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- 详细信息
- 文献和实验
- 技术资料
- 英文名：
MA104
- 库存：
1x10^6/cell
- 供应商：
上海酶研
- 肿瘤类型：
无
- 细胞类型：
MA104
- 品系：
MA104
- 组织来源：
罗猴胎肾细胞 MA104
- 相关疾病：
无
- 物种来源：
罗猴
- 免疫类型：
详询
- 细胞形态：
贴壁/悬浮
- 是否是肿瘤细胞：
否
- 器官来源：
罗猴胎肾细胞 MA104
- 运输方式：
顺丰快递
- 年限：
无限
- 生长状态：
生长良好
- 规格：
瓶
MA104、MA104、MA104罗猴胎肾细胞 MA104
Cell line name MA-104
Synonyms Ma-104; MA 104; MA104; Microbiological Associates-104
Accession CVCL_3845
Resource Identification Initiative To cite this cell line use: MA-104 (RRID:CVCL_3845)
Comments Group: Non-human primate cell line.
Problematic cell line: Misidentified. Originally thought to be of Rhesus macaque origin but found to be from African Green monkey (PubMed=4043530; PubMed=20143388) and more precisely from Chlorocebus pygerythrus (PubMed=34737324).
Registration: International Cell Line Authentication Committee, Register of Misidentified Cell Lines; ICLAC-00077.
Virology: Susceptible to infection by many viruses (arboviruses, reoviruses, rotaviruses, etc.).
Virology: Susceptible to infection by SARS coronavirus (SARS-CoV). Produces a lytic infection (PubMed=15731278; PubMed=16494729).
Virology: Susceptible to infection by SARS coronavirus 2 (SARS-CoV-2) (COVID-19) (PubMed=33389257).
Derived from site: In situ; Fetal kidney; UBERON=UBERON_0002113.
Species of origin Chlorocebus pygerythrus (Vervet monkey) (Cercopithecus pygerythrus) (NCBI Taxonomy: 60710)
Hierarchy Children:
CVCL_1K12 (9009B) CVCL_A0XU (CL2621) CVCL_3846 (MA-104 Clone 1)
CVCL_4540 (MARC-145) CVCL_3774 (PSP-36)
Sex of cell Sex unspecified
Age at sampling Fetus
Category Spontaneously immortalized cell line
PubMed=4626908; DOI=10.1128/am.24.1.62-69.1972; PMCID=PMC380548
Myers M.G., Vincent M.M., Hensen S.A., Tauraso N.M.
Problems in the laboratory isolation of simian hemorrhagic fever viruses and isolation of the agent responsible for the Sussex/69 epizootic.
Appl. Microbiol. 24:62-69(1972)
PubMed=4043530
Whitaker A.M., Hayward C.J.
The characterization of three monkey kidney cell lines.
Dev. Biol. Stand. 60:125-131(1985)
PubMed=15731278; DOI=10.1128/JVI.79.6.3846-3850.2005; PMCID=PMC1075706
Mossel E.C., Huang C., Narayanan K., Makino S., Tesh R.B., Peters C.J.
Exogenous ACE2 expression allows refractory cell lines to supps replication.
J. Virol. 79:3846-3850(2005)
PubMed=16494729; DOI=10.3201/eid1201.050496; PMCID=PMC3291385
Kaye M., Druce J., Tran T., Kostecki R., Chibo D., Morris J., Catton M., Birch C.
SARS-associated coronavirus replication in cell lines.
Emerg. Infect. Dis. 12:128-133(2006)
PubMed=19941903; DOI=10.1016/j.jviromet.2009.11.022
Karger A., Bettin B., Lenk M., Mettenleiter T.C.
Rapid characterisation of cell cultures by matrix-assisted laser desorption/ionisation mass spectrometric typing.
J. Virol. Methods 164:116-121(2010)
PubMed=20143388; DOI=10.1002/ijc.25242
Capes-Davis A., Theodosopoulos G., Atkin I., Drexler H.G., Kohara A., MacLeod R.A.F., Masters J.R.W., Nakamura Y., Reid Y.A., Reddel R.R., Freshney R.I.
Check your cultures! A list of cross-contaminated or misidentified cell lines.
Int. J. Cancer 127:1-8(2010)
PubMed=26235236; DOI=10.1016/j.jviromet.2015.07.016
Otto P.H., Reetz J., Eichhorn W., Herbst W., Elschner M.C.
Isolation and propagation of the animal rotaviruses in MA-104 cells -- 30 years of practical experience.
J. Virol. Methods 223:88-95(2015)
PubMed=28046048; DOI=10.1371/journal.pone.0169391; PMCID=PMC5207746
Dotti S., Lombardo T., Villa R., Cacciamali A., Zanotti C., Andreani N.A., Cinotti S., Ferrari M.
Transformation and tumorigenicity testing of simian cell lines and evaluation of poliovirus replication.
PLoS ONE 12:E0169391-E0169391(2017)
PubMed=33389257; DOI=10.1007/s10096-020-04106-0; PMCID=PMC7778494
Wurtz N., Penant G., Jardot P., Duclos N., La Scola B.
Culture of SARS-CoV-2 in a panel of laboratory cell lines, permissivity, and differences in growth profile.
Eur. J. Clin. Microbiol. Infect. Dis. 40:477-484(2021)
PubMed=34737324; DOI=10.1038/s41598-021-00779-5; PMCID=PMC8569163
Lung O., Candlish R.C., Nebroski M., Kruckiewicz P., Buchanan C., Moniwa M.
High-throughput sequencing for species authentication and contamination detection of 63 cell lines.
Sci. Rep. 11:21657-21657(2021)
Cross
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文献和实验*发表【中文论文】请标注：由上海酶研生物科技有限公司提供；
*发表【英文论文】请标注：From Shanghai EK-Bioscience Biotechnology Co., Ltd.
续的节段组成。在轮状病毒外衣壳上具有型特异性抗原，在内衣壳上共同抗原。根据病毒 rna 各节段在聚丙烯酰胺凝胶电泳中移动距离的差别，可将人轮状病毒到少分为四个血清型，引起人类腹泻的主要是 a 型和 b 型。 轮状病毒在一般组织培养中不适应，需选用特殊的细胞株培养（如恒河猴胚肾细胞 ma104 株和非洲绿猴肾传代细胞 cv-1 株）。培养前应先用胰酶处理病毒，以降解病毒多肽 vp3 ，该多肽能限制病毒在细胞中的增殖，在培养时细胞维持液中也应含有一定浓度的胰蛋白
Marc 145细胞培养和维持有关资料综述一、 细胞及培养1、Marc145细胞上皮样细胞，来源于猴肾细胞，从母细胞（MA 104细胞）克隆而得到，可连续培养。2、生长培养基DMEM（高糖型，含4500mg/L D－葡萄糖、L-谷氨酰胺，和110mg/L丙酮酸钠，不含碳酸氢钠）＋5－10％新生牛血清+ 1%双抗（青霉素和链霉素）的培养液。3、冻存液生长培养基＋10% DMSO4、细胞健康生长的几项注意事项（1）细胞没有支原体等外源因子的感染。（2）培养液的pH值可在7.0－7.3，以7.2为佳
淋巴细胞性脉络膜脑膜炎病毒lymphocyticchoriomeningitis virus
。在鸡胚、鼠胎、猴肾细胞上增殖，而且一般不出现细胞变性。
技术资料