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- 详细信息
- 文献和实验
- 技术资料
- 供应商:
复祥生物
- 细胞类型:
普通细胞株-科研实验
- 物种来源:
人
- 运输方式:
常温或干冰
- 生长状态:
良好
- 库存:
大量
Daudi 人Burkitt's淋巴瘤细胞
RPMI-1640(GIBCO)+10%胎牛血清。细胞货期8-10个工作日
上海复祥生物提供 ATCC 细胞|细胞系|细胞株|肿瘤细胞|细胞|贴壁细胞|悬浮细胞|,细胞库管理规范,提供的细胞株背景清楚,提供参考文献和最优培养条件,网站上有细胞照片,欢迎各位老师来电咨询!联系电话400-821-8510 手机15000266580
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ATCC® Number: CCL-213™
Designations: Daudi
Depositors: G Klein
Isotype: IgM
Biosafety Level: 2 [Cells Contain HERPESVIRUS ]
Shipped: frozen
Medium & Serum: See Propagation
Growth Properties: suspension
Organism: Homo sapiens (human)
Morphology: lymphoblast
Source: Organ: peripheral blood
Disease: Burkitt's lymphoma
Cell Type: B lymphoblast;
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.
Isolation: Isolation date: May, 1967
Applications: transfection host (Roche FuGENE® Transfection Reagents)
Receptors: complement, expressed
Fc, expressed
Tumorigenic: Yes
Reverse Transcript: negative
DNA Profile (STR): Amelogenin: X,Y
CSF1PO: 12
D13S317: 11,12
D16S539: 10,12
D5S818: 8,13
D7S820: 8,10
THO1: 6,7
TPOX: 8,11
vWA: 15,17
Cytogenetic Analysis: Male human karyotype with stemline number of 46. The karyotype is diploid in 66% of the cells and is stable within the stemline.
Isoenzymes: G6PD, B
Age: 16 years
Gender: male
Ethnicity: Black
Comments: The Daudi line was derived from a 16-year-old Black male with Burkitt's lymphoma by E. Klein and G. Klein in May, 1967. The cells are negative for beta-2-microglobulin. They are positive for EBNA, VCA and Surface immunoglobulin (sIg+).The line carries Epstein-Barr virus. The Daudi is a well characterized B lymphoblast cell line which has been employed extensively in studies of mechanisms of leukemogenesis.
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 the addition of fresh medium or replacement of medium. Alternatively, cultures can be established by centrifugation with subsequent resuspension at 3 to 5 X 10(5) viable cells/ml.
Interval: Maintain cell density between 3 X 10(5) and 2 to 3 X 10(6) viable cells/ml.
Medium Renewal: Add fresh medium every 2 to 3 days (depending on cell density)
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 30-2001
recommended serum:ATCC 30-2020
References: 22550: Ohsugi Y, et al. Tumorigenicity of human malignant lymphoblasts: comparative study with unmanipulated nude mice, antilymphocyte serum-treated nude mice, and X- irradiated nude mice. J. Natl. Cancer Inst. 65: 715-718, 1980. PubMed: 6932523
23017: Klein E, et al. Surface IgM-kappa specificity on a Burkitt lymphoma cell in vivo and in derived culture lines. Cancer Res. 28: 1300-1310, 1968. PubMed: 4174339
26046: Huber C, et al. Surface receptors on human haematopoietic cell lines. Clin. Exp. Immunol. 25: 367-378, 1976. PubMed: 963908
26047: Nilsson K, et al. Tumorigenicity of human hematopoietic cell lines in athymic nude mice. Int. J. Cancer 19: 337-344, 1977. PubMed: 14896
28315: Gao Y, et al. Induction of an exceptionally high-level, nontranslated, Epstein-Barr virus-encoded polyadenylated transcript in the uurkitts lymphoma line Daudi. J. Virol. 71: 84-94, 1997. PubMed: 8985326
32286: Cuthbert JA, Lipsky PE. Regulation of proliferation and Ras localization in transformed cells by products of mevalonate metabolism. Cancer Res. 57: 3498-3504, 1997. PubMed: 9270019
32830: Yamaguchi Y, et al. Biochemical characterization and intracellular localization of the Menkes disease protein. Proc. Natl. Acad. Sci. USA 93: 14030-14035, 1996. PubMed: 8943055
33091: Lewis JA, et al. Inhibition of mitochondrial function by interferon. J. Biol. Chem. 271: 13184-13190, 1996. PubMed: 8662694
33115: Montoya JG, et al. Human CD4+ and CD8+ T lymphocytes are both cytotoxic to Toxoplasma gondii-infected cells. Infect. Immun. 64: 176-181, 1996. PubMed: 8557337
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文献和实验[6] 。本研究目的在于利用基因工程方法将鼠源性单克隆抗CD20抗体HI47可变区和人源抗体恒定区连接起来,构建嵌合抗CD20抗体Fab′和F(ab)′2片段,以降低鼠源性抗体的免疫源性。我们构建了人源化的抗CD20抗体Fab′和F(ab)′2片段的载体,可在大肠杆菌中高效可溶性分泌表达,并比较了二者的体外活性,结果均证实了Fab′和F(ab)′2片段具有抑制B淋巴肿瘤细胞生长的活性,这无疑为B淋巴瘤的临床治疗提供了有利的工具。一、实验材料与方法1、细胞与蛋白人B淋巴瘤细胞系Raji与Daudi细胞由本室保存
人类组织肿瘤细胞 10104 人淋巴瘤细胞(B类)A-204 人横纹肌肉瘤A375 人皮肤黑色素瘤细胞A431 人皮肤基底细胞癌A549 人肺癌细胞A875 人黑色素瘤细胞BeWo 人胎盘绒毛癌细胞BGC-823 人胃腺癌细胞BT474 人乳腺导管瘤CACO-2 人结肠癌细胞CaLu-3 人肺腺癌细胞CASKI 人宫颈癌Colo205 人结肠癌Colo320DM 人结肠癌D341 Med 人髓母细胞瘤Daudi 人B淋巴细胞瘤DMF7 双位点HC-KIT
来自B细胞。瘤细胞间散在多数吞噬各种细胸碎屑的巨噬细胞,形成所谓满天星图像(图11-4)。 图11-4 Burkitt淋巴瘤 瘤细胞由小无核裂滤泡中心细胞组成,细胞大小相似,核圆形。瘤细胞间散在多数吞噬细胞呈“满天星”图像 ×280 Burkitt淋巴瘤对化疗效果较好,缓解期长。本病原因尚不清楚,由于常发生在温暖潮湿地带,故有人认为可能与蚊子或其他昆虫传播的病毒性感染有关。非洲流行区EB病毒感染率很高。约95%非洲Burkitt淋巴瘤细胞有EB病毒
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