Phospho-Synapsin I (Ser553) Rabbit Monoclonal Antibody

Phospho-Synapsin I (Ser553) Rabbit Monoclonal Antibody

Cat: AMRe87651
Size1:50μL Price1:$188
Size2:100μL Price2:$338
Application:WB

Reactivity:Human,Mouse,Rat
Conjugate:Unconjugated
Optional conjugates: Biotin, FITC (free of charge).
See other 26 conjugates.

Gene Name:Phospho-Synapsin I (Ser553)
Category: Recombinant Monoclonal Antibody Tags: , , , , ,

Summary

Production Name

Phospho-Synapsin I (Ser553) Rabbit Monoclonal Antibody

Description

Rabbit Monoclonal antibody

Host

Rabbit

Application

WB

Reactivity

Human,Mouse,Rat

 

Performance

Conjugation

Unconjugated

Modification

Phosphorylated

Isotype

IgG

Clonality

Monoclonal Antibody

Form

Liquid

Storage

Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.

Buffer

Supplied in 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40% Glycerol, 0.01% sodium azide and 0.05% protective protein . Stable for 12 months from date of receipt.

Purification

Affinity Purification

 

Immunogen

Gene Name

Phospho-Synapsin I (Ser553)

Alternative Names

SYNI; SYN1a; SYN1b

Gene ID

6853, 20964, 24949

SwissProt ID

P17600, O88935, P09951

 

Application

Dilution Ratio

WB: 1:2000-1:20000

Molecular Weight

Calculated MW:74 kDa; Observed MW:77 kDa

 

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]

 

Research Area