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Peroxiredoxin 1 Mouse mAb (bsm-33118M)  
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50ul/1180.00元
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200ul/2800.00元
200ug(PBS only)/5600.00元
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產(chǎn)品編號(hào) bsm-33118M
英文名稱(chēng) Peroxiredoxin 1 Mouse mAb
中文名稱(chēng) 過(guò)氧化還原酶1單克隆抗體
別    名 Peroxiredoxin-1; Peroxiredoxin 1; Prdx 1; Prdx1; PRDX1_HUMAN; Hbp23; Heme binding 23 kDa protein; Macrophage 23 Kd stress protein; Macrophage 23kDa stress protein; Macrophase stress protein 22kDa; Macrophase stress protein 23 kd; MSP23; Natural killer cel  
研究領(lǐng)域 腫瘤  細(xì)胞生物  免疫學(xué)  
抗體來(lái)源 Mouse
克隆類(lèi)型 Monoclonal
克 隆 號(hào) 10F9
交叉反應(yīng) Human,Mouse,Rat
產(chǎn)品應(yīng)用 WB=1:500-1000,IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500,Flow-Cyt=0.5ug/Test,ICC/IF=1:25
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 22 kDa
檢測(cè)分子量
細(xì)胞定位 細(xì)胞漿 細(xì)胞膜 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 Recombinant human Peroxiredoxin 1 Protein 
亞    型 IgG
純化方法 affinity purified by Protein G
緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事項(xiàng) This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產(chǎn)品介紹 This gene encodes a member of the peroxiredoxin family of antioxidant enzymes, which reduce hydrogen peroxide and alkyl hydroperoxides. The encoded protein may play an antioxidant protective role in cells, and may contribute to the antiviral activity of CD8(+) T-cells. This protein may have a proliferative effect and play a role in cancer development or progression. Four transcript variants encoding the same protein have been identified for this gene. [provided by RefSeq, Jan 2011].

Function:
Involved in redox regulation of the cell. Reduces peroxides with reducing equivalents provided through the thioredoxin system but not from glutaredoxin. May play an important role in eliminating peroxides generated during metabolism. Might participate in the signaling cascades of growth factors and tumor necrosis factor-alpha by regulating the intracellular concentrations of H(2)O(2). Reduces an intramolecular disulfide bond in GDPD5 that gates the ability to GDPD5 to drive postmitotic motor neuron differentiation.

Subunit:
Homodimer; disulfide-linked, upon oxidation. May form heterodimers with AOP2. Interacts with GDPD5; forms a mixed-disulfide with GDPD5 (By similarity).

Subcellular Location:
Cytoplasm. Melanosome.

Post-translational modifications:
Phosphorylated on Thr-90 during the M-phase, which leads to a more than 80% decrease in enzymatic activity.

Similarity:
Belongs to the AhpC/TSA family.
Contains 1 thioredoxin domain.

SWISS:
Q06830

Gene ID:
5052

Database links:

Entrez Gene: 281997 Cow

Entrez Gene: 5052 Human

Entrez Gene: 18477 Mouse

Entrez Gene: 117254 Rat

Omim: 176763 Human

SwissProt: Q9JKY1 Chinese Hamster

SwissProt: Q06830 Human

SwissProt: P35700 Mouse

SwissProt: Q63716 Rat

Unigene: 180909 Human

Unigene: 30929 Mouse

Unigene: 2845 Rat



產(chǎn)品圖片
Sample: Lane 1: Mouse Spleen tissue lysates Lane 2: Mouse Liver tissue lysates Lane 3: Mouse Cerebrum tissue lysates Lane 4: Rat Spleen tissue lysates Lane 5: Rat Cerebrum tissue lysates Lane 6: Human Jurkat cell lysates Lane 7: Human Raji cell lysates Lane 8: Human MCF-7 cell lysates Lane 9: Human A431 cell lysates Lane 10: Human Hela cell lysates Primary: Anti-Peroxiredoxin 1 (bsm-33118M) at 1/1000 dilution Secondary: IRDye800CW Goat Anti-Mouse IgG at 1/20000 dilution Predicted band size: 22 kD Observed band size: 23 kD
Paraformaldehyde-fixed, paraffin embedded (Human brain glioma); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with (Peroxiredoxin 1) Monoclonal Antibody, Unconjugated (ascites of bsm-33118M 10F9) at 1:2000 overnight at 4°C, followed by a conjugated secondary (sp-0024) for 20 minutes and DAB staining.
MCF7 cell; 4% Paraformaldehyde-fixed; Triton X-100 at room temperature for 20 min; Blocking buffer (normal goat serum, C-0005) at 37°C for 20 min; Antibody incubation with (Peroxiredoxin 1) polyclonal Antibody, Unconjugated (bsm-33118M) 1:25, 90 minutes at 37°C; followed by a conjugated Goat Anti-Mouse IgG antibody at 37°C for 90 minutes, DAPI (blue, C02-04002) was used to stain the cell nuclei.
Blank control(black line):Hela. Primary Antibody (green line): Mouse Anti-Peroxiredoxin 1 antibody (bsm-33118M) Dilution:0.5ug/Test; Secondary Antibody(white blue line): Goat anti-mouse IgG-FITC Dilution: 0.5ug/Test. Isotype control(orange line): Normal Mouse IgG Protocol The cells were fixed with 4% PFA (10min at room temperature)and then permeabilized with 90% ice-cold methanol for 20 min at -20℃, The cells were then incubated in 5%BSA to block non-specific protein-protein interactions for 30 min at room temperature .Cells stained with Primary Antibody for 30 min at room temperature. The secondary antibody used for 40 min at room temperature. Acquisition of 20,000 events was performed.
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