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Anti-Pseudomonas aeruginosa Ex

otoxin A antibody, Mouse monoclonalSIGMA:SAB4200871-100UL
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  • ¥3846
  • SIGMA
  • SAB4200871-100UL
  • 2026年01月07日
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    说明

    一般描述

    Pseudomonas aeruginosa is a rod shaped, gram negative, monoflagellated, aerobic to facultative anaerobe bacteria which commonly inhabits soil and aqueous environments.1,2 Pseudomonas Exotoxin A (PE) is the most potent virulence factor secreted by some strains of P. aeruginosa It is composed of three structural domains, N-terminal domain (I) responsible for the toxin binding to its host cell receptor, middle domain (II) has a role in toxin translocation across the membrane, and C-terminal domain (III) which has ADP-ribosylation activity.4,5

    特异性

    Monoclonal Anti-Exotoxin A from Pseudomonas aeruginosa antibody specifically recognizes Exotoxin A from Pseudomonas aeruginosa (ETA, PE) and has no cross reactivity with staphylococcal enterotoxin A and B (SEA, SEB) and cholera toxin.

    应用

    The antibody may be used in various immunochemical techniques including Immunoblotting (70 kDa) and ELISA.

    生化/生理作用

    P.aeruginosa is considered an opportunistic human pathogen mainly causing disease in immunocompromised patients. It is especially fatal in cystic fibrosis (CF) patients, but also presents a major problem in chronic wounds, burn wounds and infection of implanted biomaterials such as catheters.3The genome of P. aeruginosa encodes a vast arsenal of virulence factors such as, Type 3 secretion system (T3SS), type 4 pilli and several secreted proteases, lipases and phospholipases.1 The Exotoxin A ADP-ribosylation activity inhibits host elongation factor 2 (EF2), and protein synthesis.1 Due to its toxin ADP-ribosylation activity PE is considered as a selective agent for the elimination of specific cell populations resulting in the irreversible shut down of protein synthesis leading to cell death. To reduce the adverse effects of natural PE, mutated PE was used in several attempts to develop recombinant toxin-antibody or cytokines fusion fragments for therapeutic application including cancer immunotherapy.5-9

    外形

    Supplied as a solution in 0.01 M phosphate buffered saline pH 7.4, containing 15 mM sodium azide as a preservative.

    储存及稳定性

    For continuous use, store at 2-8°C for up to one month. For extended storage, freeze in working aliquots. Repeated freezing and thawing is not recommended. If slight turbidity occurs upon prolonged storage, clarify the solution by centrifugation before use. Working dilution samples should be discarded if not used within 12 hours.

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    图标文献和实验
    该产品被引用文献

    Pseudomonas aeruginosa: new insights into pathogenesis and host defenses.

    Shaan L Gellatly et al.

    Pathogens and disease, 67(3), 159-173 (2013-04-27)

    相关实验
    • 【翻译】Development trends for monoclonal antibody cancer therapeutics

      include various modified versions of Pseudomonas exotoxin, Staphylococcus enterotoxin, neocarzinostatin, and the plant-derived molecules ricin (and ricin A chain) and gelonin. Small molecules incorporated in therapeutic immunotoxins included vinblastine

    • Immunohistochemisty-Fluorescence Protocol

      polyclonal activators such as phorbol 12-myristate 13 acetate/ionomycin, anti-CD3+CD28 monoclonal antibody, LPS or bacterial superantigens such as staphylococcal enterotoxin A (SEA), staphylococcal enterotoxin B (SEB) or streptococcal pyrogenic exotoxin

    • Immunohistochemistry: Fluorescence Protocol 2.0

      by centrifugation (400 x g for 5 minutes). Incubate the cells for 30 minutes at room temperature with 50 µL of a biotinylated secondary antibody (either biotin-donkey anti-goat IgG Fab2 diluted 1:700 or biotin-goat anti-mouse IgG1 or IgG2A or IgG2B diluted

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