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        當前位置:首頁 >產品中心>細胞系>人源細胞系>HTB-37人結腸腺癌細胞

        人結腸腺癌細胞

        簡要描述:HTB-37 Caco-2 人結腸腺癌細胞,
        原代細胞|細胞系|細胞株|菌種;細胞庫管理規范,
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        • 產品型號:HTB-37
        • 廠商性質:生產廠家
        • 更新時間:2025-12-01
        • 訪  問  量:2724

        詳細介紹

        HTB-37 Caco-2 人結腸腺癌細胞

        ATCC® Number: HTB-37™

        Designations: Caco-2

        Depositors: J Fogh

        Biosafety Level: 1

        Shipped: frozen

        Medium & Serum: See Propagation

        Growth Properties: adherent

        Organism: Homo sapiens (human)

        Morphology: epithelial

        HTB-37 Caco-2 人結腸腺癌細胞

        Source: Organ: colon

        Disease: colorectal adenocarcinoma

        Cellular Products: keratin

        retinoic acid binding protein 1

        retinol binding protein 2

        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.


        Restrictions: The cells are distributed for research purposes only. The Memorial Sloan-Kettering Cancer Center releases the line subject to the following: 1.) The cells or their products must not be distributed to third parties. Commercial interests are the exclusive property of Memorial Sloan-Kettering Cancer Center. 2.) Any proposed commercial use of these cells must first be negotiated with The Director, Office of Industrial Affairs, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10021; phone (212) 639-6181; (212) 717-3439.

        Applications: transfection host (Nucleofection technology from Lonza

        Roche FuGENE® Transfection Reagents)

        Receptors: heat stable enterotoxin (Sta, E. coli), expressed

        epidermal growth factor (EGF), expressed

        Virus Susceptibility: Human immunodeficiency virus 1

        Tumorigenic: Yes

        Reverse Transcript: N

        DNA Profile (STR): Amelogenin: X

        CSF1PO: 11

        D13S317: 11,13,14

        D16S539: 12,13

        D5S818: 12,13

        D7S820: 11,12

        TH01: 6

        TPOX: 9,11

        vWA: 16,18

        Cytogenetic Analysis: The stemline modal chromosome number is 96, occurring at 16% with polyploidy at 3.2%. Ten common markers were detected i.e., t(1q;?), 10q-, t(11q17q) and 7 others. The t(1q17q) and M11 were found in a portion of cells. The ins(2), 10q-, and t(15q;?) were generally paired, and t(11q;17q) and t(21q;?) were mostly three-copied. Normal N9 was absent, and N21 was lost in some cells. One to 4 small acrocentric chromosomes were detected. No Y chromosome with bright distal q-band was detected by Q-observation.

        Isoenzymes: AK-1, 1

        ES-D, 1

        G6PD, B

        GLO-I, 1

        Me-2, 1

        PGM1, 1

        PGM3, 1

        Age: 72 years adult

        Gender: male

        Ethnicity: Caucasian

        HeLa Markers: N

        Comments: Upon reaching confluence, the cells express characteristics of enterocytic differentiation [PubMed ID: 1939345]. Caco-2 cells express retinoic acid binding protein I and retinol binding protein II [PubMed ID: 9040537].

        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 20%.

        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 which 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 37C 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.The recommended inoculum is 1 X 10(4) viable cells/cm2. Subculture cells when they are about 80% confluent, at a cell concentration between 8 X 10(4) and 1 X 10(5) cell/cm2.

        Incubate cultures at 37C.

        Subc*tion Ratio: A subc*tion ratio of 1:4 to 1:6 is recommended

        Medium Renewal: 1 to 2 times per week

        Preservation: Freeze medium: Complete growth medium, 95%; DMSO, 5%

        Storage temperature: liquid nitrogen vapor temperature

        Doubling Time: about 62 hours

        Related Products: Recommended medium (without the additional supplements or serum described under ATCC Medium):ATCC 30-2003

        recommended serum:ATCC 30-2020

        derivative:ATCC CRL-2102

        0.25% (w/v) Trypsin - 0.53 mM EDTA in Hank' BSS (w/o Ca++, Mg++):ATCC 30-2101

        Cell culture tested DMSO:ATCC 4-X

        References: 18385: Didier ES, et al. Characterization of Encephalitozoon (Septata) intestinailis isolates cultured from nasal mucosa and bronchoalveolar lavage fluids of two AIDS patients. J. Eukaryot. Microbiol. 43: 34-43, 1996. PubMed: 8563708

        22409: Jumarie C, Malo C. Caco-2 cells cultured in serum-free medium as a model for the study of enterocytic differentiation in vitro. J. Cell. Physiol. 149: 24-33, 1991. PubMed: 1939345

        22536: Fogh J, et al. Absence of HeLa cell contamination in 169 cell lines derived from human tumors. J. Natl. Cancer Inst. 58: 209-214, 1977. PubMed: 833871

        22539: Fogh J, et al. One hundred and twenty-seven cultured human tumor cell lines producing tumors in nude mice. J. Natl. Cancer Inst. 59: 221-226, 1977. PubMed: 327080

        22564: Adachi A, et al. Productive, persistent infection of human colorectal cell lines with human immunodeficiency virus. J. Virol. 61: 209-213, 1987. PubMed: 3640832

        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

        23009: Cohen MB, et al. Receptors for Escherichia coli heat stable enterotoxin in human intestine and in a human intestinal cell line (Caco-2). J. Cell. Physiol. 156: 138-144, 1993. PubMed: 8100232

        HTB-37 Caco-2



















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