Calnexin (Endoplasmic Reticulum Marker) (CANX/1541), Biotin conjugate, 0.1mg/mL, Clone: [CANX/1541], Mouse, Monoclonal

Artikelnummer: BOT-BNCB1541-100
Artikelname: Calnexin (Endoplasmic Reticulum Marker) (CANX/1541), Biotin conjugate, 0.1mg/mL, Clone: [CANX/1541], Mouse, Monoclonal
Artikelnummer: BOT-BNCB1541-100
Hersteller Artikelnummer: BNCB1541-100
Alternativnummer: BOT-BNCB1541-100-100UL
Hersteller: Biotium
Wirt: Mouse
Kategorie: Antikörper
Applikation: FC, IF, IHC, WB
Spezies Reaktivität: Human
Immunogen: Recombinant N-terminal fragment of human Calnexin protein (exact sequence is proprietary)
Konjugation: Biotin
Alternative Synonym: Calnexin, CANX, IP90, Major histocompatibility complex class I antigen-binding protein p88
Calnexin is a type-I integral membrane protein of the endoplasmic reticulum (ER). It is a calcium-binding chaperone protein that interacts transiently with newly synthesized N-linked glycoproteins, facilitating protein folding and assembly. It may also play a central role in the quality control of protein folding by retaining incorrectly folded protein subunits within the ER for degradation. Primary antibodies are available purified, or with a selection of fluorescent CF Dyes and other labels. CF Dyes offer exceptional brightness and photostability. Note: Conjugates of blue fluorescent dyes like CF405S and CF405M are not recommended for detecting low abundance targets, because blue dyes have lower fluorescence and can give higher non-specific background than other dye colors.
Klonalität: Monoclonal
Konzentration: 0.1 mg/mL
Klon-Bezeichnung: [CANX/1541]
Molekulargewicht: 67 kDa (predicted), 80-90 kDa (observed)
UniProt: P27824
Puffer: PBS, 0.1% BSA, 0.05% azide
Quelle: Animal
Anwendungsbeschreibung: Higher concentration may be required for direct detection using primary antibody conjugates than for indirect detection with secondary antibody|Immunofluorescence: 0.5-1 ug/mL|Immunohistology (formalin) 1-2 ug/mL|Staining of formalin-fixed tissues is enhanced by boiling tissue sections in 10 mM Tris, 1 mM EDTA pH 9.0 for 10-20 min followed by cooling at RT for 20 min|Flow Cytometry 0.5-1 ug/million cells/0.1 mL|Western blotting 0.5-1 ug/mL|Optimal dilution for a specific application should be determined by user