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BrdU(Proliferation Marker) Mouse mAb (bsm-0917M)  
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50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
200ug(PBS only)/5600.00元
大包裝/詢價

產(chǎn)品編號 bsm-0917M
英文名稱 BrdU(Proliferation Marker) Mouse mAb
中文名稱 5-溴脫氧尿嘧啶核苷(增殖標志物)單克隆抗體
別    名 Bromodeoxyuridine; Bromodeoxyuridine; 5-Bromo-2′-deoxyuridine; 5-BrdU; Proliferation Marker; 5-Bromo-2-deoxyUridine.  
Specific References  (8)     |     bsm-0917M has been referenced in 8 publications.
[IF=8.025] Wei Hao. et al. Ginger polysaccharides relieve ulcerative colitis via maintaining intestinal barrier integrity and gut microbiota modulation. INT J BIOL MACROMOL. 2022 Oct;219:730  IF ;  Mouse.  
[IF=5.4] Zhao, Lan, et al. "Acupuncture Improves Cerebral Microenvironment in Mice with Alzheimer’s Disease Treated with Hippocampal Neural Stem Cells."Molecular Neurobiology (2016): 1-11.  IHC-F, IF(ICC) ;  Mouse.  
[IF=3.17] Liu, Yang, et al. "Amelioration of Stroke-Induced Neurological Deficiency by Lyophilized Powder of Catapol and Puerarin." International Journal of Biological Sciences 10.4 (2014): 448-456.  IHC-P ;  Mouse.  
[IF=2.959] Zhuang M et al. Reelin regulates male mouse reproductive capacity via the sertoli cells.(2018) J. Cell. Biochem. 2018 Oct 18  WB ;  Mouse.  
[IF=2.88] Li, Hongwei, et al. "Regular treadmill running improves spatial learning and memory performance in young mice through increased hippocampal neurogenesis and decreased stress." Brain Research (2013).  Mouse.  
[IF=2.645] Xiao H et al. Osthole ameliorates cognitive impairments via augmenting neuronal population in APP/PS1 transgenic mice. Neurosci Res . 2020 Apr 14;S0168-0102(20)30008-0.  ICC,WB ;  mouse.  
[IF=1.984] Du Y et al. Jieyu Anshen Granule, a Chinese Herbal Formulation, Exerts Effects on Poststroke Depression in Rats. Evidence-Based Complementary and Alternative Medicine, 2020, 1–12.  IHF ;  Rat.  
[IF=1.89] Wang, N., et al. "Sodium hyaluronate-CNTF gelatinous particles promote axonal growth, neurogenesis and functional recovery after spinal cord injury." Spinal Cord (2014).  IHC-F ;  Rat.  
產(chǎn)品類型 小分子抗體 
研究領(lǐng)域 細胞生物  免疫學  發(fā)育生物學  染色質(zhì)和核信號  神經(jīng)生物學  藥物及化合物  細胞類型標志物  
抗體來源 Mouse
克隆類型 Monoclonal
克 隆 號 1A7
交叉反應 Species independent
產(chǎn)品應用 ICC/IF=1:100
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 0.3071 kDa
檢測分子量
細胞定位 細胞核 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated Brdu 
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 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 Proliferation Marker
Bromodeoxyuridine (BrdU) is a thymidine analog and is specifically incor-porated into DNA during DNA synthesis. Anti-bromodeoxyuridine monoclonal antibody is used to identify cells that have incorporated BrdU. This immunological detection scheme has several advantages over the use of radioactive thymidine incorporation for identifying cells under-going replication. Labeling and detection can be performed the same day instead of waiting several days, as required for autoradiography of tritium-labeled cells, and the necessity of using multiple specimens for obtaining the optimal exposure time is eliminated. In addition, anti-bromodeoxyuridine staining with flow cytometric analysis allows multiple parameters to be evaluated simultaneously. Anti-bromodeoxyuridine monoclonal antibody has been used for identi-fying proliferating cells in blood (Campana et al., 1988), tissues (Schutte et al., 1987; Hayashi, et al., 1988), tumors (Hoshino et al., 1986; Morstyn et al., 1983), as well as for determining plasma cell labeling indices (Greipp et al., 1985).

Subcellular Location:
Nuclear.

增殖標志物
BrdU(溴化脫氧尿嘧啶核苷)可以在體內(nèi)和體外摻入到處于S期的細胞所合成的DNA鏈中。此抗體可以與摻入到任何種屬細胞中的BrdU反應,與碘脫氧尿嘧啶有交叉反應,標記摻有BrdU的S期細胞,主要用于研究各種不同的因素對正常/腫瘤組織的細胞增殖及動力學的研究。
用FITC標記的抗BrdU IgG可用于流式細胞術(shù)定量檢測增值細胞。
產(chǎn)品圖片
4% Paraformaldehyde-fixed Hela(treated with 10uM BrdU for 24 hours) (H) cells; 2M HCL at r.t. for 20 min; Antibody incubation with (BrdU ) monoclonal Antibody, unconjugated (bsm-0917M) 1:100, 90 min at 37°C; followed by conjugated Goat Anti-Mouse IgG antibody (green, bs-0296G-FITC) at 37°C for 90 min, DAPI (blue, C02-04002) was used to stain the cell nuclei.
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