MStem Cell Laboratories

Ann Arbor, MI

Purchase Stem Cell Lines

The following disease-affected hESC lines and genetically normal hESC lines developed by MStem Cell Laboratories are available for purchase:

  1. UM150-1 PGD Actin Nemaline Myopathy
  2. UM150-3 PGD Actin Nemaline Myopathy
  3. UM150-4 PGD Actin Nemaline Myopathy
  4. UM112-1 PGD Adrenoleukodystrophy
  5. UM112-2 PGD Adrenoleukodystrophy
  6. UM153-1 PGD Adrenoleukodystrophy
  7. UM141-6 PGD ALS/Frontotemporal Dementia C9orf 72
  8. UM217-1 PGD ALS/Frontotemporal Dementia C9orf 72
  9. UM217-2 PGD ALS/Frontotemporal Dementia C9orf 72
  10. UM281-1 PGD ALS/Frontotemporal Dementia C9orf 72
  11. UM29-2 PGD Aniridia
  12. UM29-3 PGD Aniridia
  13. UM66-3 PGD Aniridia
  14. UM11-1 PGD Charcot Marie Tooth, Type 1A
  15. UM59-2 PGD Charcot Marie Tooth, Type 1A
  16. UM59-4 PGD Charcot Marie Tooth, Type 1A
  17. UM89-3 PGD Charcot Marie Tooth, Type 1A
  18. UM89-5 PGD Charcot Marie Tooth, Type 1A
  19. UM159-1 PGD Cystic Fibrosis
  20. UM90-14 PGD Duchenne-Becker, XX Carrier
  21. UM139-2 PGD Fragile X Syndrome
  22. UM9-1 PGD Hemophilia B
  23. UM17-1 PGD Huntington’s Disease
  24. UM103-1 PGD Huntington’s Disease
  25. UM314-1 PGD Huntington’s Disease
  26. UM314-2 PGD Huntington’s Disease
  27. UM15-4 PGD Hydroxysteroid Dehydrogenase Deficiency
  28. UM38-2 PGD Hypertrophic Cardiomyopathy
  29. UM245-2 PGD Incontinentia Pigmenti
  30. UM245-3 PGD Incontinentia Pigmenti
  31. UM197-1 PGD Kennedy Spinal Bulbar Muscular Atrophy
  32. UM89-1 PGD Marfan Syndrome
  33. UM89-4 PGD Marfan Syndrome
  34. UM57-1 PGD Multiple Endocrine Neoplasia, Type 2A
  35. UM57-3 PGD Multiple Endocrine Neoplasia, Type 2A
  36. UM207-3 PGD Neurofibromatosis, Type 2
  37. UM207-4 PGD Neurofibromatosis, Type 2
  38. UM161-1 PGD Niemann Pick, Type C
  39. UM181-1 PGD Non-syndromic Hearing Loss
  40. UM274-1 PGD Retinoblastoma
  41. UM76-1 PGS Robertsonian Translocation
  42. UM302-1 PGD Smith-Lemli-Optiz Syndrome
  43. UM206-2 PGD Spastic Paraplegia, Type 31
  44. UM134-1 PGD Spinocerebellar Ataxia, Type 3
  45. UM204-1 PGD Stickler Syndrome
  46. UM204-4 PGD Stickler Syndrome
  47. UM204-7 PGD Stickler Syndrome
  48. UM90-12 PGS Trisomy 16
  49. UM152-1 PGS Trisomy 21
  50. UM202-1 PGS Trisomy 21
  51. UM229-1 PGS Trisomy 21
  52. UM305-1 PGS Turner Syndrome

Genetically Normal hESC Lines:

  1. UM4-6
  2. UM4-9
  3. UM4-11
  4. UM4-12
  5. UM14-1
  6. UM14-2
  7. UM14-3
  8. UM22-2
  9. UM25-2
  10. UM33-4
  11. UM63-1
  12. UM76-2
  13. UM77-2
  14. UM78-2
  15. UM89-2
  16. UM114-10
  17. UM121-7
  18. UM160-3
  19. UM178-1
  20. UM126-2
  21. UM127-1
  22. UM205-1
  23. UM263-1
  24. UM300-1
  25. UM300-2

For more information, contact MStem Cell at (734)764-4134 or (734)615-1522; email: mstemcell@med.umich.edu.