DJ-1 (D29E5) XP® Rabbit mAb

DJ-1 (D29E5) XP® Rabbit mAb

价格: 询价

品牌:Cell Signaling Technology 品牌认证

货号:5933

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抗体英文名 :DJ-1 (D29E5) XP® Rabbit mAb

抗原 :synthetic peptide corresponding to residues surrounding Lys148 of human DJ-1 protein

应用范围 :W, IP, IF-IC

适应物种 :H,M,R,Hm,Mk

保质期 :详见说明书

供应商 :CST

库存 :大量

级别 :详见MSDS文件

是否单克隆 :多克隆

保存条件 :-20°c

规格 :40 ul (4 western blots)/100 ul (10 western blots)/carrier free & custom formulation / quantity

pathwaymore infoapplication referencesdatasheet PDFMSDS PDFprotocols

Applications Key: W=Western Blotting IP=Immunoprecipitation IF-IC=Immunofluorescence (Immunocytochemistry)
Reactivity Key: H=Human M=Mouse R=Rat Hm=Hamster Mk=Monkey
Species cross-reactivity is determined by western blot. Species enclosed in parentheses are predicted to react based on 100% sequence homology.

Applications Reactivity Sensitivity MW (kDa) Isotype
W IP IF-IC H M R Hm Mk Endogenous 22 Rabbit IgG
Protocols
Specificity / Sensitivity

DJ-1 (D29E5) XP® Rabbit mAb recognizes endogenous levels of total DJ-1 protein.

Source / Purification

Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Lys148 of human DJ-1 protein.

Western Blotting

Western Blotting

Western blot analysis of extracts from MEF wild-type, MEF DJ-1 (-/-), HeLa, and C6 cells using DJ-1 (D29E5) XP® Rabbit mAb (upper) and β-Actin (D6A8) Rabbit mAb #8457 (lower). (MEF wild-type and MEF DJ-1 (-/-) cells were kindly provided by Dr. Philipp Kahle, University of Tübingen, Germany).

IF-IC

IF-IC

Confocal immunofluorescent analysis of MEF wild-type (left) or MEF DJ-1 (-/-) (right) cells using DJ-1 (D29E5) XP® Rabbit mAb (green). Actin filaments were labeled with DY-554 phalloidin (red). Blue pseudocolor = DRAQ5® #4084 (fluorescent DNA dye). (MEF wild-type and MEF DJ-1 (-/-) cells were kindly provided by Dr. Philipp Kahle, University of Tübingen, Germany).

Background

Parkinson's disease (PD) is characterized by the presence of Lewy bodies (intracellular inclusions) and by the loss of dopaminergic neurons. Research studies have shown that mutations in α-synuclein, Parkin, and DJ-1 are linked to PD (1). α-synuclein is a major component of the aggregates found in Lewy bodies. Parkin is involved in protein degradation through the ubiquitin-proteasome pathway, and investigators have shown that mutations in Parkin cause early onset of PD (1). Loss-of-function mutations in DJ-1 cause early onset of PD, but DJ-1 is associated with multiple functions: it cooperates with Ras to increase cell transformation, it positively regulates transcription of the androgen receptor, and it may function as an indicator of oxidative stress (2-5). Dopamine D2 receptor-mediated functions are greatly impaired in DJ-1 (-/-) mice, resulting in reduced long-term depression (6).

  1. Borrelli, E. (2005) Neuron 45, 479-81.
  2. Bonifati, V. et al. (2003) Science 299, 256-9.
  3. Nagakubo, D. et al. (1997) Biochem. Biophys. Res. Commun. 231, 509-13.
  4. Takahashi, K. et al. (2001) J. Biol. Chem. 276, 37556-63.
  5. Mitsumoto, A. and Nakagawa, Y. (2001) Free Radic. Res. 35, 885-93.
  6. Goldberg, M.S. et al. (2005) Neuron 45, 489-96.
Application References

Have you published research involving the use of our products? If so we'd love to hear about it. Please let us know!

Companion Products

For Research Use Only. Not For Use In Diagnostic Procedures.

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