O

Synapsin I (Phospho Ser553) Rabbit pAb

-YP1207

Catalog: YP1207
Size
Price
Status
Qty.
200μL
$600.00
In stock

0

100μL
$340.00
In stock

0

50μL
$190.00
In stock

0

Add to cart

Collected

Collect

Customized Service
Main Information
Target

Synapsin I Phospho Ser553

Host Species

Rabbit

Reactivity

Human, Mouse, Rat

Applications

WB, IHC, ELISA

MW

75kD (Observed)

Conjugate/Modification


Phospho

Detailed Information
Recommended Dilution Ratio
WB 1:500-2000; IHC 1:50-300; ELISA 5000-1:20000;
Formulation
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Specificity
Phospho-Synapsin-1 (S553) Polyclonal Antibody detects endogenous levels of Synapsin-1 around the phosphorylation site of S553 protein.The name of modified sites may be influenced by many factors, such as species (the modified site was not originally found in human samples) and the change of protein sequence (the previous protein sequence is incomplete, and the protein sequence may be prolonged with the development of protein sequencing technology). When naming, we will use the "numbers" in historical reference to keep the sites consistent with the reports. The antibody binds to the following modification sequence (lowercase letters are modification sites):SPsPQ
Purification
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Storage
-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration
1 mg/ml
MW(Observed)
75kD
Modification
Phospho
Clonality
Polyclonal
Isotype
IgG
Related Products
Primary Antibodies
Synapsin I Rabbit pAb
YT5737

More→

Primary Antibodies
Synapsin I Rabbit pAb
YT4483

More→

Primary Antibodies
Synapsin I Rabbit pAb
YT4482

More→

Primary Antibodies
Synapsin I (Phospho Ser553) Rabbit pAb
YP1207

More→

Primary Antibodies
Synapsin I (Phospho Ser605) Rabbit pAb
YP1149

More→

Primary Antibodies
Synapsin I (Phospho Ser62) Rabbit pAb
YP0672

More→

Primary Antibodies
Synapsin I (Phospho Ser9) Rabbit pAb
YP0257

More→

ELISA Kits
Total Synapsin1 Cell-Based Colorimetric ELISA Kit
KA4297C

More→

ELISA Kits
Synapsin1 (Phospho Ser9) Cell-Based Colorimetric ELISA Kit
KA1661C

More→

ELISA Kits
Synapsin1 (Phospho Ser62) Cell-Based Colorimetric ELISA Kit
KA1339C

More→

Antigen&Target Information
Immunogen:
Synthesized phospho-peptide around the phosphorylation site of human Synapsin-1 (phospho Ser553)
show all
Specificity:
Phospho-Synapsin-1 (S553) Polyclonal Antibody detects endogenous levels of Synapsin-1 around the phosphorylation site of S553 protein.The name of modified sites may be influenced by many factors, such as species (the modified site was not originally found in human samples) and the change of protein sequence (the previous protein sequence is incomplete, and the protein sequence may be prolonged with the development of protein sequencing technology). When naming, we will use the "numbers" in historical reference to keep the sites consistent with the reports. The antibody binds to the following modification sequence (lowercase letters are modification sites):SPsPQ
show all
Gene Name:
SYN1
show all
Protein Name:
Synapsin-1
show all
Other Name:
SYN1 ;
Synapsin-1 ;
Brain protein 4.1 ;
Synapsin I
show all
Database Link:
Organism Gene ID SwissProt
Human 6853; P17600;
Mouse 20964; O88935;
Rat 24949; P09951;
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. [provided by RefSeq, Jul 2008],
show all
Function:
Disease: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 PRNP.,
show all
Cellular Localization:
Cell junction, synapse. Golgi apparatus .
show all
Tissue Expression:
Catalog: YP1207
Size
Price
Status
Qty.
200μL
$600.00
In stock

0

100μL
$340.00
In stock

0

50μL
$190.00
In stock

0

Add to cart

Collected

Collect

Customized Service

Toggle night Mode

{{pinfoXq.title || ''}}

Catalog: {{pinfoXq.catalog || ''}}
Filter:

All

{{item.name}}

{{pinfo.title}}
-{{pinfo.catalog}}

Filter:

{{item.descr}}

Main Information
Target
{{pinfo.target}}
Reactivity
{{pinfo.react}}
Applications
{{pinfo.applicat}}
Conjugate/Modification
{{pinfo.coupling}}/{{pinfo.modific}}
MW (kDa)
{{pinfo.mwcalc}}
Host Species
{{pinfo.hostspec}}
Isotype
{{pinfo.isotype}}
Learn more
Product {{index}}/{{pcount}}
Prev
Next

{{pvTitle}}

Scroll wheel zooms the picture
{{pvDescr}}