SCO2 Antikörper (C-Term)

Produktnummer ABIN1536825

Dieses Anti-SCO2-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von SCO2 in WB. Geeignet für Human.

Kurzübersicht für SCO2 Antikörper (C-Term) (ABIN1536825)

Target: SCO2 (SCO2 Cytochrome C Oxidase Assembly Protein (SCO2))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser SCO2 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Klon: RB30400

Produktdetails anti-SCO2 Antikörper

Bindungsspezifität: AA 196-224, C-Term

Homologie: B, M

Aufreinigung: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This SCO2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 196-224 amino acids from the C-terminal region of human SCO2.

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: WB: 1:1000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

Konservierungsmittel: Sodium azide

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

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: SCO2 Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

Haltbarkeit: 6 months

Details zu SCO2

Target: SCO2 (SCO2 Cytochrome C Oxidase Assembly Protein (SCO2))

Andere Bezeichnung: SCO2

Hintergrund: Cytochrome c oxidase (COX) catalyzes the transfer of electrons from cytochrome c to molecular oxygen, which helps to maintain the proton gradient across the inner mitochondrial membrane that is necessary for aerobic ATP production. Human COX is a multimeric protein complex that requires several assembly factors, this gene encodes one of the COX asembly factors. The encoded protein is a metallochaperone that is involved in the biogenesis of cytochrome c oxidase subunit II. Mutations in this gene are associated with fatal infantile encephalocardiomyopathy.

Molekulargewicht: 29810

Gen-ID: 9997

NCBI Accession: NP_001162580, NP_001162581, NP_001162582, NP_005129

UniProt: O43819

Pathways: Transition Metal Ion Homeostasis, Warburg Effekt