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SYP

GeneName

SYP

Summary

SYP, also known as synaptophysin or BM89 antigen, is a 34 kDa integral membrane protein primarily expressed in neurons. It is a key component of synaptic vesicles, localised to the presynaptic membrane and involved in the organisation and maturation of synaptic vesicles. SYP plays a crucial role in synaptic transmission by regulating synaptic vesicle priming and endocytosis, thereby influencing both short-term and long-term neuronal synaptic plasticity. Its presence at excitatory synapses and neuromuscular junctions highlights its importance in neurotransmitter release and neuronal communication.

Importance

SYP is relevant to: - Understanding synaptic mechanisms in neurodegenerative diseases, as alterations in synaptic vesicle dynamics can contribute to neuronal dysfunction. - Research on synaptic plasticity, which is fundamental to learning and memory processes. - Investigating the role of synaptic proteins in psychiatric disorders, where synaptic transmission may be disrupted. - The development of targeted therapies for neurological conditions by providing insights into synaptic vesicle biology and its regulatory pathways.

Top Products

For researchers investigating SYP, we highly recommend the Anti-Synaptophysin antibody [YE269] (ab32127). This top-selling recombinant antibody has garnered an impressive 430 citations, underscoring its reliability and trust within the scientific community. It has been validated in knockout models and is suitable for a variety of applications, including Western blotting (WB), immunohistochemistry (IHC), and immunocytochemistry (ICC). This versatility makes it an excellent choice for those seeking consistent and effective detection of synaptophysin in their studies. The Anti-Synaptophysin antibody [SP11] - Synaptic Marker ELISA Kit (ab16659), supported by 33 citations, is an excellent option for researchers looking to accurately measure synaptophysin levels in their samples.

Abcam Product Citation Summary

The data indicates a significant focus on the use of SYP antibodies in various studies related to synaptic function and plasticity, particularly in mouse and rat models. The applications primarily involve Western blotting and immunohistochemistry, highlighting the importance of SYP in understanding neurological conditions and synaptic changes. Studies also explore the effects of different treatments and conditions, such as stress, Alzheimer's disease, and neuronal differentiation.

Abcam Product Citation Table

ab14692
Mouse
IHC
Effects of glutamine supplementation on stress-induced changes
322249
ab14692
Mouse
IHC
Chronic immobilization stress
32224923
ab14692
Mouse
WB
Plasticity-related proteins
32087004
ab14692
Mouse
WB
Hippocampal neuronal stimulation
32087004
ab14692
Mouse
WB
Aβo-induced impairments in plasticity-related proteins
32087004
ab178412
Rat
WB
Neurite outgrowth markers and synaptic connection
32308720
ab32127
Human
WB
Androgen-deprivation and neuroendocrine transdifferentiation in prostate cancer
31959826
ab32127
Rat
WB
Effect of FMT on cognition
32357144
ab32127
Rat
WB
Cognition changes in aged rats
32357144
ab32127
Human
WB
Alzheimer's disease progression
32514860
ab32127
Mouse
WB
Synaptic protein levels in CaMKIIα‐tTA/A53T α‐syn dTg mice
31990455
ab52636
Rat
ICC-IF
Effects of AgNPs on synaptic structures
23782671
ab8049
Rat
IHC
Alzheimer's disease
26610600
ab8049
Mouse
WB
Presynaptic protein levels
32047191
ab8049
Mouse
WB
Synaptic density in APP/PS1 mice
32392535
ab8049
Mouse
WB
Tau oligomers and synaptic dysfunction
21645391
ab8049
Mouse
WB
Hippocampal protein expression
33168800
ab8049
Human
WB
Alzheimer's disease
33139712

Domain

The calcium-binding activity is thought to be localized in the cytoplasmic tail of the protein.

Function

Possibly involved in structural functions as organizing other membrane components or in targeting the vesicles to the plasma membrane. Involved in the regulation of short-term and long-term synaptic plasticity (By similarity).

Involvement in disease

Intellectual developmental disorder, X-linked 96

XLID96

A disorder characterized by significantly below average general intellectual functioning associated with impairments in adaptive behavior and manifested during the developmental period.

None

The disease is caused by variants affecting the gene represented in this entry.

Post-translational modifications

Ubiquitinated; mediated by SIAH1 or SIAH2 and leading to its subsequent proteasomal degradation.

Phosphorylated by SRC.

Sequence Similarities

Belongs to the synaptophysin/synaptobrevin family.

Tissue Specificity

Expressed in the brain, with expression in the hippocampus, the neuropil in the dentate gyrus, where expression is higher in the outer half of the molecular layer than in the inner half, and in the neuropil of CA4 and CA3 (PubMed:8838578). Expressed in the putamen (at protein level) (PubMed:17296554).

Cellular localization

Alternative names

Synaptophysin, Major synaptic vesicle protein p38, SYP

swissprot:P08247 omim:313475 entrezGene:6855