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Cat.# | Name | Description | Price |
---|---|---|---|
ABC-SC2068 |
HighQC™ Human IPSC From B-Lymphocyte-Ceroid Lipofuscinosis(Neuronal 2-Late Infantile Type) |
Ceroid Lipofuscinosis(Neuronal 2-Late Infantile Type); CLN2 CLN2 GENE; CLN2; Subcollection: Heritabl...more | +inquiry |
ABC-SC2066 |
HighQC™ Human IPSC From Fibroblast-Phenylketonuria |
Phenylketonuria; Subcollection: Heritable Diseases; Affected: YES; Cells are only guaranteed with pu...more | +inquiry |
ABC-SC2065 |
HighQC™ Human IPSC From Fibroblast-Hutchinson-Gilford Progeria Syndrome |
Hutchinson-Gilford Progeria Syndrome; HGPS; Subcollection: Heritable Diseases; Affected: YES; Cells ...more | +inquiry |
ABC-SC2064 |
HighQC™ Human IPSC From Fibroblast-Congenital Disorder Of Deglycosylation |
Congenital Disorder Of Deglycosylation; CDDG N-GLYCANASE 1; NGLY1 MALIGNANT HYPERTHERMIA SUSCEPTIBIL...more | +inquiry |
ABC-SC2063 |
HighQC™ Human IPSC From Fibroblast-Wolman Disease |
Wolman Disease; Subcollection: Heritable Diseases; Affected: YES; Cells are only guaranteed with pur...more | +inquiry |
ABC-SC2062 |
HighQC™ Human IPSC From Fibroblast-Pitt-Hopkins Syndrome |
Pitt-Hopkins Syndrome; PTHS TRANSCRIPTION FACTOR 4; TCF4; Subcollection: Heritable Diseases PIGI Con...more | +inquiry |
ABC-SC2059 |
HighQC™ Human IPSC From Fibroblast-Werner Syndrome |
Werner Syndrome; WRN REPLICATION FOCUS-FORMING ACTIVITY 1, INCLUDED; FFA1, INCLUDED LAMIN A/C; LMNA ...more | +inquiry |
ABC-SC2058 |
HighQC™ Human IPSC From Fibroblast-Choroideremia |
Choroideremia; CHM CHM GENE; CHM; Subcollection: Heritable Diseases PIGI Consented Sample; Affected:...more | +inquiry |
ABC-SC2057 |
HighQC™ Human IPSC From Fibroblast-Lesch-Nyhan Syndrome |
Lesch-Nyhan Syndrome; LNS HYPOXANTHINE GUANINE PHOSPHORIBOSYLTRANSFERASE 1; HPRT1; HPRT; Subcollecti...more | +inquiry |
ABC-SC2056 |
HighQC™ Human IPSC From Fibroblast-Huntington Disease |
Huntington Disease; HD; Subcollection: Heritable Diseases; Affected: YES; Cells are only guaranteed ...more | +inquiry |
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-SC2050 |
HighQC™ Human IPSC From Fibroblast-Alzheimer Disease |
Alzheimer Disease; AD; Subcollection: Heritable Diseases; Affected: YES; Cells are only guaranteed w...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-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 |