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      當前位置:首頁 >產品中心>細胞庫>人腫瘤細胞、癌細胞>CRL-5974 SNU-16 人胃癌細胞 腹水

      CRL-5974 SNU-16 人胃癌細胞 腹水

      簡要描述:CRL-5974 SNU-16 人胃癌細胞 腹水,
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      CRL-5974 SNU-16 人胃癌細胞 腹水

      ATCC® Number: CRL-5974™ Price: $425.00

      Designations: SNU-16

      Depositors: J Park

      Biosafety Level: 1

      Shipped: frozen

      Medium & Serum: See Propagation

      Growth Properties: suspension, multicell aggregates

      Organism: Homo sapiens (human)

      Morphology: epithelial

      Source: Organ: stomach

      Disease: gastric carcinoma

      Derived from metastatic site: ascites

      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.


      CRL-5974 SNU-16 人胃癌細胞 腹水

      Isolation: Isolation date: 1987

      Receptors: vasoactive intestinal peptide (VIP), expressed [23078]

      Oncogene: myc +; erb B2 +

      Antigen Expression: Blood Type A; Rh +

      The cells express the surface glycoproteins carcinoembryonic antigen (CEA) and TAG 72.

      DNA Profile (STR): Amelogenin: X

      CSF1PO: 12

      D13S317: 8,12

      D16S539: 11,13

      D5S818: 10,13

      D7S820: 12

      THO1: 6,9

      TPOX: 11

      vWA: 16

      Cytogenetic Analysis: This is a human cell line with the bimodal chromosome number distributions. Both modal populations were hypotetraploid. Cells with higher ploidies occurred at 1%. Nine marker chromosomes were common to all cells: t(4q21q); der(5)t(2;5) (q11.2;q13); i(5p); del(17) (p11.2); del(10) (q22.1) and four others. Of these, del(17) generally had two copies per cell. Seven or more other marker chromosomes including HSR(11) (p15.1) were found in some cells only. Multiple copies of DMs were present in most cells. Consistently there were three normal X chromosomes per cell. N7 had six copies and N14, five copies per cell. Normal N12 was not found.

      Age: 33 years

      Gender: female

      Ethnicity: Asian

      Comments: SNU-16 was line derived in 1987 by J. Park and associates from ascites of a patient with poorly differentiated carcinoma of the stomach. The line was established from cells taken prior to chemotherapy. The cells express the surface glycoproteins carcinoembryonic antigen (CEA) and TAG-72. The cells are L-dopa decarboxylase (DDC) positive. SNU-16 cells were positive for VIP receptors but lacked gastrin receptors. No evidence of amplification or rearrangements was noted in the N-myc, L-myc, myb and EGF receptor genes. The c-myc proto-oncogene was apmplified, but expressed c-erb-B-2 RNA that were comparable to other cell lines. There was no expression of the following genes: N-myc, L-myc, c-cis, IGF-2, or gastrin releasing peptide.

      Propagation: ATCC complete growth medium: The base medium for this cell line is ATCC-formulated RPMI-1640 Medium, Catalog No. 30-2001. 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: Cultures can be maintained by addition of fresh medium or replacement of medium. Alternatively, cultures can be established by centrifugation of the suspension with subsequent resuspension in fresh medium. Add medium as the cell density increases.

      Medium Renewal: Add fresh medium every 3 to 4 days (depending on cell density)

      Preservation: Freeze medium: Complete growth medium supplemented with 5% (v/v) DMSO

      Storage temperature: liquid nitrogen vapor phase

      Doubling Time: 27 hrs

      References: 23078: Park JG, et al. Characteristics of cell lines established from human gastric carcinoma. Cancer Res. 50: 2773-2780, 1990. PubMed: 2158397

      23570: . NCI-Navy Medical Oncology Branch Cell Line Supplement. J. Cell. Biochem. suppl. 24: 1996..

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      Make a Deposit

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      ATCC® Number: CRL-5974™ Price: $425.00

      Designations: SNU-16

      Depositors: J Park

      Biosafety Level: 1

      Shipped: frozen

      Medium & Serum: See Propagation

      Growth Properties: suspension, multicell aggregates

      Organism: Homo sapiens (human)

      Morphology: epithelial

      CRL-5974 SNU-16 人胃癌細胞 腹水

      Source: Organ: stomach

      Disease: gastric carcinoma

      Derived from metastatic site: ascites

      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.

      Isolation: Isolation date: 1987

      Receptors: vasoactive intestinal peptide (VIP), expressed [23078]

      Oncogene: myc +; erb B2 +

      Antigen Expression: Blood Type A; Rh +

      The cells express the surface glycoproteins carcinoembryonic antigen (CEA) and TAG 72.

      DNA Profile (STR): Amelogenin: X

      CSF1PO: 12

      D13S317: 8,12

      D16S539: 11,13

      D5S818: 10,13

      D7S820: 12

      THO1: 6,9

      TPOX: 11

      vWA: 16

      Cytogenetic Analysis: This is a human cell line with the bimodal chromosome number distributions. Both modal populations were hypotetraploid. Cells with higher ploidies occurred at 1%. Nine marker chromosomes were common to all cells: t(4q21q); der(5)t(2;5) (q11.2;q13); i(5p); del(17) (p11.2); del(10) (q22.1) and four others. Of these, del(17) generally had two copies per cell. Seven or more other marker chromosomes including HSR(11) (p15.1) were found in some cells only. Multiple copies of DMs were present in most cells. Consistently there were three normal X chromosomes per cell. N7 had six copies and N14, five copies per cell. Normal N12 was not found.

      Age: 33 years

      Gender: female

      Ethnicity: Asian

      Comments: SNU-16 was line derived in 1987 by J. Park and associates from ascites of a patient with poorly differentiated carcinoma of the stomach. The line was established from cells taken prior to chemotherapy. The cells express the surface glycoproteins carcinoembryonic antigen (CEA) and TAG-72. The cells are L-dopa decarboxylase (DDC) positive. SNU-16 cells were positive for VIP receptors but lacked gastrin receptors. No evidence of amplification or rearrangements was noted in the N-myc, L-myc, myb and EGF receptor genes. The c-myc proto-oncogene was apmplified, but expressed c-erb-B-2 RNA that were comparable to other cell lines. There was no expression of the following genes: N-myc, L-myc, c-cis, IGF-2, or gastrin releasing peptide.

      Propagation: ATCC complete growth medium: The base medium for this cell line is ATCC-formulated RPMI-1640 Medium, Catalog No. 30-2001. 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: Cultures can be maintained by addition of fresh medium or replacement of medium. Alternatively, cultures can be established by centrifugation of the suspension with subsequent resuspension in fresh medium. Add medium as the cell density increases.

      Medium Renewal: Add fresh medium every 3 to 4 days (depending on cell density)

      Preservation: Freeze medium: Complete growth medium supplemented with 5% (v/v) DMSO

      Storage temperature: liquid nitrogen vapor phase

      Doubling Time: 27 hrs

      References: 23078: Park JG, et al. Characteristics of cell lines established from human gastric carcinoma. Cancer Res. 50: 2773-2780, 1990. PubMed: 2158397

      23570: . NCI-Navy Medical Oncology Branch Cell Line Supplement. J. Cell. Biochem. suppl. 24: 1996..

      Related Links

      NCBI Entrez Search

      Make a Deposit

      Frequently Asked Questions

      Material Transfer Agreement

      Technical Support

      Related Cell Culture Products



















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