MYL3/CMLC1 Antikörper

Produktnummer ABIN2430489

Produktdetails anti-MYL3/CMLC1 Antikörper

Target: MYL3/CMLC1 (MYL3) (Myosin, Light Chain 3 (MYL3))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser MYL3/CMLC1 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunohistochemistry (IHC), ELISA

Aufreinigung: Affinity purification

Immunogen: Recombinant protein of human MYL3

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:1000-1:5000, IHC 1:50-1:200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.4 mg/mL

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

Konservierungsmittel: Sodium azide

Handhabung: Avoid freeze / thaw cycles.

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Avoid freeze / thaw cycles.

Details zu MYL3/CMLC1

Target: MYL3/CMLC1 (MYL3) (Myosin, Light Chain 3 (MYL3))

Andere Bezeichnung: MYL3 (MYL3 Produkte)

Synonyme: CMD1S antikoerper, CMH1 antikoerper, MPD1 antikoerper, MYHCB antikoerper, SPMD antikoerper, SPMM antikoerper, B-MHC antikoerper, MyHC-I antikoerper, Myhc-b antikoerper, Myhcb antikoerper, beta-MHC antikoerper, MLC1s antikoerper, MLC1v antikoerper, Mylc antikoerper, VLC1 antikoerper, Mylc1v antikoerper, CMH8 antikoerper, MLC1SB antikoerper, MLC1V antikoerper, mlc1v antikoerper, myl3-a antikoerper, myl3-b antikoerper, myl3.L antikoerper, zgc:103441 antikoerper, myosin heavy chain 7 antikoerper, myosin, heavy polypeptide 7, cardiac muscle, beta antikoerper, myosin, light polypeptide 3 antikoerper, myosin light chain 3 antikoerper, myosin light chain 3 S homeolog antikoerper, cardiac myosin light chain-1 antikoerper, MYH7 antikoerper, Myh7 antikoerper, Myl3 antikoerper, MYL3 antikoerper, myl3.S antikoerper, cmlc1 antikoerper

Hintergrund: MYL3 encodes myosin light chain 3, an alkali light chain also referred to in the literature as both the ventricular isoform and the slow skeletal muscle isoform. Mutations in MYL3 have been identified as a cause of mid-left ventricular chamber type hypertrophic cardiomyopathy.

Molekulargewicht: Calculated MW: 22 kDa