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, 15 May 2013 12:07

    NATtrol CT.NG External Run Controls

    PRODUCT DESCRIPTION:
    NATtrol™ CT.NG External Run Controls (NATCT (434)-6MC, NATNG-6MC and NATCT.NGNEG-6MC) are formulated with purified, intact bacterial particles that have been chemically modified to render them non-infectious and refrigerator stable*. Each control pack contains 6 x 1.0 mL vials of C.trachomatis NATtrolTM, N.gonorrhoeae NATtrolTM or CT.NG Negative NATtrolTM. 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 External Run Controls are full process controls designed to evaluate the performance of nucleic acid tests for determination of the presence of CT.NG DNA. NATCT(434)-6MC, NATNG-6MC and NATCT.NGNEG-6MC can also be used for quality control of clinical assays and training of laboratory personnel.
    - NATCT(434)-6MC, NATNG-6MC and NATCT.NGNEG-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 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 #:NATNG-6MC
    Catalog #:NATCT(434)-6MC
    Catalog #:NATCT.NGNEG-6MC

    For more information download PDF file

    Wednesday, 15 May 2013 11:16

    NATtrol BC.GP Panel

    PRODUCT DESCRIPTION:
    NATtrol™ BC.GP Panel (NATBC.GP-NNS) is formulated with purified, intact bacterial particles that have been chemically modified to render them non-infectious and refrigerator stable*. NATBC.GP-NNS contains 11 x 0.75 mL vials of bacterial NATtrol™ targets 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™ BC.GP Panel is designed to evaluate the performance of nucleic acid tests for determination of the presence of bacterial nucleic acids. NATBC.GP-NNS can also be used for verification of clinical assays, development of diagnostic tests and training of laboratory personnel.
    - NATBC.GP-NNS 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.

    PRECAUTIONS:
    - Although NATBC.GP-NNS contains inactivated organisms, it should be handled as if potentially infectious.
    - Use Universal Precautions when handling this product.
    - To avoid cross-contamination, use separate pipette tips for all reagents.

    Catalog #: NATBC.GP-NNS 

    For more information donwload PDF file


    A MUST FOR:

    • - Mouse-On-Mouse
    • - Human and Animal IHC
    • - Immunofluorescence
    • - in-situ Hybridization


    background busterBackground Buster is highly effective for quenching background fluorescence and is easy to use: 

    For Fluorescence:

    • Apply Background Buster for 15 minutes prior to application of the first antibody (unlabeled or fluorescence-labeled antibody).
    • Rinse with PBS for 1 minute.
    • Apply unlabeled antibody for indirect method or fluorescence labeled antibody for direct method and continue with usual protocol.

     

    Background Buster can be used for IHC:

     background buster ihc

     

    Background or non-specific staining is often observed in a variety of immunoassays, in immunohistochemistry and other immunoassay types such as immunofluorescence, ELISA and flow cytometric assays, background staining can be prevented by the use of INNOVEX Recombinant Protein Technology,Background Buster.


    Background Buster is also applicable to eliminating non-specific binding in immunofluorescence, ELISA and flow cytometric assays.


    ADVANCED & UNIQUE FEATURES:

    • Allows staining of identical species antibodies and tissues (e.g., mouse antibody on mouse tissue, rat-on-rat, rabbit-on-rabbit, etc.).
    • Short 10 minute incubation step prior to applying primary antibody or in-situ probe at room temperature
    • Delivers complete eradication of general background staining
    • Replaces the use of normal serum, powdered milk, casein, and other blocking agents and renders complete success
    • Excellent for both frozen and paraffin sections
    • Excellent for in situ application
    • A must for animal tissue staining

    Download datasheet PDF file

    Thursday, 09 May 2013 14:38

    25OH Vitamin D Total, ELISA, 96 tests

    The Gentaur 25OH Vitamin D Total ELISA is a solid phase Enzyme Linked Immunosorbent Assay performed on microtiterplates. During a first 2 hours incubation step, at room temperature, total 25OH Vitamin D (D2 and D3) present in calibrators, controls and samples is dissociated from binding serum proteins to fix on binding sites of a specific monoclonal antibody. After 1 washing step, a fixed amount of 25OH Vitamin D-labelled with biotin in presence of horseradish peroxidise (HRP), compete with unlabelled 25OH Vitamin D2 and 25OH Vitamin D3 present on the binding sites of the specific monoclonal antibody. After a 30 minutes incubation at room temperature, the microtiterplate is washed to stop the competition reaction. The Chromogenic solution (TMB) is added and incubated for 15 minutes. The reaction is stopped with the addition of Stop Solution and the microtiterplate is then read at the appropriate wavelength. The amount of substrate turnover is determined colourimetrically by measuring the absorbance, which is inversely proportional to the total 25OH Vitamin D (D2 and D3) concentration. A calibration curve is plotted and the total 25OH Vitamin D (D2 and D3) concentrations of the samples are determined by dose interpolation from the calibration curve.

      

    Price: 250 €Order Button1

      

    Technical spec.:

    Catalog # KAP1971
    Format ELISA
    Label HRP
    Size 96 tests
    Sample Type Serum
    Sample Volume 50 µL
    Controls 2 levels
    Range 0-180 ng/mL
    Sensitivity 1,4 ng/mL
    Incubation 120min./30 min./15 min
    Shelf Life (weeks) 32

    pdfDownload "Instructions for Use": KAP1971.pdf

    PRODUCT DESCRIPTION: Each frozen aliquot contains 1 mL of a pure, titered culture of Enterococcus faecium. The identification of this organism was confirmed by 16S sequencing. The purity of the culture was monitored by Gram staining and by additional culturing. The titer was performed on one aliquot after freezing. The freezing medium contains 15% glycerol as a cryoprotectant. Please see the Certificate of Analysis for the specific freezing medium used.

    INTENDED USE: Live, titered microorganisms can be used to determine a limit of detection (LOD), in diagnostic assay development or crossreactivity studies. When used as a control for nucleic acid tests, the same protocols as those used to amplify clinical specimens should be employed.

    BIOSAFETY: Enterococcus faecium is a biosafety level 2 microorganism and must be used within Biological Safety Level 2 facility or cabinet. Please consult your institution’s regulations regarding the use of this organism.

    PRECAUTIONS:
    - Use Universal Precautions, this organism is potentially biohazardous.
    - Repetitive freezing and thawing is not recommended (aliquot material if necessary). Titer will be altered by a single freeze-thaw.
    - To avoid cross-contamination, use separate pipette tips for all reagents.

    RECOMMENDED STORAGE:
    Titered material should be stored at -65°C or below.

    DO NOT USE IN HUMANS:
    These products are intended for research, product development, or quality assurance. These products are NOT intended for use in the manufacture or processing of injectable products subject to licensure under section 351 of the Public Health Service Act or for any other product intended for administration to humans.

    Catalog #: 0801892

    Contact us for additional information

    PRODUCT DESCRIPTION: Each frozen aliquot contains 1 mL of a pure, titered culture of Corynebacterium diphtheriae. The identification of this organism was confirmed by 16S sequencing. The purity of the culture was monitored by Gram staining and by additional culturing. The titer was performed on one aliquot after freezing. The freezing medium contains 15% glycerol as a cryoprotectant. Please see the Certificate of Analysis for the specific freezing medium used.

    INTENDED USE: Live, titered microorganisms can be used to determine a limit of detection (LOD), in diagnostic assay development or crossreactivity studies. When used as a control for nucleic acid tests, the same protocols as those used to amplify clinical specimens should be employed.

    BIOSAFETY: Corynebacterium diphtheriae is a biosafety level 2 microorganism and must be used within Biological Safety Level 2 facility or cabinet. Please consult your institution’s regulations regarding the use of this organism.

    PRECAUTIONS:
    - Use Universal Precautions, this organism is potentially biohazardous.
    - Repetitive freezing and thawing is not recommended (aliquot material if necessary). Titer will be altered by a single freeze-thaw.
    - To avoid cross-contamination, use separate pipette tips for all reagents.

    RECOMMENDED STORAGE:
    Titered material should be stored at -65°C or below.

    DO NOT USE IN HUMANS:
    These products are intended for research, product development, or quality assurance. These products are NOT intended for use in the manufacture or processing of injectable products subject to licensure under section 351 of the Public Health Service Act or for any other product intended for administration to humans.

    Catalog #: 0801882

    Contact us for additional information 

    PRODUCT DESCRIPTION: Each frozen aliquot contains 1 mL of a pure, titered culture of Staphylococcus simulans. The identification of this organism was confirmed by 16S sequencing. The purity of the culture was monitored by Gram staining and by additional culturing. The titer was performed on one aliquot after freezing. The freezing medium contains 15% glycerol as a cryoprotectant. Please see the Certificate of Analysis for the specific freezing medium used.

    INTENDED USE: Live, titered microorganisms can be used to determine a limit of detection (LOD), in diagnostic assay development or crossreactivity studies. When used as a control for nucleic acid tests, the same protocols as those used to amplify clinical specimens should be employed.

    BIOSAFETY: Staphylococcus simulans is a biosafety level 2 microorganism and must be used within Biological Safety Level 2 facility or cabinet. Please consult your institution’s regulations regarding the use of this organism. 

    PRECAUTIONS:
    - Use Universal Precautions, this organism is potentially biohazardous.
    - Repetitive freezing and thawing is not recommended (aliquot material if necessary). Titer will be altered by a single freeze-thaw.
    - To avoid cross-contamination, use separate pipette tips for all reagents.

    RECOMMENDED STORAGE:
    Titered material should be stored at -65°C or below.

    DO NOT USE IN HUMANS:
    These products are intended for research, product development, or quality assurance. These products are NOT intended for use in the manufacture or processing of injectable products subject to licensure under section 351 of the Public Health Service Act or for any other product intended for administration to humans.

    Catalog #: 0801728

    Contact us for additional information 

    PRODUCT DESCRIPTION: Each frozen aliquot contains 1 mL of a pure, titered culture of Staphylococcus lugdunensis. The identification of this organism was confirmed by 16S sequencing. The purity of the culture was monitored by Gram staining and by additional culturing. The titer was performed on one aliquot after freezing. The freezing medium contains 15% glycerol as a cryoprotectant. Please see the Certificate of Analysis for the specific freezing medium used.

    INTENDED USE: Live, titered microorganisms can be used to determine a limit of detection (LOD), in diagnostic assay development or crossreactivity studies. When used as a control for nucleic acid tests, the same protocols as those used to amplify clinical specimens should be employed.

    BIOSAFETY: Staphylococcus lugdunensis is a biosafety level 2 microorganism and must be used within Biological Safety Level 2 facility or cabinet. Please consult your institution’s regulations regarding the use of this organism. 

    PRECAUTIONS:
    - Use Universal Precautions, this organism is potentially biohazardous.
    - Repetitive freezing and thawing is not recommended (aliquot material if necessary). Titer will be altered by a single freeze-thaw.
    - To avoid cross-contamination, use separate pipette tips for all reagents.

    RECOMMENDED STORAGE:
    Titered material should be stored at -65°C or below.

    DO NOT USE IN HUMANS:
    These products are intended for research, product development, or quality assurance. These products are NOT intended for use in the manufacture or processing of injectable products subject to licensure under section 351 of the Public Health Service Act or for any other product intended for administration to humans.

    Catalog #: 0801555

    Contact us for additional information

    Monday, 29 April 2013 10:11

    Candida albicans Z006, DNA (1 μg)

    PRODUCT DESCRIPTION: Each aliquot contains 1 μg of DNA extracted from a pure culture of Candida albicans. The identification of this organism was confirmed by rDNA sequencing. The purity of the culture was monitored by additional culturing and Gram staining to detect any contaminating bacteria. The DNA was extracted from the cells following a protocol based on the yeast protocol provided in the Qiagen® Genomic DNA Handbook and using Qiagen® Genomic DNA Buffers with a 500/G genomic tip. DNA concentration and OD260/280 ratios are determined using a NanoDrop ND- 1000®. The extracted DNA also tested positive on an in-house real time PCR assay.

    INTENDED USE: Purified Genomic DNA is designed for use as an amplification and/or detection control for nucleic acid testing of Candida albicans. It can also be used to determine a limit of detection (LOD), in diagnostic assay development, cross-reactivity studies or genomic sequencing. When used as a control for nucleic acid tests, the same protocols as those used to amplify extracted clinical specimens should be employed.

    PRECAUTIONS:
    - Use Universal Precautions when handling Genomic DNA.
    - The material may be re-frozen after thawing. Repetitive freezing and thawing is not recommended (aliquot material if necessary).
    - To avoid cross-contamination, use separate pipette tips for all reagents.

    RECOMMENDED STORAGE:
    This control is supplied in TE Buffer and should be frozen at -20°C or below.

    DO NOT USE IN HUMANS:
    These products are intended for research, product development, quality assurance or manufacturing use. These products are NOT intended for use in the manufacture or processing of injectable products subject to licensure under section 351 of the Public Health Service Act or for any other product intended for administration to humans.

    Catalog #: 0801504DNA-1μg

    Contact us for additional information

     

    PRODUCT CHARACTERISTICS

    Each lot of IL-2/TCGF is analyzed for its ability to stimulate proliferation of seven to ten day old PHA-transformed human T- lymphocytes. When used at a final concentration of approximately 10% (v/v), IL-2/TCGF will induce a minimum five- fold increase in cell concentration of such cells when seeded at a density of 2.0 x 105/ ml. IL- 2/TCGF, a glycoprotein with a molecular weight of approximately 15,000 kDa, is produced from pooled human PHA-stimulated T-lymphocytes. IL-2/TCGF is purified by several chromatographic steps to remove PHA and interferon.

    CONTENTS

    Each 50 ml bottle contains approximately 25,000 BRMP (Biological Response Modifier Program) units of IL-2/TCGF at a concentration of approximately 500 BRMP units/ml. It is supplied as a sterile solution in 25mM HEPES buffered RPMI 1640 culture medium which is free of serum. IL-2/TCGF protein concentration ranges from 8-22 µg/ml.

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    PDF-IconDownload Natural Human Interleukin-2 (IL-2) / T-Cell Growth Factor (TCGF) Datasheet

    PDF-IconDownload SeroDetect West Nile Virus Panel