SPG7 Antikörper (AA 1-250)
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- Target Alle SPG7 Antikörper anzeigen
- SPG7 (Spastic Paraplegia 7 (SPG7))
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Bindungsspezifität
- AA 1-250
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Reaktivität
- Human
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser SPG7 Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB), Immunohistochemistry (IHC)
- Sequenz
- MAVLLLLLRA LRRGPGPGPR PLWGPGPAWS PGFPARPGRG RPYMASRPPG DLAEAGGRAL QSLQLRLLTP TFEGINGLLL KQHLVQNPVR LWQLLGGTFY FNTSRLKQKN KEKDKSKGKA PEEDEEERRR RERDDQMYRE RLRTLLVIAV VMSLLNALST SGGSISWNDF VHEMLAKGEV QRVQVVPESD VVEVYLHPGA VVFGRPRLAL MYRMQVANID KFEEKLRAAE DELNIEAKDR IPVSYKRTGF
- Kreuzreaktivität
- Human, Maus, Ratte
- Produktmerkmale
- Polyclonal Antibodies
- Immunogen
- Recombinant fusion protein containing a sequence corresponding to amino acids 1-250 of human SPG7 (NP_003110.1).
- Isotyp
- IgG
- Top Product
- Discover our top product SPG7 Primärantikörper
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- Applikationshinweise
- WB,1:1000 - 1:2000,IHC,1:50 - 1:200
- Kommentare
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HIGH QUALITY
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- 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
- SPG7 (Spastic Paraplegia 7 (SPG7))
- Andere Bezeichnung
- SPG7 (SPG7 Produkte)
- Synonyme
- CAR antikoerper, CMAR antikoerper, PGN antikoerper, SPG5C antikoerper, AI452278 antikoerper, AU015315 antikoerper, Cmar antikoerper, SPG7, paraplegin matrix AAA peptidase subunit antikoerper, SPG7 antikoerper, Spg7 antikoerper
- Hintergrund
- This gene encodes a mitochondrial metalloprotease protein that is a member of the AAA 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. Mutations in this gene cause autosomal recessive spastic paraplegia 7. Two transcript variants encoding distinct isoforms have been identified.,SPG7,CAR,CMAR,PGN,SPG5C,Cell Biology & Developmental Biology,Ubiquitin,Neuroscience,Neurodegenerative Diseases,SPG7
- Molekulargewicht
- 53 kDa/88 kDa
- Gen-ID
- 6687
- UniProt
- Q9UQ90
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