Tanaris Power, TPHX, Profile, Summary

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Tanaris Power, TPHX, Profile, Summary

 

Tanaris Power develops Smart Lithium-Ion batteries and power solutions for various industrial applications. We design, engineer and produce some of the worlds safest, highest performance, most reliable and flexible Lithium-Ion batteries.

 

Tanaris Power lithium-ion batteries feature best-In-class safety, reliability, performance and flexibility for your industrial power applications

All Tanaris Power battery packs are based on Lithium-ion battery technology. Each of our batteries incorporates our advanced Battery Management System (BMS) along with numerous redundant safety and performance features to ensure that our batteries are the safest, most reliable, best performing and flexible batteries available

 

Tanaris Power Lithium-Ion Benefits

Our lithium-ion batteries offer numerous benefits over conventional lead-acid batteries, including:

  • Significantly improved vehicle performance

  • Significantly longer run time between charges

  • Short duration charging has no negative effects

  • 3x to 5x longer life span than lead-acid batteries

  • 65-70% less weight than similar lead-acid packs

  • Completely maintenance free operation

  • No acid vapor, maintenance or storage risks

  • Integrated BMS for system monitoring and safety

  • Ruggedized design for extreme outdoor use

 

 

Safety

  • Your safety is at the core of every design decision and component selection we make

  • All of the Lithium-Ion cells we use must meet international UN38.3 standards for safe transportation and usage

  • We use the Lithium-Iron-Phosphate chemistry for our cells, which provides a level of thermal stability that some other cell chemistries do not offer

  • Every battery we make incorporates a dedicated advanced Battery Management System (BMS) along with other redundant intelligent monitoring circuitry that monitors each individual cells' operation and temperature to ensure that the whole pack operates safely

  • Each and every battery incorporates numerous additional safety features such as an integrated battery isolation fault monitoring system, redundant fuses, sealed safety relays, audible alarms and much more

     

Reliability

  • We only use the best quality automotive grade components to ensure maximum reliability

  • Each and every one of our batteries and the components that go into them, go through extensive burn-in and testing processes before they make it into any Tanaris Power battery

  • Every batch of Lithium-Ion cells are subjected to an array of standardized tests to ensure they are well qualified before they go into any battery

  • All cells are are secured using specialized hold-down mechanisms within the battery to reduce shock and vibration

  • BMS and all electronics are designed to strict automotive standards, using only automotive and industrial grade components, for the highest level of reliability in all operating environments

  • All battery cases and electronic connectors are sealed to ensure the battery will work in all weather conditions

     

Performance

  • Rigorous in-house cell testing and characterization allows us to manage and optimize the cell selection for each battery application, ensuring optimal power delivery for the life of the system

  • We test and evaluate cells from a wide variety of manufacturers to find the best performing cells

  • Our advanced Battery Management System maintains peak performance of all cells in real time

  • Proprietary cell balancing algorithms ensure that all battery cells maintain their balance at all times

  • All aspects of battery charging are under real time monitoring and direct control of the BMS which means the BMS selects the appropriate charging profile in order to extend battery life

  • Cell behavior is learned with usage, which allows the system to better predict vehicle demands and understand overall battery health flexibility

  • The BMS calculates and compares cell-by-cell performance to ensure peak battery performance

     

Flexibility

  • Battery packs are available in industry standard voltage levels such as 24V, 36V, 48V, 72V and 80V

  • Battery capacity can be selected to match application requirements at each voltage level, from 40Ah to 900Ah

  • Single or multi-module battery pack configurations are available depending on specific space or layout requirements

  • Physical dimensions of many battery modules can be customized to client specific needs

  • Integrated CAN bus communications can be customized to interface with other intelligent equipment such as on-board chargers, charging stations, motor controllers, driver displays, etc.

  • BMS control logic can be customized to interact with and control other vehicle equipment such as emergency stop button, key-switches, analog or digital gauges, mode selection switches, buzzers, sirens, lights and more

 

Sources: The Company OxBridge Research, OTCKING, DailyStockDeals, OTCstockIQ

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Amedica Corporation, AMDA, Profile, Summary

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Amedica Corporation, AMDA, Profile, Summary

 

Amedica Corporation, AMDA, is a commercial biomaterial company. The Company is focused on using its silicon nitride technology platform to develop, manufacture and sell a range of medical devices. The Company markets spinal fusion products and are developing products for use in total hip and knee joint replacements.

 

Biomaterials are synthetic or natural materials available in a variety of forms that are used in virtually every medical specialty. The Company markets its Valeo family of silicon nitride interbody spinal fusion devices in the United States and Europe for use in the cervical and thoracolumbar areas of the spine. In addition, to its silicon nitride-based spinal fusion products, it markets a complementary line of non-silicon nitride spinal fusion products which allows providing surgeons and hospitals with a range of products. The Company produces its silicon nitride advanced ceramic in four forms: a fully dense, load-bearing solid, referred to as MC2; a porous bone-like cancellous structured form, referred to as CSC; a composite incorporating both its solid MC2 material and its porous CSC material intended to promote an environment for bone growth; and a coating for application onto other biomaterials.

 

The Company competes with Medtronic, Inc.; DePuy Synthes Companies, a group of Johnson & Johnson companies; Stryker Corporation; Biomet, Inc.; Zimmer Holdings, Inc.; Smith & Nephew plc; Aesculap Inc; CeramTec, Kyocera, and CoorTek, Inc.

 

 

OSTEOPROMOTIVE: DELIVERS ENHANCED OSTEOGENIC RESPONSE

  • Enhanced osteopromotion: The surface chemistry and nanostructure topography of Si3N4 provides an optimal environment for stimulation of osteoprogenitor cells to differentiate into osteoblasts.

  • Greater protein adsorption: Si3N4 demonstrates significantly greater protein adsorption (fibronectin, laminin and vitronectin) in comparison to PEEK and titanium. (1)

  • Greater new bone formation: Si3N4 implants demonstrate greater new bone formation at 3, 7, 14 and 90 days compared to PEEK and titanium in in vivo study; regenerated bone associated with Si3N4 implants is 2 to 3 times that of PEEK and titanium implants at 3 months after surgery.(2)

  • Increased osteointegration: Si3N4 implants demonstrate increased osteointegration at 3, 7, 14 and 90 days compared to PEEK and titanium in in vivo studies; percent of bone at Si3N4 implant interface is 2 to 6 times that of PEEK and titanium implants at 3 months after surgery.(2)

DEMONSTRATED ANTI-INFECTIVE PROPERTIES

  • Superior antibacterial function: Si3N4 inhibits biofilm formation and bacterial colonization. Si3N4 demonstrates significantly lower biofilm formation at 4, 24, 48 and 72 hours as compared to PEEK and titanium; live bacteria (S. epidermidis, S. aureus, P. aeruginosa, E. coli and Enterococcus) associated with Si3N4 implants are 8 to 30 times lower than PEEK and titanium.(1)

  • Demonstrated bacteriostatic agent: In in vivo studies, no infection is observed with bacteria-inoculated Si3N4 implants at 3 months, whereas both PEEK and titanium implants maintain a septic state. Si3N4 demonstrates this property even in the absence of antibiotics.(2)

EXCELLENT IMAGING PROPERTIES

  • Compatible with all imaging modalities: Si3N4 implants are semi-radiolucent with clearly visible boundaries, and produce no distortion under MRI and no scattering under CT; this enables an exact view of the implant for precise intraoperative placement and postoperative fusion assessment.

 

Sources: The Company, OxBridge Research, OTCKING, DailyStockDeals, OTCstockIQ

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Disclaimer/Disclosure: we received or expecting compensation from the featured company. Our firm, principals and staff may own/buy/sell/trade stock/securities of this company. Always Read the full Disclosure/Disclaimer. Thanks.

If you would like your company featured or want to learn more, please don't hesitate to contact the Editor. editor [@] OxBridgeResearch.com

 

Station Digital, SDIG, Profile, Summary

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StationDigital Corporation

Multimedia Digital Broadcasting

 

StationDigital, SDIG, is a multimedia digital broadcast company that offers free music streaming of over 30 million songs. StationDigital features both genre-based and artist-based music discovery stations to suit an endless variety of musical tastes, and a personal recommendation service to its more than 2.4 million unique listeners – all available both online and through its iOS and Andriod mobile apps. StationDigital’s users can customize their listening experience by selecting playlists and stations based on themes, interests and location, as well as favorite artists, songs, genre, and by providing feedback on the music they hear.

 

StationDigital is the first truly next generation digital media broadcast platform.

 

StationDigital’s primary identity is as a sophisticated pure play music discovery Internet radio service, offering a competitive, state of the art product to capture market share in the Internet radio space. The Company has a unique, industry first value proposition - the StationDigital Listener Rewards Program, where all registered users earn listener rewards points:

 

> Every time users listen to StationDigital, either on the web or through their mobile apps

> Every time users share StationDigital with friends through social media

 

Key Features:

 

Social features and network effect – feedback on music, share music with friends and family, recommendations, post favorites on timeline, and earn reward points. Users can gain followers and build their own music social network of friends and fans.

 

Unique personalization of music to user’s taste – choose genre, artist, decade and ability to narrow search to a very specific target to get to songs faster. Features include ability to adjust music preferences, create a station playlist, and leverage songs from community of users.

 

Music discovery – with over 30 million songs and hundreds of stations providing a wide variety of categories and genres, users are always able to discover something new. Add/remove stations with one touch, smooth intuitive song catalog, 30 million songs, choose decade, genre, artist.

 

 

StationDigital will become the first agnostic, multimedia, global broadcast platform – available on any device, from anywhere, at anytime.

 

Investment Highlights

Opportunity to invest in an innovative, early stage next generation multimedia broadcast company with a unique and differentiated service and business model aimed at a rapidly growing and large market opportunity

The Company’s music streaming service has over 30 million songs for its 2.4 million users that offers customized listening, music discovery, a personal recommendation engine, a value-added social layer, and e-commerce platform

Key competitive differentiation factors are its unique listener rewards program/online store and wide variety of entertainment content options beyond music

Music streaming industry is still in its early stages and is experiencing rapid growth and market share capture from a large addressable $15 billion US radio market

Our valuation analysis results in a target price of $0.81 per share which represents significant upside of over 2 times the current stock price

 

see Investment Thesis click here

 

VALUATION

Starting with Pandora’s market cap per user of $38.63 and then applying a 65% discount to account for Pandora’s first mover advantage, dominant competitive position, and execution track record, we arrived at a market cap per user of $13.52. Based on management’s aggressive marketing plan, it can be estimated that StationDigital will have approximately 5 million monthly active users by the end of 2016. Applying this $13.52 market cap per user to 5 million monthly active user results in a StationDigital target market capitalization of $67.6 million or price per share of $0.81.

 

Our target price of $0.81 is over 2.0 times the current share price of $0.40 providing significant upside price potential while also being only 35% above the Company’s recent high of $0.60 last October.

 

learn more about this great opportunity,

download the full research report now! click here

visit the company website www.StationDigitial.com

Start Enjoying the Music You Love!

 

Sources: The Company, OxBridge Research, OTCKING, DailyStockDeals, OTCstockIQ

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Disclaimer/Disclosure: we received or expecting compensation from the featured company. Our firm, principals and staff may own/buy/sell/trade stock/securities of this company. Always Read the full Disclosure/Disclaimer. Thanks.

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please don't hesitate to contact the Editor. editor [@] OxBridgeResearch.com

 

Aethlon Medical, AEMD, Profile, Summary

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Aethlon Medical, AEMD, Profile, Summary
 

Aethlon Medical (AEMD) is developing innovative medical devices to address unmet medical needs in cancer, infectious disease, and other life-threatening conditions. Aethlon’s ADAPT™ platform provides the technology foundation for a new class of therapeutics that target the selective removal of disease enabling particles from the entire circulatory system. The Aethlon ADAPT™ product pipeline includes the Hemopurifier®, a first-in-class medical device with broad-spectrum capabilities against exosomes that contribute to the progression of cancer and infectious viral pathogens such as HIV and Hepatitis C.

 

HER2 Protein and Breast Cancer

Breast cancer is the most common form of cancer in women, accounting for 20% of cancer deaths with approximately 180,000 women diagnosed annually in the United States (Merrill, R. M., and A. Sloan. 2011. Risk-adjusted female breast cancer incidence rates in the United States. Cancer Epidemiol.). Over-expression of the human epidermal growth factor receptor 2 (HER2; ErbB2) gene occurs in approximately 25% of breast cancers and has been linked to poor prognosis (Slamon, D. J., G. M. Clark, S. G. Wong, W. J. Levin, A. Ullrich, and W. L. McGuire. 1987. Human breast cancer: correlation of relapse and survival with amplification of the HER-2/neu oncogene. Science 235:177-182). HER2 is a receptor tyrosine kinase, member of the EGF receptor family, which possesses proliferative and anti-apoptotic activities.

 

The standard of treatment for women diagnosed with HER2+ breast cancer includes the humanized monoclonal antibody trastuzumab (marketed as Herceptin®) directed against the extracellular domain of HER2. Trastuzumab binding to HER2 mediates direct growthinhibition of tumor cells and induces antibody-dependent cell cytotoxicity (ADCC), a major anti-cancer mechanism by which natural killer (NK) cells lyse antibody-coated tumor cells (Nahta, R., D. Yu, M. C. Hung, G. N. Hortobagyi, and F. J. Esteva. 2006. Mechanisms of disease: understanding resistance to HER2-targeted therapy in human breast cancer. Nat Clin Pract Oncol 3:269-280).

 

In patients with metastatic breast cancer undergoing chemotherapy, treatment with trastuzumab augments overall response rates and increases median survival time by 25% (Baselga, J. 2001. Clinical trials of Herceptin® (trastuzumab). Eur J Cancer 37 Suppl 1:18-24). However, response rates to trastuzumab range from 12% to 34% with median duration of 9 months due to development of resistance. Despite co-treatment with other HER2 targeting therapies (e.g. the tyrosine kinase inhibitor lapatinib) and chemotherapy, patients with metastatic breast cancer experience a limited duration of benefit; therefore, novel treatment strategies that act synergistically or overcome drug resistance are urgently needed (Sachdev, J. C., and M. Jahanzeb. 2011. Blockade of the HER Family of Receptors in the Treatment of HER2-Positive Metastatic Breast Cancer.

 

The Evolution of Therapeutic Filtration to Improve Hepatitis-C Virus (HCV) Treatment Outcomes

 

Therapeutic filtration of HCV from the entire circulatory system with a medical device has been clinically demonstrated to improve treatment outcomes when administered at the outset of standard of care (SOC) drug therapy. This summary overview, which includes an introduction to the Aethlon Hemopurifier®, is for informational purposes only.

 

About HCV Infection

The U.S. National Institutes of Health (NIH) reports an estimated 180 million people worldwide are afflicted with chronic HCV infection. Of people infected, 55 to 85% of will develop chronic infection, and 75% of those will develop chronic liver disease. Standard of care (SOC) drug therapy is represented by a two drug combination of interferon and ribavirin. The primary goal of SOC drug therapy is the achievement of a sustained virologic response (SVR), defined as undetectable viral load six months after completion of SOC drug therapy. According to the NIH, 15-25% of HCV infected patients will recover

completely.

 

SOC Drug Therapy Outcomes

The largest study of HCV infected individuals pursuing 48-week SOC drug

therapy was a study of 4,469 genotype 1 patients published by McHutchison in The New England Journal of Medicine in August of 2009.

31% (1,399 of 4,469) of patients screened for participation were excluded from the study.

54% (1,654 of 3,070) of treated patients completed the SOC treatment regimen.

39.6% (1,215 of 3,070) of treated patients who completed SOC therapy

achieved a SVR.

27% (1,215 of 4,469) of the total patients screened for study participation

achieved a SVR.

No data recorded for patients who may have relapsed after achieving a SVR.

 

The Hemopurifier®

The first medical device to selectively remove HCV and related immunosuppressive proteins from circulation. A Study of the Hemopurifier® + SOC Drug Therapy is Now Underway

 

Patient enrollment has been initiated at the Medanta Medicity Institute in India - www.medanta.org

Additional details can be accessed from the Clinical Trials Registry - India (CTRI) link: http://ctri.nic.in/clinicaltrials/index.jsp

Up to 30 patients / up to 6 treatments in first 3 days of SOC

Early clinical endpoints include:

Immediate Virologic Response (IVR)

Rapid Virologic Response (RVR)

Early Virologic Response (EVR)

 

The Hemopurifier® Other Selected Quick Facts

 

70 human treatment experiences administered to date

An Investigation Device Exemption (IDE) to initiate U.S. studies has been filed with FDA

Substantial viral load reductions have also been observed in a human HIV study performed in the absence of antiviral drugs

GMP manufacturing has been established in an FDA approved facility

The Hemopurifier® has proven broad-spectrum capabilities against viral bioterror and pandemic threats

The device has been discovered to capture tumor-secreted exosomes known to suppress the immune system of cancer patients

 

 

Sources: The Company, OxBridge Research, OTCKING, DailyStockDeals, OTCstockIQ

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Disclaimer/Disclosure: we received or expecting compensation from the featured company. Our firm, principals and staff may own/buy/sell/trade stock/securities of this company. Always Read the full Disclosure/Disclaimer. Thanks.

If you would like your company featured or want to learn more, please don't hesitate to contact the Editor. editor [@] OxBridgeResearch.com

ALS, Hepatitis C, Traumatic Brain Injury, Blood Sepsis,breast cancer,HIV,HPV,HCV,SOC, dialysis,DOD,UNT,USPTO, NFL,SOCCOR,MILITARY,COMBAT MISSIONS,PTSD, Ebola

 
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