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Showing 34 of 34 products
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HighQC™ Human IPSC From Fibroblast-Kearns-Sayre SyndromeABC-SC2039HighQC™ Human IPSC From Fibroblast-Kearns-Sayre Syndrome
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Human iPSC From Blood-Helsmoortel-Van Der Aa SyndromeABC-SC130GHuman iPSC From Blood-Helsmoortel-Van Der Aa Syndrome
1 Vial
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Human iPSC From Fibroblast-Rett Syndrome, Congenital VariantABC-SC138GHuman iPSC From Fibroblast-Rett Syndrome, Congenital Variant
1 Vial
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Human iPSC From Fibroblast-Rett SyndromeABC-SC161GHuman iPSC From Fibroblast-Rett Syndrome
1 Vial
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HighQC™ Human IPSC From Fibroblast-Hutchinson-Gilford Progeria SyndromeABC-SC2065HighQC™ Human IPSC From Fibroblast-Hutchinson-Gilford Progeria Syndrome
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HighQC™ Human IPSC From Fibroblast-Long QT Syndrome 2ABC-SC2053HighQC™ Human IPSC From Fibroblast-Long QT Syndrome 2
1 Vial
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Human iPSC From Fibroblast-Alagille Syndrome 1ABC-SC146GHuman iPSC From Fibroblast-Alagille Syndrome 1
1 Vial
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Human iPSC From Blood-Cerebral Creatine Deficiency Syndrome 2ABC-SC148GHuman iPSC From Blood-Cerebral Creatine Deficiency Syndrome 2
1 Vial
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HighQC™ Human IPSC From Fibroblast-Long QT Syndrome 3ABC-SC2054HighQC™ Human IPSC From Fibroblast-Long QT Syndrome 3
1 Vial
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HighQC™ Human IPSC From Fibroblast-Miller-Dieker Lissencephaly SyndromeABC-SC2029HighQC™ Human IPSC From Fibroblast-Miller-Dieker Lissencephaly Syndrome
1 Vial
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Human iPSC From Fibroblast-Isogenic Control GLUT1 Deficiency Syndrome 1ABC-SC124GHuman iPSC From Fibroblast-Isogenic Control GLUT1 Deficiency Syndrome 1
1 Vial
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Human iPSC From Blood-Isogenic Control, Nescav SyndromeABC-SC147GHuman iPSC From Blood-Isogenic Control, Nescav Syndrome
1 Vial
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Human iPSC From Blood-Multicentric Carpotarsal Osteolysis SyndromeABC-SC159GHuman iPSC From Blood-Multicentric Carpotarsal Osteolysis Syndrome
1 Vial
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HighQC™ Human IPSC From Fibroblast-Charcot-Marie-Tooth SyndromeABC-SC2076HighQC™ Human IPSC From Fibroblast-Charcot-Marie-Tooth Syndrome
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Human iPSC From Blood-Chromosome XP11.3 Deletion SyndromeABC-SC120GHuman iPSC From Blood-Chromosome XP11.3 Deletion Syndrome
1 Vial
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Human iPSC From Blood-Nescav SyndromeABC-SC132GHuman iPSC From Blood-Nescav Syndrome
1 Vial
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Human iPSC From Fibroblast-Isogenic Control, Vici SyndromeABC-SC141GHuman iPSC From Fibroblast-Isogenic Control, Vici Syndrome
1 Vial
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Human iPSC From Fibroblast-Leigh SyndromeABC-SC152GHuman iPSC From Fibroblast-Leigh Syndrome
1 Vial
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Human iPSC From Fibroblast-Miller-Dieker Lissencephaly SyndromeABC-SC155GHuman iPSC From Fibroblast-Miller-Dieker Lissencephaly Syndrome
1 Vial
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Human iPSC From Fibroblast-GLUT1 Deficiency Syndrome 1ABC-SC156GHuman iPSC From Fibroblast-GLUT1 Deficiency Syndrome 1
1 Vial
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HighQC™ Human IPSC From Fibroblast-Werner SyndromeABC-SC2059HighQC™ Human IPSC From Fibroblast-Werner Syndrome
1 Vial
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HighQC™ Human IPSC From Fibroblast-Lesch-Nyhan SyndromeABC-SC2057HighQC™ Human IPSC From Fibroblast-Lesch-Nyhan Syndrome
1 Vial
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Human iPSC From Fibroblast-Long QT Syndrome 3ABC-SC140GHuman iPSC From Fibroblast-Long QT Syndrome 3
1 Vial
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Human iPSC From Blood-Cerebral Creatine Deficiency Syndrome 3ABC-SC170GHuman iPSC From Blood-Cerebral Creatine Deficiency Syndrome 3
1 Vial
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Human iPSC From Fibroblast-Isogenic Control, Long QT Syndrome 2ABC-SC173GHuman iPSC From Fibroblast-Isogenic Control, Long QT Syndrome 2
1 Vial
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Human iPSC From Fibroblast-Scheie SyndromeABC-SC182GHuman iPSC From Fibroblast-Scheie Syndrome
1 Vial
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Human iPSC From Fibroblast-Isogenic Control, Rett Syndrome, Congenital VariantABC-SC127GHuman iPSC From Fibroblast-Isogenic Control, Rett Syndrome, Congenital Variant
1 Vial
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Human iPSC From Fibroblast-Cockayne Syndrome Type AABC-SC144GHuman iPSC From Fibroblast-Cockayne Syndrome Type A
1 Vial
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Human iPSC From Fibroblast-Schuurs-Hoeijmakers SyndromeABC-SC165GHuman iPSC From Fibroblast-Schuurs-Hoeijmakers Syndrome
1 Vial
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Human iPSC From Fibroblast-Hurler SyndromeABC-SC172GHuman iPSC From Fibroblast-Hurler Syndrome
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HighQC™ Human IPSC From Fibroblast-Vici SyndromeABC-SC2035HighQC™ Human IPSC From Fibroblast-Vici Syndrome
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HighQC™ Human IPSC From Fibroblast-Pitt-Hopkins SyndromeABC-SC2062HighQC™ Human IPSC From Fibroblast-Pitt-Hopkins Syndrome
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Human iPSC From Blood-Turner SyndromeABC-SC219GHuman iPSC From Blood-Turner Syndrome
1 Vial
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Human iPSC From Fibroblast-Rett Syndrome, Congenital VariantABC-SC126GHuman iPSC From Fibroblast-Rett Syndrome, Congenital Variant
1 Vial
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