UBC13 Antibody, Goat, Polyclonal

Artikelnummer: ROC-600-101-342
Artikelname: UBC13 Antibody, Goat, Polyclonal
Artikelnummer: ROC-600-101-342
Hersteller Artikelnummer: 600-101-342
Alternativnummer: ROC-600-101-342
Hersteller: Rockland Immunochemicals
Wirt: Goat
Kategorie: Antikörper
Applikation: ELISA, WB
Spezies Reaktivität: Human
Immunogen: This affinity purified antibody was prepared from whole rabbit serum produced by repeated immunizations with a synthetic peptide corresponding to an internal region near amino acids 30-55 of human UBC13 protein.
Konjugation: Unconjugated
Alternative Synonym: goat anti-UBC13 antibody, UBEN2, BLU, Ubch13, UBC 13, UbCH ben antibody, Ube 2N antibody, ubiquitin carrier protein N antibody, Ubiquitin conjugating enzyme E2N antibody, ubiquitin protein ligase N antibody, Ubiquitin-conjugating enzyme E2 N antibody
Klonalität: Polyclonal
Konzentration: 1.25 mg/mL by UV absorbance at 280 nm
NCBI: 7334
UniProt: P61088
Puffer: 0.02 M Potassium Phosphate, 0.15 M Sodium Chloride, pH 7.2
Formulierung: Liquid (sterile filtered)
Target-Kategorie: Human
Antibody Type: Primary Antibody
Application Verdünnung: ELISA: 1:5,000 - 1:25,000, WB: 1:500 - 1:2,000
Anwendungsbeschreibung: This affinity purified antibody has been tested for use in ELISA and western blot. Specific conditions for reactivity should be optimized by the end user. Expect a band approximately 17 kDa in size corresponding to UBC13 protein by western blotting in th
Western blot using Rocklands affinity purified anti-UBC13 antibody shows detection of UBC13 protein in human small intestine lysate (lane 1) but not in mouse thymus lysate (lane 2). The heavily stained band in lane 1 (arrowhead) indicates this particular gel was overloaded with protein. The identity of minor reactive bands is unknown but could represent E2 complexes. Each lane contains approximately 20 ug of lysate. Primary antibody was used at a 1:500 dilution. The membrane was washed and reacted with a 1:10,000 dilution of Alexa FluorTM 680 conjugated Rb-a-Goat IgG. Molecular weight estimation was made by comparison to prestained MW markers indicated at the left (lane M). Other detection systems will yield similar results.