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Stem Cells
Stem Cells, also calls Progenitor Cells, are a kind of self-replicating pluripotent cells, which can differentiate into multiple functional cells under certain conditions. Given this characteristic, some diseases can be cured by transplanting stem cells or related derivatives into patients to replace damaged cells. Stem cells have become the frontier and hotspot of life science and medical research at the beginning of this century because of the broad application prospects in the fields of disease treatment and regenerative medicine.
AcceGen offers a wide range of high-quality human/animal stem cells, click on the selected item to view the products:
| Cat.# | Name | Description | Price |
|---|---|---|---|
| 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 |
| 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 |
