AFG3L2 Antikörper (AA 161-245)

Produktnummer ABIN7825258

Der Kaninchen-Polyklonal Anti-AFG3L2-Antikörper wurde für WB validiert. Er ist geeignet zum Nachweis von AFG3L2 in Proben aus Zebrafisch (Danio rerio). }

Kurzübersicht für AFG3L2 Antikörper (AA 161-245) (ABIN7825258)

Target: AFG3L2 (AFG3-Like Protein 2 (AFG3L2))

Reaktivität: Zebrafisch (Danio rerio)

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser AFG3L2 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Produktdetails anti-AFG3L2 Antikörper

Bindungsspezifität: AA 161-245

Verwendungszweck: Anti-Zebrafish AFG3L2 Antibody

Produktmerkmale: Anti-Zebrafish AFG3L2 Antibody catalog # AZA9JRG9. Tested in WB applications. This antibody reacts with Zebrafish. This is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications.

Aufreinigung: Immunogen affinity purified.

Immunogen: E.coli-derived zebrafish AFG3L2 recombinant protein (Position: G161-D245).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: Western blot, 0.25-0.5 μg/mL, Zebrafish

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Lyophilized

Rekonstitution: Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

Konzentration: 500 μg/mL

Buffer: Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.

Details zu AFG3L2

Target: AFG3L2 (AFG3-Like Protein 2 (AFG3L2))

Andere Bezeichnung: AFG3L2

Hintergrund: AFG3L2 is the catalytic subunit of the m-AAA protease, an ATP-dependent proteolytic complex of the mitochondrial inner membrane that degrades misfolded proteins and regulates ribosome assembly. In humans, it is encoded by the AFG3L2 gene. This gene encodes a protein localized in mitochondria and closely related to paraplegin. The paraplegin gene is responsible for an autosomal recessive form of hereditary spastic paraplegia. And this gene is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders as well as spastic ataxia-neuropathy syndrome.

Gen-ID: 569168

Pathways: Skeletal Muscle Fiber Development