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Human - AcceGen
Cat.# | Name | Description | Price |
---|---|---|---|
ABC-SC2082 |
HighQC™ Human IPSC From Corneal Epithelial Cells-Control |
Cell Type iPSC Primary Tissue Corneal epithelial cells Reprogramming Method Episomal Plasmid; Cells ...more | +inquiry |
ABC-SC2081 |
HighQC™ Human IPSC From PBMC-Crohn’s Disease |
Cell Type: iPSC; Primary Tissue: PBMC; Reprogramming Method: Episomal Plasmid ; Disease: Crohn’s Dis...more | +inquiry |
ABC-SC2079 |
HighQC™ Human IPSC From Fibroblast-Skeletal Displasia |
Cell Type: iPSC; Primary Tissue: Fibroblast; Reprogramming Method: Episomal Plasmid; Disease: Skelet...more | +inquiry |
ABC-SC2078 |
HighQC™ Human IPSC From LCL-Spondylometaphyseal Displasia, Kozlowski Type |
Cell Type: iPSC; Primary Tissue: LCL; Reprogramming Method: Episomal Plasmid; Disease: Spondylometap...more | +inquiry |
ABC-SC2076 |
HighQC™ Human IPSC From Fibroblast-Charcot-Marie-Tooth Syndrome |
Cell Type: iPSC; Primary Tissue: Fibroblast; Reprogramming Method: Episomal Plasmid; Disease: Charco...more | +inquiry |
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-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 |