PIPA585691
Synapsin 1 Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA585691-Each-of-1 | In Stock | ₹ 46,502.50 |
PIPA585691 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 46,502.50
GST (18%): ₹ 8,370.45
Total Price: ₹ 54,872.95
Antigen
Synapsin 1
Classification
Polyclonal
Conjugate
Unconjugated
Gene
SYN1
Gene Alias
Brain protein 4.1, SYN1, Syn-1, SYN1a, SYN1b, Syn1-S, synapsin 1, synapsin I, synapsin Ia, synapsin Ib, synapsin-1, SYNI, truncated synapsin 1-S
Host Species
Rabbit
Purification Method
Antigen affinity chromatography
Regulatory Status
RUO
Gene ID (Entrez)
20964, 6853
Content And Storage
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Form
Liquid
Applications
Western Blot
Concentration
0.23 mg/mL
Formulation
PBS with 1% BSA, 20% glycerol and 0.025% ProClin 300, pH 7
Gene Accession No.
O88935, P17600
Gene Symbols
SYN1
Immunogen
Recombinant protein encompassing a sequence within the center region of human Synapsin I.
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human, Mouse
Product Type
Antibody
Isotype
IgG
Related Products
Description
- Keep as concentrated solution
- Predicted reactivity: Mouse (100%), Rat (100%), Xenopus laevis (86%), Pig (99%), Bovine (98%)
- Positive Control: mouse brain
- Store product as a concentrated solution
- Centrifuge briefly prior to opening the vial
- SYN1 (synapsin 1) is a member of the synapsin gene family
- Synapsins encode neuronal phosphoproteins that associate with the cytoplasmic surface of synaptic vesicles
- Family members are characterized by common protein domains and are implicated in synaptogenesis and the modulation of neurotransmitter release, suggesting a potential role in several neuropsychiatric diseases
- Synapsin 1 plays a role in regulation of axonogenesis and synaptogenesis
- It 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.