SOD1 Antikörper

Produktnummer ABIN7384493

Dieses Kaninchen Monoklonal-Antikörper erkennt spezifisch SOD1 in WB und IHC (p). Er zeigt eine Reaktivität gegenüber Human und Ratte.

Kurzübersicht für SOD1 Antikörper (ABIN7384493)

Target: SOD1 (Superoxide Dismutase 1, Soluble (SOD1))

Reaktivität: Human, Ratte

Wirt: Kaninchen

Klonalität: Monoklonal

Konjugat: Dieser SOD1 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Klon: R08-5A5

Produktdetails anti-SOD1 Antikörper

Aufreinigung: Affinity Purified

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:500-1:1000 IHC 1:50-1:100

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Konzentration: 300 μg/mL

Buffer: 50 mM Tris-Glycine( pH 7.4), 0.15M NaCl, 40 % Glycerol, 0.01 % Sodium azide and 0.05 % BSA

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.

Details zu SOD1

Target: SOD1 (Superoxide Dismutase 1, Soluble (SOD1))

Andere Bezeichnung: Superoxide Dismutase 1

Hintergrund: ALS,ALS1,Amyotrophic lateral sclerosis 1 adult,Cu/Zn SOD,Cu/Zn superoxide dismutase,Epididymis secretory protein Li 44,HEL S 44,Homodimer,hSod1,Indophenoloxidase A,IPOA,Mn superoxide dismutase,SOD,SOD soluble,SOD1,SOD2,SODC,SODC,Superoxide dismutase [Cu-Zn],Superoxide dismutase 1,Superoxide dismutase 1 soluble,Superoxide dismutase Cu Zn,Superoxide dismutase cystolic,The protein encoded by this gene binds copper and zinc ions and is one of two isozymes responsible for destroying free superoxide radicals in the body. The encoded isozyme is a soluble cytoplasmic protein, acting as a homodimer to convert naturally-occuring but harmful superoxide radicals to molecular oxygen and hydrogen peroxide. The other isozyme is a mitochondrial protein. Mutations in this gene have been implicated as causes of familial amyotrophic lateral sclerosis. Rare transcript variants have been reported for this gene. 

Molekulargewicht:

Observed_MW: 16kDa

Calculated_MW: 16kDa

Gen-ID: 6647

UniProt: P00441

Pathways: Sensory Perception of Sound, Transition Metal Ion Homeostasis