CD14 (Monocyte / Macrophage Marker) (LPSR/2385), 0.2mg/mL, Clone: [LPSR/2385], Mouse, Monoclonal

Catalog Number: BOT-BNUB2385-500
Article Name: CD14 (Monocyte / Macrophage Marker) (LPSR/2385), 0.2mg/mL, Clone: [LPSR/2385], Mouse, Monoclonal
Biozol Catalog Number: BOT-BNUB2385-500
Supplier Catalog Number: BNUB2385-500
Alternative Catalog Number: BOT-BNUB2385-500-500UL
Manufacturer: Biotium
Host: Mouse
Category: Antikörper
Application: FC, IHC, WB
Species Reactivity: Human
Immunogen: Recombinant fragment of human CD14 protein (around aa 25-148) (exact sequence is proprietary)
Alternative Names: Lipopolysaccharide receptor, LPS-R, LPSR, Mo2, Monocyte Differentiation Antigen 14, Myeloid cell-specific leucine-rich glycoprotein
This antibody recognizes a protein of 55 kDa, identified as CD14 (also known lipopolysaccharide receptor). CD14 is expressed strongly on monocytes and macrophage and weakly on the surface of neutrophils. CD14 is anchored to cells by linkage to glycosylphosphatidylinositol (GPI) and functions as a high affinity receptor for complexes of LPS and LPS binding protein (LBP). Soluble CD14, also binding to LPS, acts at physiological concentration as an LPS agonist and has, at higher concentrations, an LPS antagonizing effect in cell activation.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.
Clonality: Monoclonal
Concentration: 0.2 mg/mL
Clone Designation: [LPSR/2385]
Molecular Weight: 55 kDa
UniProt: P08571
Buffer: PBS, 0.05% BSA, 0.05% azide
Source: Animal
Application Notes: Higher concentration may be required for direct detection using primary antibody conjugates than for indirect detection with secondary antibody|Immunohistology (formalin): 1-2 ug/mL for 30 minutes at RT|Staining of formalin-fixed tissues requires boiling tissue sections in 10 mM citrate buffer, pH 6.0, for 10-20 minutes followed by cooling at RT for 20 minutes|Optimal dilution for a specific application should be determined by user