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.
Applications:

WB, IP

REACTIVITY:

H

SENSITIVITY:

Endogenous

MW (kDa):

21

Source/Isotype:

Rabbit IgG

UniProt ID:

#Q06830

Entrez-Gene Id:

5052

Product Information

Product Usage Information

Application Dilution
Western Blotting 1:1000
Immunoprecipitation 1:50

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

Phospho-Prdx1 (Tyr194) (D1T9C) Rabbit mAb recognizes endogenous levels of Prdx1 protein only when phosphorylated at Tyr194. This antibody may cross react with other activated receptor tyrosine kinases including EGFR.

Species Reactivity:

Human

Species predicted to react based on 100% sequence homology

Mouse, Rat

Source / Purification

Monoclonal antibody is produced by immunizing animals with a synthetic phosphopeptide corresponding to residues surrounding Tyr194 of human Prdx1 protein.

Background

Prdx1 belongs to a family of non-seleno peroxidases that function as H2O2 scavengers. All 6 Prdx isoforms share a conserved N-terminal cysteine (Cys51) that is oxidized by H2O2 to form cysteine-sulfenic acid (Cys51-SOH) and, in turn, reacts with Cys172-SH of another Prdx protein, forming a disulfide dimer and protecting it from degradation (1-3). Abnormally high levels of H2O2 cause Prdx1 to form an oligomeric chaperone that loses its peroxidase activity (4). Prdx family members have been reported to bind to JNK and c-Abl and regulate their kinase activity (5,6). Prdx1 was shown to bind to PTEN and regulate its phosphatase activity in conditions of mild or no cellular stress, hence preventing Akt-driven transformation by protecting PTEN from oxidation-induced inactivation (7).
The transient phosphorylation of Prdx1 at Tyr194 leads to inactivation of Prdx1 that in turn promotes localized hydrogen peroxide accumulation (8). Evidence suggests that the Tyr194 phosphorylation of Prdx1 is prominent at the wound edge during repair of cutaneous injury in mice (8,9).

  1. Wood, Z.A. et al. (2003) Trends Biochem Sci 28, 32-40.
  2. Chae, H.Z. et al. (1994) J Biol Chem 269, 27670-8.
  3. Chae, H.Z. et al. (1994) Proc Natl Acad Sci U S A 91, 7022-6.
  4. Jang, H.H. et al. (2004) Cell 117, 625-35.
  5. Wen, S.T. and Van Etten, R.A. (1997) Genes Dev 11, 2456-67.
  6. Kim, Y.J. et al. (2006) Cancer Res 66, 7136-42.
  7. Cao, J. et al. (2009) EMBO J 28, 1505-17.
  8. Woo, H.A. et al. (2010) Cell 140, 517-28.
  9. Singer, A.J. and Clark, R.A. (1999) N Engl J Med 341, 738-46.

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.
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 1
#14041

Phospho-Prdx1 (Tyr194) (D1T9C) Rabbit mAb

Western Blotting Image 1: Phospho-Prdx1 (Tyr194) (D1T9C) Rabbit mAb Expand Image
使用 Phospho-Prdx1 (Tyr194) (D1T9C) Rabbit mAb(上图)和 Prdx1 (D5G12) Rabbit mAb #8499(下图),对未经处理或已经 EGF(50 ng/ml,15 分钟)和 λ 磷酸酶(13333 单位/ml,过夜)处理的 A-431 细胞的提取物进行蛋白质印迹分析。
Immunoprecipitation Image 1: Phospho-Prdx1 (Tyr194) (D1T9C) Rabbit mAb Expand Image
使用 Rabbit (DA1E) mAb XP® Isotype control #3900(泳道 2)或 Phospho-Prdx1 (Tyr194) (D1T9C) Rabbit mAb(泳道 3),对已经 EGF 处理(50 ng/ml,15 分钟)的 A-431 细胞的磷酸 Prdx1 (Tyr194) 蛋白进行免疫沉淀。泳道 1 是 10% 输入对照。使用 Phospho-Prdx1 (Tyr194) (D1T9C) Rabbit mAb 进行蛋白质印迹分析。