Revision 3

#80471Store at -20C

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.
Applications:

WB, IP

REACTIVITY:

H M R

SENSITIVITY:

Endogenous

MW (kDa):

80-100

Source/Isotype:

Rabbit IgG

UniProt ID:

#O60313

Entrez-Gene Id:

4976

Product Information

Product Usage Information

Application Dilution
Western Blotting 1:1000
Immunoprecipitation 1:100

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.

Specificity / Sensitivity

OPA1 (D6U6N) Rabbit mAb recognizes endogenous levels of total OPA1 protein.

Species Reactivity:

Human, Mouse, Rat

Source / Purification

Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Leu821 of human OPA1 protein.

Background

Changes in mitochondrial dynamics regulated by environmental cues affect mitochondrial size and shape and have been shown to dramatically impact mitochondrial metabolism, apoptosis, and autophagy (1). These processes are largely controlled by mitochondrial dynamin-related GTPases, including mitofusin-1, mitofusin-2, OPA1, and DRP1. DRP1 regulates mitochondrial fission, while the mitofusins and OPA1 control fusion at the outer and inner mitochondrial membrane, respectively.

OPA1, or Optic Atrophy 1, was originally identified as a genetic cause for Autosomal Dominant Optic Atrophy, a neuropathy resulting in progressive visual loss (2,3). OPA1 is a widely expressed protein localized to the inner mitochondrial membrane, which regulates mitochondrial fusion and cristae morphology and protects against apoptosis (4-6). OPA1 activity is tightly regulated through alternative splicing and post-translational modifications including complex proteolytic processing by multiple proteases (7-12). In addition, OPA1 expression can be induced under conditions of metabolic demand through a pathway involving Parkin induced NF-κB activation (13).

  1. Kasahara, A. and Scorrano, L. (2014) Trends Cell Biol 24, 761-70.
  2. Delettre, C. et al. (2000) Nat Genet 26, 207-10.
  3. Alexander, C. et al. (2000) Nat Genet 26, 211-5.
  4. Frezza, C. et al. (2006) Cell 126, 177-89.
  5. Olichon, A. et al. (2003) J Biol Chem 278, 7743-6.
  6. Griparic, L. et al. (2004) J Biol Chem 279, 18792-8.
  7. Delettre, C. et al. (2001) Hum Genet 109, 584-91.
  8. Olichon, A. et al. (2007) Cell Death Differ 14, 682-92.
  9. Ishihara, N. et al. (2006) EMBO J 25, 2966-77.
  10. Cipolat, S. et al. (2006) Cell 126, 163-75.
  11. Griparic, L. et al. (2007) J Cell Biol 178, 757-64.
  12. Merkwirth, C. et al. (2008) Genes Dev 22, 476-88.
  13. Müller-Rischart, A.K. et al. (2013) Mol Cell 49, 908-21.

Species Reactivity

Species reactivity is determined by testing in at least one approved application (e.g., western blot).

Western Blot Buffer

IMPORTANT: For western blots, incubate membrane with diluted primary antibody in 5% w/v BSA, 1X TBS, 0.1% Tween® 20 at 4°C with gentle shaking, overnight.

Applications Key

WB: Western Blotting IP: Immunoprecipitation

Cross-Reactivity Key

H: human M: mouse R: rat Hm: hamster Mk: monkey Vir: virus Mi: mink C: chicken Dm: D. melanogaster X: Xenopus Z: zebrafish B: bovine Dg: dog Pg: pig Sc: S. cerevisiae Ce: C. elegans Hr: horse GP: Guinea Pig Rab: rabbit All: all species expected

Trademarks and Patents

Cell Signaling Technology is a trademark of Cell Signaling Technology, Inc.
SignalSilence is a registered trademark of Cell Signaling Technology, Inc.
XP 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.

限制使用

除非 CST 的合法授书代表以书面形式书行明确同意,否书以下条款适用于 CST、其关书方或分书商提供的书品。 任何书充本条款或与本条款不同的客书条款和条件,除非书 CST 的合法授书代表以书面形式书独接受, 否书均被拒书,并且无效。

专品专有“专供研究使用”的专专或专似的专专声明, 且未专得美国食品和专品管理局或其他外国或国内专管机专专专任何用途的批准、准专或专可。客专不得将任何专品用于任何专断或治专目的, 或以任何不符合专专声明的方式使用专品。CST 专售或专可的专品提供专作专最专用专的客专,且专用于研专用途。将专品用于专断、专防或治专目的, 或专专售(专独或作专专成)或其他商专目的而专专专品,均需要 CST 的专独专可。客专:(a) 不得专独或与其他材料专合向任何第三方出售、专可、 出借、捐专或以其他方式专专或提供任何专品,或使用专品制造任何商专专品,(b) 不得复制、修改、逆向工程、反专专、 反专专专品或以其他方式专专专专专品的基专专专或技专,或使用专品开专任何与 CST 的专品或服专专争的专品或服专, (c) 不得更改或专除专品上的任何商专、商品名称、徽专、专利或版专声明或专专,(d) 只能根据 CST 的专品专售条款和任何适用文档使用专品, (e) 专遵守客专与专品一起使用的任何第三方专品或服专的任何专可、服专条款或专似专专

Revision 3
#80471

OPA1 (D6U6N) Rabbit mAb

Western Blotting Image 1: OPA1 (D6U6N) Rabbit mAb Expand Image
使用 OPA1 (D6U6N) Rabbit mAb (上图)或 β-Actin (D6A8) Rabbit mAb #8457(下图),对野生型 (-) 和 OPA 敲除型 (OPA-/-; +) 小鼠的 MEF 提取物进行蛋白质印迹分析。
Western Blotting Image 2: OPA1 (D6U6N) Rabbit mAb Expand Image
使用 OPA1 (D6U6N) Rabbit mAb (上图)或 β-Actin (D6A8) Rabbit mAb #8457(下图),对转染 100 nM SignalSilence® Control siRNA (Unconjugated) #6568 (-)、SignalSilence® OPA1 siRNA I (+) 或 SignalSilence® OPA1 siRNA II 的 HeLa 细胞提取物进行蛋白质印迹分析。OPA1 (D6U6N) Rabbit mAb 确认 OPA1 表达沉默,而 β-Actin (D6A8) Rabbit mAb 则用作上样对照。
Western Blotting Image 3: OPA1 (D6U6N) Rabbit mAb Expand Image
使用 OPA1 (D6U6N) Rabbit mAb 对未经处理 (-) 或已经羰基氰化物间氯苯腙 (CCCP; +) 处理的 MCF7 和 HeLa 细胞的提取物进行蛋白质印迹分析。
Western Blotting Image 4: OPA1 (D6U6N) Rabbit mAb Expand Image
使用 OPA1 (D6U6N) Rabbit mAb 对不同细胞系的提取物进行蛋白质印迹分析。
Immunoprecipitation Image 1: OPA1 (D6U6N) Rabbit mAb Expand Image
对 MCF7 细胞提取物 OPA1 进行免疫沉淀。泳道 1 为10% input,泳道 2 为 Rabbit (DA1E) mAb IgG XP® Isotype Control #3900,泳道 3 为 OPA1 (D6U6N) Rabbit mAb。使用 OPA1 (D6U6N) Rabbit mAb 进行蛋白质印迹分析。构象特异性二抗用于避免与 IgG 的反应性。