ATP2A1/SERCA1 Antikörper

Produktnummer ABIN7243562

Produktdetails anti-ATP2A1/SERCA1 Antikörper

Target: ATP2A1/SERCA1 (ATP2A1) (ATPase, Ca++ Transporting, Cardiac Muscle, Fast Twitch 1 (ATP2A1))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser ATP2A1/SERCA1 Antikörper ist unkonjugiert

Applikation: ELISA, Immunohistochemistry (IHC)

Produktmerkmale: Polyclonal Antibody

Aufreinigung: Affinity purification

Immunogen: Synthetic peptide of human ATP2A1

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IHC 1:50-1:200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.7 mg/mL

Buffer: PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4

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 ATP2A1/SERCA1

Target: ATP2A1/SERCA1 (ATP2A1) (ATPase, Ca++ Transporting, Cardiac Muscle, Fast Twitch 1 (ATP2A1))

Andere Bezeichnung: ATP2A1 (ATP2A1 Produkte)

Synonyme: cb279 antikoerper, serca antikoerper, serca1 antikoerper, wu:cegs655 antikoerper, wu:fb17h11 antikoerper, wu:fb19b10 antikoerper, zgc:92110 antikoerper, ATP2A1 antikoerper, atp2a antikoerper, atp2a2 antikoerper, atp2b antikoerper, ca-p60a antikoerper, dar antikoerper, serca2 antikoerper, SERCA1 antikoerper, ATP2A3 antikoerper, SERCA1a antikoerper, Serca1 antikoerper, ATP2A antikoerper, ATPase, Ca++ transporting, cardiac muscle, fast twitch 1 antikoerper, ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 1 antikoerper, ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 S homeolog antikoerper, atp2a1 antikoerper, ATP2A1 antikoerper, atp2a2.S antikoerper, Atp2a1 antikoerper

Hintergrund: This gene encodes one of the SERCA Ca(2+)-ATPases, which are intracellular pumps located in the sarcoplasmic or endoplasmic reticula of muscle cells. This enzyme catalyzes the hydrolysis of ATP coupled with the translocation of calcium from the cytosol to the sarcoplasmic reticulum lumen, and is involved in muscular excitation and contraction. Mutations in this gene cause some autosomal recessive forms of Brody disease, characterized by increasing impairment of muscular relaxation during exercise. Alternative splicing results in three transcript variants encoding different isoforms.

NCBI Accession: NP_775293

UniProt: O14983

Pathways: Ribonucleoside Biosynthetic Process