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Crohn’s Disease - AcceGen
| Cat.# | Name | Description | Price |
|---|---|---|---|
| ABC-SC2075 | HighQC™ Human IPSC From Fibroblast-Familial Alzheimer’s Disease | Cell Type: iPSC; Primary Tissue: Fibroblast; Reprogramming Method: Episomal Plasmid; Disease: Famili...more | +inquiry |
| ABC-SC2073 | HighQC™ Human IPSC From PBMC-ALS | Cell Type: iPSC; Primary Tissue: PBMC; Disease: Amyotrophic Lateral Sclerosis(ALS); Cells are only g...more | +inquiry |
| ABC-SC2072 | HighQC™ Human IPSC From Fibroblast-Monocarboxylate Transporter 9-Specific Thyroid Hormone Cell Transporter Deficiency | Cell Type: iPSC; Primary Tissue: Fibroblast; Reprogramming Method: Episomal Plasmid; Disease: Monoca...more | +inquiry |
| ABC-SC2071 | HighQC™ Human IPSC From Fibroblast-Monocarboxylate Transporter 8-Specific Thyroid Hormone Cell Transporter Deficiency | Cell Type: iPSC; Primary Tissue: Fibroblast; Reprogramming Method: Episomal Plasmid; Disease: Monoca...more | +inquiry |
| ABC-SC2070 | HighQC™ Human IPSC From PBMC-Control | Cell Type: iPSC; Primary Tissue: PBMC Reprogramming Method: Episomal Plasmid; Disease: Control; Cell...more | +inquiry |
| ABC-SC2069 | HighQC™ Human IPSC From B-Lymphocyte-Apparently Healthy Individual | Apparently Healthy Individual; Subcollection: Apparently healthy iPSCs Apparently Healthy Collection...more | +inquiry |
| 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 |
