Ordering Information
Model: 177313 - Electric Driven TK-3e
Scale Units: 01 - English
Power Cord Type: 01 - American
The TK-3 Proximity System Test Kit simulates shaft vibration and position for calibrating Bently Nevada monitors. It verifies the operating condition of the monitor readouts as well as the condition of the proximity transducer system. A properly calibrated system ensures that the transducer inputs and the resulting monitor readings are accurate.
The TK-3 uses a removable spindle micrometer assembly to check the transducer system and position monitor calibration. This assembly features a universal probe mount that will accommodate probe diameters from 5 mm to 19mm (0.197 in to 0.75 in). The mount holds the probe while the user moves the target toward or away from the probe tip in calibrated increments and records the output from the Proximitor* Sensor using a voltmeter. The spindle micrometer assembly also features a convenient magnetic base for ease of use in the field.
Vibration monitors are calibrated using the motor-driven wobble plate. A swingarm assembly located over the wobble plate holds the proximity probe in place. This assembly uses a universal probe mount, identical to that used with the spindle micrometer assembly. By using the absolute scale factor of the proximity probe in conjunction with a multimeter, the user adjusts the probe to find a position where the desired amount of mechanical vibration (as determined by peak-to-peak DC voltage output) is present. No oscilloscope is needed.
The user can then compare a vibration monitorâ??s reading to the known
mechanical vibration signal input viewed by the proximity probe. The
mechanical vibration signal from the TK-3 can range from 50 to 254 �¼m (2 to 10
mils) peak-to-peak.
Estimated Lead Time: In stock. Usually ships in 5 - 7 working days.
Shipping Weight: 6 Kg
Peanut Hay Pellets are produced from Sun Cured Peanut Hay of Indian Origin. The Hay is passed through a Complex Process of Production, wherein required Steam and Cooking of the Hay is done. Removal of Toxic and Hazardous Contents is done to maximum possible extent. Being an Agro-Based Derivative, the nutritional value of the Hay Pellets is highly volatile in Nature. Due to efficient Production System the Volume of the Hay is densified to a maximum possible extent. The final product is absolutely� suitable for feeding Dairy and Meat Livestock and other Domestic Farm Animals.
Product Details:
Crude Protein : 12% to 16%
Crude Fat : 1.5% to 3%
Crude Fibre : 15% to 20%
Ash : 3.5 to 5%
Moisture : 12% Maximum
GENERAL DETAILSÃ? Ã?Â
Ingredients : Sun Cured Peanut Hay of Indian Origin
Ingredient Profile : 100% Vegetarian
Moisture (% Maximum) : 12
Product Form : Pellet Form
Product Branding : HAF�®
Net Weight : 39 Kgs When Packed
Product Pricing : On Unit Basis (for each 39 Kgs Packing)
Factory Visit : Not Permissible
Fumigation : Aluminum Phosphide or Methyl Bromide (or any as per buyer specification)
Clinical Test Methodology : As per IS:2052 Proximate Analysis on Dry Matter Basis
We are amongst the trusted manufacturer supplier distributor exporter and wholesaler of excellent quality array of Duck Finisher Feed Our duck finisher feeds are contain best combination of nutrients and vitamins for providing duck excellent growth rate and build their muscles These duck finisher feeds gives the duck excellent body mass to combat various diseases Our duck finisher feeds are easily digested in the duck system providing faster growth Avail from us our duck finisher feeds at market leading prices
The COVID-19 RT-PCR Detection Kit is a real-time RT-PCR test intended for the qualitative detection of nucleic acid from the SARS-CoV-2 in upper and lower respiratory specimens (such as anterior nasal swabs, mid-turbinate nasal swabs, nasopharyngeal swabs, oropharyngeal swabs, sputum, lower respiratory tract aspirates, bronchoalveolar lavage, and nasopharyngeal wash/aspirate or nasal
aspirate) from individuals suspected of COVID-19 by their healthcare provider. Testing is limited to laboratories certified under the Clinical Laboratory Improvement Amendments (CLIA) of 1988, 42 U.S.C.
263a, to perform high complexity tests.
Results are for the identification of SARS-CoV-2 RNA. The SARS-CoV-2 RNA is generally detectable in upper and lower respiratory specimens during the acute phase of infection. Positive results are indicative of the presence of SARS-CoV-2 RNA; clinical correlation with patient history and other diagnostic information is necessary to determine patient infective status. The agent detected may not be
the definite cause of disease. Positive results do not rule out bacterial co-infection with other viruses.
Laboratories within the United States and its territories are required to report all positive results to the appropriate public health authorities.
Negative results do not preclude SARS-CoV-2 infection and should not be used as the sole basis for patient management decisions. Negative results must be combined with clinical observations, patient history, and epidemiological information.
The COVID-19 RT-PCR Detection Kit is intended for use by qualified trained clinical laboratory personnel specifically instructed and trained in the techniques of real-time PCR and in vitro diagnostic procedures. The COVID-19 RT-PCR Detection Kit is only for use under the Food and Drug Administration's Emergency Use Authorization.
PRINCIPLE OF DETECTION
This product is a fluorescent probe-based Taqman RT-PCR assay system. Firstly, the RNA of SARS-CoV-2 will be reverse transcribed into cDNA by reverse transcriptase, and then PCR amplification will be performed with cDNA as template. During amplification of the template, the TaqMan probe will
be degraded due to the 5'-3 polymerase activity and exonuclease activity of Taq DNA polymerase, then the separation of fluorescent reporter and quencher enables the fluorescent signal to be detected by instrument. The ORF1ab gene of SARS-CoV-2 will be detected qualitatively by FAM channel, the N
gene of SARS-CoV-2 will be detected qualitatively by JOE channel, the E gene of SARS-CoV-2 will be detected qualitatively by ROX channel, and the internal reference will be detected by CY5 channel.
dUTP and UNG enzyme are used in the kit to prevent contamination of the amplified products.
Internal reference is used in the kit for quality control starting from sample collection
Introducing our Rapid Malaria Testing Kit, a breakthrough in diagnosing malaria with speed and accuracy. This cutting-edge kit is designed for easy and quick detection of the malaria parasite, revolutionizing the way healthcare professionals identify this life-threatening disease.
With a user-friendly approach, it requires only a small blood sample to deliver results within minutes, enabling swift and informed medical decisions. Our kit boasts high sensitivity and specificity, ensuring reliable diagnoses even in low-infection scenarios. Its compact design and portability make it ideal for remote and resource-limited settings. Trust our Rapid Malaria Testing Kit for fast, dependable, and life-saving malaria diagnosis, providing critical support in the fight against this global health challenge.
813 Bently Nevada Proximity System Test Kit Tk 3E Suppliers
Short on time? Let Bently Nevada Proximity System Test Kit Tk 3E sellers contact you.
Our Rapid Typhoid Testing Kit is a cutting-edge solution for swift and accurate diagnosis of typhoid fever. This advanced kit is designed for quick detection of the Salmonella Typhi bacteria, streamlining the diagnostic process for healthcare professionals.
With a user-friendly approach, it requires a small blood sample and delivers results within minutes, enabling rapid treatment decisions. The kit exhibits exceptional sensitivity and specificity, ensuring reliable diagnoses even in low-infection scenarios. Its compact, portable design makes it ideal for remote and resource-limited areas. Trust our Rapid Typhoid Testing Kit for fast, dependable, and life-saving typhoid fever diagnosis, enhancing patient care and containment of this infectious disease.
Product Name:
Surplex(R)-COVID-19 IgM/IgG Rapid test
Product Description:
Surplex(R)-COVID-19 IgM/IgG Rapid test is a serology test intended for the qualitative detection of IgM and IgG antibodies of the novel coronavirus (the SARS-COV-2 virus) in human serum, plasma or whole blood. It is CE marked and approved in Brazil (ANVISA approved).
We are motivated to aggressively price our product and ready to send 20 tests (one box) to qualified buyers for evaluation, free of charge.
Price of product:
FOB USD $1.50 - $2.50 per test, volume dependent.
Product origin :
China.
Key Specifications/Special Features :
- Competitively priced and ready to ship in volume.
- Currently shipping in volume to Brazil.
- Highly accurate and specific - performance independently confirmed.
- Results ready in 15 minutes.
- Harmonization System (HS) Code: 382200.
- We provide a full support during regulatory application.
Minimum Order Size and Packaging details:
MOQ: Flexible.
Box of 20 or 50 test kits.
Storage: 2-30C.
Shelf Life: 10 months.
The KAiRA 2019-nCoV PCR Detection Kit is a one step RT-PCR reagent system, based on real-time PCR technology, for the qualitative detection and differentiation of lineage B-beta Coronavirus and severe acute respiratory syndrome coronavirus 2 specific RNA.
The test kit has FDA and CE Approval and comes in packs of 100 tests. In combination with Dr PCR the test results for PCR Testing can be given in under an hour and are compatible for use for international travel requirements.
The product is based on the principle of antigen-antibody reaction and immunoassay technique. The test device contains colloidal gold labeled SARS-CoV-2 recombinant protein, mouse-anti human IgG antibody immobilized in G test area, mouse-anti human IgM antibody immobilized in M test area and the corresponding antibody in quality control area (C).
During the test, when the SARS-CoV-2 IgM antibody level in the sample is at or above the limit of detection of the test, the SARS-CoV-2 IgM antibody in the sample binds to the colloidal gold labeled SARS-CoV-2 recombinant protein which is pre-coated on a gold label pad. The conjugates migrate upward through capillary effect and would be captured by mouse-anti human IgM antibody immobilized in M test area subsequently and this produces a purple-red band appears in the M test area. When the SARS-CoV-2 IgG antibody level in the sample is at or above the limit of detection of the test, the SARS-CoV-2 IgG antibody in the sample binds to the colloidal gold labeled SARS-CoV-2 recombinant protein which is pre-coated on a gold label pad. Theconjugates migrate upward through capillary effect and would be captured by mouse-anti human IgG antibody immobilized in G test area subsequently and this produces a purple-red band appears in the G test area. If it is a negative sample, there is not a purple-red band appeared in the M and G test area. Regardless of the presence or absence of the SARS-CoV-2 antibody in the sample, a purple-red band will appear in the quality control area (C). The purple-red band in the quality control area (C) is a criterion for judging whether there is enough sample and whether the chromatography process is normal. It also serves as the internal control standard for reagents.
Super long life refrigeration sheet modified by special process;
Precision temperature control technology ensures that the temperature fluctuation of each hole is less than 0.1 ;
Ultra high sensitivity PMT system combined with precision optical system ensures accuracy;
New automatic hot cover technology can effectively prevent reagent evaporation;
Maximum 6 channels fluorescence detection, no cross interference between channels;
Intelligent operating system, flexible program setting, comprehensive analysis and report function;
RAPID ANTIBODY/Finger Prick 10 to 15 Minute Results
An antibody test is also known as a serology test looks for the presence of antibodies, which are specific proteins made in response to infections. It is effective at detecting the recent past SARS-CoV2 infection. This test can detect the body's IgM Antibody response in as little as 7 days (IgG in 14 days) from infection with CDC validated 100% specificity and 100% sensitivity.
The highest accuracy serological test on the market
FDA EUA Approved
Manufactured by one of the leaders in lateral flow technology
COVID finger prick, rapid antigen test, or rapid test, is a rapid diagnostic test suitable for point-of-care testing that directly detects the presence or absence of an antigen. It is commonly used for the detection of SARS-CoV-2, the virus that causes COVID-19. Rapid tests are a type of lateral flow tests that detect protein, distinguishing it from other medical tests that detect antibodies or nucleic acid, of either laboratory or point-of-care types. Rapid tests generally give a result in 1 to 15 minutes, require minimal training or infrastructure, and have significant cost advantages. NO Lab Required for results.
1. Generic Name: Novel Coronavirus COVID-19 IgG Antigen Test Kit
2. Brand Name: NIL
3. Notified Category: Other than above substances intended for qualitative determination of COVID-19 infection
4. Class of Medical Device: Class D
5. Shelf life :15 months
6. Sterile/Non-Sterile: Non-Sterilized
7. Contains Drugs: No
8. Medical Device Grouping Category: IVD-Kit
9. Grouping Description: Intended for qualitative determination of COVID-19 infection
10. Intended Use: The Novel Coronavirus COVID-19 IgG Kit is intended for the qualitative detection of human anti-COVID- 19 IgG antibody in human serum/plasma. Any reactive specimen with the Novel Coronavirus COVID-19 IgG Kit must be confirmed with alternative testing method(s).
11. Product Description: Assay controls and 1:10 diluted human serum samples are added to the microtiter wells of a microplate that was coated with COVID-19 recombinant full length recombinant protein. After the first incubation period, the unbound protein matrix is removed with a subsequent washing step. A horseradish peroxidase (HRP) labeled polyclonal goat anti-human IgG tracer antibody is added to each well. After an incubation period, an immunocomplex of "COVID-19 recombinant antigen-human anti-COVID-19 IgG antibody - HRP labeled anti human IgG tracer antibody" is formed if there is specific Coronavirus IgG antibody present in the tested specimen. The unbound tracer antibody is removed by the subsequent washing step. HRP-Labeled tracer antibody bound to the well is then incubated with a substrate solution in a timed reaction and then measured in a spectrophotometric microplate reader. The enzymatic activity of the tracer antibody bound to the anti-COVID-19 IgG on the wall of the microtiter well is proportional to the amount of the anti-COVID-19 IgG antibody level in the tested specimen.
SALIENT FEATURES:
â?¢ Recombinant COVID-19 Spike subunit Protein coated on Microwell Plate
â?¢ HRP Conjugated Polyvalent Anti-Human IgG
â?¢ Assay Time: 80 mins (30mins+30 Mins+20mins)
â?¢ Strip Format Microwell Plate
â?¢ Ready to use Substrate and Controls
â?¢ Only 20 pL of human serum is required for measurement in duplicate.
â?¢ Works on any open ELISA system
â?¢ Assay procedure is easy to automate
OUR TEST:
â?¢ Principle: Indirect ELISA
â?¢ The normal healthy patients with samples collected prior to the COVID-19 outbreak [December 3, 2019] (n = 150) and RT-PCR confirmed positive patients in after the second week of the onset of the disease (n = 32). The Positive sample evaluation was done at external Approved Lab. The results are as follows:
â?¢ Diagnostic sensitivity is 100% (>98%)
â?¢ Diagnostic specificity is 98.67% (>97%)
â?¢ PPV: 94.12�°/0
â?¢ NPV: 100%
Please contact us for more information and product details.
Ionebio produces the iLAMP Novel-CoV19 Detection Kit, a real-time Reverse Transcription LAMP-PCR assay system. The test kits are widely used in South Korea, including at ports of entry into the country. Ionebio has secured a facility in the United States which can produce 1 million test per day. This PCR has a 20 minute test time.
ThermoFisher Scientific Accula System Rapid & Reliable RT-PCR Test for Corona in 30mins
Product Details:
Number of Reactions(Preps)/Kit : 25
Brand : Thermo
Test Method : (SARS-CoV-2) RT-PCR
Sample Type : Nasal Swab
Test Time 30 min
The Accula System from Thermo Fisher Scientific is a rapid diagnostic platform that combines the accuracy of RT-PCR with the simplicity, convenience, and procedural familiarity of traditional rapid immunoassays. The Acculaâ?¢ SARS-CoV-2 Test has received an Emergency Use Authorization (EUA) from the FDA for the detection of SARS-CoV-2 in Clinical Laboratory Improvement Amendments (CLIA) waived environments. Designed for use with the palm-sized Accula Dock, the Accula SARS-CoV-2 Test provides reliable, qualitative results in approximately 30 minutes
Product Name
Neutrophil Gelatinase-Associated Lipid Carrier Protein (NGAL)Test Kit (Immunofluorescence Chromatography)
Purpose
To detect the NGAL in human plasma/serum/whole blood in vitro quantitatively.For Professional Use only.
Principles of Detection
The NGAL Test is a fluorescent lateral flow immunoassay. The test consists of: 1) a conjugate pad containing NGAL antibody conjugated with fluorescent microspheres and a control antibody (goat anti-chicken IgY antibody) conjugated with fluorescence microspheres, 2) a nitrocellulose membrane strip containing a test line (T line) and a control line (C line). The T line is pre-coated with anotherNGAL antibody, and the C line is pre-coated with a control line antibody (chicken IgY antibody).
NGAL concentration in specimen is positively correlated with the fluorescent density of the microspheres, after the measure and calculation of the quantitative fluorescence immunoassay analyzer, then the analyzer would calculate the concentration of NGAL according to the preset calibration curve in the machine and display the result, detection unit is ng/mL. C line should appear in any cases, which indicates the reaction system is effective.
Reference range
Reference value: 37-180ng/mL; The reference value is verified by referring to similar products on the market. Due to ethnic and regional differences, each laboratory can establish its own reference interval according to the actual situation.
Product Details:
Number of Reactions(Preps)/Kit 10 T
Brand CTK BioTech
Test Type Rapid test
Sample human serum, plasma, or whole blood
Test time 10 Min
Cat No : R0253C
The OnSite TORCH Panel Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection and differentiation of antibodies (IgG and IgM) to Toxoplasma gondii (T. gondii), rubella virus, cytomegalovirus (CMV), herpes simplex virus 1 (HSV-1), and herpes simplex virus 2 (HSV-2) in human serum, plasma, or whole blood.
This test is intended to be used by professionals as a screening test and provides a preliminary test result to aid in the diagnosis of infection with T. gondii, rubella virus, CMV, HSV-1 and HSV-2. Any interpretation or use of this preliminary test result must also rely on other clinical findings as well as on the professional judgment of health care providers. Alternative test method(s) should be considered to confirm the test result obtained by this device.
Recommended for use:
Any person presenting with clinical signs or symptoms consistent with TORCH infection.
Women who are pregnant or who are planning to become pregnant
Individuals with a compromised immune system
The OnSite TORCH Panel Rapid Test detects and differentiates IgG and IgM antibodies for all 5 TORCH infections. In general, a negative test result indicates that the individual is at risk for acquiring a primary infection. A positive IgM result only indicates acute infection, a positive IgM and IgG test indicate acute, late phase infection, and a positive IgG test result only indicates past or chronic infection.
The presence of IgM anti-rubella virus or high titers of IgG anti-rubella virus (> 200 IU/mL) are suggestive of acute rubella infection. Lower titers of IgG anti-rubella virus (â?¥ 10-15 IU/mL) are suggestive of previous exposure and protective immunity. An individual with an IgG anti-rubella virus titer less than 10-15 IU/mL is considered to be at risk of acquiring a rubella virus infection.
The TORCH Panel Rapid test also differentiates between HSV-1 and HSV-2 antibodies using HSV-1 specific glycoprotein G1 and HSV-2 specific glycoprotein G2.
Product Specification :
Individually sealed foil pouches containing:
One cassette device
Two desiccants
Plastic droppers
Sample diluent (REF SB-R0253, 5 mL/bottle)
One package insert (instruction for use)
Our HCG Strips are a reliable and user-friendly solution for at-home pregnancy testing. These highly sensitive strips are designed to detect the presence of human chorionic gonadotropin (HCG) hormone in urine, a hormone produced during pregnancy.
With their simple, dip-and-read design, these strips provide quick and accurate results within minutes. A clearly visible test and control line make interpretation effortless, even for first-time users. Our HCG Strips are manufactured with precision, ensuring consistent and dependable results. These strips offer privacy and convenience, empowering individuals to confirm pregnancy discreetly and with confidence in the comfort of their own homes.
813 Bently Nevada Proximity System Test Kit Tk 3E Suppliers
Short on time? Let Bently Nevada Proximity System Test Kit Tk 3E sellers contact you.
