GLU I (PR-2) antibody
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- 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
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- Application Notes
- Recommended Dilution: 8 ug/mL with standard ECL (WB).
- Comment
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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
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- Format
- Lyophilized
- Reconstitution
- For reconstitution add 100 µL of sterile water.
- Buffer
- PBS pH 7.4 (without Ca++)
- Preservative
- Without preservative
- Handling Advice
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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
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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).
: "
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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).
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- 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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