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CA46細胞

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產品名稱: CA46細胞
產品型號: CA46
產品展商: HZbscience
產品文檔: 無相關文檔

簡單介紹

CA46細胞應如何避免細胞污染,細胞污染的種類可分成**、酵母菌、霉菌、病毒和霉漿菌。主要的污染原因為無菌操作技術不當、操作室環境不佳、污染之血清和污染之細胞等。嚴格之無菌操作技術、清潔的環境、與品質良好之細胞來源和培養基配制是減低污染之*好方法。CA46細胞何時須更換培養基?視細胞生長密度而定,或遵照細胞株基本數據上之更換時間,按時更換培養基即可。


CA46細胞  的詳細介紹

CA46細胞

細胞類型: B**細胞

ATCC Number: CRL-1648?

相關**: **瘤

是否是腫瘤細胞: 1

物種來源: 人

生長狀態: 懸浮生長

運輸方式: 凍存運輸

數量: 大量

細胞形態: **樣

**類型: IgM; kappa light chain

CA46細胞Designations: CA46

Depositors: IT Magrath

Isotype: IgM; kappa light chain

Biosafety Level: 1

Shipped: frozen

Medium & Serum: See Propagation

Growth Properties: suspension

Organism: Homo sapiens

Morphology: lymphoblast


Source: Disease: Burkitt's lymphoma

Cell Type: B lymphocyte;

Cellular Products: immunoglobulin (surface and secreted)

Permits/Forms: CA46細胞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.

Receptors: complement

Antigen Expression: HLA B27 (the patient was HLA A2, A11, B17, B27)

DNA Profile (STR): Amelogenin: X

CSF1PO: 10,12

D13S317: 8,12

D16S539: 11,12

D5S818: 13

D7S820: 11,12

THO1: 7,9

TPOX: 8,9

vWA: 15,16

CA46細胞Cytogenetic Analysis: 46, XO, XY, dup1(q21-32), t(8;14) (8pter --> 8q23 :: 14q32 --> 14qter; 14pter --> 14q32 :: 8q23 --> 8qter), 13q+, +16

Gender: male

Comments: The cells are EBNA negative and are negative for Fc receptors.

Approximately 12% of the cells express commplement receptors.

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 20%.

Temperature: 37.0°C

Subculturing: Medium Renewal: Every 2 to 3 days

Cultures can be maintained by the addition of fresh medium or replacement of medium. Alternatively, cultures can be established by centrifugation with subsequent resuspension at 2 to 3 X 10 exp5 viable cells/ml.

A saturation density of 2 X 10 exp6 is obtainable.

Preservation: culture medium 95%; DMSO, 5%

Doubling Time: 16 hrs

Related Products: CA46細胞Recommended medium (without the additional supplements or serum described under ATCC Medium):ATCC 30-2001

recommended serum:ATCC 30-2020

References: 1093: Benjamin D, et al. Immunoglobulin secretion by cell lines derived from African and American undifferentiated lymphomas of Burkitt's and non-Burkitt's type. J. Immunol. 129: 1336-1342, 1982. PubMed: 6286763

22548: Magrath IT, et al. Characterization of lymphoma-derived cell lines: comparison of cell lines positive and negative for Epstein-Barr virus nuclear antigen. I. Physical, cytogenetic, and growth characteristics. J. Natl. Cancer Inst. 64: 465-476, 1980. PubMed: 6243721

22549: Magrath IT, et al. Characterization of lymphoma-derived cell lines: comparison of cell lines positive and negative for Epstein-Barr virus nuclear antigen. II. Surface markers. J. Natl. Cancer Inst. 64: 477-483, 1980. PubMed: 6243722

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