Antibodies

ELISA

Western Blot

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fliD

Target

Human

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AdipoGen Life Sciences

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Monoclonal

Clonality

IgG1

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Research Use Only

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881775

Gene ID

Business Unit

anti-FliD (Pseudomonas aeruginosa), mAb (rec.) (SH1579-B7) for ELISA, WB in Bacteria by AdipoGen Life Sciences. Order at Bio-Connect.

AG-27B-6322 anti-FliD (Pseudomonas aeruginosa), mAb (rec.)...

anti-FliD (Pseudomonas aeruginosa), mAb (rec.) (SH1579-B7)

Pathogenic bacteria cause a multitude of deadly human diseases. Pseudomonas aeruginosa is a predominant organism within the hospital environment, an increasingly multidrug-resistant microbe, and the most common gram-negative pathogen causing nosocomial pneumonia in the United States. Nearly all P. aeruginosa infections are associated with compromised host defenses, which may include patients with severe burns, diabetes, cancer, organ transplants or additional immunodeficiencies. Many of these pathogenic bacteria possess flagella, molecular machines responsible for cell motility, adherence to host cells, and pathogenicity. Flagella are helix-shaped hollow attachments formed predominantly by thousands of copies of the protein flagellin (also called FliC), anchored in the bacterial membrane by a hook (or joint) that is attached to the basal body and that is composed of rotary motor proteins. A FliD (also called HAP2) oligomer forms the cap protein complex that is located at the tip of the flagellar filament. This complex controls the distal growth of the filament by regulating the assembly of FliC molecules, which are transported through the hollow filament from the cytoplasm to the tip of the flagellum. In the absence of FliD, flagella are not formed, resulting in impaired motility and infectivity. - Recombinant Antibody. Recognizes FliD from Pseudomonas aeruginosa. Applications: ELISA, WB. Clone: SH1579-B7. Isotype: Human IgG1. Formulation: Liquid. In PBS. Pathogenic bacteria cause a multitude of deadly human diseases. Pseudomonas aeruginosa is a predominant organism within the hospital environment, an increasingly multidrug-resistant microbe, and the most common gram-negative pathogen causing nosocomial pneumonia in the United States. Nearly all P. aeruginosa infections are associated with compromised host defenses, which may include patients with severe burns, diabetes, cancer, organ transplants or additional immunodeficiencies. Many of these pathogenic bacteria possess flagella, molecular machines responsible for cell motility, adherence to host cells, and pathogenicity. Flagella are helix-shaped hollow attachments formed predominantly by thousands of copies of the protein flagellin (also called FliC), anchored in the bacterial membrane by a hook (or joint) that is attached to the basal body and that is composed of rotary motor proteins. A FliD (also called HAP2) oligomer forms the cap protein complex that is located at the tip of the flagellar filament. This complex controls the distal growth of the filament by regulating the assembly of FliC molecules, which are transported through the hollow filament from the cytoplasm to the tip of the flagellum. In the absence of FliD, flagella are not formed, resulting in impaired motility and infectivity.

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