Controls

Products

UTAK Benzodiazepines Plus

UTAK Benzodiazepines Plus

The UTAK 100% REAL StoryThe best way to give you an idea as to the quality of UTAK 100% REAL Controls is to tell you what IS, and what is NOT used to make them. The UTAK Control Freaks use 100% REAL Human Matrices – serum, urine and whole blood. We do not add preservatives or stabilizers to ourmatrices. Nor do we fortify our human matrix pools with “constituents of animal origin”. And we definitely do not use stripped or “human-based” matrices

UTAK Pain Management

UTAK Pain Management

The UTAK 100% REAL StoryThe best way to give you an idea as to the quality of UTAK 100% REAL Controls is to tell you what IS, and what is NOT used to make them. The UTAK Control Freaks use 100% REAL Human Matrices – serum, urine and whole blood. We do not add preservatives or stabilizers to ourmatrices. Nor do we fortify our human matrix pools with “constituents of animal origin”. And we definitely do not use stripped or “human-based” matrices
The UTAK 100% REAL StoryThe best way to give you an idea as to the quality of UTAK 100% REAL Controls is to tell you what IS, and what is NOT used to make them. The UTAK Control Freaks use 100% REAL Human Matrices – serum, urine and whole blood. We do not add preservatives or stabilizers to ourmatrices. Nor do we fortify our human matrix pools with “constituents of animal origin”. And we definitely do not use stripped or “human-based” matrices

Seracare Serology Controls

ACCURUN serology controls have been a long trusted source of reliable and consistent QC material for clinical laboratories worldwide. SeraCare’s ACCURUN controls are weakly reactive to help challenge your serology assays and provide additional confidence in your laboratory test results. Monitoring your assay performance can help you avoid costly repeats and, more importantly, avoid false-negative and false-positive results. With ACCURUN controls, you can troubleshoot your test methods and isolate system errors in your laboratory.

  • Mimics a patient sample, therefore treated like a patient sample, reducing additional steps in your workflow
  • Reliable and ready-to-use, eliminates the hassle of locating external controls to meet laboratory compliance requirements
  • Single-analyte and multi-analyte formats offer you cost-effective options to conserve your laboratory budget

Challenges your assay more effectively
A low positive control challenges your assay more than a medium-to-high control since it is closer to the assay cut-off; therefore, any variability in the assay will be easier to detect. Assay monitoring with ACCURUN single and multi-analyte controls improves confidence in your serology test results.

ACCURUN Controls

Consistent accuracy is non-negotiable.

Serology Controls

  • Specifically formulated as a low level positive sample for manual and automated platforms
  • Ready to use—no reconstitution or special handling required; most stable at refrigerated temperatures
  • Enable your lab to meet compliance requirements of regulatory agencies and professional organizations

 

Nucleic Acid Controls: our comprehensive line of PCR and hybrid-capture

NAT controls are formulated using intact virus or microorganisms

  • Help your lab monitor all aspects of sample testing—sample lysis and extraction through target or signal amplification to detection
  • Formulated at different levels to effectively challenge assay performance and monitor results at clinical decision points

 

Genetic Controls: setting a new standard for error detection

  • Muliple alleles per vial allow your lab to run more samples and fewer controls
    • Optimizes instrument capacity, especially for multiplexed assays
  • Eliminate more test errors, run more samples and fewer controls

Custom Controls

If you cannot find a stock product to meet your needs, ELITechGroup Benelux will partner with you to manufacture custom controls according to your exact specifications

It’s this straightforward, you make the choices that fit your needs, ELITechGroup Benelux works closely with you to produce the controls you require. You choose the Matrix, Analyte, Concentration, Volume Fill Size per Vial and Liquid-stable Frozen or Freeze Dried Consistency. We make your choices a reality, and we do it at a competitive cost.

Cycler Validation

Validation tools for testing PCR thermal cyclers according to legal requirements

Validation tools for testing PCR thermal cyclers according to legal requirements

 Thermal Cycler Validation Kits available for both conventional endpoint PCR and real-time PCR (qPCR) cyclers False negative PCR results are highly critical and might be caused by a defect PCR cycler. Verification of the correct temperature control of the used equipment is usually a stressful issue. To comply with quality management systems is not easy to fulfill for PCR cyclers.

Principle

The Traditional/qPCR Thermal Cycler Validation Kits provide temperature sensitive PCR reactions to monitor an upper and lower temperature range in one run. The primer sequences in the Traditional Thermal Cycler Validiation Kit respectively the primer/probe sequences in the qPCR Thermal Cycler Validation Kit in combination with a regular PCR protocol were designed to react extremely sensitive to incorrect temperature control, temperature homogeneity, precision and timing. Amplification will completely drop out at temperature differences of more than 2 °C. The cycler performance is tested at standard PCR settings to reflect most users applications. In addition, the pre-adjusted target concentrations are only amplified at high PCR efficiencies as an additional indicator for accurate temperature control of the thermal cycler.

Benefits

  • No extra equipment, instrument or software needed.
  • Applicable with any block PCR cycler or qPCR cycler used in a research or industrial quality assurance lab for the reliability testing of instrument performance and reliability.
  • In the qPCR Thermal Cycler Validiation Kit the probes of each amplification system are labeled with different fluorescent dyes (FAM™ and ROX™) to allow individual evaluation of each temperature range.
  • Includes all you need: Freeze-dried primer/probe sets, polymerase, nucleotides and rehydration buffer

Cat.-No. 57-2102
Traditional Thermal Cylcer Validation Kit (6 strips, 8 vials each)

Cat.-No. 57-2103
Traditional Thermal Cylcer Validation Kit (100 reactions)

PCR Thermal Cycler Color Compensation Kit

For real-time PCR (qPCR) thermal cyclers with optical unit equipped with filter sets for FAM™ and ROX™

Description

As real-time qPCR cyclers may vary in their fluorescence detection sensitivity, color compensation experiments must be performed on each specific multiplex PCR instrument. The Color Compensation Kit is designed for generating color compensation files on qPCR cyclers to allow proper interpretation of multiplex experiments. To generate a color compensation object, the labeled calibration dyes are used in an initial color compensation run. The calibration dyes contain labeled oligonucleotides for the determination of crosstalk corresponding to each individual dye being used in a multiplex assay, and a blank reaction buffer without dye for the determination of background fluorescence of the buffer. The result evaluation is performed by measuring the fluorescence signal with your qPCR cycler.

Kit Components

  • Freeze-dried calibration dyes for 3 different wavelengths (FAM, ROX and VIC)
  • Rehydration Buffer

Cat.-No. 57-0010
10 calibrations (25 μl each)

Molecular Controls

Molecular Controls & QCMD Past Panels

Qnostics’ Molecular ‘Q’ Controls are positive run controls intended to help laboratories monitor their molecular diagnostic assay on a run to run basis within customer derived limits.

Product Code(s)

ADVQC01
Product: ‘Q’ Control
Pathogen: Adenovirus

ADVMQP01
Product: Molecular ‘Q’ Panel
Pathogen: Adenovirus

BKVQC01
Product: ‘Q’ Control
Pathogen: BK Virus

BKVMQP01
Product: Molecular ‘Q’ Panel
Pathogen: BK Virus

CMVQC01
Product: ‘Q’ Control
Pathogen: Cytomegalovirus

CMVMQP01
Product: Molecular ‘Q’ Panel
Pathogen: Cytomegalovirus

EBVQC01
Product: ‘Q’ Control
Pathogen: Epstein-Barr Virus

EBVMQP01
Product: Molecular ‘Q’ Panel
Pathogen: Epstein-Barr Virus

HHV6QC01
Product: ‘Q’ Control
Pathogen: Human Herpes Virus 6

HHV6MQP01
Product: Molecular ‘Q’ Panel
Pathogen: Human Herpes Virus 6

HSV1QC01
Product: ‘Q’ Control
Pathogen: Human Herpes Virus 1

HSV1MQP01
Product: Molecular ‘Q’ Panel
Pathogen: Human Herpes Virus 1

HSV2QC01
Product: ‘Q’ Control
Pathogen: Human Herpes Virus 2

HSV2MQP01
Product: Molecular ‘Q’ Panel
Pathogen: Human Herpes Virus 2

INFAQC01
Product: ‘Q’ Control
Pathogen: Influenza A Virus

INFBQC01
Product: ‘Q’ Control
Pathogen: Influenza B Virus

RSVQC01
Product: ‘Q’ Control
Pathogen: Respiratory Syncytial Virus

JCVQC02
Product: ‘Q’ Control
Pathogen: JC Virus

JCVMQP02
Product: Molecular ‘Q’ Panel
Pathogen: JC Virus

PINFQC01
Product: ‘Q’ Control
Pathogen: Parainfluenza Virus

VZVQC01
Product: ‘Q’ Control
Pathogen: Varicella Zoster Virus

VZVMQP01
Product: Molecular ‘Q’ Panel
Pathogen: Varicella Zoster Virus

QCMD Past EQA/PT Panels

External Quality Assessment (EQA) / Proficiency Testing (PT) is recognized within ISO15189:2012 as an essential part of a laboratory’s quality management. It helps monitor and improve quality within the laboratory

  • Adenovirus
  • Aspergillus
  • B19
  • Borrelia burgdorferi
  • BK virus
  • Bordetella pertussis
  • Candida albicans
  • Chlamydia trachomatis A
  • Chlamydia trachomatis B
  • Chlamydophila pneumoniae & Mycoplasma pneumoniae
  • Clostridium difficile
  • Cytomegalovirus Dried Blood Spot
  • Cytomegalovirus Whole Blood
  • Cytomegalovirus
  • Coronavirus
  • Dengue Virus
  • Enterovirus
  • Epstein Barr virus
  • ENVA HIV Drug Resistance
  • ENVA HIV Drug Resistance Typing (Integrase)
  • Extended Spectrum β-lactamase and Carbapenemase
  • Viral Gastroenteritis
  • Bacterial Gastroenteritis
  • Parasitic Gastroenteritis
  • Hepatitis A virus
  • Hepatitis B virus
  • Hepatitis B virus Drug Resistance
  • Hepatitis B virus Genotype
  • Hepatitis C virus
  • Hepatitis C virus Genotype
  • Hepatitis C virus Drug Resistance
  • Hepatitis E virus
  • Human Immunodeficiency Virus DNA B
  • Human Immunodeficiency Virus RNA A
  • Human Immunodeficiency Virus RNA B
  • Herpes Simplex Virus
  • Human Papillomavirus
  • Human Herpes virus 6
  • Influenza virus A and B
  • Influenza Haemaglutinin typing
  • JC virus
  • JC virus and BK virus
  • Legionella pneumophila
  • MALDI-TOF Bacterial
  • Metapneumovirus
  • Methicillin Resistant S. aureus
  • Methicillin Resistant S. aureus SPA
  • Methicillin Resistant S. aureus Typing
  • Mycobacterium tuberculosis
  • Neisseria gonorrhoeae
  • Norovirus
  • Parechovirus RNA
  • Parainfluenzavirus
  • Respiratory Syncytial virus
  • Rhinovirus
  • Toxoplasma gondii
  • Vancomycin Resistant Enterococci
  • Varicella-Zoster virus
  • West Nile virus

Recipe HPLC & LC-MS Calibrators, Controls and Standards

IVD/CE labelelled test- and reference materials

RECIPE provides a wide range of IVD/CE labelled test- and reference materials. Our products help to ensure a coherent QA process including the testing of the analytical system (ClinTest®), calibration (ClinCal®) and quality control (ClinChek®).

ClinTest® Standard and Test Solutions are matrix-free and thus are ready to use. ClinCal® Calibrators and ClinChek® Controls are available in different matrices (urine, plasma, serum, whole blood) and are prepared for analysis like the patient samples.

SERO Autonorm

SERO Autonorm

  • Animal-based control serum for precision control of the most important components in clinical chemistry laboratories
  • Product documentation with approximate value list for about 40 components
  • Component levels mainly in the borderline between normal and pathological range
  • Pharmaca free
  • Freeze-dried material, offering long shelf life
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