logo
News

iPSC Cell Bank (Cell line list)

 

We Offer iPSCs to You
 

(1) iPSC Consortium offers research-grade normal and disease human-derived iPSCs for general public and commercial industries. All available cell lines are listed below.
(2) For more information of each specific cell lines/clones (e.g. characterization results, suggested culture methods, etc.), please click corresponding purchase links on the right column of the table below.
(3) We also provide donor-customized iPSC generation service. Please refer to Service iPSC-1 and iPSC-2 in Service Item and Charge
(4) Our cell bank is also included and ranked fifth in the Stemcell Knowledge & Information Portal (SKIP) created by Dr. Wataru Fujibuchi’s group (CiRA, University of Kyoto). SKIP is a stem cell information database that provides access to cell banks worldwide and information of stem cell-related researches. For further information, please click on the following link:
https://skip.stemcellinformatics.org/en/

Donor Status

Donor Status in Chinese

iPSC Clone Number

Note

Gender

Age

Donor Cells

Mutations

Purchase Links

Purchase Links

Feeder-Dependent

Feeder-Free

Normal Lines

無已知疾病之健康捐贈者

IBMS-iPSC-001-02

---

F

33

PBMCs

---

Click

Click

IBMS-iPSC-002-07

---

M

22

PBMCs

---

Click

Click

IBMC-iPSC-003-06

---

F

31

PBMCs

---

Click

Click

IBMS-iPSC-004-02

---

M

32

PBMCs

---

Click

Click

NTUH-iPSC-001-05

---

F

45

PBMCs

---

Click

Click

NTUH-iPSC-002-02

---

M

52

PBMCs

---

Click

Click

TVGH-iPSC-001-04

---

F

25

PBMCs

---

Click

Click

TVGH-iPSC-002-07

---

M

26

PBMCs

---

Click

Click

FIRDI-iPSC-002-30

---

M

39

PBMCs

---

Click

Click

NHRI-iPSC-001-01

---

M

27

PBMCs

---

Click

Click

Polycystic Kidney Disease (PKD)

多囊性腎臟病

IBMS-iPSC-012-012

---

M

35

PBMCs

Chr16: 2160801_2delTC (p.Ser1457fs)

Click

Click

IBMS-iPSC-013-07

---

M

36

PBMCs

Not sent for mutation sequencing (shared same patient origin with IBMS-iPSC-013-06)

Click

Click

IBMS-iPSC-014-05

---

F

63

PBMCs

 PKD2/R803X, Chr4: 88989098 C>T

Click

Click

Atrial Fibrillation (AF)

心房顫動

IBMS-iPSC-015-06

---

M

53

PBMCs

---

---

Click

IBMS-iPSC-016-06

---

M

34

PBMCs

---

---

Click

IBMS-iPSC-017-02

---

F

32

PBMCs

---

---

Click

Parkinson's Disease (PD)

帕金森氏症

IBMS-iPSC-018-09

---

M

44

PBMCs

LRRK2 p. G2385R rs34778348 /chromosome 12q12

---

Click

IBMS-iPSC-019-11

---

F

67

PBMCs

Heterozygous LRRK2 p. I2012T rs34015634  /chromosome 12q12

Click

Click

IBMS-iPSC-020-01

---

M

53

PBMCs

LRRK2 p. G2385R rs34778348 /chromosome 12q12

Click

Click

IBMS-iPSC-042-01

---

F

60

PBMCs

LRRK2  p. I1371V

---

Click

IBMS-iPSC-043-05

---

F

32

PBMCs

PLA2G6 C.G991T (p. D331Y)

---

Click

ALDH2 mutation

乙醛脫氫酶突變

IBMS-iPSC-021-04

---

M

47

PBMCs

 ALDH2 rs671 G>A p.Glu504Lys

 ---

Click

IBMS-iPSC-022-01

---

M

57

PBMCs

 ALDH2 rs671 G>A p.Glu504Lys

 ---

Click

IBMS-iPSC-023-03

---

F

74

PBMCs

 ALDH2 rs671 G>A p.Glu504Lys

 ---

Click

Fabry Disease

法布瑞氏症

IBMS-iPSC-024-03

---

M

28

PBMCs

p. E398DfsX6

---

Click

IBMS-iPSC-025-03

---

M

66

PBMCs

IVS4+919G>A

Click

Click

IBMS-iPSC-026-02

---

M

67

PBMCs

IVS4+919G>A

---

Click

Aromatic L-Amino Acid Decarboxylase Deficiency (AADC)

芳香族L-胺基酸類脫羧基酶缺乏症

IBMS-iPSC-027-01

---

M

11

PBMCs

IVS6+4/IVS6+4

---

Click

IBMS-iPSC-028-01

---

M

41

PBMCs

IVS6+4/WT

---

Click

IBMS-iPSC-029-01

---

F

10

PBMCs

IVS6+4/IVS6+4

Click

Click

Mitochondrial DNA mutation

粒線體DNA突變

IBMS-iPSC-030-06

Sensorineural Hearing Loss

F

39

PBMCs

MTRNR1, mtDNA1555A>G (A: 15.3%, G: 84.7%)

Click

Click

IBMS-iPSC-031-05

Deafness

F

40

Fibroblasts

 A8344G mutation in the mitochondrial tRNALys gene (A: 70.2%, G: 29.8%)

Click

Click

 TVGH-iPSC-025-06

---

M

28

Fibroblasts

A3243G transition in mitochondrial DNA

---

Click

 TVGH-iPSC-026-11

---

M

32

Fibroblasts

A3243G transition in mitochondrial DNA

---

Click

Sialidosis Disease

涎酸酵素缺乏症

IBMS-iPSC-033-02

---

F

16

PBMCs

NEU1/chromosome 6p21.33, A544G mutation (Exon3 p.Ser182Gly) and 667-679 deletion (Exon4)

Click

Click

Short QT syndrome (SQTS)

QT综合症

IBMS-iPSC-044-05

---

F

65

PBMCs

SCN3A

---

Click

IBMS-iPSC-045-02

---

M

81

PBMCs

DSP g. Chr6: 7585411G>A | c. 7916G>A | p. R2639Q

---

Click

Huntington's Disease (HD)

亨丁頓舞蹈症

IBMS-iPSC-053-02

---

F

60

PBMCs

---

---

Click

IBMS-iPSC-053-05

---

F

60

PBMCs

---

---

Click

Premature Ovarian Failure (POF)

卵巢早衰症

NTUH-iPSC-003-40

Turner syndrome

F

32

PBMCs

---

---

Click

NTUH-iPSC-004-06

Turner syndrome

F

34

PBMCs

---

---

Click

NTUH-iPSC-005-02

---

F

33

PBMCs

---

---

Click

Familial Amyloid Neuropathy (FAP)

家族性類澱粉多發性神經病變

NTUH-iPSC-007-03

---

M

64

PBMCs

---

---

Click

NTUH-iPSC-008-11

---

M

61

PBMCs

---

---

Click

NTUH-iPSC-009-07

---

F

77

PBMCs

---

---

Click

Type 1 Diabetes

1型糖尿病

NTUH-iPSC-010-06

---

F

33

PBMCs

---

---

Click

NTUH-iPSC-011-05

---

F

51

PBMCs

---

---

Click

NTUH-iPSC-012-04

---

M

26

PBMCs

---

---

Click

Prader-Willi Syndrome (PWS)

普瑞德威利症候群 (小胖威利)

NTUH-iPSC-013-01

---

F

11

PBMCs

---

---

Click

NTUH-iPSC-014-01

---

F

5

PBMCs

---

---

Click

Spinocerebellar Ataxia (SCA)

脊髓小腦萎縮症

TVGH-iPSC-003-12

SCA3

M

37

PBMCs

---

---

Click

TVGH-iPSC-004-13

SCA36

F

58

PBMCs

---

---

Click

TVGH-iPSC-005-05

SCA36

M

64

PBMCs

---

---

Click

IBMS-iPSC-046-06

SCA22

F

62

PBMCs

c. 679_681delTTC

---

Click

IBMS-iPSC-047-03

SCA22

F

52

PBMCs

c. 679_681delTTC

---

Click

IBMS-iPSC-050-04

SCA3

F

46

PBMCs

---

---

Click

IBMS-iPSC-050-05

SCA3

F

46

PBMCs

---

---

Click

IBMS-iPSC-051-02

SCA2

F

47

PBMCs

---

---

Click

IBMS-iPSC-051-05

SCA2

F

47

PBMCs

---

---

Click

IBMS-iPSC-052-01

SCA2

M

61

PBMCs

---

---

Click

Leber's Hereditary Optic Neuropathy (LHON)

雷伯氏遺傳性視神經病變

TVGH-iPSC-006-06

---

M

47

PBMCs

---

---

Click

TVGH-iPSC-007-08

---

F

42

PBMCs

---

---

Click

TVGH-iPSC-010-09

---

F

61

PBMCs

Mitochondrial MT-ND4 gene/m.11778G > A (A:95.71%, G:4.29%)

---

Click

Juvenile Macular Degeneration (JMD)

青少年黄斑部病變

TVGH-iPSC-012-04

Best Dystrophy

M

11

PBMCs

(BEST1 (VMD2)) 11q12.3

---

Click

TVGH-iPSC-013-05

X-linked Juvenile Retinoschisis

M

16

PBMCs

g.488G>A mutation of RS1 gene, p.W163X

---

Click

TVGH-iPSC-014-05

---

M

13

PBMCs

---

---

Click

Facioscapulohumeral Muscular Dystrophy (FSHD)

顏面肩胛肱骨型肌肉失養症

TVGH-iPSC-019-07

---

M

21

PBMCs

---

---

Click

TVGH-iPSC-020-10

---

M

55

PBMCs

---

---

Click

TVGH-iPSC-024-42

---

M

22

PBMCs

---

---

Click

Monogenic Diabetes

單基因糖尿病

TVGH-iPSC-015-16

---

M

13

PBMCs

---

---

Click

TVGH-iPSC-016-01

---

M

11

PBMCs

---

---

Click

TVGH-iPSC-017-08

---

F

14

PBMCs

---

---

Click

Frontotemporal Dementia (FTD)

額顳葉型失智症

TVGH-iPSC-021-10

---

F

64

PBMCs

---

---

Click

TVGH-iPSC-022-04

---

F

57

PBMCs

---

---

Click

TVGH-iPSC-023-02

---

F

54

PBMCs

---

---

Click

Schizophrenia

思覺失調症

NHRI-iPSC-003-04

---

M

64

PBMCs

---

---

Click

NHRI-iPSC-004-03

---

F

61

PBMCs

---

---

Click

NHRI-iPSC-005-01

---

F

42

PBMCs

---

---

Click

NHRI-iPSC-006-01

---

F

57

PBMCs

---

---

Click

NHRI-iPSC-007-01

---

M

25

PBMCs

---

---

Click

NHRI-iPSC-008-01

---

M

25

PBMCs

---

---

Click

Bardet-Biedl Syndrome

巴德-畢德氏症候群

IBMS-iPSC-063-06

---

M

37

PBMCs

C534+1G>T

---

Click

Motor Neuron Disease (ALS)

運動神經元疾病(漸凍症)

IBMS-iPSC-068-02

---

M

53

PBMCs

---

---

Click

IBMS-iPSC-069-05

---

M

75

PBMCs

---

---

Click

Copyright ©2015 All rights reserved. NCFB