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GLU I (PR-2) antibody

Reactivity: Nicotiana tabacum, Potato IL, WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN190719
  • Target
    GLU I (PR-2)
    Reactivity
    Nicotiana tabacum, Potato
    Host
    Rabbit
    Clonality
    Polyclonal
    Application
    Immunolocalization (IL), Western Blotting (WB)
    Cross-Reactivity (Details)
    No cross-reactivity with: Arabidopsis thaliana
    Characteristics
    Expected / apparent Molecular Weight of the Antigene: 37 / 33 kDa
    Purification
    affinity purified
    Immunogen
    purified tobacco class I, basic ß-1,3-glucanase. Purified GLU I consists of a mixture of closely related polypeptides encoded by a family of GLU I genes comprising GLA B5APL3 derived from the sylvestris ancestor of tobacco, GLB P27666 derived from the tomentosiformis ancestor of tobacco and homeologous recombinants (Sperisen et al., 1991). Mature GLU I is processed from a pre-pro-polypeptide (Shinshi et al., 1988).
    Isotype
    IgG
  • Application Notes
    Recommended Dilution: 8 ug/mL with standard ECL (WB).
    Comment

    Important note: for blocking 5 % skim milk in PBS without Ca++ should be used.This antibody is purified by affinity chromarography on Portein G.

    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    For reconstitution add 100 µL of sterile water.
    Buffer
    PBS pH 7.4 (without Ca++)
    Preservative
    Without preservative
    Handling Advice
    Please, remember to spin tubes briefly prior to opening them to avoid any losses that might occur from lyophilized material adhering to the cap or sides of the tubes.
    Once reconstituted make aliquots to avoid repreated freeze-thaw cycles.
    Storage
    -20 °C
  • Beffa, Neuhaus, Meins: "Physiological compensation in antisense transformants: specific induction of an \" glucan endo-1,3-beta-glucosidase in plants infected with necrotizing viruses." in: Proceedings of the National Academy of Sciences of the United States of America, Vol. 90, Issue 19, pp. 8792-6, (1993) (PubMed).

  • Target
    GLU I (PR-2)
    Background
    Pathogenesis-related (PR) proteins, are induced in response to the infection of plants with microbial pathogens. Combinations of glucanase I and chitinase I are potent inhibitors of fungal growth in vitro however precise mechanism of that is still not known. Glucanase I and chitinase I contribute to defense against fungal infection and are currently used as markers for innate immunity, and in particular the ethylene/jasmonate signalling pathway in pathogenesis. Alternative names of the protein: basic beta-1,3-glucanase
    Molecular Weight
    expected: 37 kDa, apparent: 33 kDa
    UniProt
    P27666
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