Phospho-Dab1 (Tyr232) Rabbit Polyclonal Antibody
Catalog #:EAB10715
Host / Isotype Clonality Applications MW (kDa) Reactivity
Rabbit IgG Polyclonal WB, IF/ICC, ELISA 64 Human, Mouse, Rat
Application Key

WB-Western Blot IP-Immunoprecipitation IHC-Immunohistochemistry IF-Immunofluorescence ICC-Immunocytochemistry FC-Flow Cytometry

Reactivity Key

H-Human M-Mouse R-Rat Mk-Monkey B-Bovine Pg-Pig Hm-Hamster Dg-Dog C-Chicken X-Xenopus Z-Zebrafish Hr-Horse All-All Species Expected

Applications Dilutions
The application notes include recommended starting dilutions;optimal dilutions/concentrations should be detemined by the end user.
WB(Westem Blotting)
IHC-P(Immunohistochemistry-Paraffin)
IF/ICC(Immunofluorescence/Immunocytochemistry)
ELISA(Enzyme-linked Immunosorbent Assay)
WB=1:500-2000 
IF/ICC=1:50-300 
Product Information
Conjugate Unconjugate
Specificity Phospho-Dab1 (Tyr232) Rabbit Polyclonal Antibody detects endogenous levels of Dab1 protein only when phosphorylated at Tyr232.
Purification Affinity purification
Concentration 1mg/ml
Format Liquid
Formulation In PBS, pH 7.4, containing 0.02% sodium azide,0.5% BSA and 50% glycerol.
Shipping Gel Pack
Storage Store at -20°C least 1 year from the date of shipment. avoid repeated freeze/thaw cycles. Aliquots may be stored at +4°C for 1-2 weeks.
UniProt ID

O75553

Entrez Gene ID

8674

Product Description

Dab1 also known as SCA37 is a homolog of the Drosophila Disabled protein. Dab1 plays a crucial role as an adaptor protein in neural development, particularly during the rapid expansion of the developing nervous system. Located primarily in the cytoplasm, Dab1 undergoes tyrosine phosphorylation, which is essential for its function in signaling pathways that guide the positioning of neurons. This phosphorylation allows Dab1 to interact with other proteins, notably through its PTB-like domain, facilitating its role in the Reelin signaling pathway. Reelin, a secreted protein, is vital for the proper migration and layering of neurons in the brain, and Dab1 acts downstream of Reelin, mediating its effects. Mutations in Dab1 can lead to significant brain abnormalities, mirroring the defects observed in Reelin mutants, underscoring the importance of Dab1 in maintaining neural architecture and function.

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For Research Use Only, Not For Diagnostic Or Therapeutic Procedures.
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