HighQC™ Human IPSC From Fibroblast-Wolman Disease
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quantity
Produktdetaljer
Katalognummer: 870 - ABC-SC2063
Produktkategori: Företag och industri > Vetenskap och laboratorium
Gentaur
Storlek: 1 vial
ABC-SC2063
HighQC™ Human IPSC From Fibroblast-Wolman Disease
Wolman Disease; Subcollection: Heritable Diseases; Affected: YES; Cells are only guaranteed with purchase of Gentaur Media and Gentaur Extra Cellular Matrix for appropriate cell culture, for 30 days from the date of shipment.
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ABC-SC2050
HighQC™ Human IPSC From Fibroblast-Alzheimer Disease
Alzheimer Disease; AD; Subcollection: Heritable Diseases; Affected: YES; Cells are only guaranteed with purchase of Gentaur Media and Gentaur Extra Cellular Matrix for appropriate cell culture, for 30 days from the date of shipment.
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ABC-SC2056
HighQC™ Human IPSC From Fibroblast-Huntington Disease
Huntington Disease; HD; Subcollection: Heritable Diseases; Affected: YES; Cells are only guaranteed with purchase of Gentaur Media and Gentaur Extra Cellular Matrix for appropriate cell culture, for 30 days from the date of shipment.
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ABC-SC0015T
HighQC™ Human IPSC From Foreskin Fibroblast (Skin Fibroblasts Of A Cystinosis Patient)
iPSC (induced Pluripotent Stem cells) reprogrammed from human Skin Fibroblasts of a Cystinosis patient.This iPS cell line was created using a normal human skin fibroblast from a male patient suffering from Cystinosis. The iPS cell line was generated using an episomal reprogramming containing a prprietary mix of vectors, containing Oct-4, Sox-2, Klf-4 along with p53 Anti-sense, EBNA-1.The cell line was validated for pluripotency based on colony morphology, alkaline phosphatase expression, and expression of SSEA-4.iPS colonies exhibit classical morphology and growth.Absence of Mycoplasma was confirmed.The cell line is shipped on dry ice.
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ABC-SC0016T
HighQC™ Human IPSC From Foreskin Fibroblast (Fibroblasts Of A Cystic Fibrosis Patient)
iPSC (induced Pluripotent Stem cells) reprogrammed from human Fibroblasts of a cystic fibrosis patient.This iPS cell line was created using a normal human fibroblast of a male adult patient suffering from Cystic Fibrosis. The iPS cell line was generated using an episomal reprogramming containing a prprietary mix of vectors, containing Oct-4, Sox-2, Klf-4 along with p53 Anti-sense, EBNA-1.The cell line was validated for pluripotency based on colony morphology, alkaline phosphatase expression, and expression of SSEA-4.iPS colonies exhibit classical morphology and growth.Absence of Mycoplasma was confirmed.The cell line is shipped on dry ice.
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ABC-SC2040
HighQC™ Human IPSC From Fibroblast-Epidermolysis Bullosa: Dystrophic, Junctional, Or Simplex Types
Epidermolysis Bullosa: Dystrophic, Junctional, Or Simplex Types; Subcollection: Heritable Diseases; Affected: YES; Cells are only guaranteed with purchase of Gentaur Media and Gentaur Extra Cellular Matrix for appropriate cell culture, for 30 days from the date of shipment.