Leishmania LPG antibody | CA7AE
Image caption:
The inhibition of the V-ATPase acquisition on phagosomes is specific for the promastigote stage. A–C, BMM cells were infected with either WT promastigotes or amastigotes for 2 h and 24 h, fixed and stained for V-ATPase (green), LPG (red) and DNA (blue) (A) or V-ATPase (green), LAMP-1 (red) and DNA (blue) (B). A and B, Confocal images illustrating V-ATPase acquisition on parasite-containing phagosomes (white arrowheads). C, V-ATPase acquisition was determined on at least 100 phagosomes for each condition and expressed as a percentage of recruitment. Three independent experiments were performed and the bars show the standard deviations of one representative triplicate (**, p≤0.005; p values compare the acquisition of V-ATPase on phagosomes containing promastigotes vs amastigotes parasites). Bar, 3 µm.
From: Vinet AF, Fukuda M, Turco SJ, Descoteaux A (2009)
The Leishmania donovani Lipophosphoglycan Excludes the Vesicular Proton-ATPase from Phagosomes by Impairing the Recruitment of Synaptotagmin V.
PLoS Pathog 5(10): e1000628.
This is from an open access article distributed under the terms of the Creative Commons Attribution License.
Image caption:
CsA-treated L. donovani promastigotes show altered morphology. Promastigotes were incubated with 0.15% ethanol or 15 μM (B, C) or 20 μM (A) CsA at 26°C, pH 7.4 for 72 hours. Axenic amastigotes were prepared as described in experimental procedure. 107 cells were fixed with either methanol for Giemsa staining (A), or 2.5% glutaraldehyde for scanning electron microscopy (B). The bar corresponds to 1 μm (B) and 5 μm (A). Two independent experiments were performed and representative fields are shown. (C) Flagellum length measurement. CsA-treated and solvent treated cells L. donovani promastigotes were fixed in methanol and stained with anti-tubulin monoclonal antibody. Flagellum length was measured from a total of 180 cells each for control and CsA-treated samples. Only cells with a single flagellum that was completely visible and fully in focus were taken into account. Samples were observed with a DMR Leica microscope and images were captured with a Cool Snap HQ camera (Roper Scientific). Images were analysed using the IPLab Spectrum 3.9 software (Scanalytics & BD Biosciences) and flagellum length was measured using ImageJ (NIH). (D) Immunoblot analysis of CsA treated parasites. Parasites were treated with solvent or 15 μM CsA for 72 hours, lysed in 1× Laemmli buffer, and lysates equal to 2×107 cells were analyzed by immunoblotting. Promastigote specific marker LPG (upper), amastigote specific marker A2 (middle) and α-tubulin (lower) were analyzed. Two independent experiments which gave identical results were performed.
From: Yau W-L, Blisnick T, Taly J-F, Helmer-Citterich M, Schiene-Fischer C, et al. (2010)
Cyclosporin A Treatment of Leishmania donovani Reveals Stage-Specific Functions of Cyclophilins in Parasite Proliferation and Viability.
PLoS Negl Trop Dis 4(6): e729.
This is from an open access article distributed under the terms of the Creative Commons Attribution License.
Image caption
Recruitment of Syt V is impaired on phagosomes containing LPG-coated Zymosan. A and B, BMM were allowed to internalize Zym or LPG-Zym during 15 min (A) or 2 h (B), and prepared for confocal analysis. Presence (left y axis) and P/C ratio levels (right y axis) were determined for EEA1 (A) or LAMP-1 (B). C and D, BMM cells were allowed to internalize Zym or LPG-Zym for 10 min, 30 min or 2 h, fixed and stained for either endogenous Syt V (green) and LPG (red). The presence of Syt V and LPG on phagosomes is illustrated by confocal images (C). D. Quantification of Syt V recruitment (left panel) and relative Syt V levels (P/C ratio) on these phagosomes (right panel) were determined. E. Syt V-GFP cells were allowed to internalize Zym or LPG-Zym for 10 min, 30 min or 2 h, fixed and stained for LPG. Quantification of Syt V- recruitment (left panel) and relative Syt V levels on these phagosomes (right panel) were determined. The recruitment of EEA1, LAMP1 and Syt V was determined on at least 100 phagosomes for each condition, at least three independent experiments were performed and the bars show the standard deviations of one representative triplicate (*, p≤0.05; **, p≤0.005). Bar, 3 μm.
From: Vinet AF, Fukuda M, Turco SJ, Descoteaux A (2009)
The Leishmania donovani Lipophosphoglycan Excludes the Vesicular Proton-ATPase from Phagosomes by Impairing the Recruitment of Synaptotagmin V.
PLoS Pathog 5(10): e1000628.
This is from an open access article distributed under the terms of the Creative Commons Attribution License.
Image caption
Exclusion of Syt V is restricted to the LPG insertion sites on the phagosome membrane. A and B, BMM were allowed to internalize Zym or Zym-LPG during 30 min or 2 h, and stained for Syt V (green) and LPG (red). Green arrowheads indicate a localized Syt V recruitment on phagosome membrane and red arrowheads indicate a localized LPG insertion into phagosome membrane (A). C and D, Syt V-GFP cells were allowed to internalize Zym or Zym-LPG for 30 min or 2 h, fixed and stained for LPG (red). Green arrowheads indicate a localized Syt V-GFP recruitment on phagosome membrane and red arrowheads indicate a localized LPG insertion into phagosome membrane (C). A rim around a representative phagosome formed in BMM (B) or in SytV-GFP cells (D) from A and C respectively, was manually traced with a one pixel width and fluorescence intensity profile of Syt V in green and LPG in red were represented in a graph for each phagocytosis time point. Bar, 3 μm.
From: Vinet AF, Fukuda M, Turco SJ, Descoteaux A (2009)
The Leishmania donovani Lipophosphoglycan Excludes the Vesicular Proton-ATPase from Phagosomes by Impairing the Recruitment of Synaptotagmin V.
PLoS Pathog 5(10): e1000628.
This is from an open access article distributed under the terms of the Creative Commons Attribution License.
Image caption
Recruitment of Syt V to GM1-containing microdomains of phagosome membranes is prevented by LPG. A, BMM were allowed to internalize Zym for 30 min, fixed and stained for endogenous Syt V (green) and GM1 (red). White arrowheads indicate examples of colocalization between Syt V and GM1-positive microdomains, indicating a Syt V enrichment on these microdomains. B and C, BMM were either left untreated or treated with 10 mmol/L MβCD for 1 h before the internalization of Zym for 30 and 120 min. Cells were then fixed and stained for Syt V and LAMP-1. Representative confocal images of Syt V recruitment on cells with or without MβCD treatment is presented (B), white arrowheads indicate phagosomes. Syt V acquisition is expressed as a percentage of phagosome recruitment for Syt V. At least 100 phagosomes for each condition were assessed. Three independent experiments were performed and the bars show the standard deviations of one representative triplicate (C) (**, p≤0.005). D, BMM were allowed to internalize Zym-LPG for 30 min, fixed and stained for LPG (green) and GM1 (red). White arrowheads indicate a colocalization between LPG and GM1-positive rafts. BMM were allowed to internalize Zym (E, upper panel) or LPG-Zym (E, lower panel) for 30 min, fixed and stained for Syt V (blue), LPG (green) and GM1 (red). Blue arrowheads indicate a local Syt V acquisition on phagosome membrane and yellow arrowheads indicate a local colocalization between GM1 microdomains and LPG. A rim around each phagosome was manually traced with a one pixel width and fluorescence intensity profile of Syt V in blue, LPG in green and GM1 in red were represented in a graph (F). Bars, 3 μm (A, B and D) or 1 μm (E).
From: Vinet AF, Fukuda M, Turco SJ, Descoteaux A (2009)
The Leishmania donovani Lipophosphoglycan Excludes the Vesicular Proton-ATPase from Phagosomes by Impairing the Recruitment of Synaptotagmin V.
PLoS Pathog 5(10): e1000628.
This is from an open access article distributed under the terms of the Creative Commons Attribution License.
Image caption
The inhibition of the V-ATPase acquisition on phagosomes is specific for the promastigote stage. A–C, BMM cells were infected with either WT promastigotes or amastigotes for 2 h and 24 h, fixed and stained for V-ATPase (green), LPG (red) and DNA (blue) (A) or V-ATPase (green), LAMP-1 (red) and DNA (blue) (B). A and B, Confocal images illustrating V-ATPase acquisition on parasite-containing phagosomes (white arrowheads). C, V-ATPase acquisition was determined on at least 100 phagosomes for each condition and expressed as a percentage of recruitment. Three independent experiments were performed and the bars show the standard deviations of one representative triplicate (**, p≤0.005; p values compare the acquisition of V-ATPase on phagosomes containing promastigotes vs amastigotes parasites). Bar, 3 μm.
From: Vinet AF, Fukuda M, Turco SJ, Descoteaux A (2009)
The Leishmania donovani Lipophosphoglycan Excludes the Vesicular Proton-ATPase from Phagosomes by Impairing the Recruitment of Synaptotagmin V.
PLoS Pathog 5(10): e1000628.
This is from an open access article distributed under the terms of the Creative Commons Attribution License.
Mouse anti Leishmania lipophosphoglycan antibody, clone CA7AE recognizes lipophosphoglycan (LPG) the major cell surface glycoconjugate of Leishmania parasites. Mouse anti Leishmania lipophosphoglycan antibody, clone CA7AE recognizes the repeat carbohydrate epitope of most species of Leishmania LPG. The epitope is also found on the excreted acid phosphatase of Leishmania and is expressed on the surface of Leishmania infected macrophages (Tolson et al. 1990).
Mouse anti Leishmania lipophosphoglycan antibody, clone CA7AE recognizes the promastigotes of Leishmania donovani but not those of the related species L. tropica (Jaffe and Sarfstein 1987, Sundar et al. 2001). Mouse anti Leishmania lipophosphoglycan antibody, clone CA7AE does however recognize a broad range of L. donovani and L. major strains and related species including L. infantum, L. m. mexicana, L. aethiopica and L. b. panamensis (Tolson et al. 1994).
Mouse anti Leishmania lipophosphoglycan antibody, clone CA7AE recognizes the promastigotes of Leishmania donovani but not those of the related species L. tropica (Jaffe and Sarfstein 1987, Sundar et al. 2001). Mouse anti Leishmania lipophosphoglycan antibody, clone CA7AE does however recognize a broad range of L. donovani and L. major strains and related species including L. infantum, L. m. mexicana, L. aethiopica and L. b. panamensis (Tolson et al. 1994).
Product Details
- Target Species
- Protozoan
- Product Form
- Ascites - lyophilised
- Reconstitution
- Reconstitute with 0.5 ml distilled water
Care should be taken during reconstitution as the protein may appear as a film at the bottom of the vial. Bio-Rad recommend that the vial is gently mixed after reconstitution. For long term storage the addition of 0.09% sodium azide is recommended. - Preservative Stabilisers
- None present
- Immunogen
- Heat killed Leishmania donovani promastigotes.
- Fusion Partners
- Spleen cells from immunised BALB/c mice were fused with cells of the murine SP2/0 myeloma cell line.
Storage Information
- Storage
- Prior to reconstitution store at +4oC.
After reconstitution store at -20oC.
Storage in frost-free freezers is not recommended. This product should be stored undiluted. Avoid repeated freezing and thawing as this may denature the antibody. - Guarantee
- 12 months from date of despatch
More Information
- Regulatory
- For research purposes only
Applications of Leishmania LPG antibody
| Application Name | Verified | Min Dilution | Max Dilution |
|---|---|---|---|
| ELISA | 1/1000 | ||
| Immunoblotting | |||
| Immunofluorescence | 1/500 | 1/1000 |
Where this product has not been tested for use in a particular technique this does not necessarily exclude its use in such procedures. Suggested working dilutions are given as a guide only. It is recommended that the user titrates the product for use in their own system using appropriate negative/positive controls.
Copyright © 2021 Bio-Rad Antibodies (formerly AbD Serotec)
Product Specific References
References for Leishmania LPG antibody
-
Sundar, S. et al. (2001) Resistance to treatment in Kala-azar: speciation of isolates from northeast India.
Am J Trop Med Hyg. 65: 193-6. -
Tolson, D.L. et al. (1990) Expression of a repeating phosphorylated disaccharide lipophosphoglycan epitope on the surface of macrophages infected with Leishmania donovani.
Infect Immun. 58: 3500-7. -
Butcher, B.A. et al. (1996) Deficiency in beta1,3-galactosyltransferase of a Leishmania major lipophosphoglycan mutant adversely influences the Leishmania-sand fly interaction.
J Biol Chem. 271: 20573-9. -
Goyard, S. et al. (2003) An in vitro system for developmental and genetic studies of Leishmania donovani phosphoglycans
Mol Biochem Parasitol. 130: 31-42. -
Soares, R.P. et al. (2004) Leishmania tropica: intraspecific polymorphisms in lipophosphoglycan correlate with transmission by different Phlebotomus species.
Exp Parasitol. 107: 105-14. -
Amprey, J.L. et al. (2004) Inhibition of CD1 expression in human dendritic cells during intracellular infection with Leishmania donovani.
Infect Immun. 72: 589-92. -
Coelho-Finamore, J.M. et al. (2011) Leishmania infantum: Lipophosphoglycan intraspecific variation and interaction with vertebrate and invertebrate hosts.
Int J Parasitol. 41: 333-42. -
Capul, A.A. et al. (2007) Two Functionally Divergent UDP-Gal Nucleotide Sugar Transporters Participate in Phosphoglycan Synthesis in Leishmania major
J Biol Chem. 282: 14006-17. -
Vinet, A.F. et al. (2009) The Leishmania donovani lipophosphoglycan excludes the vesicular proton-ATPase from phagosomes by impairing the recruitment of synaptotagmin V.
PLoS Pathog. 5: e1000628.
Fluorescent Spectraviewer
Watch the Tool Tutorial Video ▸How to Use the Spectraviewer
Watch the Tool Tutorial Video ▸- Start by selecting the application you are interested in, with the option to select an instrument from the drop down menu or create a customized instrument
- Select the fluorophores or fluorescent proteins you want to include in your panel to check compatibility
- Select the lasers and filters you wish to include
- Select combined or multi-laser view to visualize the spectra
