responsible for surfactant production and homeostasis." [https://www.sciencedirect.com/topics/medicine-and-dentistry/alveolar-type-i-cells]

The alveolar epitheliumis a major target in toxic exposures of the lung because of its structural delicacy and proximity to inhaled toxicants. Type II epithelial cellsare important in maintaining the integrity of alveolar epitheliumand normal lung function.

MCMV: mouse cytomegalovirus, unstained Icon

MCMV: mouse cytomegalovirus, unstained

MCMV: mouse cytomegalovirus, unstained

HCMV Human cytomegalovirus, unstained Icon

HCMV Human cytomegalovirus, unstained

HCMV human cytomegalovirus, unstained

"The glycoprotein gO (UL74) of human cytomegalovirus (HCMV) forms a complex with gH/gL. Virus mutants with a deletion of gO show a defect in secondary envelopment with the consequence that virus spread is restricted to a cell-associated pathway." [https://www.ncbi.nlm.nih.gov/pubmed/20181688]

NK92 cells natural killer cells (human cell line) same samples microwell plate. Icon

NK92 cells natural killer cells (human cell line) same samples microwell plate.

NK92 cells natural killer cells (human cell line) same samples microwellplate

"Natural killer cells, or NK cells, are a type of cytotoxic lymphocyte critical to the innate immune system. Typically, immune cells detect major histocompatibility complex (MHC) presented on infected cell surfaces, triggering cytokine release, causing lysis or apoptosis." [https://en.wikipedia.org/wiki/Natural_killer_cell]

Foci assay: Very large Foci Icon

Foci assay: Very large Foci

Foci assay: very large Foci

"The focus forming assay (FFA) is a variation of the plaque assay, but instead of relying on cell lysis in order to detect plaque formation, the FFA employs immunostaining techniques using fluorescently labeled antibodies specific for a viral antigen to detect infected host cells and infectious virus particles before an actual plaque is formed." [https://en.wikipedia.org/wiki/Virus_quantification]

Plaque assay extremely large spots Icon

Plaque assay extremely large spots

Plaque assay with extremely large spots

"The TCID50 (Median Tissue Culture Infectious Dose) is one of the methods used when verifying viral titer. TCID50 signifies the concentration at which 50% of the cells are infected when a test tube or well plate upon which cells have been cultured is inoculated with a diluted solution of viral fluid." [https://www.zeomic.co.jp/en/glossary/virus/71]

CV Plaque assay.Example with large and fuzzy plaques Icon

CV Plaque assay.Example with large and fuzzy plaques

CV Plaque assay; example with large and fuzzy plaques

Cells were infected and covered with an overlay. Surviving cells stained with CV. Cells killed by the virus.

TCID50 viral assay Icon

TCID50 viral assay

Various media/strain combinations on petridishes Icon

Various media/strain combinations on petridishes

Various media/strain combinations on petridishes

Dual Transgene assay Icon

Dual Transgene assay

Dual Transgene assay

A segment of DNA introduced to some other organism. See [https://en.wikipedia.org/wiki/Transgene]

Various colonies in 6 well plates and Petridishes 35 mm - 100 mm Icon

Various colonies in 6 well plates and Petridishes 35 mm - 100 mm

Various colonies in 6 well plates

Organoids Icon

Organoids

Organoids

"An organoid is a miniaturized and simplified version of an organ produced in vitro in three dimensions that shows realistic micro-anatomy. The technique for growing organoids has rapidly improved since the early 2010s." [https://en.wikipedia.org/wiki/Organoid]

Detection of Marek's disease virus Plaques after staining with specific anti-MDV antibodies and Alexa 488 labelled secondary antibodies Icon

Detection of Marek's disease virus Plaques after staining with specific anti-MDV antibodies and Alexa 488 labelled secondary antibodies

Detection of Marek's disease virus

Plaques after staining with specific anti-MDV antibodies and Alexa 488 labelled secondary antibodies

"Marek's disease is a highly contagious viral neoplastic disease in chickens. The disease is characterized by the presence of T cell lymphoma as well as infiltration of nerves and organs by lymphocytes. Viruses related to MDV appear to be benign and can be used as vaccine strains to prevent Marek's disease." [https://en.wikipedia.org/wiki/Marek's_disease]

Detection of Marek's disease virus Plaques after staining with specific anti-MDV antibodies and Alexa 568 labelled secondary antibodies Icon

Detection of Marek's disease virus Plaques after staining with specific anti-MDV antibodies and Alexa 568 labelled secondary antibodies

Detection of Marek's disease virus but Alexa 568 labelled

"Marek's disease is a highly contagious viral neoplastic disease in chickens. The disease is characterized by the presence of T cell lymphoma as well as infiltration of nerves and organs by lymphocytes. Viruses related to MDV appear to be benign and can be used as vaccine strains to prevent Marek's disease. " [https://en.wikipedia.org/wiki/Marek's_disease]

Neutralization assay Accepted Plaques are surrounded Icon

Neutralization assay Accepted Plaques are surrounded

Neutralization assay

Accepted Plaques are surrounded

"The plaque reduction neutralization test is used to quantify the titer of neutralizing antibody for a virus. The serum sample or solution of antibody to be tested is diluted and mixed with a viral suspension." [https://en.wikipedia.org/wiki/Plaque_reduction_neutralization_test]

Neutralization assay Icon

Neutralization assay

Neutralization assay

"The plaque reduction neutralization test is used to quantify the titer of neutralizing antibody for a virus. The serum sample or solution of antibody to be tested is diluted and mixed with a viral suspension." [https://en.wikipedia.org/wiki/Plaque_reduction_neutralization_test]

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