Methods for detecting
Disclosed are Bacillus thuringiensis strains comprising novel crystal proteins which exhibit insecticidal activity against coleopteran insects including red flour beetle larvae ( Tribolium castaneum ) and Japanese beetle larvae ( Popillia japonica ). Also disclosed are novel B. thuringiensis crystal toxin genes, designated cryET33 and cryET34, which encode the colepteran-toxic crystal proteins, CryET33 (29-kDa) crystal protein, and the cryET34 gene encodes the 14-kDa CryET34 crystal protein. The CryET33 and CryET34 crystal proteins are toxic to red flour beetle larvae and Japanese beetle larvae. Also disclosed are methods of making and using transgenic cells comprising the novel nucleic acid sequences of the invention.
1. A purified antibody that binds to a CryET33 peptide, wherein the CryET33 peptide is SEQ ID NO:3.
2. The purified antibody of claim 1 generated by using a peptide according to SEQ ID NO:3 as an immunogen.
3. The purified antibody of claim 1 produced by a hybridoma, wherein a peptide according to SEQ ID NO:3 is used to generate the hybridoma producing the antibody.
4. A method for detecting a CryET33 peptide in a biological sample, comprising the steps of:
(a) obtaining a biological sample suspected of containing the peptide;
(b) contacting the sample with an antibody of claim 1 , that binds to the peptide, under conditions effective to allow the formation of complexes; and
(c) detecting the complexes so formed.
5. The method of claim 4 , wherein the antibody is generated by using a peptide according to SEQ ID NO:3 as an immunogen.
6. An immunodetection kit comprising, in suitable container means, an antibody of claim 1 that binds to a CryET33 peptide, and an immunodetection reagent
7. The immunodetection kit of claim 6 , wherein the antibody is generated by using a peptide of SEQ ID NO:3 as an immunogen.