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Human - AcceGen
| Cat.# | Name | Description | Price |
|---|---|---|---|
|
ABC-SC2055 |
HighQC™ Human IPSC From Fibroblast-Tuberous Sclerosis 2 |
Tuberous Sclerosis 2; TSC2 TSC2 GENE; TSC2; Subcollection: Heritable Diseases; Affected: YES; Cells ...more | +inquiry |
|
ABC-SC2054 |
HighQC™ Human IPSC From Fibroblast-Long QT Syndrome 3 |
Long QT Syndrome 3; LQT3 SODIUM CHANNEL, VOLTAGE-GATED, TYPE V, ALPHA SUBUNIT; SCN5A; Subcollection:...more | +inquiry |
|
ABC-SC2053 |
HighQC™ Human IPSC From Fibroblast-Long QT Syndrome 2 |
Long QT Syndrome 2; LQT2 POTASSIUM CHANNEL, VOLTAGE-GATED, SUBFAMILY H, MEMBER 2; KCNH2; Subcollecti...more | +inquiry |
|
ABC-SC2052 |
HighQC™ Human IPSC From Fibroblast-Krabbe Disease-Galactosylceramidase |
Krabbe Disease, Galactosylceramidase; GALC; Subcollection: Heritable Diseases Lysosomal Storage Dise...more | +inquiry |
|
ABC-SC2051 |
HighQC™ Human IPSC From B-Lymphocyte-Personal Genome Project |
Personal Genome Project; Subcollection: Apparently Healthy Collection Apparently healthy iPSCs PIGI ...more | +inquiry |
|
ABC-SC2050 |
HighQC™ Human IPSC From Fibroblast-Alzheimer Disease |
Alzheimer Disease; AD; Subcollection: Heritable Diseases; Affected: YES; Cells are only guaranteed w...more | +inquiry |
|
ABC-SC2048 |
HighQC™ Human IPSC From Fibroblast-Dystrophia Myotonica 1 |
Dystrophia Myotonica 1; DM1; Subcollection: Heritable Diseases Muscular Dystrophies; Affected: YES; ...more | +inquiry |
|
ABC-SC2044 |
HighQC™ Human IPSC From Fibroblast-Spinal Muscular Atrophy, TYPE II |
Spinal Muscular Atrophy, TYPE II; SMA2; Subcollection: Heritable Diseases ; Affected: YES; Cells are...more | +inquiry |
|
ABC-SC2042 |
HighQC™ Human IPSC From Fibroblast-Apparently Healthy Individual |
Apparently Healthy Individual; Subcollection: Apparently healthy iPSCs Apparently Healthy Collection...more | +inquiry |
|
ABC-SC2041 |
HighQC™ Human IPSC From Fibroblast-Diabetes Mellitus, Juvenile-Onset RI-Dependent |
Diabetes Mellitus, Juvenile-Onset RI-Dependent; IDDM; Subcollection: Heritable Diseases; Affected: Y...more | +inquiry |
|
ABC-SC2040 |
HighQC™ Human IPSC From Fibroblast-Epidermolysis Bullosa: Dystrophic, Junctional, Or Simplex Types |
Epidermolysis Bullosa: Dystrophic, Junctional, Or Simplex Types; Subcollection: Heritable Diseases; ...more | +inquiry |
|
ABC-SC2039 |
HighQC™ Human IPSC From Fibroblast-Kearns-Sayre Syndrome |
Kearns-Sayre Syndrome; KSS; Subcollection: Heritable Diseases; Affected: YES; Cells are only guarant...more | +inquiry |
|
ABC-SC2038 |
HighQC™ Human IPSC From Fibroblast-Niemann-Pick Disease, Type C1 |
Niemann-Pick Disease, Type C1; NPC1 NPC1 GENE; NPC1; Subcollection: Heritable Diseases Lysosomal Sto...more | +inquiry |
|
ABC-SC2037 |
HighQC™ Human IPSC From Fibroblast(Niemann-Pick Disease, Type A |
Human IPSC From Fibroblast-Niemann-Pick Disease, Type A Sphingomyelin Phosphodiesterase 1, Acid Lyso...more | +inquiry |
|
ABC-SC2036 |
HighQC™ Human IPSC From B-Lymphocyte(Facioscapulohumeral Muscular Dystrophy 1) |
Facioscapulohumeral Muscular Dystrophy 1; FSHD1; Subcollection: Heritable Diseases Muscular Dystroph...more | +inquiry |
|
ABC-SC2035 |
HighQC™ Human IPSC From Fibroblast-Vici Syndrome |
Vici Syndrome; VICIS ECTOPIC P-GRANULES AUTOPHAGY PROTEIN 5, C. ELEGANS, HOMOLOG OF; EPG5; Subcollec...more | +inquiry |
|
ABC-SC2034 |
HighQC™ Human IPSC From Fibroblast-Muscular Dystrophy, Duchenne Type |
Muscular Dystrophy, Duchenne Type; DMD DYSTROPHIN; DMD; Subcollection: Heritable Diseases Muscular D...more | +inquiry |
|
ABC-SC2033 |
HighQC™ Human IPSC From Fibroblast(Mucopolysaccharidosis Type IIIA N-Sulfoglucosamine Sulfohydrolase) |
Mucopolysaccharidosis Type IIIA N-Sulfoglucosamine Sulfohydrolase; SGSH; Subcollection: Heritable Di...more | +inquiry |
|
ABC-SC2029 |
HighQC™ Human IPSC From Fibroblast-Miller-Dieker Lissencephaly Syndrome |
Miller-Dieker Lissencephaly Syndrome; MDLS; Subcollection: Heritable Diseases Chromosome Abnormaliti...more | +inquiry |
|
ABC-TC5593 |
JY |
This cell line is an Epstein-Barr Virus (EBV) transformed lymphoblastoid line and is part of the Hum...more | +inquiry |
