Synapsin I (phospho Ser9) rabbit pAb

Synapsin I (phospho Ser9) rabbit pAb

AO-06-ES1410-100

Synapsin I (phospho Ser9) rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES1410
Product nameSynapsin I (phospho Ser9) rabbit pAb
ReactivityHuman;Mouse;Rat
ApplicationsWB;IHC;IF;ELISA
Other nameSYN1; Synapsin-1; Brain protein 4.1; Synapsin I
Size100μL
Unit price ($)248
Human gene ID6853
Human Swiss-ProtP17600
SourceRabbit
IsotypeIgG
TargetSynapsin I
Fields
Gene nameSYN1
Protein nameSynapsin-1
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID20964
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtO88935
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID24949
Rat gene linkView Rat Gene
Rat Swiss-ProtP09951
Rat Swiss linkView Rat Swiss-Prot
ImmunogenThe antiserum was produced against synthesized peptide derived from human Synapsin around the phosphorylation site of Ser9. AA range:3-52
SpecificityPhospho-Synapsin I (S9) Polyclonal Antibody detects endogenous levels of Synapsin I protein only when phosphorylated at S9.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. Immunofluorescence: 1/200 - 1/1000. ELISA: 1/20000. Not yet tested in other applications.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)77kD
BackgroundThis 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. [provided by RefSeq, Jul 2008],
Functiondisease:Defects in SYN1 are a cause of epilepsy X-linked with variable learning disabilities and behavior disorders [MIM:300491]. XELBD is characterized by variable combinations of epilepsy, learning difficulties, macrocephaly, and aggressive behavior.,function:Neuronal phosphoprotein that coats synaptic vesicles, binds to the cytoskeleton, and is believed to function in the regulation of neurotransmitter release. The complex formed with NOS1 and CAPON proteins is necessary for specific nitric-oxid functions at a presynaptic level.,PTM:Substrate of at least four different protein kinases. It is probable that phosphorylation plays a role in the regulation of synapsin-1 in the nerve terminal. Phosphorylated upon DNA damage, probably by ATM or ATR.,similarity:Belongs to the synapsin family.,subunit:Homodimer. Interacts with CAPON. Forms a ternary complex with NOS1. Isoform Ib interacts with
Subcellular locationCell junction, synapse. Golgi apparatus .
ExpressionBrain,Brain cortex,

Additional Images

Image 1
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Western Blot analysis of various cells using Phospho-Synapsin I (S9) Polyclonal Antibody diluted at 1:1000
Image 2
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Western Blot analysis of 3T3 cells using Phospho-Synapsin I (S9) Polyclonal Antibody diluted at 1:1000
Image 3
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Western blot analysis of HELA KB 293T 3T3 lysis using Phospho-Synapsin I (S9) antibody. Antibody was diluted at 1:1000
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Western blot analysis of lysates from 293 cells treated with PMA 200nM 30', using Synapsin (Phospho-Ser9) Antibody. The lane on the right is blocked with the phospho peptide.
: AO-06-ES1410-100
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