HighQC™ Human IPSC From Fibroblast-Werner Syndrome
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quantity
Produktdetaljer
Katalognummer: 870 - ABC-SC2059
Produktkategori: Företag och industri > Vetenskap och laboratorium
Gentaur
Storlek: 1 vial
ABC-SC2059
HighQC™ Human IPSC From Fibroblast-Werner Syndrome
Werner Syndrome; WRN REPLICATION FOCUS-FORMING ACTIVITY 1, INCLUDED; FFA1, INCLUDEDLAMIN A/C; LMNAIPSC; 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-SC2035
HighQC™ Human IPSC From Fibroblast-Vici Syndrome
Vici Syndrome; VICIS ECTOPIC P-GRANULES AUTOPHAGY PROTEIN 5, C. ELEGANS, HOMOLOG OF; EPG5; Subcollection: Heritable DiseasesPIGI Consented Sample; 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-SC2039
HighQC™ Human IPSC From Fibroblast-Kearns-Sayre Syndrome
Kearns-Sayre Syndrome; KSS; 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-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.
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BR1001
Human Foreskin Fibroblast iPSC Expansion Bundle
Cryopreserved vial of human foreskin fibroblast iPS cells containing ≥ 500,000 cells and companion iPS Cell Growth Media Kit