Flow cytometric analysis of contactin associated protein 1 expression in HepG2 cells using contactin associated protein 1 antibody. Green, isotype control; red, contactin associated protein 1.
Immunocytochemical staining of HepG2 cells with Contactin associated protein 1 antibody. Nuclei were stained blue with DAPI; Contactin associated protein 1 was stained magenta with Alexa Fluor? 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: Medium. Scale bar, 20 μm.
Western blotting analysis using contactin associated protein 1 antibody. Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with contactin associated protein 1 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively.
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貨期:
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用途:
For Research Use Only. Not for use in diagnostic or therapeutic procedures.
Required, with CNTNAP2, for radial and longitudinal organization of myelinated axons. Plays a role in the formation of functional distinct domains critical for saltatory conduction of nerve impulses in myelinated nerve fibers. Demarcates the paranodal region of the axo-glial junction. In association with contactin involved in the signaling between axons and myelinating glial cells.
基因功能參考文獻(xiàn):
E. coli exploits Caspr1 as a host receptor for penetration of the blood-brain barrier, resulting in meningitis PMID: 29895952
In two brothers with severe congenital hypotonia and foot deformities, we identified compound heterozygous variants in CNTNAP1, reporting the first causative missense variant, p.(Cys323Arg). Motor nerve conductions were markedly decreased. PMID: 27782105
CNTNAP1 mutations were found to induce characteristic ultrastructural lesions of the paranodal region. PMID: 27818385
report a consanguineous Arab family from Qatar with three children having an early lethal form of arthrogryposis multiplex congenita and a novel frameshift mutation in CNTNAP1 PMID: 28254648
Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defects PMID: 24319099
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相關(guān)疾病:
Lethal congenital contracture syndrome 7 (LCCS7)
亞細(xì)胞定位:
Membrane; Single-pass type I membrane protein. Cell junction, paranodal septate junction.
蛋白家族:
Neurexin family
組織特異性:
Predominantly expressed in brain. Weak expression detected in ovary, pancreas, colon, lung, heart, intestine and testis.