Carousel Ovarian Cancer Cell Model
CB-0101
1 Each
Frozen Cell Suspension
This product is discontinued
Product Details
Carousel Ovarian Cancer Cell Model - CB-0101
patient derived tumor, tumor models, carcinoma cell lines
Target Details
All lots are tested for microbial and viral contamination, cell line cross - contamination, mycoplasma, and consistent growth capabilities.
Application Details
Tumor sample diagnosis was confirmed by histology and immunohistochemical detection of tumor markers. Immunofluorescence detection of lineage markers confirm epithelial phenotype using CK7 with DAPI overlay. Spontaneous formation of tumorspheres under low-attachment conditions.
Cell Line Data
Human - Endometrioid adenocarcinoma of the ovary
Viable Cells
RETM Complete with 7% HI-FBS
Cells should be maintained ~80% confluent in RETM Media with 7% HI-FBS, 100 nM Estrogen, 125 uL Cholera Toxin; media change every 2-3 days; seeding density 1.2x10^4 cell per cm2.
37°C incubator with 5% CO2 and 5% O2
Formulation
1.0 million cells/vial Count By Hemocytometer
Shipping & Handling
Dry Ice
Store frozen in liquid nitrogen.
This product MAY be stable for up to four (4) weeks if properly stored and handled.
Carousel Ovarian Cell Model originates from endometrioid adenocarcinoma of the ovary of a 65-69 yr old Caucasian female collected in the United States in 2013.
STR Profile: AMEL: X; CSF1PO: 10, 11; D13S317: 9, 11; D16S539: 12; D18S51: 14, 15; D21S11: 30, 31.2; D3S1358: 15, 18; D5S818: 11, 12; D7S820: 10, 12; D8S1179: 14; FGA: 19, 26; Penta D: 8, 12; Penta E: 7, 11; TH01: 7, 9; TPOX: 8; vWA: 18, 19.
Manufactured by Cellaria, LLC.
No test method can provide total assurance that the hepatitis B virus, hepatitis C virus, human immunodeficiency virus, or any other infectious agents are absent. Thus, all blood products, including purified proteins derived from human blood sources, should be handled at Biosafety Level 2 as recommended by the CDC\NIH manual entitled Biosafety in Microbiological and Biomedical Laboratories for potentially infectious human serum, blood specimens or proteins derived from same. Source material for the human blood product supplied to your facility has been tested for the detection of HIV antibody, Hepatitis B surface antigen, antibody to Hepatitis C, HIV 1 antigen(s), antibody to HTLV - I/II, and syphilis by FDA guidelines. All units were found to be non-reactive/negative for these tests. All human blood source material is collected in FDA licensed centers and is tested with FDA approved test kits.; This product is for research use only and is not intended for therapeutic or diagnostic applications. Please contact a technical service representative for more information. All products of animal origin manufactured by Rockland Immunochemicals are derived from starting materials of North American origin. Collection was performed in United States Department of Agriculture (USDA) inspected facilities and all materials have been inspected and certified to be free of disease and suitable for exportation. All properties listed are typical characteristics and are not specifications. All suggestions and data are offered in good faith but without guarantee as conditions and methods of use of our products are beyond our control. All claims must be made within 30 days following the date of delivery. The prospective user must determine the suitability of our materials before adopting them on a commercial scale. Suggested uses of our products are not recommendations to use our products in violation of any patent or as a license under any patent of Rockland Immunochemicals, Inc. If you require a commercial license to use this material and do not have one, then return this material, unopened to: Rockland Inc., P.O. BOX 5199, Limerick, Pennsylvania, USA.
