Induced Pluripotent Stem Cells (iPSCs)

• 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

• Chicken
• Human
• Mouse
• PND 35 Oct4-GFP Mice

• Alagille Syndrome 1
• Albino
• Alzheimer Disease
• Alzheimer's Disease
• Alzheimer’s Disease
• Alzheimer’s Presenilin-1 Mutation
• Amyotrophic Lateral Sclerosis
• Amyotrophic Lateral Sclerosis (ALS)
• Apparently Healthy Individual
• Breast Cancer
• Canavan Disease
• Cancer of the Breast
• Central Core Disease of Muscle
• Cerebral Creatine Deficiency Syndrome 2
• Cerebral Creatine Deficiency Syndrome 3
• Ceroid Lipofuscinosis
• Ceroid Lipofuscinosis, Neuronal 2,
• Charcot-Marie-Tooth Disease
• Charcot-Marie-Tooth Syndrome
• Choroideremia
• Chromosome XP11.3 Deletion Syndrome
• Cockayne Syndrome Type A
• Congenital Disorder Of Deglycosylation
• Crohn's Disease
• Cystic Fibrosis
• Developmental And Epileptic Encephalopathy 2
• Diabetes
• Diabetes (mellitus)
• Diabetes Mellitus
• Diabetes Mellitus, Juvenile-Onset RI-Dependent
• Diabetes Type II
• Disease
• Dystrophia Myotonica 1
• Epidermolysis Bullosa
• Epidermolysis Bullosa: Dystrophic, Junctional, Or Simplex Types
• Epilepsy
• Epileptic Encephalopathy
• Facioscapulohumeral Muscular Dystrophy 1
• Familial Alzheimer's Disease
• Fibroblasts Of A Cystic Fibrosis
• Fibrodysplasia Ossificans Progressiva
• Friedreich Ataxia 1
• Gaucher Syndrome (Morbus Gaucher)
• Gaucher’s Type 1
• Glioblastoma
• GLUT1 Deficiency Syndrome 1
• Glycogen Storage Disease II
• Helsmoortel-Van Der Aa Syndrome
• Huntington Disease
• Huntington's Disease Like
• Hurler Syndrome
• Hutchinson-Gilford Progeria Syndrome
• Isogenic Control Congenital Disorder Of Deglycosylation
• Isogenic Control GLUT1 Deficiency Syndrome 1
• Kearns-Sayre Syndrome
• Krabbe Disease
• Leigh Syndrome
• Lesch-Nyhan Syndrome
• Lingual Cancer
• Long QT Syndrome 2
• Long QT Syndrome 3
• Maturity Onset Diabetes
• Mental Retardation
• Mental Retardation, Autosomal Dominant 40
• Miller-Dieker Lissencephaly Syndrome
• Monocarboxylate Transporter 8-Specific Thyroid Hormone Cell Transporter Deficiency
• Monocarboxylate Transporter 9-Specific Thyroid Hormone Cell Transporter Deficiency
• Mucopolysaccharidosis Type II
• Mucopolysaccharidosis Type IIIA N
• Mucopolysaccharidosis Type IVA
• Multicentric Carpotarsal Osteolysis Syndrome
• Muscular dystrophy
• Muscular Dystrophy, Becker Type
• Muscular Dystrophy, Duchenne Type
• Myopathy
• Nemaline Myopathy 2
• Nemaline Myopathy 3
• NESCAV Syndrome
• Neuroaxonal Dystrophy
• Neurodegeneration With Brain Iron Accumulation 5
• Neurodevelopmental Disorder
• Neuropathy, Hereditary Sensory And Autonomic, Type III
• Niemann Pick Type C
• Niemann-Pick Disease
• Niemann-Pick Disease, Type A
• Niemann-Pick Disease, Type C1
• Normal
• Normal or Disease
• Osteogenesis Imperfecta, Type IV
• Parkinson
• Parkinson Disease
• Parkinson's Disease
• Parkinson’s Disease
• Phenylketonuria
• Pitt-Hopkins Syndrome
• Primary Keratocytes-Keratoconus
• Primary Lateral Sclerosis
• Rett Syndrome
• Scheie Syndrome
• Schizophrenia
• Schuurs-Hoeijmakers Syndrome
• Selenon-Related Myopathy
• Severe Combined Immunodeficiency
• Skeletal Displasia
• Skin Fibroblasts Of A Cystinosis
• Spinal Muscular Atrophy I
• Spinal Muscular Atrophy, TYPE II
• Spondylometaphyseal Displasia, Kozlowski Type
• Tay-sachs
• Tay-Sachs Disease
• Trisomy 21
• Trisomy X
• Tuberous Sclerosis 1
• Tuberous Sclerosis 2
• Turner Syndrome
• Type 2 Diabetes
• Vici Syndrome
• Werner Syndrome
• Wolman Disease
• Xeroderma Pigmentosum

• Activated Fibroblast
• Adipose
• Adipose Mesenchymal Stromal
• B-Lymphocyte
• Blood
• Bone Marrow
• Brain
• Cord Blood
• Corneal Epithelial Cell
• Embryo
• Epithelium
• Fibroblast
• Fibroblasts
• Foreskin
• Heart
• Hippocampus
• Human Foreskin Fibroblasts
• Induced Pluripotent Stem Cell
• LCL
• Limbal Epithelial Cell
• Lingual
• Nervous Tissue
• PBMC
• Periodontal Ligament
• Primary Human Fibroblast
• Skin
• Skin Fibroblasts
• Ventral Horns

• Atrial Cardiomyocyte
• Cancer Stem Cell
• Cardiac Cell
• Endothelial
• Endothelial Colony Forming Cell
• Endothelial Stem Cell
• Fibroblast
• Hematopoietic Progenitor Cell
• Hepatocyte
• Induced Pluripotent Stem Cell
• Melanocyte
• Mesenchymal Stem Cell
• Microglia
• Neural Progenitor
• Neural Stem Cell
• Neuron
• Neuronal Stem Cell
• NK Cell
• Pancreatic Beta Cell
• Periodontal Ligament Stem Cell
• Retinal Pigment Epithelium
• Sebocyte
• Stem Cell
• Stem Cells
• T Cell
• Ventricular Cardiomyocyte