Anti-MAP1LC3A antibody [BS405] - Autophagosome Marker
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(2 Publications)
Mouse Monoclonal Microtubule-associated proteins 1A/1B light chain 3A antibody. Suitable for WB, ICC/IF, Flow Cyt (Intra) and reacts with Human, Rat samples. Cited in 2 publications. Immunogen corresponding to Synthetic Peptide within Human MAP1LC3A aa 1-50.
View Alternative Names
Microtubule-associated proteins 1A/1B light chain 3A, Autophagy-related protein LC3 A, Autophagy-related ubiquitin-like modifier LC3 A, MAP1 light chain 3-like protein 1, MAP1A/MAP1B light chain 3 A, Microtubule-associated protein 1 light chain 3 alpha, MAP1A/MAP1B LC3 A, MAP1LC3A
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-MAP1LC3A antibody [BS405] - Autophagosome Marker (AB244210)
Flow cytometry analysis of SH-SY5Y (Human neuroblastoma cell line from bone marrow) cells of MAP1LC3A with ab244210.
Fixing / permeabilization of cells : Absolute methanol / 0.1% Tween-20 in PBS.
Primary antibody : ab244210 at 2 μg per ~106 cells for 15 minutes at room temperature.
Secondary antibody : Goat anti-mouse PE labeled secondary antibody (1/1000) with incubation for 15 minutes in dark at room temperature.
Non-specific Control IgG, clone X63 was used under same conditions as negative control (black dashed).
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-MAP1LC3A antibody [BS405] - Autophagosome Marker (AB244210)
Immunofluorescence analysis of MAP1LC3A expression in SH-SY5Y (human neuroblastoma cell line from bone marrow) cells.
Fixed (4% formaldehyde), permeabilized, and blocked (10% normal horse serum, 0.1% Triton X-100) C6 cells were incubated with ab244210 at 2 μg/mL, (green) for 1 hour. Primary antibody binding was visualized with a secondary donkey anti-mouse-CF488A antibody (4 μg/mL, 1 hour incubation). Cell nuclei were stained with Hoechst dye (blue).
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-MAP1LC3A antibody [BS405] - Autophagosome Marker (AB244210)
Immunofluorescence analysis of MAP1LC3A expression in C6 (rat glial tumor cell line) cells.
Fixed (4% formaldehyde), permeabilized, and blocked (10% normal horse serum, 0.1% Triton X-100) C6 cells were incubated with ab244210 at 2 μg/mL, (green) for 1 hour. Primary antibody binding was visualized with a secondary donkey anti-mouse-CF488A antibody (4 μg/mL, 1 hour incubation). Cell nuclei were stained with Hoechst dye (blue).
- WB
Supplier Data
Western blot - Anti-MAP1LC3A antibody [BS405] - Autophagosome Marker (AB244210)
SDS-PAGE : 4-20% Bis-Tris denatured.
All lanes:
Western blot - Anti-MAP1LC3A antibody [BS405] - Autophagosome Marker (ab244210) at 10 µg/mL
All lanes:
SH-SY5Y (human neuroblastoma cell line from bone marrow) cell lysate at 20 µg
Secondary
All lanes:
Anti-mouse-HRP, 2 hrs at RT at 1/10000 dilution
Predicted band size: 14 kDa
true
Reactivity data
Properties and storage information
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Reconstitution
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Publications (2)
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Cells 14: PubMed40643462
2025
Applications
Unspecified application
Species
Unspecified reactive species
Molecular and cellular biology 44:87-102 PubMed38520226
2024
Applications
Unspecified application
Species
Unspecified reactive species
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