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      亞膜漢遜酵母

      簡要描述:亞膜漢遜酵母,感謝您使用本單位的微生物菌種,我們有可用于科研、教學、生產的菌種約2500株,基本覆蓋了環境、工業、農業、分析、食、藥用真菌行業各類生產和科研用微生物,其中許多優良菌株的生產性能具有較高水平。

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      亞膜漢遜酵母


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      亞膜漢遜酵母

      ATCC® Number:  CL-188™

      Designations:  LS 174T

      Depositors:   Northwestern University

      Biosafety Level: 1

      Shipped:  frozen

      Medium & Serum:  See Propagation

      Growth Properties: adherent

      Organism: Homo sapiens (human)

      Morphology: epithelial


      Source: Organ: colon

      Tumor Stage: Dukes' type B

      Disease: colorectal adenocarcinoma

      Cellular Products: carcinoembryonic antigen (CEA) (The production of CEA in the ATCC seed stock was 1944 ng per 10(6) cells in 10 days.)

      interleukin 10 (IL-10) [22511]

      interleukin 6 (IL-6)

      mucin

      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 ultimay responsible for obtaining the permits. Please click here for information regarding the specific requirements for shipment to your location.


      Tumorigenic: Yes

      Reverse Transcript: negative

      Oncogene: myc +; myb + ; ras +; fos +; p53 +; sis -; abl -; ros -; src -

      Antigen Expression: serologically defined colon cancer antigen 3; Homo sapiens, expressed

      HLA A2, B13, B50; Blood type O

      Cytogenetic Analysis: 45,X; one X chromosome missing; no other chromosomal aberrations

      Isoenzymes:  ADA, 1

      ES-D, 1

      G6PD, B

      PEP-D, 1

      PGD, A

      PGM1, 1

      PGM3, 2

      Age:  58 years

      Gender:  female

      Ethnicity:  Caucasian

      Comments: LS 174T is a variant of LS 180 (ATCC CL-187) that has been maintained by using trypsin in the subculture protocol. It is more easily subc*ted than that parent line and, like LS 180, it is reported to produce large amounts of carcinoembryonic antigen (CEA).

      Electron microscopic studies revealed abundant microvilli and intracytoplasmic mucin vacuoles [Pubmed ID: 1262041].

      They are negative for p53 antigen expression, but positive for mRNA expression.

      LS 174T cells stain positively for cytokeratins.

      The line is positive for expression of c-myc, N-myc, H-ras, N-ras.

      Myb, and fos oncogenes.

      K-ras and sis oncogene expression were not detected.

      Propagation:  ATCC complete growth medium: The base medium for this cell line is ATCC-formulated Eagle's 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%.

      Atmosphere: air, 95%; carbon dioxide (CO2), 5%

      Temperature: 37.0°C

      Subculturing:  Protocol:

      Remove and discard culture medium.

      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.

      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.

      Add 6.0 to 8.0 ml of complete growth medium and aspirate cells by gently pipetting.

      Add appropriate aliquots of the cell suspension to new culture vessels.

      Incubate cultures at 37°C.

      Subc*tion Ratio: A subc*tion ratio of 1:2 to 1:4 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

      derived from same individual:ATCC CL-187

      References: 2148: Tom BH, et al. Human colonic adenocarcinoma cells. I. Establishment and description of a new line. In Vitro 12: 180-191, 1976. PubMed: 1262041

      3524: Tom BH, et al. Process of producing carcinoembryonic antigen. US Patent 4,228,236 dated Oct 14 1980

      22147: Chen TR, et al. Intercellular karyotypic similarity in near-diploid cell lines of human tumor origins. Cancer Genet. Cytogenet. 10: 351-362, 1983. PubMed: 6652615

      22511: Gastl GA, et al. Interleukin-10 production by human carcinoma cell lines and its relationship to interleukin-6 expression. Int. J. Cancer 55: 96-101, 1993. PubMed: 8344757

      22861: Trainer DL, et al. Biological characterization and oncogene expression in human colorectal carcinoma cell lines. Int. J. Cancer 41: 287-296, 1988. PubMed: 3338874

      32265: Tsao H, et al. Novel mutations in the p16/CDKN2A binding region of the Cyclin-dependent Kinase-4 gene. Cancer Res. 58: 109-113, 1998. PubMed: 9426066

      32377: Shibata D, et al. Genomic instability in repeated sequences is an early somatic event in colorectal tumorigenesis that persists after transformation. Nat. Genet. 6: 273-281, 1994. PubMed: 8012390

      32794: Kutchera W, et al. Protaglandin H synthase 2 is expressed abnormally in human colon cancer: evidence for a transcriptional effect. Proc. Natl. Acad. Sci. USA 93: 4816-4820, 1996. PubMed: 8643486




















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