SYN1 Antikörper (AA 362-511)
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- Target Alle SYN1 Antikörper anzeigen
- SYN1 (Synapsin I (SYN1))
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Bindungsspezifität
- AA 362-511
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Reaktivität
- Human, Maus, Ratte
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Wirt
- Maus
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Klonalität
- Monoklonal
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Konjugat
- Dieser SYN1 Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Immunocytochemistry (ICC), Flow Cytometry (FACS)
- Aufreinigung
- purified
- Immunogen
- Purified recombinant fragment of human SYN1 (AA: 362-511) expressed in E. coli.
- Klon
- 7B1D9
- Isotyp
- IgG1
- Top Product
- Discover our top product SYN1 Primärantikörper
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- Applikationshinweise
- ELISA: 1:10000, WB: 1:500 - 1:2000, IHC: , ICC: 1:200 - 1:1000, FCM:
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Buffer
- Purified antibody in PBS with 0.05 % sodium azide
- Konservierungsmittel
- Sodium azide
- Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Lagerung
- 4 °C/-20 °C
- Informationen zur Lagerung
- 4°C, -20°C for long term storage
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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
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Description: 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.,
Aliases: SYNI, SYN1a, SYN1b
- Molekulargewicht
- 74.1 kDa
- Gen-ID
- 6853
- HGNC
- 6853
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