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Irvine Scientific Offers Cell Therapy Products

SANTA ANA, Calif.--(BUSINESS WIRE)--

Irvine Scientific, a leading cell culture media/ medical device company for more than 40 years, announced their newly launched cell therapy PRIME-XV product portfolio as part of the companys commitment to accelerate basic research and clinical applications in cell therapy and regenerative medicine. Using their expertise in cell culture media development, PRIME-XV products were designed to function as part of an integrated workflow solution in culturing primary cells, where all products have been pre-validated to decrease end user qualification time. Initially, PRIME-XV products will comprise of a serum-free medium for the expansion of human mesenchymal stromal/ stem cells (MSCs), biopreservation solutions and extracellular matrix proteins. However, Irvine Scientific intends to expand this product line to offer other cell culture media and reagents, such as stem cell qualified fetal bovine serum, tumorsphere and neural progenitor cell expansion media. Examples of existing PRIME-XV products include:

PRIME-XV MatrIS F: a recombinant human matrix protein intended for the culture of human stem/ progenitor cells under serum-free conditions. PRIME-XV MatrIS F provides an alternative substrate to the PRIME-XV Human Fibronectin product, which has a wide variety of applications in primary cell spreading and attachment.

PRIME-XV MSC EXPANSION SFM: a complete, serum-free expansion medium specifically designed for the culture of primary human MSCs derived from bone marrow and adipose tissues. This medium is supplied as a convenient one 250mL bottle and is ready-to-use without the need of additional cytokine/ growth factor supplements. MSCs cultured in PRIME-XV MSC EXPANSION SFM out performed serum-containing medium as well as leading competitors in cell expansion studies without losing their multipotent characteristics or immune modulation functions.

PRIME-XV Hypothermic Biopreservation Solution: a protein-free, defined solution intended for storage and stable shipping of cells and tissue samples under hypothermic (2-8C) condition. By preserving cells above freezing temperature, it reduces cellular stress response associated from chilling and re-warming of cells and tissues, and retains high culture viabilities after recovery. Simply replace the culture medium with this animal component-free, cGMP manufactured product for short term storage. To recover from preservation, PRIME-XV Hypothermic Biopreservation Solution is removed and replaced with growth medium of choice.

As an alternative to the PRIME-XV Hypothermic Biopreservation Solution, Irvine Scientific also carries a protein-free, defined PRIME-XV Cryogenic Preservation Solution, which allows for cryopreservation of biologics at -80C to -196C.

About Irvine Scientific

Irvine Scientific, a member of JX group, is a worldwide leader in the design, manufacture and distribution of medical devices, including Cell Therapy, Industrial Cell Culture, Cytogenetic and Assisted Reproductive Technology products. We are a large scale producer of advanced quality cell culture media for the cell therapy, industrial bioprocess, medical and diagnostic markets. Our companys extensive experience in the design of culture media, compliance with ISO and FDA regulations for class II/III medical devices and industrial scale manufacturing capacity provides our customers with unique capabilities and support. Irvine Scientific delivers products worldwide to the biopharmaceutical industry, research and medical laboratory communities.

For more information:

- Visit http://www.irvinesci.com

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Irvine Scientific Offers Cell Therapy Products

FAQ-4 of 19: What Is My Chance of Success With Stem Cells in Stem Cell Therapy – Video


FAQ-4 of 19: What Is My Chance of Success With Stem Cells in Stem Cell Therapy
youtu.be When considering stem cell treatment, it is natural to wonder what one #39;s chances of success are. This short video explains several key factors in assuring successful stem cell therapy. For more detailed information, visit StemCell-Asia.infoFrom:Karridine1Views:0 0ratingsTime:01:28More inPeople Blogs

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FAQ-4 of 19: What Is My Chance of Success With Stem Cells in Stem Cell Therapy - Video

FAQ-4 of 19: What Chance That Stem Cells Will Help Me When I Get Stem Cell Therapy – Video


FAQ-4 of 19: What Chance That Stem Cells Will Help Me When I Get Stem Cell Therapy
youtu.be When considering stem cell treatment, it is only natural to wonder what one #39;s chances of success are. This brief video explains several of the key factors in assuring successful stem cell therapy. For more detailed information, visit StemCell-Asia.infoFrom:John PepperViews:0 0ratingsTime:01:28More inPeople Blogs

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FAQ-4 of 19: What Chance That Stem Cells Will Help Me When I Get Stem Cell Therapy - Video

George Brown of Kool


George Brown of Kool The Gang Talks About His Stem Cell Treatment At MetroMD Hollywood
Musician George Brown, an original member of the jazz funk band, Kool and The Gang, talks with us about his day at MetroMD. George was in Los Angeles on tour with rockers Van Halen David Lee Roth in June 2012. George had an orthopedic stem cell treatment performed by Dr. Alex Martin MD at about noon and was on stage performing 8 hours later. For more info, visit us at MetroMD.net or call (323) 285-5300. The MetroMD Institute of Regenerative Medicine is located in Hollywood at the heart of Los Angeles.From:MetroMDViews:6 0ratingsTime:02:02More inScience Technology

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George Brown of Kool

Cecelia fights generalized hypoxia with her MS – Video


Cecelia fights generalized hypoxia with her MS
After the FDA ruling that her own banked stem cells taken from her fat tissue are a "biological drug" and her expected stem cell treatment to repair her circulation and relieve her pain has been halted, Cecelia Johnson tries to update on her condition.From:Cecelia JohnsonViews:111 5ratingsTime:06:27More inPeople Blogs

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Cecelia fights generalized hypoxia with her MS - Video

Federal government renews contract for collecting and maintaining national stem cell transplantation database

Public release date: 1-Nov-2012 [ | E-mail | Share ]

Contact: Rachel Mosey rmosey@mcw.edu Medical College of Wisconsin

The Medical College of Wisconsin (MCW) Center for International Blood and Marrow Transplant Research (CIBMTR) successfully competed for, and was awarded, renewal of the Stem Cell Therapeutics Outcomes Database contract with the U.S. Health Resources and Services Administration (HRSA). The CIBMTR administers the database as a key component of the national hematopoietic cell transplantation program. Hematopoietic stem cells are the cells responsible for continual regeneration of circulating blood cells throughout life; they are not embryonic stem cells.

The HRSA first awarded the contract to CIBMTR in 2006 to develop and maintain the national Stem Cell Therapeutic Outcomes Database (SCTOD), which is a standardized outcomes registry of allogeneic (related and unrelated donor cells) marrow and cord blood transplants performed in the United States. Funding for the first year of this new contract is $3.8 million, with an additional four years of negotiable funding.

The outcomes registry of the CIBMTR currently contains the status of 330,000 transplant recipients, as well as critical information to continually evaluate the operations of the national transplant program. All U.S. transplant centers that perform allogeneic marrow and cord blood transplants are required to provide patient outcomes data to the registry.

"CIBMTR is privileged to continue to operate the Outcomes Database on behalf of the C.W. Bill Young Cell Transplantation Program," said J. Douglas Rizzo, M.D., M.S., professor of medicine at MCW, associate scientific director at CIBMTR and principal investigator of the SCTOD. "CIBMTR delivers value by using the Outcomes Database to provide clinicians, scientists, patients and policymakers the information they need to make the best possible clinical decisions. It is a beneficial platform to expand important research to advance the field, plan clinical trials, facilitate quality improvement and perform studies on behalf of policymakers. The major goal of the program is to make blood and marrow transplants available to all who need them, and to increase their safety and effectiveness."

Congress first enacted HRSA's C.W. Bill Young Cell Transplantation Program in 2005, which led to the creation of the Stem Cell Therapeutic Outcomes Database. Congress reauthorized the Program in 2010. It is named after U.S. Congressman C.W. Bill Young of Florida, who was instrumental in founding a national marrow donor registry that could provide potentially life-saving treatment for those diagnosed with leukemia and other blood diseases.

The Medical College's CIBMTR is a partnership formed through an affiliation of the Medical College's International Bone Marrow Transplant Registry and the National Marrow Donor Program (NMDP). Since 1972, the Center has collected outcomes data provided voluntarily by transplant centers worldwide on both allogeneic (related and unrelated donor cells) and autologous (patient's own cells) hematopoietic stem cell transplants, and has made these data available to investigators and physicians worldwide to perform research to advance the field. The CIBMTR has published nearly 800 peer-reviewed papers (more than 45 in the past year alone) and is conducting more than 250 observational studies. It also has helped to coordinate 28 national clinical trials in HCT, 18 of which have completed accrual.

In addition to the Stem Cell Therapeutic Outcomes Database, HRSA recently awarded other C.W. Bill Young Cell Transplantation Program contracts to the NMDP, in order to continue the Program's work as the Office of Patient Advocacy/Single Point of Access for transplant patients, the Bone Marrow Coordinating Center and the Cord Blood Coordinating Center.

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Federal government renews contract for collecting and maintaining national stem cell transplantation database