Suppliers
Contact Us
GENTAUR Europe BVBA Voortstraat 49, 1910 Kampenhout BELGIUM Tel 0032 16 58 90 45 Fax 0032 16 50 90 45 This email address is being protected from spambots. You need JavaScript enabled to view it.">This email address is being protected from spambots. You need JavaScript enabled to view it. |
GENTAUR BULGARIA
53 Iskar Str. 1191 Kokalyane, Sofia
Tel 0035924682280
Fax 0035929830072
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GENTAUR France SARL
9, rue Lagrange, 75005 Paris
Tel 01 43 25 01 50
Fax 01 43 25 01 60
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GmbH Marienbongard 20
52062 Aachen Deutschland
Tel (+49) 0241 56 00 99 68
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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 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 BV
Kuiper 1
5521 DG Eersel Nederland
Tel 0208-080893
Fax 0497-517897
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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
Tel 0911876558
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Genprice 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
Serbia, Macedonia,
Montenegro, Croatia:
Tel 0035929830070
Fax 0035929830072
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GENTAUR Romania
Tel 0035929830070
Fax 0035929830072
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GENTAUR Greece
Tel 00302111768494
Fax 0032 16 50 90 45
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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
AccuPower ProFi Taq PCR PreMix
AccuPower® ProFi Taq PCR PreMix for high efficiency and amplification of long range PCR.
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
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
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
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)
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
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
AccuPower 2X Greenstar master mix solution
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.
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
rHu IL 2, 3MIU, Lot 200908F02
- 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.
- Indication
- Indicated for the treatment of adults with metastatic renal cell carcinoma (metastatic RCC).
- Indicated for the treatment of adults with metastatic melanoma.
- 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%
- Composition
Active ingredient: Recombinant Human Interleukin 2 (rHuIL-2)
Inactive ingredients: Glacial Acetic Acid, Mannitol, Polysorbate-80 and Sodium Acetate.
- 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
mGMP GM-CSF, 50ug batch20040823
Product number | 04-RHUGM-CSF-50UG | |||||||||||||||||||||||||||||||||||||||||||||
Product name | mGMP GM-CSF, 50ug batch20040823 | |||||||||||||||||||||||||||||||||||||||||||||
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For more information Contact us
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.
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.
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.
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.
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.
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
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
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
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