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SMC-327D-APC

SHANK Antibody, Clone N23b/49: APC

Cannot supply to this region.

SKU:
SMC-327D-APC
Additional Names:
Cortactin binding protein 1, Cortactin SH3 domain-binding protein, Cortactin-binding protein 1, CortBP1, CTTNBP1, GKAP/SAPAP interacting protein, GKAP/SAPAP-interacting protein, KIAA1022, Proline rich synapse associated protein 1, Proline-rich synapse-associated protein 1, ProSAP1, SH3 and multiple ankyrin repeat domains protein 2, SHAN2_RAT, Shank2, SPANK-3
Application:
IHC, WB, IF, ICC, IP, Microarray
Concentration:
1 mg/ml
Species Reactivity:
Rat
Purification:
Protein G Purified
Storage Conditions:
See Manual
Supplier:
StressMarq Biosciences
Host:
Mouse
Reactivities:
Human, Mouse, Rat
ABP:
IMP-GEN-2015-06 < 10% Serum <100ml
Buffer:
95.46mM Phosphate, 2.48mM MES and 2mM EDTA
Immunogen:
Fusion protein amino acids 84-309 of rat Shank2
Clone:
N23b/49 (Formerly sold as S23b-49)
Uniprot:
Q9QX74
Synonyms:
cortactin-binding protein 1;CortBP1;GKAP/SAPAP-interacting protein;proline-rich synapse-associated protein 1;ProSAP1;SH3 and multiple ankyrin repeat domains protein 2;SH3 and multiple ankyrin repeat domains protein 2-like;SH3/ankyrin domain gene 2;Spank-3
Extra Details:
SHANK proteins are a family of postsynaptic scaffolding proteins that organize receptor and signaling complexes at excitatory synapses. They contain multiple protein interaction domains, including ankyrin repeats, SH3, PDZ, and SAM domains, enabling them to link neurotransmitter receptors to the actin cytoskeleton. SHANK proteins regulate synaptic strength, dendritic spine morphology, and receptor trafficking. Disruption of SHANK-mediated scaffolding impairs glutamate receptor localization and contributes to synaptic loss-a key feature of Alzheimer's disease. SHANK family members also influence receptor tyrosine kinase signaling and are involved in neurodevelopmental processes. Their dysregulation has been associated with autism spectrum disorders, schizophrenia, and intellectual disability, making them central to both neurodevelopmental and neurodegenerative research.
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