SYN1 antibody (clone 4F6), anti-human
€435.00
In stock
SKU
AC-AT4119a
Catalog Number: AC-AT4119a
Size: 100 µg
Isotype: mouse IgG2a Kappa
Applications: WB
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Size: 100 µg
Isotype: mouse IgG2a Kappa
Applications: WB
Request Information AC-AT4119a">Request Information
Background:
This gene is a member of the synapsin gene family. Synapsins encode neuronal phosphoproteins which associate with the cytoplasmic surface of synaptic vesicles. Family members are characterized by common protein domains, and they are implicated in synaptogenesis and the modulation of neurotransmitter release, suggesting a potential role in several neuropsychiatric diseases. This member of the synapsin family plays a role in regulation of axonogenesis and synaptogenesis. The protein encoded serves as a substrate for several different protein kinases and phosphorylation may function in the regulation of this protein in the nerve terminal. Mutations in this gene may be associated with X-linked disorders with primary neuronal degeneration such as Rett syndrome. Alternatively spliced transcript variants encoding different isoforms have been identified.
Other Names:
Synapsin-1, Brain protein 41, Synapsin I, SYN1
Antigen Type:
Recombinant Protein
Gene Name: SYN1
Gene ID: 6853
NCBI Accession: NP_008881.2;NP_598006.1
Primary Accession: P17600
Other Accession: NM_006950
Format: Clear, colorless solution in phosphate buffered saline, pH 7.2 .
This gene is a member of the synapsin gene family. Synapsins encode neuronal phosphoproteins which associate with the cytoplasmic surface of synaptic vesicles. Family members are characterized by common protein domains, and they are implicated in synaptogenesis and the modulation of neurotransmitter release, suggesting a potential role in several neuropsychiatric diseases. This member of the synapsin family plays a role in regulation of axonogenesis and synaptogenesis. The protein encoded serves as a substrate for several different protein kinases and phosphorylation may function in the regulation of this protein in the nerve terminal. Mutations in this gene may be associated with X-linked disorders with primary neuronal degeneration such as Rett syndrome. Alternatively spliced transcript variants encoding different isoforms have been identified.
Other Names:
Synapsin-1, Brain protein 41, Synapsin I, SYN1
Antigen Type:
Recombinant Protein
Gene Name: SYN1
Gene ID: 6853
NCBI Accession: NP_008881.2;NP_598006.1
Primary Accession: P17600
Other Accession: NM_006950
Format: Clear, colorless solution in phosphate buffered saline, pH 7.2 .
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