Revision 1
Cell Signaling Technology

Orders: 877-616-CELL (2355) [email protected]

Support: 877-678-TECH (8324)

Web: [email protected] cellsignal.com

3 Trask LaneDanversMassachusetts01923USA
For Research Use Only. Not for Use in Diagnostic Procedures.
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UniProt ID:

#O75385

Entrez-Gene Id:

8408

Product Includes Quantity Reactivity MW(kDa) Isotype
ULK1 (D8H5) Rabbit mAb 8054 100 µl H M R Mk 150 Rabbit IgG
Phospho-ULK1 (Ser555) (D1H4) Rabbit mAb 5869 100 µl H M 140-150 Rabbit IgG

Please visit cellsignal.com for individual component applications, species cross-reactivity, dilutions, protocols, and additional product information.

Description

PhosphoPlus® Duets from Cell Signaling Technology (CST) provide a means to assess protein activation status. Each Duet contains an activation-state and total protein antibody to your target of interest. These antibodies have been selected from CST's product offering based upon superior performance in specified applications.

Storage

Supplied in 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 µg/ml BSA, 50% glycerol and less than 0.02% sodium azide. Store at –20°C. Do not aliquot the antibody.

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).

Phosphorylation of ULK1 by AMPK at Ser555 is critical for starvation-induced autophagy, cell survival under conditions of low nutrients and energy, and mitochondrial homeostasis (17).

  1. Ogura, K. et al. (1994) Genes Dev 8, 2389-400.
  2. Kuroyanagi, H. et al. (1998) Genomics 51, 76-85.
  3. Yan, J. et al. (1998) Biochem Biophys Res Commun 246, 222-7.
  4. Yan, J. et al. (1999) Oncogene 18, 5850-9.
  5. Zhou, X. et al. (2007) Proc Natl Acad Sci USA 104, 5842-7.
  6. Tomoda, T. et al. (2004) Genes Dev 18, 541-58.
  7. Matsuura, A. et al. (1997) Gene 192, 245-50.
  8. Chan, E.Y. et al. (2007) J Biol Chem 282, 25464-74.
  9. Reggiori, F. and Klionsky, D.J. (2002) Eukaryot Cell 1, 11-21.
  10. Codogno, P. and Meijer, A.J. (2005) Cell Death Differ 12 Suppl 2, 1509-18.
  11. Stephan, J.S. and Herman, P.K. (2006) Autophagy 2, 146-8.
  12. Okazaki, N. et al. (2000) Brain Res Mol Brain Res 85, 1-12.
  13. Young, A.R. et al. (2006) J Cell Sci 119, 3888-900.
  14. Kamada, Y. et al. (2000) J Cell Biol 150, 1507-13.
  15. Lee, S.B. et al. (2007) EMBO Rep 8, 360-5.
  16. Hara, T. et al. (2008) J Cell Biol 181, 497-510.
  17. Egan, D.F. et al. (2011) Science 331, 456-61.

Background References

    Trademarks and Patents

    Cell Signaling Technology is a trademark of Cell Signaling Technology, Inc.
    PhosphoPlus is a registered trademark of Cell Signaling Technology, Inc.
    All other trademarks are the property of their respective owners. Visit cellsignal.com/trademarks for more information.

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    Revision 1
    #97094

    PhosphoPlus® ULK1 (Ser555) Antibody Duet

    PhosphoPlus® ULK1 (Ser555) Antibody Duet: Image 1 Expand Image
    对来自 MCF7 细胞提取物的 ULK1 进行免疫沉淀分析。泳道 1 为 10% input,泳道 2 用 Rabbit (DA1E) mAb IgG XP® Isotype Control #3900 进行沉淀,泳道 3 为 ULK1 (D8H5) Rabbit mAb #8054。使用 ULK1 (D8H5) Rabbit mAb 进行蛋白质印迹分析。
    PhosphoPlus® ULK1 (Ser555) Antibody Duet: Image 2 Expand Image
    使用 ULK1 (D8H5) Rabbit mAb #8054 对 RD 细胞的裂解物 (0.1 mg/mL) 进行 Simple Western™ 分析。虚拟泳道式图像(左图)显示一抗稀释比例为 1:50 和 1:250 时的单一靶标条带(如图所示)。对应的电泳图(右图)为一抗稀释比例在 1:50(蓝线)和 1:250(绿线)时沿毛细血管内分子量的化学发光结果。在还原条件下,使用 12-230 kDa 分离模块在 ProteinSimple(BioTechne 品牌)的 Jess™ Simple Western 仪器上进行该实验。
    PhosphoPlus® ULK1 (Ser555) Antibody Duet: Image 3 Expand Image
    使用 Phospho-ULK1 (Ser555) (D1H4) Rabbit mAb(上图)、ULK1 (D8H5) Rabbit mAb #8054(中图)或 GAPDH (D16H11) XP® Rabbit mAb #5174(下图)对未经处理 (-) 或已经过 AMPK 激活剂 991(50μM,1 小时;+)处理的对照 U-2 OS 细胞或 CRISPR/Cas9 ULK1 敲除型 (KO) U-2 OS 细胞的提取物进行蛋白质印迹法分析。ULK1 KO 细胞中没有信号证实了抗体对 ULK1 的特异性。ULK1 敲除型细胞由加利福尼亚州拉霍亚索尔克生物研究所的 Reuben Shaw 博士惠赠。
    PhosphoPlus® ULK1 (Ser555) Antibody Duet: Image 4 Expand Image
    使用 ULK1 (D8H5) Rabbit mAb(上图)、Phospho-ULK1 (Ser555) (D1H4) Rabbit mAb #5869 (中图)或 GAPDH (D16H11) XP® Rabbit mAb #5174(下图)对未经处理 (-) 或已经过 AMPK 激活剂 991(50μM,1 小时;+)处理的对照 U-2 OS 细胞或 CRISPR/Cas9 ULK1 敲除型 (KO) U-2 OS 细胞的提取物进行蛋白质印迹法分析。ULK1 KO 细胞中没有信号,这证实了抗体对 ULK1.ULK1 敲除型细胞的特异性,该细胞由加州拉霍亚 Salk 生物研究所的 Reuben Shaw 博士惠赠。
    PhosphoPlus® ULK1 (Ser555) Antibody Duet: Image 5 Expand Image
    使用 Phospho-ULK1 (Ser555) (D1H4) Rabbit mAb 对未处理的或经 oligomycin #9996(0.5 μM,持续30 分钟)处理的 MCF7 细胞提取物,以及未处理的或经过氧化氢(10 mM,持续5分钟)处理的 C2C12 细胞提取物进行蛋白质印迹分析。
    PhosphoPlus® ULK1 (Ser555) Antibody Duet: Image 6 Expand Image
    使用 ULK1 (D8H5) Rabbit mAb 对不同细胞系提取物进行蛋白质印迹分析。
    PhosphoPlus® ULK1 (Ser555) Antibody Duet: Image 7 Expand Image
    使用 Phospho-ULK1 (Ser555) (D1H4) Rabbit mAb(左图)对未处理的或经 oligomycin #9996(0.5 µM,持续30 分钟)处理的 MCF7 细胞提取物进行蛋白质印迹分析。使用磷酸化(中间图)或在 ULK1 的 Ser555 周围区域的非磷酸化肽(右图)来预孵育抗体,从而证实磷酸化的特异性。
    PhosphoPlus® ULK1 (Ser555) Antibody Duet: Image 8 Expand Image
    使用 ULK1 (D8H5) Rabbit mAb(上图)和 β-Actin (D6A8) Rabbit mAb #8457(下图)对野生型 MEF 和 ULK1 (-/-) MEF 细胞提取物进行蛋白质印迹分析。MEF 细胞由 Reuben Shaw 博士 (Salk Institute, La Jolla, CA) 惠赠。
    PhosphoPlus® ULK1 (Ser555) Antibody Duet: Image 9 Expand Image
    使用 Phospho-ULK1 (Ser555) (D1H4) Rabbit mAb(上图)或 ULK1 (D8H5) Rabbit mAb #8054(下图)对未处理的 (-) 或经羰基氰化物3-氯苯腙(CCCP)(100 μM,持续2 小时; +)处理的 MCF7 细胞提取物进行蛋白质印迹分析。