Mouse Monoclonal Salmonella LPS antibody. Suitable for WB, ELISA and reacts with Salmonella enteritidis, Purified native protein - Salmonella enteritidis, Salmonella typhimurium samples.
pH: 6 - 8.5
Constituents: 50% Glycerol (glycerin, glycerine), 50% PBS
WB | ELISA | |
---|---|---|
Purified native protein - Salmonella enteritidis | Tested | Not recommended |
Salmonella enteritidis | Tested | Tested |
Salmonella typhimurium | Expected | Expected |
Species | Dilution info | Notes |
---|---|---|
Species Salmonella enteritidis | Dilution info 1/1000.00000 - 1/2000.00000 | Notes - |
Species Purified native protein - Salmonella enteritidis | Dilution info 1/1000.00000 - 1/2000.00000 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Salmonella typhimurium | Dilution info 1/1000.00000 - 1/2000.00000 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Salmonella enteritidis | Dilution info - | Notes (assay dependent) |
Species | Dilution info | Notes |
---|---|---|
Species Salmonella typhimurium | Dilution info - | Notes (assay dependent) |
Species | Dilution info | Notes |
---|---|---|
Species Purified native protein - Salmonella enteritidis | Dilution info - | Notes - |
Mouse Monoclonal Salmonella LPS antibody. Suitable for WB, ELISA and reacts with Salmonella enteritidis, Purified native protein - Salmonella enteritidis, Salmonella typhimurium samples.
pH: 6 - 8.5
Constituents: 50% Glycerol (glycerin, glycerine), 50% PBS
Reacts with LPS of Salmonella enteritidis and Salmonella typhimurium. Does not react with other gram-negative food-poisoning bacteria like E. coli ,V. parahaemolyticus and Campylobacter species.
This antibody recognizes common antigenic determinants that are found in the structural components of Salmonella LPS.
Purified from TCS.
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Salmonella LPS often referred to as lipopolysaccharide is an important component of the outer membrane of Salmonella bacteria. It consists of three main parts: lipid A a core oligosaccharide and an O-antigen polysaccharide. The lipid A portion is known for its endotoxic properties and typically has a mass around 2 kDa. Salmonella LPS is expressed on the surface of Salmonella spp. facilitating the interaction with host cells during infection. Its recognition is pivotal for the innate immune response and is commonly studied in the context of Western blot analysis with anti-Salmonella antibodies.
Salmonella LPS plays a critical role in bacterial virulence and survival. It is part of the outer membrane layer contributing to the structural integrity of the bacterium and protecting against hostile environmental conditions. Additionally LPS is important in the formation of biofilms enabling the bacteria to adhere to surfaces and resist antimicrobial agents. The molecule also forms complexes with proteins on the host's immune cells triggering strong immune reactions. The interactions often lead to inflammatory responses via cytokine release making it an important player in immune modulation.
The functions of Salmonella LPS are notably involved in the toll-like receptor (TLR) signaling pathway and the NF-kappa B pathway. In the TLR pathway LPS binds to TLR4 on immune cells activating downstream signaling that leads to the production of pro-inflammatory cytokines. The NF-kappa B pathway gets activated as a consequence further amplifying the immune response. Proteins like MyD88 and TRIF are closely related to Salmonella LPS in these pathways as they serve as intermediaries in signal transduction.
Salmonella LPS is linked to conditions like septic shock and gastroenteritis. The endotoxin property of the lipid A component can lead to severe inflammatory responses which might cause septic shock when the bacterial infection becomes systemic. Salmonella LPS also plays a role in gastroenteritis a result of inflammation of the stomach and intestines primarily caused by infection. It interacts with immune receptors like TLR4 and CD14 which modulate the inflammatory response that ultimately contributes to the disease pathology.
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This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
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Terms & Conditions.
Blocked with 5 % skimmed milk.
They showed similar band patterns characteristic of LPS, O-chain repeating unit.
All lanes: Western blot - Anti-Salmonella LPS antibody [se-01] (ab243104) at 1/250 dilution
Lane 1: Crude extract of S. enteritidis cells at 1 µg
Lane 2: Purified LPS of S. enteritidis cells at 1 µg
The plate was coated with indicated amounts of the extract of S. Enteriditis cells. ab243104 was used at a 1/500 dilution.
Lane 1: S. Enteritidis
Lane 2: V. Parahaemolyticus
Lane 3: E. Coli
Lane 4: E. Coli O157:H7
Panel B: Extracts of each strain of food poisoning bacteria were coated onto 5 areas of a nitrocellulose membrane. The membrane was soaked and reacted with ab243104.
SE: S. Enteritidis, EC: E. Coli, CJ: C, Jejuni, VP: V, Parahaemolyticus.
All lanes: Western blot - Anti-Salmonella LPS antibody [se-01] (ab243104)
The wells of the plate were coated with crude extract of S. Enteritidis (100 μL, 1 μg/mL). After blocking with 5% skimmed milk, 100 μl of antibody at the indicated dilution was added to the each well. HRP-conjugate goat anti-mouse IgG (100 μL, X2000 dilution) was added. Color was developed with orthophenylenediamine as substrate. Optical densities (OD) measured at 490nm.
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