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Crohn’s Disease - AcceGen
| Cat.# | Name | Description | Price |
|---|---|---|---|
| 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-TC5598 | ATDC5 | ATDC5 cells are derived from mouse teratocarcinoma and possess chondrogenic potential, meaning they ...more | +inquiry |
| ABC-TC5597 | NB2a | Mouse cell line derived from neuroblastoma ...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 |
| ABC-TC5592 | TR146 | TR146 was derived from the neck node of a 67 year-old female (primary tumour was sited in buccal muc...more | +inquiry |
| ABC-TC5591 | OE19 | The cell line OE19, also known as JROECL19, was established in 1993 from an adenocarcinoma of gastri...more | +inquiry |
