Spastin Antikörper
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- Target Alle Spastin (SPAST) Antikörper anzeigen
- Spastin (SPAST)
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Reaktivität
- Maus, Human, Ratte
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser Spastin Antikörper ist unkonjugiert
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Applikation
- ELISA, Immunohistochemistry (IHC)
- Produktmerkmale
- Polyclonal Antibody
- Aufreinigung
- Affinity purification
- Immunogen
- Synthetic peptide of human SPAST
- Isotyp
- IgG
- Top Product
- Discover our top product SPAST Primärantikörper
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- Applikationshinweise
- IHC 1:50-1:200
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- 0.6 mg/mL
- Buffer
- PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
- 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
- Spastin (SPAST)
- Andere Bezeichnung
- SPAST (SPAST Produkte)
- Synonyme
- CG5977 antikoerper, D-spastin antikoerper, Dmel\\CG5977 antikoerper, Dspastin antikoerper, Spas antikoerper, zgc:85952 antikoerper, SPAST antikoerper, spg4 antikoerper, LOC100224472 antikoerper, ADPSP antikoerper, FSP2 antikoerper, SPG4 antikoerper, Spg4 antikoerper, mKIAA1083 antikoerper, spastin antikoerper, spastin S homeolog antikoerper, spas antikoerper, spast antikoerper, SPAST antikoerper, Spast antikoerper, spast.S antikoerper
- Hintergrund
- This gene encodes a member of the AAA (ATPases associated with a variety of cellular activities) protein family. Members of this protein family share an ATPase domain and have roles in diverse cellular processes including membrane trafficking, intracellular motility, organelle biogenesis, protein folding, and proteolysis. The encoded ATPase may be involved in the assembly or function of nuclear protein complexes. Two transcript variants encoding distinct isoforms have been identified for this gene. Other alternative splice variants have been described but their full length sequences have not been determined. Mutations associated with this gene cause the most frequent form of autosomal dominant spastic paraplegia 4.
- NCBI Accession
- NP_055761
- UniProt
- Q9UBP0
- Pathways
- Microtubule Dynamics, M Phase, Regulation of Cell Size
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