YH653-MUT-1C8-HET, DYT1-HET-1C8
UCSFi001-A-49
General
Cell Line |
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hPSCreg name | UCSFi001-A-49 |
Cite as: | UCSFi001-A-49 (RRID:CVCL_A8PL) |
Alternative name(s) |
YH653-MUT-1C8-HET, DYT1-HET-1C8
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Cell line type | Human induced pluripotent stem cell (hiPSC) |
Similar lines |
UCSFi001-A-50 (YH653-MUT-H6-HET, DYT1-HET-H6) UCSFi001-A-51 (YH653-MUT-2F2-HOMO, DYT1-HOMO-2F2) UCSFi001-A (wtc11, Wtc11, WTC, WTC11, GM25256) UCSFi001-A-74 (FUS-P525L HET 2D1) UCSFi001-A-75 (FUS-P525L HOM 2D2) UCSFi001-A-72 (FUS-R521G HET 2B10, LSUHSi004-A-72) UCSFi001-A-73 (FUS-R521G HOM 1D9) UCSFi001-A-64 (P633L RBM20 iPSCs) UCSFi001-A-3 (AICS-0016-184) UCSFi001-A-4 (AICS-0075-085) UCSFi001-A-63 (AICS-0082-001) UCSFi001-A-5 (AICS-0011-027) UCSFi001-A-6 (AICS-0013-210) UCSFi001-A-66 (AICS-0114-032) UCSFi001-A-67 (AICS-0114-035) UCSFi001-A-40 (AICS-094-024) UCSFi001-A-7 (AICS-0017-065) UCSFi001-A-41 (AICS-0034-062) UCSFi001-A-8 (AICS-0010-055) UCSFi001-A-9 (AICS-0014-006) UCSFi001-A-10 (AICS-0023-020) UCSFi001-A-11 (AICS-0024-080) UCSFi001-A-12 (AICS-0036-006) UCSFi001-A-13 (AICS-0022-037) UCSFi001-A-14 (AICS-0025-001) UCSFi001-A-15 (AICS-0025-044) UCSFi001-A-16 (AICS-0031-035) UCSFi001-A-17 (AICS-0032-019) UCSFi001-A-55 (AICS-0078-079) UCSFi001-A-18 (AICS-0030-022) UCSFi001-A-69 (AICS-0083-005) UCSFi001-A-56 (AICS-0088-083) UCSFi001-A-19 (AICS-0033-115) UCSFi001-A-70 (AICS-0083-124) UCSFi001-A-57 (AICS-0099-020) UCSFi001-A-20 (AICS-0040-013) UCSFi001-A-21 (AICS-0040-035) UCSFi001-A-22 (AICS-0053-016) UCSFi001-A-23 (AICS-0054-091) UCSFi001-A-24 (AICS-0057-050) UCSFi001-A-25 (AICS-0058-067) UCSFi001-A-26 (AICS-0037-172) UCSFi001-A-27 (AICS-0048-039) UCSFi001-A-39 (AICS-089-061) UCSFi001-A-28 (AICS-0061-036) UCSFi001-A-29 (AICS-0052-003) UCSFi001-A-78 (WTC11-KL-GFP) UCSFi001-A-30 (AICS-0046-051) UCSFi001-A-2 (AICS-0012-105) |
Last update | 13th September 2021 |
User feedback | |
Provider |
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Generator | University of Louisiana at Lafayette (ULL) |
External Databases |
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BioSamples | SAMEA8868384 |
Cellosaurus | CVCL_A8PL |
Wikidata | Q108821427 |
General Information |
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Publications | |
* Is the cell line readily obtainable for third parties? |
No |
Subclone of |
Donor Information
General Donor Information |
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Sex | male |
Ethnicity | Asian |
Phenotype and Disease related information (Donor) |
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Diseases | No disease was diagnosed.
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Family history | N/A |
Is the medical history available upon request? | No |
Is clinical information available? | Limited clinical information - EKG |
Karyotyping (Donor) |
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Has the donor karyotype been analysed? |
Yes
normal karyotype, 46, XY
Karyotyping method:
G-Banding
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Other Genotyping (Donor) |
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Is there genome-wide genotyping or functional data available? |
No
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Donor Relations |
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Other cell lines of this donor | |
External Databases (Donor) |
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BioSamples | SAMEA5843920 |
Ethics
Also have a look at the ethics information for the parental line
UCSFi001-A
.
For generation of the cell line, who was the supplier of any recombined DNA vectors or commercial kits used? |
hIPSC Derivation
General |
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The source cell information can be found in the parental cell line
UCSFi001-A.
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Reprogramming method |
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Vector type | None |
Vector free reprogramming |
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Type of used vector free reprogramming factor(s) |
mRNA
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Other |
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Derived under xeno-free conditions |
Unknown |
Derived under GMP? |
Unknown |
Available as clinical grade? |
No |
Culture Conditions
Surface coating | Matrigel/Geltrex |
Feeder cells |
No |
Passage method |
Enzyme-free cell dissociation
Gentle Cell Dissociation Reagent
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Medium |
mTeSR™ 1
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Has Rock inhibitor (Y27632) been used at passage previously with this cell line? | Yes |
Has Rock inhibitor (Y27632) been used at cryo previously with this cell line? | Yes |
Has Rock inhibitor (Y27632) been used at thaw previously with this cell line? | Yes |
Characterisation
No characterisation data could be found for this subclone. Please open parental cell line UCSFi001-A .Genotyping
Karyotyping (Cell Line) |
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Has the cell line karyotype been analysed? |
Yes
Normal 46, XY
Karyotyping method:
G-Banding
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Other Genotyping (Cell Line) |
Genetic Modification
Disease/phenotype related modifications |
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