Escherichia coli Lipopolysaccharide (LPS) Antibody (Biotin)

416€ (200 µl)
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935106861
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name
Escherichia coli Lipopolysaccharide (LPS) Antibody (Biotin)
category
Primary Antibodies
provider
Abbexa
reference
abx274403
tested applications
ELISA
Description
Lipopolysaccharide (LPS) Antibody (Biotin) is a rabbit polyclonal antibody (
Documents del producto
Instrucciones
Data sheet
Product specifications
Category | Primary Antibodies |
Immunogen Target | Escherichia coli Lipopolysaccharide (LPS) |
Host | Rabbit |
Reactivity | General |
Recommended Dilution | IHC (Predicted): 5-20 µg/ml, IF/ICC (Predicted): 5-20 µg/ml. Optimal dilutions/concentrations should be determined by the end user. |
Clonality | Polyclonal |
Conjugation | Biotin |
Isotype | IgG |
Purification | Purified by antigen-specific affinity chromatography. |
Size 1 | 200 µl |
Size 2 | 1 ml |
Form | Liquid |
Tested Applications | ELISA |
Buffer | 0.01 M PBS, pH 7.4, containing 0.05% Proclin-300, 50% glycerol. |
Availability | Shipped within 5-15 working days. |
Storage | Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles. Avoid repeated freeze/thaw cycles. |
Dry Ice | No |
Alias | LPS |
Background | Antibody anti-LPS |
Status | RUO |
Descripción
Lipopolysaccharides (LPS) are large molecules found in the outer membrane of Gram-negative bacteria, playing a crucial role in the structural integrity of bacterial cells and acting as a potent activator of the immune system. Composed of lipid A, a core oligosaccharide, and an O-antigen polysaccharide, LPS is a critical factor in bacterial pathogenicity. Lipid A is the bioactive component that triggers immune responses by binding to the Toll-like receptor 4 (TLR4) complex on immune cells, leading to the activation of nuclear factor-kappa B (NF-κB) and the release of pro-inflammatory cytokines such as IL-6 and TNF-alpha. While LPS is essential for host defense, its excessive activation can result in septic shock, characterized by systemic inflammation, organ failure, and high mortality. Therapeutic strategies targeting LPS-TLR4 signaling pathways are being explored to manage sepsis and other inflammatory conditions.
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