SPG7 Antikörper (AA 71-120)

Produktnummer ABIN7231494

Der Kaninchen Polyklonal anti-SPG7 Antikörper (ABIN7231494) detektiert spezifisch SPG7 in WB und ELISA. Dieser Antikörper reagiert spezifisch mit Proben aus Human, Maus und Ratte.

Kurzübersicht für SPG7 Antikörper (AA 71-120) (ABIN7231494)

Target: SPG7 (Spastic Paraplegia 7 (SPG7))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser SPG7 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA

Produktdetails anti-SPG7 Antikörper

Bindungsspezifität: AA 71-120

Verwendungszweck: Rabbit Anti-SPG7 Polyclonal Antibody

Spezifität: The antibody detects endogenous levels of SPG7 protein

Aufreinigung: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogen: Synthesized peptide derived from part region of human SPG7 protein at AA range: 71-120

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-2000,ELISA 1:5000-20000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 mg/mL

Buffer: PBS, 50 % glycerol, 0.05 % Proclin 300, 0.05 %BSA

Konservierungsmittel: ProClin

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

Lagerung: -20 °C

Informationen zur Lagerung: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Haltbarkeit: 12 months

Details zu SPG7

Target: SPG7 (Spastic Paraplegia 7 (SPG7))

Andere Bezeichnung: SPG7

Hintergrund: Paraplegin, Cell matrix adhesion regulator, Spastic paraplegia 7 proteinSPG7 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 SPG7 cause autosomal recessive spastic paraplegia 7. Two transcript variants encoding distinct isoforms have been identified.

Molekulargewicht: 87kD

Gen-ID: 6687

UniProt: Q9UQ90