Cell No. : Cell Name
HPS0177 :
update : 2023/06/07
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Comment | Disease specific iPS cell line derived from a patient : Pompe's disease. HPS0175 and HPS0176 were derived from the same patient. iPS cells were created using the Sendai virus vector. Cryopreserved by vitrification method. |
Comment from the depositor | |
Terms and conditions | 1) The iPS cells created using the Sendai virus vector are now available must be observed when using SeV-iPS cells. 2) In relation to the for-profit organizations, please contact iPS Academia Japan, Inc., prior to the utilization of iPS cells. 3) The RECIPIENT of BIOLOGICAL RESOURCE shall obtain a prior written consent on use of it from the APPROVER. 4) Contact Us : RIKEN Cell Bank |
Remarks | |
Order Form |
Order Form(C-0042.pdf)
 
Approval Form(C-0057.pdf)
 
MTA(C-0007.pdf)
 
MTA(C-0007p.pdf)
 
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Regarding MTA between user institutions and RIKEN BRC, there are two kinds of MTA, not-for-profit academic purpose (C-XXXX) and for-profit research purpose (C-XXXXp) , depending on the sort of user institutions and the purposes of use. Please use an appropriate MTA(to see). In relation to commercial use and use for patent filing, first of all Please contact RIKEN BRC (cellbank.brc@riken.jp).
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Basic information
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Animal |
_human
< Mammals
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Genus |
Homo
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Species |
sapiens
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Race |
Japanese
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Gender |
Female
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Age at sampling |
1-9 years
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Tissue |
skin
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Disease name |
Glycogen storage disease
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Classification |
iPS
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Recombinant |
recombinant
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Exogene |
SeV18+HS-OCT3/4/TSΔF, SeV18+HS-SOX2/TSΔF, SeV18+HS-KLF4/TSΔF, SeV18(HNL)c-MYCQC/TSΔF
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Lifespan |
infinite
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Morphology |
ES-like
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Cellosaurus(Expasy) |
CVCL_T934
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deposit info |
lot info |
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Medium |
Medium List |
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Culture type |
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Adherent cells
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Culture medium |
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DMEM/HamF12 (2mM L-Glutamine) + 20% KSR + 0.1mM NEAA + 0.1mM 2-Mercaptoethanol + 5ng/ml human basic FGF
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Antibiotics |
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Free
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Passage method |
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0.25% Trypsin + 0.1% collagenase type IV + 20% KSR + 1mM CaCl2 + PBS(-)
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Coating dish |
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0.1% gelatin coated dish
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Culture information
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Passage ratio |
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1 : 3-5 split
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SC frequency |
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Subculture : once/4-6 days, Medium Renewal : every day
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Temperature |
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37
℃
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CO2 concentration |
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3
%
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Feeder cells |
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MEF
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Feeder treatment |
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X-rays 5000R (or MMC)
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Feeder seed cells |
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3-5 x 10 5 cells/60 mm dish
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Freeze medium |
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DAP213 : Medium + 2M DMSO + 1M Acetamide + 3M Propyleneglycol
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Freezing method |
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Vitrification
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Mycoplasma/Acholeplasma |
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(-)
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STR(human) |
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OK
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Images |
deposit info | lot info |
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Relational File |
deposit info | lot info |
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Reference information |
Reference |
0
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User's Publication |
2
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User's Publication |
14036
Sato Y, Kobayashi H, Higuchi T, Shimada Y, Ida H, Ohashi T.
TFEB overexpression promotes glycogen clearance of Pompe disease iPSC-derived skeletal muscle
Mol Ther Methods Clin Dev
2016
3:16054
PubMed ID: 27556060
DOI: 10.1038/mtm.2016.54
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7266
Sato Y, Kobayashi H, Higuchi T, Shimada Y, Era T, Kimura S, Eto Y, Ida H, Ohashi T.
Disease modeling and lentiviral gene transfer in patient-specific induced pluripotent stem cells from late-onset Pompe disease patient.
Mol Ther Methods Clin Dev
2015
2:15023
PubMed ID: 26199952
DOI: 10.1038/mtm.2015.23
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