Human rudimentary female parent cells are middle in the developmental routine between rudimentary branch cells and entirely differentiated cells. The cells may retain the aptitude to turn a far-reaching form of unit variety with promising applications in research, drug discovery, and promising novel regenerative branch unit therapies. The cells are comparatively easy to produce on a considerable scale and in a purified state, that may make it fitting to work with these cells compared to the send use of human rudimentary branch cells. The 7 new unit lines have markers of heterogeneous mesoderm and neural design unit variety and are directed towards W11, Z2, SK31, SM35, T36, EN51, and EN55. In add-on to gift these new unit lines, BioTime will moreover concurrently launch analogous unit enlightenment media and variance kits. Information about the products will be existing online at www.embryome.com/products.htm commencement September 1, 2010.
BioTime wishes to explain that it does not use or rely on U.S. sovereign give appropriation to rise its products, nor does the firm rely on sales to federally saved investigate projects. The most of the aim marketplace for BioTime's investigate products is and has always been researchers that are not saved by U.S. NIH grants, the usually investigate appropriation that has been dangling since the new U.S. District Court preference in Sherley v. Sebelius. These other researchers add general researchers, in isolation researchers, and researchers saved by other U.S. bureaucratic entities such as CIRM (California Institute for Regenerative Medicine).
About BioTime, Inc.
BioTime, headquartered in Alameda, California, is a biotechnology firm focused on regenerative disinfectant and blood plasma volume expanders. Its extended stage of branch unit technologies is created by subsidiaries focused on definite fields of applications. BioTime develops and markets investigate products in the margin of branch cells and regenerative disinfectant by its unconditionally owned auxiliary Embryome Sciences, Inc. BioTime's auxiliary OncoCyte Corporation focuses on the healing applications of branch unit technology in cancer. Another subsidiary, OrthoCyte Corporation, is building healing applications of branch cells to provide orthopedic diseases and injuries. BioTime skeleton to rise healing products in China is to treatment of ophthalmologic, skin, musculo-skeletal system, and hematologic diseases, inclusive the targeting of genetically mutated branch cells to tumors as a novel means of treating currently incorrigible forms of cancer, by its auxiliary BioTime Asia, Limited. BioTime's Singapore subsidiary, ES Cell International Pte Ltd, has been at the forefront of advances in human rudimentary branch ("hES") unit technology, being a of the earliest distributors of hES unit lines to the investigate community. ESI has constructed clinical-grade human rudimentary branch unit lines that were subsequent subsequent to beliefs of great production use and currently offers them for promising use in healing product development. In add-on to its branch unit products, BioTime develops blood plasma volume expanders, blood deputy solutions for hypothermic (low temperature) surgery, and technology for use in surgery, crisis mishap treatment and other applications. BioTime's lead product, Hextend(R), is a blood plasma volume expander made and distributed in the U.S. by Hospira, Inc. and in South Korea by CJ CheilJedang Corp. beneath disdainful chartering agreements. Additional data about BioTime, Embryome Sciences, OncoCyte, OrthoCyte, BioTime Asia, and ESI may be found on the web at www.biotimeinc.com .
Forward-Looking Statements
Statements regarding to future financial and/or working results, future expansion in research, technology, clinical development, and promising opportunities is to firm and its subsidiaries, along with other statements about the future expectations, beliefs, goals, plans, or prospects expressed by administration consecrate forward-looking statements. Any statements that are not chronological fact (including, but not paltry to statements that enclose difference such as "will," "believes," "plans," "anticipates," "expects," "estimates") should moreover be deliberate to be forward-looking statements. Forward-looking statements engage risks and uncertainties, including, without limitation, risks fundamental in the development and/or commercialization of promising products, doubt in the results of clinical trials or regulatory approvals, need and aptitude to get hold of future capital, and continuance of egghead skill rights. Actual results may deviate materially from the results expected in these forward-looking statements and as such should be evaluated together with the many uncertainties that start the company's business, quite those referred to in the cautionary statements found in the company's Securities and Exchange Commission filings. The firm disclaims any vigilant or responsibility to refurbish these forward-looking statements.
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SOURCE: BioTime, Inc.
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