Home > Products > Induced Pluripotent Stem Cells (iPSCs) >
Induced Pluripotent Stem Cells (iPSCs)
Human iPSCs
Animal iPSCs
Induced Pluripotent Stem Cells (iPSCs) have the same differentiation potential as embryonic stem cells, however, hiPSCs are obtained from human cells, which means they have a sufficient source of cells without any ethical problems, what’s more, hiPSCs can be produced by the patient’s own cells to reduce immune rejection.
iPSCs technology is much simpler and more efficient than other reprogramming techniques, such as somatic cell nuclear transfer or cell fusion. Since the birth of iPSCs technology, the selection of reprogramming factors, the introduction of reprogramming factors and the extensive research on cell culture conditions have made the establishment and cultivation system more perfect.
AcceGen induced Pluripotent Stem Cells use advanced reprogramming technology to provide researchers with safe and stable cell products.
| Cat.# | Name | Description | Price |
|---|---|---|---|
| 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 |
| ABC-SC2051 | HighQC™ Human IPSC From B-Lymphocyte-Personal Genome Project | Personal Genome Project; Subcollection: Apparently Healthy Collection Apparently healthy iPSCs PIGI ...more | +inquiry |
