SKIP000842
SKIP ID SKIP000842
Organism(En) -
Organism(Ja) -
Cell Type(En) -
Cell Type(Ja) -
Cell Tissue(En) -
Cell Tissue(Ja) -
Cell Origin Normal
Cell Name 1(En) TFK12(DNAVEC)
Cell Name 1(Ja) TFK12(DNAVEC)
Cell Name 2(En) -
Cell Name 2(Ja) -
Disease Name 1(Ja) -
ICD Code 1 -
Disease Name 1(En) -
OMIM1 -
Disease Name 2(Ja) -
ICD Code 2 -
Disease Name 2(En) -
OMIM 2 -
Disease Name 3(Ja) -
ICD Code 3 -
Disease Name 3(En) -
OMIM 3 -
Age 25
Age Range 20-29
Sex Male
Race(En) -
Race(Ja) -
Genetic Diagnosis --
Not Detected No
Description(En) Induced pluripotent stem cell (iPSC) line derived from peripheral blood cells, T-cells; for reprogramming, sendai viruse vectors, which contained human Oct3/4, Sox2, Klf4 and c-Myc, were used.
Healthy iPSC line.
Description(Ja) 血球系細胞(T細胞)にセンダイウイルスベクターを用いてOct3/4, Sox2, Klf4, c-Mycの4因子を導入して樹立したヒト人工多能性幹細胞株(iPSC)。
健常者由来iPS細胞株。
Cell Morphology human ES-like
Grade Research Grade
Vector Sendai virus
Transgene Sendai Virus (DNAVEC: CytoTuneTM-iPS Cat. No. DV-0301)
SeV18+HS-OCT3/4/TS Delta-F
SeV18+HS-SOX2/TS Delta-F
SeV18+HS-KLF4/TS Delta-F
SeV18(HNL)c-MYCQC/TS Delta-F
Adhesiveness -
Feeder Yes
Feeder Cell Mitomycn C-inactivated SNL feeder cells
Medium standard hESC medium (Dulbecco's modified Eagle's medium [DMEM]/F12 [Sigma] containing 20% KnockOut serum replacement [KSR; Life Technologies], nonessential amino acids [NEAA], 0.1 mM 2-mercaptoethanol [Sigma], and 4 ng/ml fibroblast growth factor 2 [FGF-2] [PeproTech])
Genome Editing -
CO2 -
Mycoplasma Unknown
Detection of Contaminants Mycoplasma -
Pluripotent Markers Yes
Pluripotent Markers Assay ICC
in vitro Differentiation Yes
in vitro Differentiation Assay -
in vivo Differentiation -
in vivo Differentiation Assay -
Other 1 Assay -
Other 1 Assay Method -
Other 2 Assay -
Other 2 Assay Method -
Other 3 Assay -
Other 3 Assay Method -
Karyotype -
Karyotype Assay -
Remaining Vector Detection -
Remaining Vector Detection Assay -
STR -
HLA -
Stem Cell Transcriptome analysis -
Stem Cell Transcriptome analysis Assay -
Author Name(En) Hideyuki Okano
Author Name(Ja) 岡野 栄之
Author Organization(En) Department of Physiology, Keio University School of Medicine
Author Organization(Ja) 慶應義塾大学 医学部 生理学教室
Author Contact Email hidokano[at]a2[dot]keio[dot]jp
PI Organization(En) Department of Physiology, Keio University School of Medicine
PI Organization(Ja) 慶應義塾大学 医学部 生理学教室
PI Name(En) Hideyuki Okano
PI Name(Ja) 岡野 栄之
PI Contact Email hidokano[at]a2[dot]keio[dot]jp
Availability Information Only
Provider Organization(En) Department of Physiology, Keio University School of Medicine
Provider Organization(Ja) 慶應義塾大学 医学部 生理学教室
Provider Email -
Provider URL -
Ethical Statement(En) -
Ethical Statement(Ja) -
Terms of Use(En) -
Terms of Use(Ja) -
PubMed ID 26905201
DOI 10.1016/j.stemcr.2016.01.010
Title Functional Neurons Generated from T Cell-Derived Induced Pluripotent Stem Cells for Neurological Disease Modeling.
Authors Matsumoto T, Fujimori K, Andoh-Noda T, Ando T, Kuzumaki N, Toyoshima M, Tada H, Imaizumi K, Ishikawa M, Yamaguchi R, Isoda M, Zhou Z, Sato S, Kobayashi T, Ohtaka M, Nishimura K, Kurosawa H, Yoshikawa T, Takahashi T, Nakanishi M, Ohyama M, Hattori N, Akamatsu W, Okano H
Journal Stem Cell Reports
Year 2016
Volume 6
Issue 3
Pages 422-35
URL http://www.ncbi.nlm.nih.gov/pubmed/26905201
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