Anti-Meloidogyne Spp. [12H7] Antibody
![Anti-Meloidogyne Spp. [12H7] Antibody](https://www.kerafast.com/MediaStorage/Product/Images/Large/4369_2001202001284643680.jpg "Anti-Meloidogyne Spp. [12H7] Antibody, 100ug")
This mouse IgG monoclonal antibody was generated against protein and recognizes Meloidogyne spp. J2 hypodermal chords and adult female dorsal gland lobe (DG), extension and ampulla.
Highlights:
- Reacts with Meloidogyne spp. J2 hypodermal chords and adult female dorsal gland lobe (DG), extension and ampulla
- May help elucidate the function of several nematodal structures in organismal development and plant parasitism by facilitating isolation of proteins from complex mixtures
- Suitable for the study of development of, and parasitism by other members of the Nematoda phylum
- Suitable for ELISA and Immunostaining applications
Members of the genus Meloidogyne (Chitwood), the root-knot nematodes, are an agronomically important group of pathogens that establish a complex parasitic relationship with a wide range of host plants. Currently, well over 2000 plants are susceptible to root-knot nematode infections, leading to over 5% of global crop loss. Substances produced in the esophageal glands of Chitwood are secreted through the stylets of feeding root-knot nematodes, modifying several root protophloem cells into elaborate feeding sites called giant-cells. Nutrients from the giant-cells are required for the growth and pronounced morphological changes that occur during nematode development from a motile, vermiform juvenile to an enlarged, rounded, sedentary adult female. These changes include a reduction in size of the two subventral esophageal gland cells and an increase in size of the single dorsal esophageal gland cell as the nematode develops to an adult female.
From the laboratories of Richard S. Hussey, PhD and Lee H. Pratt, PhD, University of Georgia.
Part of The Investigator's Annexe program.
This mouse IgG monoclonal antibody was generated against protein and recognizes Meloidogyne spp. J2 hypodermal chords and adult female dorsal gland lobe (DG), extension and ampulla.
Highlights:
- Reacts with Meloidogyne spp. J2 hypodermal chords and adult female dorsal gland lobe (DG), extension and ampulla
- May help elucidate the function of several nematodal structures in organismal development and plant parasitism by facilitating isolation of proteins from complex mixtures
- Suitable for the study of development of, and parasitism by other members of the Nematoda phylum
- Suitable for ELISA and Immunostaining applications
Members of the genus Meloidogyne (Chitwood), the root-knot nematodes, are an agronomically important group of pathogens that establish a complex parasitic relationship with a wide range of host plants. Currently, well over 2000 plants are susceptible to root-knot nematode infections, leading to over 5% of global crop loss. Substances produced in the esophageal glands of Chitwood are secreted through the stylets of feeding root-knot nematodes, modifying several root protophloem cells into elaborate feeding sites called giant-cells. Nutrients from the giant-cells are required for the growth and pronounced morphological changes that occur during nematode development from a motile, vermiform juvenile to an enlarged, rounded, sedentary adult female. These changes include a reduction in size of the two subventral esophageal gland cells and an increase in size of the single dorsal esophageal gland cell as the nematode develops to an adult female.
From the laboratories of Richard S. Hussey, PhD and Lee H. Pratt, PhD, University of Georgia.
Part of The Investigator's Annexe program.
| Catalog Number | Product | DataSheet | Size | AVAILABILITY | Price | Qty |
|---|
| Product Type: | Antibody |
| Antigen: | J2 hypodermal chords and adult female dorsal gland lobe (DG), extension and ampulla |
| Isotype: | IgG |
| Clonality: | Monoclonal |
| Clone Name: | 12H7 |
| Reactivity: | Only J2 stages of M. incognita, M. javanica, M arenariaand M.hapla, female hypodermal chords and DG |
| Immunogen: | Protein |
| Species Immunized: | Mouse |
| Purification Method: | Protein G |
| Buffer: | PBS, 0.05% (w/v) Sodium Azide |
| Tested Applications: | Immunostaining, ELISA |
| Storage: | -20C |
| Shipped: | Cold packs |
Find the best Meloidogyne spp. Antibody for your research:
| Reactivity | ||
| Antibody | J2 | Female |
| Anti-Meloidogyne Spp., J2 Stage Subventral Gland Lobe [3H11] Antibody | SvG | NB |
| Anti-Meloidogyne Spp., Female Dorsal Gland Lobe [6F11] Antibody | NB | DG |
| Anti-Meloidogyne Spp., Stage Subventral Gland Lobe [3F4] Antibody | SvG | SvG, amphids, esophageal lumen |
| Anti-Meloidogyne Spp. [12H7] Antibody | Hypodermal chords (*) | DG (#) |
(*): Also reacts withM. hapla;(#): Also reactsH. glycines.
- Davis EL, Aron, LM, Pratt, LH, Hussey, RS: Novel immunization Procedures used to Develop Monoclonal Antibodies that Bind to Specific Structures in Meloidogyne spp. (1992). Phytopathology, 82(10), 1244-1250.
If you publish research with this product, please let us know so we can cite your paper.
