Product Category
- 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
Species
- Chicken
- Human
- Mouse
- PND 35 Oct4-GFP Mice
Disease
- Alagille Syndrome 1
- Albino
- Alzheimer Disease
- Alzheimer's Disease
- Alzheimer’s Disease
- 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)
- 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
Organ
- Activated Fibroblast
- Adipose
- Adipose Mesenchymal Stromal
- B-Lymphocyte
- Blood
- Bone Marrow
- Brain
- Cord Blood
- Corneal Epithelial Cell
- Epithelium
- Fibroblast
- Fibroblasts
- Foreskin
- Heart
- Hippocampus
- Human Foreskin Fibroblasts
- LCL
- Limbal Epithelial Cell
- Lingual
- Nervous Tissue
- PBMC
- Periodontal Ligament
- Primary Human Fibroblast
- Skin
- Skin Fibroblasts
Cell Type
- 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
- 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
- T Cell
- Ventricular Cardiomyocyte
Showing all 225 results
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Stem Cells |
ABC-SC2119
HighQC™ Human iPSC-Derived Hepatocytes
Cell TypeHepatocyte
Storage ConditionLiquid Nitrogen
To Explore -
Stem Cells |
ABC-SC2118
HighQC™ Human IPSC Derived Retinal Pigment Epithelium
Cell TypeRetinal Pigment Epithelium
Storage ConditionLiquid Nitrogen
To Explore -
Stem Cells |
ABC-SC2113
HighQC™ Pancreatic Beta Cells Derived From Human Induced Pluripotent Stem Cell
Cell TypePancreatic Beta Cell
Storage ConditionLiquid Nitrogen
To Explore -
Stem Cells |
ABC-SC2111
HighQC™ Human iPSC-Derived Astrocytes
Cell TypeInduced Pluripotent Stem Cell
Storage ConditionLiquid Nitrogen
To Explore -
Stem Cells |
ABC-SC2110
HighQC™ Human iPSC-Derived Microglia
Cell TypeMicroglia
Storage ConditionLiquid Nitrogen
To Explore -
Stem Cells |
ABC-SC2108
HighQC™ IPSC Human Foreskin Fibroblast IPSC FFHFF
Cell TypeInduced Pluripotent Stem Cell
Source OrganForeskin
Storage ConditionLiquid Nitrogen
To Explore -
Stem Cells |
ABC-SC2107
HighQC™ IPSC FFGAU
Cell TypeInduced Pluripotent Stem Cell
Source OrganFibroblast
Storage ConditionLiquid Nitrogen
To Explore -
Stem Cells |
ABC-SC2105
HighQC™ Human IPS Cell Line (Episomal, CD34+, ApoE4)
Cell TypeInduced Pluripotent Stem Cell
Storage ConditionLiquid Nitrogen
To Explore -
Stem Cells |
ABC-SC2104
HighQC™ Human IPS Cell Line (Episomal, MSC)
Cell TypeInduced Pluripotent Stem Cell
Storage ConditionLiquid Nitrogen
To Explore -
Stem Cells |
ABC-SC2103
HighQC™ Human IPS Cell Line (Episomal, HFF)
Cell TypeInduced Pluripotent Stem Cell
Storage ConditionLiquid Nitrogen
To Explore