老带新
Phospho-DRP1 (Ser616) Antibody
1/6

Phospho-DRP1 (Ser616) Antibody

分享
品牌: CST
pdf 下载产品说明书
pdf 下载COA
pdf 下载SDS
用小程序,查商品更便捷
收藏
对比对比
咨询咨询
分子量:
78-82
反应种属:
Human
展开
产品介绍
产品介绍
产品信息
荧光素标记
抗原名称
DRP1
来源纯化

Polyclonal antibodies are produced by immunizing animals with a synthetic phosphopeptide corresponding to residues surrounding Ser616 of human DRP1. Antibodies are purified by protein A and peptide affinity chromatography.

宿主
Rabbit
商品描述

Product Usage Information

ApplicationDilution
Western Blotting1:1000
Simple Western™1:10 - 1:50
Immunoprecipitation1:50
Immunofluorescence (Immunocytochemistry)1:200 - 1:400
Flow Cytometry (Fixed/Permeabilized)1:50 - 1:200
分子量
78-82
内毒素水平
小鼠, 大鼠, 猴
研究领域
细胞生物学,神经科学,
应用
反应种属
Human
预测反应种属
Mouse,Rat,Monkey,
目标/特异性

Specificity/Sensitivity

Phospho-DRP1 (Ser616) Antibody detects endogenous levels of DRP1 only when phosphorylated at Ser616.

Species Reactivity:

Human

敏感性
Endogenous
背景
背景
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). 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.
研究领域
细胞生物学,神经科学,
翻译后修饰
phosphate
制备和贮存
保存方式

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

数据库链接
Entrez-Gene ID
10059
UniProt ID
O00429

参考图片

Flow cytometric analysis of Jurkat cells, untreated (left) or λ phosphatase-treated (right), using Phospho-DRP1 (Ser616) Antibody and Propidium Iodide (PI)/RNase Staining Solution #4087 to measure DNA content. Anti-rabbit IgG (H+L), F(ab')2 Fragment (Alexa Fluor® 488 Conjugate) #4412 was used as a secondary antibody.

Western blot analysis of extracts from HeLa cells, untreated or treated with Calyculin A #9902, using Phospho-DRP1 (Ser616) Antibody.

Western blot analysis of extracts from HeLa cells, untreated or nocodazole-treated for the indicated times, using Phospho-DRP1 (Ser616) Antibody.

Simple WesternTM analysis of lysates (1 mg/mL) from Hela cells treated with Nocodazole (100ng/mL, 24hr) using Phospho-DRP1 (Ser616) Antibody #3455.  The virtual lane view (left) shows a single target band (as indicated) at 1:10 and 1:50 dilutions of primary antibody.  The corresponding electropherogram view (right) plots chemiluminescence by molecular weight along the capillary at 1:10 (blue line) and 1:50 (green line) dilutions of primary antibody.  This experiment was performed under reducing conditions on the JessTM Simple Western instrument from ProteinSimple, a BioTechne brand, using the 12-230 kDa separation module.

Immunoprecipitation of Phospho-DRP1 (Ser616) from HeLa cell extracts, untreated or nocodazole-treated, using Phospho-DRP1 (Ser616) Antibody followed by western blot using the same antibody. Lanes 1 & 2 are 5% input.

Confocal immunofluorescent analysis of NCI-H1299 cells, untreated (left) or λ-phosphatase-treated (right), using Phospho-DRP1 (Ser616) Antibody (green). Actin filaments have been labeled with DY-554 phallodin (red). Blue pseudocolor = DRAQ5® (fluorescent DNA dye).

声明 :本官网所有报价均为常温或者蓝冰运输价格,如有产品需要干冰运输,需另外加收干冰运输费。
货号:
3455S
一键复制
询价
供应商现货
100ul
选择数量
当前规格1件起购 
配送至
预计5-6个工作日送达,快递: 免运费,若需干冰额外收费