Cell Signaling Technology

Product Pathways - Cytoskeletal Signaling

Phospho-DRP1 (Ser616) (D9A1) Rabbit mAb #4494

No. Size Price
4494S 100 µl ( 10 western blots ) ¥3,900.00 现货查询 购买询价
4494 carrier free & custom formulation / quantityemail request
Applications Dilution Species-Reactivity Sensitivity MW (kDa) Isotype
W 1:1000 Human, Endogenous 78-82 Rabbit IgG
F 1:1600
IF-IC 1:3200

Species cross-reactivity is determined by western blot.

Applications Key: W=Western Blotting, F=Flow Cytometry, IF-IC=Immunofluorescence (Immunocytochemistry),


Species predicted to react based on 100% sequence homology: Mouse, Rat,

Specificity / Sensitivity

Phospho-DRP1 (Ser616) (D9A1) Rabbit mAb recognizes endogenous levels of DRP1 protein only when phosphorylated at Ser616.

Phospho-DRP1 (Ser616) (D9A1)Rabbit mAb可以识别内源性 616位丝氨酸磷酸化的DRP1蛋白。

Source / Purification

Monoclonal antibody is produced by immunizing animals with a synthetic phosphopeptide corresponding to residues surrounding Ser616 of human DRP1 protein.




Confocal immunofluorescent analysis of HeLa cells, untreated (left) or λ phosphatase-treated (right), using Phospho-DRP1 (Ser616) (D9A1) Rabbit mAb (green). Actin filaments were labeled with DY-554 phalloidin (red). Blue pseudocolor = DRAQ5® #4084 (fluorescent DNA dye).使用Phospho-DRP1 (Ser616) (D9A1)Rabbit mAb和碘化丙啶(DNA content)对未处理(左)或λ phosphatase-处理(右)HeLa细胞进行激光共聚焦免疫荧光分析。肌动蛋白丝使用DY-554鬼笔环肽标记(红色)。蓝色假色= DRAQ5® #4084 (fluorescent DNA dye).

Western Blotting

Western Blotting

Western blot analysis of extracts from HeLa cells, untreated (-) or treated (+) with nocodazole (100 mg/ml, 17 hr), using Phospho-DRP1 (Ser616) (D9A1) Rabbit mAb (upper) and DRP1 (D6C7) Rabbit mAb #8570 (lower).未处理(-)或经过nocodazole (100 mg/ml, 17 hr)处理(+)的HeLa细胞提取物,使用Phospho-DRP1 (Ser616) (D9A1)Rabbit mAb(上)和DRP1 (D6C7) Rabbit mAb #8570(下)进行western blot分析。

Flow Cytometry

Flow Cytometry

Flow cytometric analysis of Jurkat cells, untreated (left) or λ phosphatase-treated (right), using Phospho-DRP1 (Ser616) (D9A1) Rabbit mAb and propidium iodide (DNA content).使用Phospho-DRP1 (Ser616) (D9A1)Rabbit mAb和碘化丙啶(DNA content)对未处理(左)或λ phosphatase-处理(右)的Jurkat细胞进行流式分析。


Dynamin-related protein 1 (DRP1) is a member of the dynamin superfamily of GTPases. Members of this family have diverse cellular functions including vesicle scission, organelle fission, viral resistance, and intracellular trafficking (reviewed in 1). DRP1 affects mitochondrial morphology and is important in mitochondrial and peroxisomal fission in mammalian cells (2-5). The yeast ortholog of DRP1 clusters into a spiral-shaped structure on the mitochondrial membrane at the site of fission (reviewed in 6), and this structure is likely conserved in mammalian cells (3). The division of the mitochondria, which is required for apoptosis, as well as normal cell growth and development is controlled, in part, by the phosphorylation of DRP1 at Ser616 by Cdk1/cyclin B and at Ser637 by protein kinase A (PKA) (reviewed in 6). When phosphorylated at Ser616, DRP1 stimulates mitochondrial fission during mitosis. Conversely, fission is inhibited when DRP1 is phosphorylated at Ser637 (reviewed in 6). Dephosphorylation at Ser637 by calcineurin reverses this inhibition (7). In addition to phosphorylation, sumoylation of DRP1 is also an enhancer of mitochondrial fission (8). Balancing fission and fusion events is essential for proper mitochondrial function. Research studies have demonstrated mitochondrial defects in a variety of neurodegenerative diseases including Alzheimer’s disease, Parkinson’s disease, and Huntington’s disease (reviewed in 6).

Dynamin-related protein 1 (DRP1)是GTPases dynamin超家族的一员。该家族的成员具有多种功能包括囊泡分离,细胞器分裂,对抗病毒以及胞内示踪(1)。DRP1影响线粒体的形态,对哺乳动物细胞中线粒体和过氧化物酶病裂变有重要作用(2-5)。DRP1的酵母同源蛋白成簇排列在线粒体分裂位置的线粒体膜螺旋状结构处(6),这个结构似乎在哺乳动物细胞中也是保守的(3)。线粒体的分裂部分通过DRP1的616位丝氨酸被Cdk1/cyclin B磷酸化和637位丝氨酸被蛋白激酶A(PKA)磷酸化调控(6),线粒体的分裂对细胞凋亡、正常细胞生长和发育都是必须的。616位丝氨酸被磷酸化后,DRP1刺激有丝分裂时的线粒体分裂。相反的,DRP1的637位丝氨酸被磷酸化后分裂受限(6)。磷酸酶去磷酸化637位丝氨酸后,抑制被翻转(7)。除了磷酸化,DRP1的SUMO化也是线粒体分裂的促进因素(8)。分裂和融合之间的平衡是正常发挥线粒体功能所必需的。研究证明线粒体缺陷会导致多种神经功能障碍包括阿尔兹海默症,帕金森病已经亨廷顿症(6)。

  1. Praefcke, G.J. and McMahon, H.T. (2004) Nat Rev Mol Cell Biol 5, 133-47.
  2. Taguchi, N. et al. (2007) J Biol Chem 282, 11521-9.
  3. Smirnova, E. et al. (2001) Mol Biol Cell 12, 2245-56.
  4. Smirnova, E. et al. (1998) J Cell Biol 143, 351-8.
  5. Koch, A. et al. (2003) J Biol Chem 278, 8597-605.
  6. Knott, A.B. et al. (2008) Nat Rev Neurosci 9, 505-18.
  7. Cereghetti, G.M. et al. (2008) Proc Natl Acad Sci USA 105, 15803-8.
  8. Zunino, R. et al. (2007) J Cell Sci 120, 1178-88.

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