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- 详细信息
- 文献和实验
- 技术资料
- 英文名:
IM-9
- 库存:
1x10^6/瓶
- 供应商:
上海酶研
- 肿瘤类型:
淋巴瘤
- 细胞类型:
IM-9
- 品系:
IM-9
- 组织来源:
人外周血B淋巴瘤细胞
- 相关疾病:
详询
- 物种来源:
人
- 免疫类型:
详询
- 细胞形态:
贴壁/悬浮
- 是否是肿瘤细胞:
是
- 器官来源:
人外周血B淋巴瘤细胞
- 运输方式:
顺丰快递
- 年限:
5年
- 生长状态:
生长良好
- 规格:
瓶
IM-9、IM-9、IM-9细胞、IM-9细胞、IM-9人外周血B淋巴瘤细胞
Cell line name IM-9
Synonyms IM 9; IM9; GM04680
Accession CVCL_1305
Resource Identification Initiative To cite this cell line use: IM-9 (RRID:CVCL_1305)
Comments Problematic cell line: Misclassified. Originally thought to be a myeloma cell line but is a B-lymphoblastoid cell line (PubMed=10516762).
Part of: Cancer Dependency Map project (DepMap) (includes Cancer Cell Line Encyclopedia - CCLE).
Part of: COSMIC cell lines project.
Population: Caucasian.
Doubling time: ~45 hours (DSMZ=ACC-117); ~1 day (Note=Lot 09172008), ~23 hours (Note=Lot 03302009) (JCRB=JCRB0024).
Microsatellite instability: Stable (MSS) (Sanger).
Transformant: NCBI_TaxID; 10376; Epstein-Barr virus (EBV).
Omics: CRISPR phenotypic screen.
Omics: Deep exome analysis.
Omics: Deep quantitative proteome analysis.
Omics: DNA methylation analysis.
Omics: SNP array analysis.
Omics: Transcriptome analysis by microarray.
Derived from site: In situ; Bone marrow; UBERON=UBERON_0002371.
Sequence variations
Mutation; HGNC; 7989; NRAS; Simple; p.Gln61Lys (c.181C>A); ClinVar=VCV000073058; Zygosity=Heterozygous (Cosmic-CLP=753563; DepMap=ACH-002247).
Genome ancestry Source: PubMed=30894373
Origin % genome
African 0
Native American 0.41
East Asian, North 0
East Asian, South 0
South Asian 0
European, North 68.16
European, South 31.43
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_B6CV (IM-9-P)
Sex of cell Female
Age at sampling Age unspecified
Category Transformed cell line
STR profile Source(s): ATCC=CCL-159; CCRID=1102HUM-NIFDC00064; Cosmic-CLP=753563; DSMZ=ACC-117; JCRB=JCRB0024; KCLB=10159
Markers:
Amelogenin X
CSF1PO 10,11
D2S1338 24,26
D3S1358 14,18
D5S818 13
D7S820 11,12
D8S1179 12,13
D13S317 9,11
D16S539 9,13
D18S51 14,17
D19S433 13,14
D21S11 30,30.2
FGA 20,23
Penta D 9,11
Penta E 13,15
TH01 6,9.3
TPOX 11
vWA 14,17
Run an STR similarity search on this cell line
Publications
PubMed=2836165; DOI=10.1210/endo-122-6-2508
DiMattia G.E., Gellersen B., Bohnet H.G., Friesen H.G.
A human B-lymphoblastoid cell line produces prolactin.
Endocrinology 122:2508-2517(1988)
PubMed=1366653; DOI=10.1007/BF00365265
Bonhoff A., Gellersen B., Held K.R., Bohnet H.G.
Clonal derivatives of a human B-lymphoblastoid cell line producing prolactin -- a cytogenetic characterization.
Cytotechnology 3:43-50(1990)
CLPUB00447
Mulivor R.A., Suchy S.F.
1992/1993 catalog of cell lines. NIGMS human genetic mutant cell repository. 16th edition. October 1992.
(In misc. document) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda; USA (1992)
PubMed=8139288; DOI=10.1016/0145-2126(94)90118-x
Sato S., Honma Y., Hozumi M., Hayashi Y., Matsuo Y., Shibata K., Omura S., Hino K.-i., Tomoyasu S., Tsuruoka N.
Effects of herbimycin A and its derivatives on growth and differentiation of Ph1-positive acute lymphoid leukemia cell lines.
Leuk. Res. 18:221-228(1994)
PubMed=7579375; DOI=10.1182/blood.V86.10.4001.bloodjournal86104001
Pellat-Deceunynck C., Amiot M., Bataille R., Van Riet I., Van Camp B., Omede P., Boccadoro M.
Human myeloma cell lines as a tool for studying the biology of multiple myeloma: a reappraisal 18 years after.
Blood 86:4001-4002(1995)
PubMed=9290701; DOI=10.1002/(SICI)1098-2744(199708)19:4<243::AID-MC5>3.0.CO;2-D
Jia L.-Q., Osada M., Ishioka C., Gamo M., Ikawa S., Suzuki T., Shimodaira H., Niitani T., Kudo T., Akiyama M., Kimura N., Matsuo M., Mizusawa H., Tanaka N., Koyama H., Namba M., Kanamaru R., Kuroki T.
Screening the p53 status of human cell lines using a yeast functional assay.
Mol. Carcinog. 19:243-253(1997)
PubMed=9510473; DOI=10.1111/j.1349-7006.1998.tb00476.x; PMCID=PMC5921588
Hosoya N., Hangaishi A., Ogawa S., Miyagawa K., Mitani K., Yazaki Y., Hirai H.
Frameshift mutations of the hMSH6 gene in human leukemia cell lines.
Jpn. J. Cancer Res. 89:33-39(1998)
PubMed=10516762; DOI=10.1038/sj.leu.2401510
Drexler H.G., Dirks W.G., MacLeod R.A.F.
False human hematopoietic cell lines: cross-contaminations and misinterpretations.
Leukemia 13:1601-1607(1999)
PubMed=10936422; DOI=10.1016/S0145-2126(99)00195-2
Drexler H.G., Matsuo Y.
Malignant hematopoietic cell lines: in vitro models for the study of multiple myeloma and plasma cell leukemia.
Leuk. Res. 24:681-703(2000)
PubMed=20164919; DOI=10.1038/nature08768; PMCID=PMC3145113
Bignell G.R., Greenman C.D., Davies H.R., Butler A.P., Edkins S., Andrews J.M., Buck G., Chen L., Beare D., Latimer C., Widaa S., Hinton J., Fahey C., Fu B.-Y., Swamy S., Dalgliesh G.L., Teh B.T., Deloukas P., Yang F.-T., Campbell P.J., Futreal P.A., Stratton M.R.
Signatures of mutation and selection in the cancer genome.
Nature 463:893-898(2010)
PubMed=20454443; DOI=10.1155/2010/904767; PMCID=PMC2861168
Uphoff C.C., Denkmann S.A., Steube K.G., Drexler H.G.
Detection of EBV, HBV, HCV, HIV-1, HTLV-I and -II, and SMRV in human and other primate cell lines.
J. Biomed. Biotechnol. 2010:904767.1-904767.23(2010)
PubMed=27397505; DOI=10.1016/j.cell.2016.06.017; PMCID=PMC4967469
Iorio F., Knijnenburg T.A., Vis D.J., Bignell G.R., Menden M.P., Schubert M., Aben N., Goncalves E., Barthorpe S., Lightfoot H., Cokelaer T., Greninger P., van Dyk E., Chang H., de Silva H., Heyn H., Deng X.-M., Egan R.K., Liu Q.-S., Miroo T., Mitropoulos X., Richardson L., Wang J.-H., Zhang T.-H., Moran S., Sayols S., Soleimani M., Tamborero D., Lopez-Bigas N., Ross-Macdonald P., Esteller M., Gray N.S., Haber D.A., Stratton M.R., Benes C.H., Wessels L.F.A., Saez-Rodriguez J., McDermott U., Garnett M.J.
A landscape of pharmacogenomic interactions in cancer.
Cell 166:740-754(2016)
PubMed=29892436; DOI=10.1098/rsos.172472; PMCID=PMC5990783
Shioda S., Kasai F., Watanabe K., Kawakami K., Ohtani A., Iemura M., Ozawa M., Arakawa A., Hirayama N., Kawaguchi E., Tano T., Miyata S., Satoh M., Shimizu N., Kohara A.
Screening for 15 pathogenic viruses in human cell lines registered at the JCRB Cell Bank: characterization of in vitro human cells by viral infection.
R. Soc. Open Sci. 5:172472-172472(2018)
PubMed=30894373; DOI=10.1158/0008-5472.CAN-18-2747; PMCID=PMC6445675
Dutil J., Chen Z.-H., Monteiro A.N.A., Teer J.K., Eschrich S.A.
An interactive resource to probe genetic diversity and estimated ancestry in cancer cell lines.
Cancer Res. 79:1263-1273(2019)
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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.
人外周血单细胞悬液制备流程 1.采集人外周血样本于抗凝管中。 离心管内加入100 μL新鲜血和2 mL 1×红细胞裂解液,混匀,4℃裂解10 min。 300 g离心5 min(裂解完立即离心,防止时间过长损伤细胞),弃上清,得到白色细胞沉淀。 PBS洗涤一次。 加入100 μL细胞染色缓冲液重悬细胞,不用计数,即可进行后续流式抗体染色实验。按照100 μL新鲜血样本制备的单细胞悬液,加入1 Test对应的流式抗体混匀进行后续实验。 注意事项: 1. 采血用抗凝管,有肝素和EDTA两种
小鼠外周血单细胞悬液制备 采集小鼠外周血样本于抗凝管中。 离心管内加入 100 μL 新鲜血,加入 1 Test 对应流式抗体,混匀,4℃ 避光孵育 30 min。 加入 2 mL 1×红细胞裂解液,混匀,4℃ 裂解 5 min。 300 g 离心 5 min(裂解完立即离心,防止时间过长损伤细胞),弃上清可得到白色的细胞沉淀。 PBS 洗涤一遍。 加入 200 μL 细胞染色缓冲液重悬细胞,用流式细胞仪进行检测和分析。 注意事项: 采血用抗凝管,有肝素和 EDTA 两种,若直接裂解
度的功能细胞。二、人外周血中 CD4 T 细胞分选实例1.产品信息: MojoSort™ Human CD4 T Cell Isolation Kit(BioLegend, Cat#480009),阴性分选试剂盒2.检测仪器型号:BD LSRⅡ3.样本:正常人外周血4.分选前后检测相关产品:PE-CD4(Biolegend, Cat# 317410)5.实验过程(1)采血之后采用达优™ 人淋巴细胞分离液分离人外周血单个核细胞。分离之后能见到明显的白膜层。(达优,Cat#DKW-KLSH-0100
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