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APG8c (MAP1LC3C) Antibody (Y105) Blocking PeptideSynthetic peptide
| Country | United States
Ordering Information
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| Catalog # | Size | Availability | Price | |
| BP1804f | 0.1 mg 400 ul | In Stock | $ 45.00 | DISCONTINED INQUIRE CLICK INQUIRE Add to cart |
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- Citiations : 0
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APG8c (MAP1LC3C) Antibody (Y105) Blocking Peptide - Product info | |
| Primary Accession | Q9BXW4 |
| Clone Names | 80317114 |
| Calculated MW | 16852 Da |
APG8c (MAP1LC3C) Antibody (Y105) Blocking Peptide - Additional info | |
| Gene ID 440738 | |
| Target/Specificity The synthetic peptide sequence used to generate the antibody AP1804f was selected from the MAP1LC3C region of human APG8c (MAP1LC3C). A 10 to 100 fold molar excess to antibody is recommended. Precise conditions should be optimized for a particular assay. | |
| Format Synthetic peptide was lyophilized with 100% acetonitrile and is supplied as a powder. Reconstitute with 0.1 ml DI water for a final concentration of 1 mg/ml. | |
| Storage Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C. | |
| Precautions This product is for research use only. Not for use in diagnostic or therapeutic procedures. | |
APG8c (MAP1LC3C) Antibody (Y105) Blocking Peptide - Protein Information | |
| Name MAP1LC3C | |
| Function Probably involved in formation of autophagosomal vacuoles (autophagosomes) (By similarity) | |
| Cellular Location Cytoplasm, cytoskeleton. Endomembrane system; Lipid-anchor. Cytoplasmic vesicle, autophagosome membrane; Lipid-anchor. Note=LC3-II binds to the autophagic membranes | |
| Tissue Location Most abundant in placenta, lung and ovary. | |
APG8c (MAP1LC3C) Antibody (Y105) Blocking Peptide - Related products
AP1804a: LC3 Antibody (APG8C) (N-term)
AP1804e: LC3 Antibody (APG8C) (T48)
AP1804f: LC3 Antibody (APG8C) (Y105)
AP3457a: Phospho-LC3C-S9 Antibody
AP3531a: Phospho-LC3C-S137/138 Antibody
AP3646a: Phospho-LC3C-T48 Antibody
AP3691a: Phospho-APG8c (MAP1LC3C)-Y105 Antibody
RI13152: MAP1LC3C predesign siRNA
BP1804a: LC3 Antibody (APG8c) (N-term) Blocking Peptide
BP1804e: APG8c (MAP1LC3C) Antibody (T48) Blocking Peptide
BP1804f: APG8c (MAP1LC3C) Antibody (Y105) Blocking Peptide
BP3457a: Phospho-LC3 (APG8c) - S9 Antibody Blocking Peptide
BP3531a: Phospho-LC3 (APG8c) - S137/138 Antibody Blocking Peptide
BP3646a: Phospho-APG8c (MAP1LC3C)-T48 Antibody Blocking Peptide
BP3647a: Phospho-APG8c (MAP1LC3C)-Y105 Antibody Blocking Peptide
BP3691a: Phospho-APG8c (MAP1LC3C)-Y105 Antibody Blocking Peptide
APG8c (MAP1LC3C) Antibody (Y105) Blocking Peptide - Research Areas
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BACKGROUND
Macroautophagy is the major inducible pathway for the general turnover of cytoplasmic constituents in eukaryotic cells, it is also responsible for the degradation of active cytoplasmic enzymes and organelles during nutrient starvation. Macroautophagy involves the formation of double-membrane bound autophagosomes which enclose the cytoplasmic constituent targeted for degradation in a membrane bound structure, which then fuse with the lysosome (or vacuole) releasing a single-membrane bound autophagic bodies which are then degraded within the lysosome (or vacuole). MAP1A and MAP1B are microtubule-associated proteins which mediate the physical interactions between microtubules and components of the cytoskeleton. These proteins are involved in formation of autophagosomal vacuoles (autophagosomes). MAP1A and MAP1B each consist of a heavy chain subunit and multiple light chain subunits. MAP1LC3c is one of the light chain subunits and can associate with either MAP1A or MAP1B. The precursor molecule is cleaved by APG4B/ATG4B to form the cytosolic form, LC3-I. This is activated by APG7L/ATG7, transferred to ATG3 and conjugated to phospholipid to form the membrane-bound form, LC3-II.
REFERENCES
Baehrecke EH. Nat Rev Mol Cell Biol. 6(6):505-10. (2005) Lum JJ, et al. Nat Rev Mol Cell Biol. 6(6):439-48. (2005) Greenberg JT. Dev Cell. 8(6):799-801. (2005) Levine B. Cell. 120(2):159-62. (2005) Shintani T and Klionsky DJ. Science. 306(5698):990-5. (2004)Tanida I., et al. Int. J. Biochem. Cell Biol. 36:2503-2518(2004)He H., et al. J. Biol. Chem. 278:29278-29287(2003)Tanida I., et al. J. Biol. Chem. 279:36268-36276(2004)