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Heritable-disease cells used for various research and medical applications.

Heritable Disease - AcceGen

Cat.#NameDescriptionPrice

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
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