Phospho-SYN1(S9) Polyclonal Antibody
€0.00
In stock
SKU
E-AB-68119
Catalog Number: E-AB-68119
Isotype: Rabbit IgG
Reactivity: human, mouse, rat
Applications: WB,IF
Datasheet, Questions? Contact us!
Isotype: Rabbit IgG
Reactivity: human, mouse, rat
Applications: WB,IF
Datasheet, Questions? Contact us!
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.
Research Area: Cancer, Neuroscience
Synonyms:
SYN1, SYN1a, SYN1b, SYNI
Immunogen: A phospho specific peptide corresponding to residues surrounding S9 of human SYN1
Swissprot: P17600
Gene ID: 6853
Calculated MW: 70 kDa/74 kDa
Observed MW: 74 kDa
Purification Method: Affinity purification
Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3
Concentration: 1 mg/mL
Dilution: "WB 1:500-1:2000 IF 1:100-1:200"
Storage:
Store at -20°C. Avoid freeze / thaw cycles.
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.
Research Area: Cancer, Neuroscience
Synonyms:
SYN1, SYN1a, SYN1b, SYNI
Immunogen: A phospho specific peptide corresponding to residues surrounding S9 of human SYN1
Swissprot: P17600
Gene ID: 6853
Calculated MW: 70 kDa/74 kDa
Observed MW: 74 kDa
Purification Method: Affinity purification
Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3
Concentration: 1 mg/mL
Dilution: "WB 1:500-1:2000 IF 1:100-1:200"
Storage:
Store at -20°C. Avoid freeze / thaw cycles.
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