Heritable Disease,HighQC™ Human IPSC From B-Lymphocyte-Ceroid Lipofuscinosis(Neuronal 2-Late Infantile Type)

• Human Primary Cells
• Animal Primary Cells
• Subcellular Fractions
• Specific Protein Expressing Cells

• Human Tumor Cell Lines
• Animal Tumor Cell Lines

• Human MicroRNA Agomir/Antagomir
• Mouse MicroRNA Agomir/Antagomir
• Rat MicroRNA Agomir/Antagomir
• Other MicroRNA Agomir/Antagomir

• Adult Stem Cells
• Cancer Stem Cells
• Embryonic Stem (ES) Cells
• Induced Pluripotent Stem Cells (iPSCs)
• Mesenchymal Stem Cells (MSC)
• Mesenchymal Stem Cells

• Knockout Stable Cell Lines
• Knockin Stable Cell Lines
• Knockdown Stable Cell Lines
• Overexpression Stable Cell Lines
• Reporter Stable Cell Lines
• Knockout Cell Lysate

• Nucleic Acid Extraction/Purification
• Nucleic Acid Transfection
• Nucleic Acid Enzyme
• Nucleic Acid Correlation

• Human

• Alzheimer's Disease
• Ceroid Lipofuscinosis
• Choroideremia
• Congenital Disorder Of Deglycosylation
• Diabetes Mellitus, Juvenile-Onset RI-Dependent
• Epidermolysis Bullosa: Dystrophic, Junctional, Or Simplex Types
• Huntington Disease
• Hutchinson-Gilford Progeria Syndrome
• Kearns-Sayre Syndrome
• Krabbe Disease
• Lesch-Nyhan Syndrome
• Long QT Syndrome 2
• Long QT Syndrome 3
• Mucopolysaccharidosis Type IIIA N
• Niemann-Pick Disease, Type A
• Niemann-Pick Disease, Type C1
• Phenylketonuria
• Pitt-Hopkins Syndrome
• Spinal Muscular Atrophy, TYPE II
• Tuberous Sclerosis 2
• Vici Syndrome
• Werner Syndrome
• Wolman Disease

• B-Lymphocyte
• Fibroblast

• Induced Pluripotent Stem Cell