Product Includes | Product # | Quantity | Mol. Wt | Isotype/Source |
---|---|---|---|---|
Phospho-AMPKα (Thr172) (40H9) Rabbit mAb | 2535 | 20 µl | 62 kDa | Rabbit IgG |
AMPKα (D63G4) Rabbit mAb | 5832 | 20 µl | 62 kDa | Rabbit  |
Phospho-Raptor (Ser792) Antibody | 2083 | 20 µl | 150 kDa | Rabbit  |
Raptor (24C12) Rabbit mAb | 2280 | 20 µl | 150 kDa | Rabbit  |
Phospho-ULK1 (Ser555) (D1H4) Rabbit mAb | 5869 | 20 µl | 140-150 kDa | Rabbit IgG |
Phospho-ULK1 (Ser757) Antibody | 6888 | 20 µl | 140-150 kDa | Rabbit  |
ULK1 (D8H5) Rabbit mAb | 8054 | 20 µl | 150 kDa | Rabbit IgG |
Anti-rabbit IgG, HRP-linked Antibody | 7074 | 100 µl | Goat  |
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Description
The ULK1 Antibody Sampler Kit provides an economical way to investigate ULK1 signaling. The kit contains enough primary antibody to perform two western blots with each primary antibody.
Storage
Background
Two related serine/threonine kinases, UNC-51-like kinase 1 and 2 (ULK1, ULK2), were discovered as mammalian homologs of the C. elegans gene unc-51 in which mutants exhibited abnormal axonal extension and growth (1-4). Both proteins are widely expressed and contain an amino-terminal kinase domain followed by a central proline/serine rich domain and a highly conserved carboxy-terminal domain. The roles of ULK1 and ULK2 in axon growth have been linked to studies showing that the kinases are localized to neuronal growth cones and are involved in endocytosis of critical growth factors, such as NGF (5). Yeast two-hybrid studies found ULK1/2 associated with modulators of the endocytic pathway, SynGAP, and syntenin (6). Structural similarity of ULK1/2 has also been recognized with the yeast autophagy protein Atg1/Apg1 (7). Knockdown experiments using siRNA demonstrated that ULK1 is essential for autophagy (8), a catabolic process for the degradation of bulk cytoplasmic contents (9,10). It appears that Atg1/ULK1 can act as a convergence point for multiple signals that control autophagy (11), and can bind to several autophagy-related (Atg) proteins, regulating phosphorylation states and protein trafficking (12-16).
Raptor mediates the binding of mTORC1 to ULK1, which phosphorylates and inhibits ULK1 under nutrient rich conditions. AMPK also associates directly with ULK1 and, upon nutrient deprivation, can readily reverse the inhibitory effect of mTORC1 by phosphorylating raptor and initiating autophagy (17,18).
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Background References
Trademarks and Patents
Limited Uses
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