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Mouse Anti-DAB1 Recombinant Antibody (13A170) (V2LY-0125-LY1047)

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Published Data

Summary

Host Animal
Mouse
Specificity
Human, Mouse, Rat, Horse, Dog
Clone
13A170
Antibody Isotype
IgG1, κ
Application
WB, IP, IF, ELISA

Basic Information

Immunogen
Amino acids 451-553 of human Dab1.
Host Species
Mouse
Specificity
Human, Mouse, Rat, Horse, Dog
Antibody Isotype
IgG1, κ
Clonality
Monoclonal Antibody
Application Notes
ApplicationNote
WB1:100-1:1,000
IP1-2 μg per 100-500 μg of total protein (1 mL of cell lysate)
ELISA1:100-1:1,000
IF(ICC)1:50-1:500

Formulations & Storage [For reference only, actual COA shall prevail!]

Format
Liquid
Buffer
Gelatin & PBS
Preservative
Sodium Azide
Concentration
0.2 mg/mL
Purity
>95% as determined by analysis by SDS-PAGE
Storage
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freezethaw cycles.

Target

Entrez Gene ID
Human1600
Mouse13131
Rat266729
UniProt ID
HumanO75553
MouseP97318
RatQ8CJH2
Function
Adapter molecule functioning in neural development. May regulate SIAH1 activity.
Biological Process
Adult walking behavior Source: Ensembl
Axon guidance Source: Reactome
cell-cell adhesion involved in neuronal-glial interactions involved in cerebral cortex radial glia guided migration Source: Ensembl
Cerebellum structural organization Source: Ensembl
Dendrite development Source: Ensembl
Golgi localization Source: Ensembl
Hippocampus development Source: Ensembl
Lateral motor column neuron migration Source: GO_Central
Midgut development Source: Ensembl
Negative regulation of astrocyte differentiation Source: Ensembl
Negative regulation of axonogenesis Source: Ensembl
Negative regulation of cell adhesion Source: Ensembl
Negative regulation of receptor signaling pathway via JAK-STAT Source: Ensembl
Positive regulation of neuron differentiation Source: Ensembl
Positive regulation of protein kinase activity Source: Ensembl
Radial glia guided migration of Purkinje cell Source: Ensembl
Response to drug Source: Ensembl
Small GTPase mediated signal transduction Source: Ensembl
Ventral spinal cord development Source: GO_Central
Cellular Location
Cytosol; Apical part of cell; Brush border; Cytoplasm; Intracellular membrane-bounded organelle; Membrane; Neuron projection; Neuronal cell body; Perinuclear region of cytoplasm; Postsynaptic density
Involvement in disease
Spinocerebellar ataxia 37 (SCA37):
A form of spinocerebellar ataxia, a clinically and genetically heterogeneous group of cerebellar disorders. Patients show progressive incoordination of gait and often poor coordination of hands, speech and eye movements, due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord. SCA37 is an autosomal dominant form characterized by adult-onset of slowly progressive gait instability, frequent falls, and dysarthria associated with cerebellar atrophy on brain imaging.
PTM
Phosphorylated on Tyr-198 and Tyr-220 upon reelin induction in embryonic neurons. Also phosphorylated on Ser-524 independently of reelin signaling.
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For research use only. Not intended for any clinical use.

Custom Antibody Labeling

We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).

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