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                SiHa(子宫↑颈癌细胞)

                SiHa(子宫颈癌细胞)
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                • SiHa(子宫颈癌细胞)
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                ATCC
                HTB-35 (株)
                上海锐聪科技发展有限公司
                上海
                详细说明

                SiHa(子宫颈癌细胞)

                SiHa(子宫颈癌细胞)
                 
                Cell Biology
                ATCC® Number: HTB-35™ Price: $203.00
                Designations:
                SiHa
                Depositors:
                Y Ito
                2 [CELLS CONTAIN PAPOVAVIRUS]
                Shipped:
                frozen
                Medium & Serum:
                Growth Properties:
                adherent
                Organism:
                Homo sapiens (human)
                Morphology:
                epithelial
                 
                Source:
                Organ: cervix
                Disease: squamous cell carcinoma
                Tumor stage: grade II
                Permits/Forms:
                In addition to the MTA mentioned above, other ATCC and/or regulatory permits may be required for the transfer of this ATCC material. Anyone purchasing ATCC material is ultimately responsible for obtaining the permits. Please click here for information regarding the specific requirements for shipment to your location.
                Applications:
                Tumorigenic:
                Yes, in nude mice; forms poorly differentiated epidermoid carcinoma (grade III)
                Oncogene:
                p53 +; pRB +
                DNA Profile
                (STR):
                Amelogenin: X
                CSF1PO: 12
                D13S317: 11
                D16S539: 12
                D5S818: 9
                D7S820: 10
                THO1: 6,9
                TPOX: 8
                vWA: 14,17
                Cytogenetic
                Analysis:
                modal number = 69; range = 51 to 72.
                This is a hypertriploid human cell line with the modal chromosome number of 71, occurring in 24% of cells. Most cells had the chromosome numbers distributed between 69 and 72. Polyploid cells occurred at 7.6%. Fifteen or more marker chromosomes were common to most cells. Among them are dup(2) (q22q31) and del(2) (q31) which probably resulted from the balanced translocation between two N2s. Most cells had two copies of del(2). M2 is an A3-sized acrocentric. M13 is a minute submetacentric with 1-3 copies per cell. Origins of both M2 and M13 are not identified. There were two copies of normal X chromosomes. N2 was absent and probably was replaced by dup(2) and del(2).
                Isoenzymes:
                AK-1, 1; ES-D, 2; G6PD, B; GLO-I, 2; Me-2, 1; PGM1, 1; PGM3, 1
                Age:
                55 years adult
                Gender:
                female
                Ethnicity:
                Asian
                Comments:
                This line was established from fragments of a primary tissue sample obtained after surgery from a Japanese patient.
                Electron microscopic observations revealed presence of typical desmosomes at the cell junctions and an abundance of tonofilaments in the cytoplasm.
                Mycoplasma contamination was detected and eliminated in 1975.
                The line is reported to contain an integrated human papillomavirus type 16 genome (HPV-16, 1 to 2 copies per cell).
                Propagation:
                ATCC complete growth medium: The base medium for this cell line is ATCC-formulated Eagles Minimum Essential Medium, Catalog No. 30-2003. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%.
                Temperature: 37.0C
                Atmosphere: air, 95%; carbon dioxide (CO2), 5%
                Subculturing:
                Protocol:
                1. Remove and discard culture medium.
                2. Briefly rinse the cell layer with 0.25% (w/v) Trypsin- 0.53 mM EDTA solution to remove all traces of serum that contains trypsin inhibitor.
                3. Add 2.0 to 3.0 ml of Trypsin-EDTA solution to flask and observe cells under an inverted microscope until cell layer is dispersed (usually within 5 to 15 minutes).
                  Note: To avoid clumping do not agitate the cells by hitting or shaking the flask while waiting for the cells to detach. Cells that are difficult to detach may be placed at 37°C to facilitate dispersal.
                4. Add 6.0 to 8.0 ml of complete growth medium and aspirate cells by gently pipetting.
                5. Add appropriate aliquots of the cell suspension to new culture vessels.
                6. Incubate cultures at 37°C.


                Subcultivation ratio: A subcultivation ratio of 1:3 to 1:8 is recommended

                Medium renewal: 2 to 3 times per week
                Preservation:
                Freeze medium: Complete growth medium supplemented with 5% (v/v) DMSO
                Storage temperature: liquid nitrogen vapor phase
                Related Products:
                Recommended medium (without the additional supplements or serum described under ATCC Medium): ATCC 30-2003
                recommended serum: ATCC 30-2020
                References:
                22565: Baker CC , et al. Structural and transcriptional analysis of human papillomavirus type 16 sequences in cervical carcinoma cell lines. J. Virol. 61: 962-971, 1987. PubMed:
                22995: Pater MM , Pater A . Human papillomavirus types 16 and 18 sequences in carcinoma cell lines of the cervix. Virology 145: 313-318, 1985. PubMed:
                23180: Yee C , et al. Presence and expression of human papillomavirus sequences in human cervical carcinoma cell lines. Am. J. Pathol. 119: 361-366, 1985. PubMed:
                23192: Friedl F , et al. Studies on a new human cell line (SiHa) derived from carcinoma of uterus. I. Its establishment and morphology. Proc. Soc. Exp. Biol. Med. 135: 543-545, 1970. PubMed:
                23324: Scheffner M , et al. The state of the p53 and retinoblastoma genes in human cervical carcinoma cell lines. Proc. Natl. Acad. Sci. USA 88: 5523-5527, 1991. PubMed:
                29988: Hendricks DT , et al. FHIT gene expression in human ovarian, endometrial, and cervical cancer cell lines. Cancer Res. 57: 2112-2115, 1997. PubMed:
                32270: Olive PL , Banath JP . Multicell spheroid response to drugs predicted with the comet assay. Cancer Res. 57: 5528-5533, 1997. PubMed:

                 

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