SYN1 Antikörper (pSer9)
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- Target Alle SYN1 Antikörper anzeigen
- SYN1 (Synapsin I (SYN1))
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Bindungsspezifität
- pSer9
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Reaktivität
- Human, Maus, Ratte
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser SYN1 Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB), Immunofluorescence (IF)
- Produktmerkmale
- Phosphorylated antibody
- Aufreinigung
- Affinity purification
- Immunogen
- A phospho specific peptide corresponding to residues surrounding S9 of human SYN1
- Isotyp
- IgG
- Top Product
- Discover our top product SYN1 Primärantikörper
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- Applikationshinweise
- WB 1:500-1:2000 IF 1:100-1:200
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- 1 mg/mL
- 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.
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- 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.
- Molekulargewicht
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Observed_MW: 74 kDa
Calculated_MW: 70 kDa/74 kDa
- Gen-ID
- 6853
- UniProt
- P17600
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