SYN1 Antikörper (pSer9)

Produktnummer ABIN3019917

Produktdetails anti-SYN1 Antikörper

Target: SYN1 (Synapsin I (SYN1))

Bindungsspezifität: pSer9

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser SYN1 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunofluorescence (IF)

Kreuzreaktivität: Human, Maus, Ratte

Produktmerkmale: Phosphorylated Antibodies

Immunogen: A phospho specific peptide corresponding to residues surrounding S9 of human SYN1

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB,1:500 - 1:2000,IF,1:100 - 1:200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Avoid freeze / thaw cycles.

Details zu SYN1

Target: SYN1 (Synapsin I (SYN1))

Andere Bezeichnung: SYN1 (SYN1 Produkte)

Synonyme: SYN1a antikoerper, SYN1b antikoerper, SYNI antikoerper, Syn-1 antikoerper, SYN I antikoerper, si:dkey-90n12.3 antikoerper, synapsin I antikoerper, synapsin I L homeolog antikoerper, SYN1 antikoerper, Syn1 antikoerper, syn1.L antikoerper, syn1 antikoerper

Hintergrund: 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.,SYN1,SYN1a,SYN1b,SYNI,Signal Transduction,G protein signaling,G2/M DNA Damage Checkpoint,Neuroscience,Cell Type Marker,Neuron marker,Synapse marker,Protein phosphorylation,SYN1

Molekulargewicht: 70 kDa/74 kDa

Gen-ID: 6853

UniProt: P17600