The following disease-affected hESC lines and genetically normal hESC lines developed by MStem Cell Laboratories are available for purchase:
- UM150-1 PGD Actin Nemaline Myopathy
- UM150-3 PGD Actin Nemaline Myopathy
- UM150-4 PGD Actin Nemaline Myopathy
- UM112-1 PGD Adrenoleukodystrophy
- UM112-2 PGD Adrenoleukodystrophy
- UM153-1 PGD Adrenoleukodystrophy
- UM141-6 PGD ALS/Frontotemporal Dementia C9orf 72
- UM29-2 PGD Aniridia
- UM29-3 PGD Aniridia
- UM66-3 PGD Aniridia
- UM11-1 PGD Charcot Marie Tooth, 1A
- UM59-2 PGD Charcot Marie Tooth, 1A
- UM59-4 PGD Charcot-Marie-Tooth, 1A
- UM89-3 PGD Charcot-Marie-Tooth,1A
- UM89-5 PGD Charcot-Marie-Tooth,1A
- UM159-1 PGD Cystic Fibrosis
- UM90-14 PGD Duchenne-Becker,XX Carrier
- UM139-2 PGD Fragile X Syndrome
- UM9-1 PGD Hemophilia B
- UM17-1 PGD Huntington’s Disease
- UM103-1 PGD Huntington’s Disease
- UM15-4 PGD Hydroxysteroid Dehydrogenase Deficiency
- UM38-2 PGD Hypertrophic Cardiomyopathy
- UM197-1 PGD Kennedy Spinal Bulbar Muscular Atrophy
- UM89-1 PGD Marfan Syndrome
- UM89-4 PGD Marfan Syndrome
- UM57-1 PGD Multiple Endocrine Neoplasia, 2A
- UM57-3 PGD Multiple Endocrine Neoplasia, 2A
- UM207-3 PGD Neurofibromatosis, Type 2
- UM207-4 PGD Neurofibromatosis, Type 2
- UM161-1 PGD Niemann Pick,Type C
- UM181-1 PGD Non-syndromic Hearing Loss
- UM76-1 PGS Robertsonian Translocation
- UM134-1 PGD Spinocerebellar Ataxia, T3
- UM204-1 PGD Stickler Syndrome
- UM90-12 PGS Trisomy 16
- UM152-1 PGS Trisomy 21
- UM202-1 PGS Trisomy 21
Genetically Normal hESC Lines:
- UM4-6
- UM4-9
- UM4-11
- UM4-12
- UM14-1
- UM14-2
- UM14-3
- UM22-2
- UM25-2
- UM33-4
- UM63-1
- UM76-2
- UM77-2
- UM78-2
- UM89-2
- UM114-10
- UM121-7
- UM160-3
- UM178-1
- UM126-2
- UM127-1
- UM205-1
For more information, contact MStem Cell at (734) 649-6557.