Contact Us

GENTAUR Europe

 GENTAUR Europe BVBA
Voortstraat 49, 1910 Kampenhout BELGIUM
Tel 0032 16 58 90 45 
Fax 0032 16 50 90 45
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Gentaur Bulgaria

 GENTAUR BULGARIA
53 Iskar Str. 1191 Kokalyane, Sofia
Tel 0035924682280 
Fax 0035929830072
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    GENTAUR France

     GENTAUR France SARL
    9, rue Lagrange, 75005 Paris 
    Tel 01 43 25 01 50 
    Fax 01 43 25 01 60
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    Gentaur Germany

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      GmbH Marienbongard 20
    52062 Aachen Deutschland
    Tel (+49) 0241 56 00 99 68 
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    Gentaur London

     GENTAUR Ltd. 
    Howard Frank Turnberry House 
    1404-1410 High Road 
    Whetstone London N20 9BH 
    Tel 020 3393 8531 
    Fax 020 8445 9411
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    GENTAUR Poland

     GENTAUR Poland Sp. z o.o. 

    ul. Grunwaldzka 88/A m.2

    81-771 Sopot, Poland
    Tel  058 710 33 44
    Fax 058 710 33 48 
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    GENTAUR Nederland

     GENTAUR Nederland BV
    Kuiper 1 
    5521 DG Eersel Nederland
    Tel 0208-080893 
    Fax 0497-517897
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    Gentaur Italy

     GENTAUR SRL IVA IT03841300167

    Piazza Giacomo Matteotti, 6, 24122 Bergamo
    Tel 02 36 00 65 93 
    Fax 02 36 00 65 94
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    GENTAUR Spain

     GENTAUR Spain
    Tel 0911876558
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    Genprice USA

    usa-flagGenprice Inc, Logistics
    547, Yurok Circle
    San Jose, CA 95123
    Phone/Fax: 

    (408) 780-0908 

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    GENPRICE Inc. invoicing/ accounting:
    6017 Snell Ave, Suite 357
    San Jose, CA. 96123

     

    Gentaur Serbia

    serbiaSerbia, Macedonia FlagMacedonia, 

    montenegro-flagMontenegro, croatiaCroatia: 
    Tel 0035929830070 
    Fax 0035929830072
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    GENTAUR Romania

    romGENTAUR Romania

    Tel 0035929830070 
    Fax 0035929830072
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    GENTAUR Greece

    grGENTAUR Greece 

    Tel 00302111768494 
    Fax 0032 16 50 90 45

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    Other countries

    Other countries
    Luxembourg +35220880274
    Schweiz Züri +41435006251
    Danmark +4569918806
    Österreich +43720880899
    Ceská republika Praha +420246019719
    Ireland Dublin +35316526556
    Norge Oslo +4721031366
    Finland Helsset +358942419041
    Sverige Stockholm +46852503438
    Magyarország Budapest +3619980547

    seal-in-search-symantec

     

     

    Wednesday, 29 May 2013 16:18

    AccuPower ProFi Taq PCR PreMix

    AccuPower® ProFi Taq PCR PreMix for high efficiency and amplification of long range PCR.

    ProFiTaqPCRPreMix f01

    AccuPower® ProFi Taq PCR PreMix is a convenient lyophilized PCR master mix containing ProFi Taq DNA polymerase, reaction buffer, dNTPs, tracking dye, and a patented stabilizer. ProFi Taq DNA polymerase in the premix is a unique recombinant Taq DNA polymerase that offers enhanced amplification efficiency and higher fidelity for PCR. AccuPower® ProFi Taq PCR PreMix is applicable to any template DNA, and especially effective in amplifying large genomic DNA fragments around 20 kb. AccuPower® ProFi Taq PCR PreMix provides accurate long-range amplification of standard and amplification of low-copy target, and is highly suitable for all PCR applications.

     

    Features and Benefits

    Long PCR: ProFi Taq is especially effective in amplifying large genomic DNA fragments around 20 kb and amplifying Lambda DNA up to 30kb.
    Easy to use: All reaction components required for PCR, including thermostable DNA polymerase and dNTPs are contained within each tube and in a lyophilized "PreMix" form.
    Reproducibility: Gentaur's strict quality controlled production system ensures that your results will be reproducible experiment after experiment.
    Convenient: Just add template and primers and start your reaction. dNTPs, buffer and enzyme are provided
    Stability: Stable at room temperature for a month and for 2 years in a -20°C freezer

     

    Specifications

    5' to 3' exonuclease: Yes
    3' to 5' exonuclease: Yes
    3' – A Overhang: Yes
    PCR product size: ~ 30kb


    Application

    - Primer extension
    - long-range amplification from genomic DNA
    - High amplification efficiency
    - Excellent performance on difficult templates
    - Amplification of low-copy targets
    - High yield and high sensitivity PCR

    Experimental data

    ProFi Taq fig1

    Figure 1. Comparison of PCR amplification efficiency between AccuPower® ProFi Taq PCR PreMix from Gentaur and other suppliers' PCR master mix

    The cycling conditions for AccuPower® ProFi Taq PCR PreMix were 95°C for 5min, 30 cycles of 95°C for 20 sec, 55°C for 20 sec and 72°C for 30 sec. PCR reactions using other suppliers' PCR master mix were performed according to each supplier's protocol.
    Target : human insulin receptor gene.
    Lane M : 100 bp DNA Ladder(Gentaur, Cat. No. D-1030)
    Lane 1 : 10 ng of human genomic DNA
    Lane 2 : 1 ng of human genomic DNA
    Lane 3 : 100 pg of human genomic DNA
    Lane 4 : 10 pg of human genomic DNA

    ProFi Taq fig2
    Figure 2. Comparison of PCR amplification efficiency between AccuPower® ProFi Taq PCR PreMix from Gentaur and other suppliers' PCR master mix

    cDNA synthesized from 10-fold serial-diluted human total RNA from 10 ng to 10 pg using AccuPower® RocketScript™ Cycle RT PreMix. (Gentaur, Cat. No K-2201) wase used as a template for PCR amplification. The cycling conditions for AccuPower® ProFi Taq PCR PreMix were 95°C for 5min, 33 cycles of 95°C for 20 sec, 55°C for 20 sec and 72°C for 30 sec. PCR reactions using other suppliers' PCR master mix were performed according to each supplier's protocol.
    Target : human GAPDH gene.
    Lane M : 100 bp DNA Ladder(Gentaur, Cat. No. D-1030)
    Lane 1 : 10 ng of human total cDNA
    Lane 2 : 1 ng of human total cDNA
    Lane 3 : 100 pg of human total cDNA
    Lane 4 : 10 pg of human total cDNA

    ProFi Taq fig3
    Figure 3. Comparison of PCR amplification of long targets between AccuPower® ProFi Taq PCR PreMix from Gentaur and other suppliers' PCR master mix

    The cycling conditions for AccuPower® ProFi Taq PCR PreMix were 95°C for 5 min, 30 cycles of 95°C for 20 sec, 65°C for 20 sec and 68°C for 4 min. PCR reactions using other suppliers' PCR master mix were performed according to each supplier's protocol.
    Lane M1 : Lambda/Hind III marker (Gentaur, Cat. No. D-1050)
    Lane M2 : 1 kb DNA Ladder (Gentaur, Cat. No. D-1040)
    Lane 1 : 2 kb fragment (human tumor protein p53 gene)
    Lane 2 : 3 kb fragment (human tumor protein p53 gene)
    Lane 3 : 4.5kb fragment (human DNA cross-link repair 1A gene)
    Lane 4 : 8 kb fragment (human hemoglobin epsilon 1 gene)

    ProFi Taq fig4
    Figure 4. Comparison of PCR amplification of long targets between AccuPower® ProFi Taq PCR PreMix from Gentaur and other suppliers' PCR master mix

    The cycling conditions for AccuPower® ProFi Taq PCR PreMix were 95°C for 5 min, 32 cycles of 95°C for 20 sec and 68°C for 15 min. PCR reactions using other suppliers' PCR master mix were performed according to each supplier's protocol. Human genomic DNA was used as a template for PCR amplification.
    Lane M1 : Lambda/Hind III marker (Gentaur, Cat. No. D-1050)
    Lane M2 : 1 kb DNA Ladder (Gentaur, Cat. No. D-1040)
    Lane 1 : 11 kb fragment
    Lane 2 : 13.5 kb fragment
    Lane 3 : 17.6 kb fragment
    Lane 4 : 21.4 kb fragment

    ProFi Taq fig5
    Figure 5. Comparison of PCR amplification of long targets between AccuPower® ProFi Taq PCR PreMix from Gentaur and other suppliers' PCR master mix

    The cycling conditions for AccuPower® ProFi Taq PCR PreMix were 95°C for 5 min, 32 cycles of 95°C for 20 sec, 65°C for40 sec, and 68°C for 20 min. PCR reactions using other suppliers' PCR master mix were performed according to each supplier's protocol. Lambda DNA was used as a template for PCR amplification.
    Lane M1 : Lambda/Hind III marker (Gentaur, Cat. No. D-1050)
    Lane M2 : 1 kb DNA Ladder (Gentaur, Cat. No. D-1040)
    Lane 1 : 15 kb fragment
    Lane 2 : 20 kb fragment
    Lane 3 : 25 kb fragment
    Lane 4 : 30 kb fragment

    Order Button1

    Ready-to-use cocktail containing all components,except primer, for the amplification and detection of DNA in real-time quantitative PCR(qPCR).

    The AccuPower® 2X Greenstar qPCR Master Mix is a ready-to-use cocktail containing all components,except primer, for the amplification and detection of DNA in real-time quantitative PCR(qPCR). It combines the automatic "Hotstart" technology of Top DNA polymerase and SYBR Green I fluorescent dye to deliver excellent sensitivity in the quantification of target sequences, with a linear dose response over a wide range of target concentration. Volumes are provided for 100 or 200 amplification reactions of 50ul each.

    accupower-greenstarmaster product f01

    Features and Benefits

    High Specificity : AccuPower® 2X Greenstar qPCR Master Mix provides more accurate Real-time PCR result by application of Hot-start method.
    Stability: The chemical stabilizer maintains enzyme activity for 2 years at -20°C
    Simplicity: Ready to use, AccuPower® 2X Greenstar qPCR Master Mix contains everything of Real-time PCR excluding primer and template.
    Reproducibility: Gentaur's strict quality controlled production system ensures that your results will be reproducible experiment after experiment

     

    Applications

    - Real-time quantification of DNA and cDNA targets
    - Gene expression profiling
    - Microbial & Viral pathogen detection

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    Wednesday, 22 May 2013 14:39

    rHu IL 2, 3MIU, Lot 200908F02

    1. Description

    Recombinant human interleukin-2 is a sterile protein product for injection. rHuIL-2 is produced by recombinant DNA technology using Yeast. It is a highly purified protein containing 133 amino acids, with cysteine mutated to alanine at 125 amino acid position, and has a molecular weight of approximately 15.4kD, non-glycosylated.

    1. Indication
      1. Indicated for the treatment of adults with metastatic renal cell carcinoma (metastatic RCC).
      2. Indicated for the treatment of adults with metastatic melanoma.
    1. Pharmaceutical particulars

    Sterile, clear and colorless liquid for injection in vial.

    Dosage: 3 million IU (0.3ml)/vial

    Reference: Current CP/Internal

    Specific activity: ≥1.7×107IU/mg

    Purity (HPLC, SDS-PAGE): ≥98%

    1. Composition

    Active ingredient: Recombinant Human Interleukin 2 (rHuIL-2)

    Inactive ingredients: Glacial Acetic Acid, Mannitol, Polysorbate-80 and Sodium Acetate.

    1. Shelf life and storage conditions

     

     Drug Product

     Storage at 2-8℃ for 2 years
     Drug Substance (Concentrated solution)  Storage at -70℃ for 12 months

     

     

    Tests

    Specifications

    Results

    Identification (Immunoblot)

    Positive

    Positive

    Appearance

    Clear, colorless solution

    Complies

    Particulate Matter

       

             Visible particles

    Free of Visible foreign particles

    Complies

             Sub-visible particles

    ≥10µm: ≤6000/vial

    ≥25µm: ≤600/vial

    162

    41

    Mass Variation

    Complies to EP 6th

    Complies

    pH

    4.00 – 5.00

    4.68

    Potency

    80% - 150% of stated value

    (2.40 – 4.50 x 106IU/vial)

    113%

    (3.40 x 106IU/vial)

    Sterility

    Sterile

    Sterile

    Abnormal Toxicity test

    Complies to EP 6th

    Complies

    Pyrogen Test (Rabbit)

    Complies to EP 6th

    Complies

    Bacterial Endotoxins

    Not more than 1 EU/ml

    Less than 1 EU/ml

    Conclusion

    Complies

    Complies

     

     

    Price: 209 EUR 

    Order Button1

    Tuesday, 21 May 2013 15:35

    mGMP GM-CSF, 50ug batch20040823

    Product number 04-RHUGM-CSF-50UG
    Product name mGMP GM-CSF, 50ug batch20040823
    Quantity  
    Supplier

    GENTAUR

     

     

    Test

    Specifications

    Results

    Identification

    Positive

    Positive

    Appearance

    Looks like a white to off-white crisp cake. After reconstitution, the solution is clear, colorless

    Complies

    Particulate Matter

     

     

               Visible particles

    Free of visible foreign particles

    Complies

     

               Sub-visible particles

    = 10µm: = 6000/vial

    = 25µm: = 600/vial

    393

    21

    Weight of content

    90% - 110% of he stated value

    Complies

    PH

    6.50 – 7.50

    7.22

    Moisture

    = 3.0%

    0.6%

    Potency

    80% - 150%

    ( 4.40-8.25x105IU/vial)

    114%

    (6.25x105IU/vial)

     

    Sterility

    Sterile

    Sterile

    Abnormal Toxicity Test

    Complies to EP 5th /CP 2005

    Complies

    Pyrogen Test (Rabbit)

    Complies to EP 5th

    Complies

    Bacterial Endotoxins

    Not more than 0.25 EU/vial

    Less than 0.25 EU/vial

    Conclusion

    Complies

    Complies

     

    For more information Contact us

    Tuesday, 21 May 2013 13:52

    Real Time PCR Kits

    RR-0306-02 Measles Virus &Rubella Virus Real Time RT-PCR Kit 600 EUR

    Measles is one of the most contagious of all human  viruses, with about forty  million infections world  wide  each  year,  and  one  to  two  million  deaths. Measles  outbreaks  are  common  in underdeveloped countries where there is lower socioecoomic status, crowding, and low access to health  care.

    PDF-IconDownload pdf

    RR-0308-02 Human Betacoronavirus 2c (2012)Real Time RT-PCR Kit 568 EUR

    Human coronaviruses (HCoVs) have been known since the late 1960s as a group of viruses capable of  infecting  humans  and  animals.  SARS-CoV,  HCoV-229E,  HCoV-OC43,HCoV-NL63,and HCoV-HKU1 have been in continuous circulation since their first isolation and every year cause a large  number  of  infections.  In  September  2012,  health  authorities  worldwide  were  notified  of  2 cases of severe respiratory disease caused by a novel hCoV.

    PDF-IconDownload pdf


    RR-0310-02 Avian influenza virus N9 Real Time RT-PCR Kit 438 EUR

    Highly  pathogenic  avian  influenza  (HPAI)  caused  by  certain  subtypes  of  influenza  A  virus  in animal  populations,  particularly  chickens,  poses  a  continuing  global  human  public  health  risk. Direct human infection by an avian influenza A (H5N1) virus was first recognized during the 1997 outbreak in Hong Kong. The avian influenza virus H7N9 is one subgroup among the larger group of H7 viruses. Some cases of human infection with H7N9 virus in China are confirmed till early April of 2013.

    PDF-IconDownload pdf


    SD-0252-02 UU/MH/MG/TV Multiplex Real Time PCR Kit 1035 EUR

    UU/MH/MG/TV Multiplex real time PCR kit contains a specific ready-to-use system for the detection of  UU,  MH,  MG  and  TV  by  polymerase  chain  reaction  in  the  real-time  PCR  system.  The  master contains  reagents  and  enzymes  for  the  specific  amplification  of  the  target  DNA.  Fluorescence  is emitted and measured by the real time systems´ optical unit during PCR. The detection of amplified Ureaplasma  urealyticum  DNA  fragment  is  performed  in  fluorimeter  channel  FAM  with  the fluorescent  quencher  BHQ1.  Detection  of  amplified  Mycoplasma  humenis  DNA  fragment  is performed in fluorimeter channel HEX/VIC/JOE with the fluorescent quencher BHQ1.

    PDF-IconDownload pdf

    Saturday, 18 May 2013 17:20

    InfectoSTOP 25ml

    Initiating a primary cell culture from a surgical tissue is often difficult because of contamination. It is therefore important to incubate the tissue in an appropriate solution containing an optimized mixture of antibiotics, each at a given concentration able to avoid infectious contamination without affecting cell viability. Furthermore, it is not always possible to initiate primary cell culture immediately after surgical excision so the tissue needs to be stored for several hours until further processed.

    Product Description

    InfectoSTOP (GENT 19 - INSTOP) is a ready-to-use solution containing an optimized mix of antibiotics against gram-negative and gram-positive bacteria, mycoplasma and fungi for cell culture applications.

    Simply dilute the necessary volume (enough to cover the tissue) of InfectoSTOP in PBS or in cell culture medium.

    Intended Use

    InfectoSTOP is intended for use in primary cell culture initiation or to extend cell viability in fresh surgical material of any tissue type.

    InfectoSTOP can also be used for decontaminating established cell cultures.

    The product should be handled under sterile conditions and is not intended for animal or human use.

    Caution: If handled improperly, some components of this product may present a health hazard. Take appropriate precautions when handling this product, including the wearing of protective clothing and eyewear. Dispose of properly

    How to use InfectoSTOP

    To initiate primary cultures from fresh surgical material

    Dilute InfectoSTOP 10x in PBS (4 °C) and put the tissue in the freshly made solution. Rinse tissue immediately twice or more and then incubate 2 hours at 4 °C. Prepare a fresh solution, rinse once and incubate overnight (or at least one week without viability loss, depending on the type of tissue) at 4 °C.

    Just before initiating primary cell culture, rinse one more with InfectoSTOP.

    To eliminate contamination in anchorage-dependant cells
    • - Entirely rinse the flask twice with a 5x diluted fresh made InfectoSTOP solution (w/o serum)
    • - Incubate at 37 °C for 1 hour
    • - Entirely rinse the flask twice with a 10x diluted freshly made InfectoSTOP solution (w/o serum)
    • - Incubate at 37 °C for 3 hours
    • - Entirely rinse the flask twice with a 10x diluted freshly made InfectoSTOP solution (w/o serum)
    • - Incubate overnight in cell culture with a 10x diluted freshly made dilution of InfectoSTOP in complete culture medium

    The above cell treatment can be repeated twice if necessary.

    The dilution and incubation time of InfectoSTOP must be adjust to your own cell culture

    To eliminate contamination in anchorage-independent cells

    Same procedure as above, but before rinsing and incubation, pellet the cells by brief centrifugation.

    Storage and Stability
    •  InfectoSTOP is stored under -20° C at our facility and is shipped on dry ice.
    •  If the product is to be used immediately, thaw in a 37° C water bath or overnight at 4° C.
    •  If thawed in a water bath, do not leave the product at 37° C for more than 1 hour.
    •  When stored at 4° C, InfectoSTOP is stable for at least 2 weeks.
    •  If the product is not to be used within 1 week after receipt, we recommend storing it at below -20° C in a freezer that is not self-defrosting.
    •  Do not thaw and refreeze more than once. When stored at below -20°C, the product is stable until the expiration date shown on the label.

    Handling:

    GLP techniques should be employed for the safe handling of this product.

    This includes observing the following practices:

    • - Wear appropriate laboratory cloches including a lab coat, gloves and safety glasses.
    • - Do not mouth pipette, inhale, ingest or allow to come into contact with open wounds. Wash thoroughly any area of the body, which comes into contact with the product.
    • - Avoid accidental autoinoculation by exercising extreme care when handling in conjunction with any injection device.
    • - Handle the product under sterile area.
    • - This product is intended for research purposes and should be handled by qualified personnel only. It is not intended for use in humans or in animals. Gentaur is not liable for any damages resulting from the misuse or handling of this product.
    Components

    One bottle of 25 ml.

    Order Button1

    Thursday, 16 May 2013 16:59

    TotalLab Quant v12.3

    1D Analysis Module

    General
    - Fully automatic, single button press complete image analysis within area of interest if required
    - Instant access to refinement of any analysis step
    - Alternative step-wise image analysis for each step
    - Facility to load and save user preferences, including parameters and display options, prior to analysis
    - Automatic PDF report generator
    - Ruler options to display lane names, numbers and MWs
    - Multiple copies of the program can now be run at the same time to better compare results

    Multiplex Analysis
    - Create multiplex gels from up to 4 channel images
    - Create lanes across all channels
    - Measurement results for each channel in all tables
    - Propagate Molecular Size results across channels or per channel

    For more information download PDF file

    Order Button1

    Wednesday, 15 May 2013 15:17

    NATtrol MRSA.SA Panel

    PRODUCT DESCRIPTION:
    NATtrol™ MRSA.SA Panel (NATMRSA.SAP-C) is formulated with purified, intact bacterial particles that have been chemically modified to render them non-infectious and refrigerator stable*. NATMRSA.SAP-C contains 5 x 0.5 mL vials of S. aureus or S. epidermidis NATtrol™ as listed in Table 1. These panels are supplied in a purified protein matrix that mimics the composition of a true clinical specimen. *NATtrol™ Patents Pending

    INTENDED USE:
    - NATtrol™ MRSA.SA Panel is designed to evaluate the performance of nucleic acid tests for determination of the presence of S. aureus DNA. NATMRSA.SAP-C can also be used for verification of clinical assays, development of diagnostic tests and training of laboratory personnel.
    - NATMRSA.SAP-C contains intact organisms and should be run in a manner identical to that used for clinical specimens.

    ETIOLOGIC STATUS/BIOHAZARD TESTING:
    - NATtrol™ inactivation was carried out on the bacterial stock used to formulate panel members. The inactivation was verified by the absence of bacterial growth in a validated growth protocol.
    - The purified protein matrix was manufactured from materials that were screened and found to be negative for HIV 1&2 Ab, HBsAg, HTLV I&II Ab, HCV Ab, HIV RNA, HBV DNA and HCV RNA using FDA cleared kits at the single donor level.

    Catalog #: NATMRSA.SAP-C

    For more information download PDF file

    Wednesday, 15 May 2013 14:33

    NATtrol Influenza External Run Controls

    PRODUCT DESCRIPTION:
    NATtrol™ Influenza External Run Controls (NATFLUA.B-6MC, NATFLUAH1N1-6MC and NATCXVA9-6MC) are formulated with purified, intact virus particles that have been chemically modified to render them non-infectious and refrigerator stable*. Each control contains 6 x 0.5 mL vials of NATtrol™ Influenza A.B or Influenza A H1N1 (2009) or Coxsackie virus A9 NATtrol™.  These controls are supplied in a purified protein matrix that mimics the composition of a true clinical specimen. *NATtrol™ Patents Pending

    INTENDED USE:
    - NATtrol™ Influenza External Run Controls are designed to evaluate the performance of nucleic acid tests for determination of the presence of respiratory virus nucleic acids. NATFLUA.B-6MC, NATFLUAH1N1-6MC and NATCXVA9-6MC can also be used for quality control of clinical assays and training of laboratory personnel.
    - NATFLUA.B-6MC, NATFLUAH1N1-6MC and NATCXVA9-6MC contain intact organisms and should be run in a manner identical to that used for clinical specimens.

    ETIOLOGIC STATUS/BIOHAZARD TESTING:
    - NATtrol™ inactivation was carried out on each control. The inactivation was verified by the absence of virus growth in a validated tissue culture based infectivity assay.
    - The purified protein matrix was manufactured from materials that were screened and found to be negative for HIV 1&2 Ab, HBsAg, HTLV I&II Ab, HCV Ab,HIV RNA, HBV DNA and HCV RNA using FDA cleared kits at the single donor level.

    Catalog #:NATFLUA.B-6MC
    Catalog #:NATFLUAH1N1-6MC
    Catalog #:NATCXVA9-6MC

    For more information download PDF file

    Wednesday, 15 May 2013 14:19

    NATtrol CT.NG Panel

    PRODUCT DESCRIPTION:
    NATtrol™ CT.NG Panel (NATCT.NGP-C) is formulated with purified, intact bacterial particles that have been chemically modified to render them non-infectious and refrigerator stable*. NATCT.NGP-C panel contains 17 x 1.2 mL vials each containing the bacterial NATtrol™ targets listed in the Expected Results. These controls are  supplied in a purified protein matrix that mimics the composition of a true clinical specimen. *NATtrol™ Patents Pending

    INTENDED USE:
    - NATtrol™ CT.NG Panel is designed to evaluate the performance of nucleic acid tests for determination of the presence bacterial DNA. NATCT.NGP-C can also be used for verification of clinical assays, development of diagnostic tests and training of laboratory personnel.
    - NATCT.NGP-C contains intact organisms and should be run in a manner identical to that used
    for clinical specimens.

    ETIOLOGIC STATUS/BIOHAZARD TESTING:
    - NATtrol™ inactivation was carried out on each member in the panel. The inactivation was verified by the absence of bacterial growth in a validated growth protocol.
    - The purified protein matrix was manufactured from materials that were screened and found to be negative for HIV 1&2 Ab, HBsAg, HTLV I&II Ab, HCV Ab, HIV RNA, HBV DNA and HCV RNA using FDA cleared kits at the single donor level.

    Catalog #: NATCT.NGP-C

    For more information download PDF file