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CDCA3 Rabbit anti-Human, Polyclonal, Proteintech
Rabbit Polyclonal Antibody
Supplier: Proteintech Group Inc 155941AP150UL
Description
Implicated as a tumor suppressor. May have a function in vesicular transport. Interaction between TSC1 and TSC2 may facilitate vesicular docking.Defects in TSC1 are the cause of tuberous sclerosis complex (TSC). The molecular basis of TSC is a functional impairement of the hamartin-tuberin complex. TSC is an autosomal domit multi-system disorder that affects especially the brain, kidneys, heart, and skin. TSC is characterized by hamartomas (benign overgrowths predomitly of a cell or tissue type that occurs normally in the organ) and hamartias (developmental abnormalities of tissue combination). Clinical symptoms can range from benign hypopigmented macules of the skin to profound mental retardation with intractable seizures to premature death from a variety of disease-associated causes.Defects in TSC1 may be a cause of focal cortical dysplasia of Taylor balloon cell type (FCDBC). FCDBC is a subtype of cortical displasias linked to chronic intractable epilepsy. Cortical dysplasias display a broad spectrum of structural changes, which appear to result from changes in proliferation, migration, differentiation, and apoptosis of neuronal precursors and neurons during cortical development.Specifications
CDCA3 | |
Polyclonal | |
Unconjugated | |
CDCA3 | |
C8, CDCA3, Gene rich cluster protein C8, GRCC8, TOME 1, TOME1 | |
Rabbit | |
Antigen Affinity Chromatography | |
RUO | |
83461 | |
-20°C | |
Liquid |
Immunohistochemistry (Paraffin), Western Blot | |
0.21 mg/mL | |
PBS with 50% glycerol and 0.1% sodium azide; pH 7.3 | |
Q99618 | |
CDCA3 | |
CDCA3 Fusion Protein Ag7951 | |
150 μL | |
Primary | |
Human | |
Antibody | |
IgG |
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