SGCA Antikörper (Middle Region)

Produktnummer ABIN5516845

Produktdetails anti-SGCA Antikörper

Target: SGCA (Sarcoglycan, alpha (50kDa Dystrophin-Associated Glycoprotein) (SGCA))

Bindungsspezifität: Middle Region

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser SGCA Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Sequenz: QVIEVTAYNR DSFDTTRQRL VLEIGDPEGP LLPYQAEFLV RSHDAEEVLP

Produktmerkmale: This is a rabbit polyclonal antibody against SGCA. It was validated on Western Blot.

Aufreinigung: Affinity purified

Immunogen: The immunogen is a synthetic peptide directed towards the middle region of Human SGCA

Anwendungsinformationen

Applikationshinweise: Optimal working dilution should be determined by the investigator.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

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: For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.

Details zu SGCA

Target: SGCA (Sarcoglycan, alpha (50kDa Dystrophin-Associated Glycoprotein) (SGCA))

Andere Bezeichnung: SGCA (SGCA Produkte)

Synonyme: Sgca antikoerper, 50-DAG antikoerper, A2 antikoerper, ADL antikoerper, DAG2 antikoerper, DMDA2 antikoerper, LGMD2D antikoerper, SCARMD1 antikoerper, adhalin antikoerper, 50DAG antikoerper, Asg antikoerper, sarcoglycan alpha antikoerper, sarcoglycan, alpha (dystrophin-associated glycoprotein) antikoerper, sarcoglycan, alpha antikoerper, SGCA antikoerper, Sgca antikoerper

Hintergrund: This gene encodes a component of the dystrophin-glycoprotein complex (DGC), which is critical to the stability of muscle fiber membranes and to the linking of the actin cytoskeleton to the extracellular matrix. Its expression is thought to be restricted to striated muscle. Mutations in this gene result in type 2D autosomal recessive limb-girdle muscular dystrophy. Multiple transcript variants encoding different isoforms have been found for this gene.

Alias Symbols: SGCA, ADL, DAG2,

Protein Size: 263

Gen-ID: 6442

NCBI Accession: NP_001129169