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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
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