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Plant/Algal cell antibodies / Compartment markers / Vacuole


PR-2 | GLU I | class I beta-1,3-glucanase

Art no: AS07 208
Price: 304
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product information

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

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).

antibody format  

rabbit

polyclonal

total IgG in PBS pH 7.4 (without Ca++)

lyophilized

quantity  

2 mg

for reconstitution add 100 µl of sterile water.

storage  

store lyophilized/reconstituted at -20°C; once reconstituted make aliquots to avoid repeated freeze-thaw cycles. 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.

tested applications  

western blot (WB), immunolocalization (IL)

related products  

AS07 207 | anti-PR-3 | CHN | class I chitinase

collection of antibodies to other proteins involved in stress response

additional information  

for more details on immunolocalization, please referr to Keefe et al (1990). Plant 182: 43-51

This antibody can be used as a marker of vacuolar contents Keefe et al. (1990). The effect of ethylene on the cell-type-specific and intracellular localization of β-1,3-glucanase and chitinase in tobacco leave. Plant 182: 43-51. 

application information

recommended dilution  

8 ug/ml with standard ECL (WB)

expected | apparent MW  

37 | 33 kDa

confirmed reactivity  

Nicotiana tabacum, Populus sp. 

predicted reactivity  

dicots including: Solanum lycopersicum, Solanum tuberosum,

not reactive in  

Arabidopsis thaliana

additional information  

Important note: for blocking 5 % skim milk in PBS without Ca++ should be used.

This antibody is purified by affinity chromarography on Portein G.

selected references  

Sticher,L., Hinz,U., Meyer,A.D., and Meins,F.Jr. (1992). Intracellular transport and processing of a tobacco vacuolar β -1,3-glucanase. Planta 188, 559-565.

Beffa et al. (1993). Physiological compensation in antisense transformants: Specific induction of an ersatz glucan endo-1,3- β -glucosidase in plants infected with necrotizing viruses. Proc. Natl. Acad. Sci. U. S. A 90, 8792-8796.


application example

western blot detection of tobacco class I beta 1,3 glucanase

 

Detection of tobacco tobacco class I ß 1,3 – glucanase in ng loaded per respective well using anti- tobacco class I ß 1,3 – glucanase antibodies. Primary antibodies have been used at 8 µg/ml.


||| For applications or usage on species others than stated as confirmed above Agrisera offers a payment-after-testing option. To learn more about this or for any questions on this product, please use the LiveChat option in the left menue bar or contact us at support@agrisera.com

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