万千商家帮你免费找货
0 人在求购买到急需产品
- 详细信息
- 文献和实验
- 技术资料
- 规格:
T25
KU812/KU812细胞系/KU812细胞株/KU812人外周血嗜碱性白血病细胞
Cell line name Ku812
Synonyms KU812; KU-812; KU.812; KU 812
Accession CVCL_0379
Resource Identification Initiative To cite this cell line use: Ku812 (RRID:CVCL_0379)
Comments Part of: Cancer Dependency Map project (DepMap) (includes Cancer Cell Line Encyclopedia - CCLE).
Part of: COSMIC cell lines project.
Part of: LL-100 blood cancer cell line panel.
Population: Japanese.
Doubling time: 25 +- 2 hours (PubMed=11264164); ~20-30 hours (ATCC=CRL-2099); ~80-100 hours (DSMZ=ACC-378).
Microsatellite instability: Stable (MSS) (Sanger).
Omics: Deep exome analysis.
Omics: Deep quantitative proteome analysis.
Omics: DNA methylation analysis.
Omics: SNP array analysis.
Omics: Transcriptome analysis by microarray.
Omics: Transcriptome analysis by RNAseq.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Cell type: Basophil progenitor cell; CL=CL_0000613.
PubMed=9644295; DOI=10.1159/000040837
Kaneko H., Horiike S., Sasai Y., Iwai T., Nakao M., Yokota S., Taniwaki M., Kashima K., Misawa S.-i.
Rare alteration of genomic structure or expression of the DPC4 gene in myelogenous leukemias.
Acta Haematol. 99:187-190(1998)
PubMed=10071072; DOI=10.1016/S0145-2126(98)00171-4
Drexler H.G., MacLeod R.A.F., Uphoff C.C.
Leukemia cell lines: in vitro models for the study of Philadelphia chromosome-positive leukemia.
Leuk. Res. 23:207-215(1999)
PubMed=10576511; DOI=10.1016/S0145-2126(99)00131-9
Uphoff C.C., Habig S., Fombonne S., Matsuo Y., Drexler H.G.
ABL-BCR expression in BCR-ABL-positive human leukemia cell lines.
Leuk. Res. 23:1055-1060(1999)
DOI=10.1016/B978-0-12-221970-2.50457-5
Drexler H.G.
The leukemia-lymphoma cell line factsbook.
(In book) ISBN 9780122219702; pp.1-733; Academic Press; London; United Kingdom (2001)
PubMed=11264164; DOI=10.1182/blood.V97.7.1999
Kano Y., Akutsu M., Tsunoda S., Mano H., Sato Y., Honma Y., Furukawa Y.
In vitro cytotoxic effects of a tyrosine kinase inhibitor STI571 in combination with commonly used antileukemic agents.
Blood 97:1999-2007(2001)
PubMed=11416159; DOI=10.1073/pnas.121616198; PMCID=PMC35459
Masters J.R.W., Thomson J.A., Daly-Burns B., Reid Y.A., Dirks W.G., Packer P., Toji L.H., Ohno T., Tanabe H., Arlett C.F., Kelland L.R., Harrison M., Virmani A.K., Ward T.H., Ayres K.L., Debenham P.G.
Short tandem repeat profiling provides an international reference standard for human cell lines.
Proc. Natl. Acad. Sci. U.S.A. 98:8012-8017(2001)
PubMed=15843827; DOI=10.1038/sj.leu.2403749
Andersson A., Eden P., Lindgren D., Nilsson J., Lassen C., Heldrup J., Fontes M., Borg A., Mitelman F., Johansson B., Hoglund M., Fioretos T.
Gene expression profiling of leukemic cell lines reveals conserved molecular signatures among subtypes with specific genetic aberrations.
Leukemia 19:1042-1050(2005)
PubMed=16408098; DOI=10.1038/sj.leu.2404081
Quentmeier H., MacLeod R.A.F., Zaborski M., Drexler H.G.
JAK2 V617F tyrosine kinase mutation in cell lines derived from myeloproliferative disorders.
Leukemia 20:471-476(2006)
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=20215515; DOI=10.1158/0008-5472.CAN-09-3458; PMCID=PMC2881662
Rothenberg S.M., Mohapatra G., Rivera M.N., Winokur D., Greninger P., Nitta M., Sadow P.M., Sooriyakumar G., Brannigan B.W., Ulman M.J., Perera R.M., Wang R., Tam A., Ma X.-J., Erlander M., Sgroi D.C., Rocco J.W., Lingen M.W., Cohen E.E.W., Louis D.N., Settleman J., Haber D.A.
A genome-wide screen for microdeletions reveals disruption of polarity complex genes in diverse human cancers.
Cancer Res. 70:2158-2164(2010)
PubMed=20809971; DOI=10.1186/1755-8166-3-15; PMCID=PMC2944125
Virgili A., Nacheva E.
Genomic amplification of BCR/ABL1 and a region downstream of ABL1 in chronic myeloid leukaemia: a FISH mapping study of CML patients and cell lines.
Mol. Cytogenet. 3:15.1-15.12(2010)
风险提示:丁香通仅作为第三方平台,为商家信息发布提供平台空间。用户咨询产品时请注意保护个人信息及财产安全,合理判断,谨慎选购商品,商家和用户对交易行为负责。对于医疗器械类产品,请先查证核实企业经营资质和医疗器械产品注册证情况。
文献和实验*发表【中文论文】请标注:由博辉生物科技(广州)有限公司提供; *发表【英文论文】请标注:From Bohui Biological Technology (Guangzhou) Co., Ltd.
Mol Cell:杨薇等揭示 DNA-PK 的激活机制以及自磷酸化对 NHEJ 通路的重要作用
DNA 双链断裂可由外在因素(电离辐射和活性氧等)或内在因素(DNA 复制错误和 V(D)J 重组等)造成,从而激发 DNA 损伤应答,包括 DNA 修复、细胞周期调控、细胞衰老和细胞凋亡等。 DNA 损伤应答由 PIKK(phosphoinositide-3-kinase-related kinase)家族蛋白激酶催化下游蛋白的磷酸化而启动,包括 DNA-PK(DNA 依赖性蛋白激酶)、ATM(Ataxia Telangiectasia Mutated)和 ATR(ATM-Related
特点是能够将两种性质完全不同的外源多肽或蛋白质,分别与T4衣壳表面上的外壳蛋白SOC(9 ku)和HOC(40 ku)融合而直接展示于T4噬菌体的表面,因此它表达的蛋白不需要复杂的蛋白纯化,避免了因纯化而引起的蛋白质变性和丢失。其病毒颗粒在宿主细胞内组装,不经过分泌途径,因而其表面展示多肽的范围更广,尤其适用于那些不能被大肠杆菌分泌的复杂蛋白质。值得关注的是,SOC与HOC蛋白的存在与否并不影响T4的生存和繁殖。SOC和HOC在噬菌体组装时可优于DNA的包装而装配于衣壳的表面。事实上,在DNA包装被抑制
(一)CA125 1983年由Bast等从上皮性卵巢癌抗原检测出可被单克隆抗体OC125结合的一种糖蛋白。分子量为200ku,加热至100℃时CA125的活性破坏,正常人血清CA125中的(RIA)阳性临界值为35ku/L. CA125是上皮性卵巢癌和子宫内膜癌的标志物,浆液性子宫内膜样癌、透明细胞癌、输卵管癌及未分化卵巢癌患者的CA125含量可明显升高。当卵巢癌复发时,在临床确诊前几个月便可呈现CA125增高,尤其卵巢癌转移患者的血清CA125更明显高于正常参考
技术资料




