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Heritable Disease - AcceGen
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 |