最近搜索:細胞培養(yǎng) 微生物學(xué) 分子生物 生物化學(xué)
    首頁>>免疫學(xué)>>一抗>>磷酸化細胞信號轉(zhuǎn)導(dǎo)分子SMAD2抗體
    磷酸化細胞信號轉(zhuǎn)導(dǎo)分子SMAD2抗體
    • 產(chǎn)品貨號:
      BN41150R
    • 中文名稱:
      磷酸化細胞信號轉(zhuǎn)導(dǎo)分子SMAD2抗體
    • 英文名稱:
      Rabbit anti-Phospho-Smad2 (Thr220) Polyclonal antibody
    • 品牌:
      Biorigin
    • 貨號

      產(chǎn)品規(guī)格

      售價

      備注

    • BN41150R-100ul

      100ul

      ¥2470.00

      交叉反應(yīng):Human(predicted:Mouse,Rat,Chicken,Dog,Cow,Horse) 推薦應(yīng)用:IHC-P,IHC-F,IF,Flow-Cyt,ELISA

    產(chǎn)品描述

    英文名稱Phospho-Smad2 (Thr220)
    中文名稱磷酸化細胞信號轉(zhuǎn)導(dǎo)分子SMAD2抗體
    別    名Smad2 (phospho T220); p-Smad2 (phospho T220); phospho-Smad2(p-Thr220); p-Smad2(Thr220); phospho-Smad2(p-Thr220); hMAD 2; hSMAD2; JV18 1; JV18; JV181; MAD; MAD Related Protein 2; MADH2; MADR2; MGC22139; MGC34440; Mothers Against Decapentaplegic Homolog 2; mothers against DPP homolog 2; SMAD 2; SMAD; SMAD2; SMAD2_HUMAN.  




    產(chǎn)品類型磷酸化抗體 
    研究領(lǐng)域腫瘤  免疫學(xué)  信號轉(zhuǎn)導(dǎo)  轉(zhuǎn)錄調(diào)節(jié)因子  
    抗體來源Rabbit
    克隆類型Polyclonal
    交叉反應(yīng)Human,  (predicted: Mouse, Rat, Chicken, Dog, Cow, Horse, )
    產(chǎn)品應(yīng)用WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 Flow-Cyt=2ug/Test IF=1:100-500 (石蠟切片需做抗原修復(fù))
    not yet tested in other applications.
    optimal dilutions/concentrations should be determined by the end user.
    分 子 量52kDa
    細胞定位細胞核 細胞漿 
    性    狀Liquid
    濃    度1mg/ml
    免 疫 原KLH conjugated Synthesised phosphopeptide derived from human Smad2 around the phosphorylation site of Thr220:PE(p-T)PP 
    亞    型IgG
    純化方法affinity purified by Protein A
    儲 存 液0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
    保存條件Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
    PubMedPubMed
    產(chǎn)品介紹Smad2 is a 58 kDa member of a family of proteins involved in cell proliferation, differentiation and development. The Smad family is divided into three subclasses: receptor-regulated Smad's, activin/TGF alpha receptor-regulated (Smad2 and 3) or BMP receptor regulated (Smad1, 5, and 8); the common partner, (Smad4) that functions via its interaction to the various Smad's; and the inhibitory Smad's, (Smad6 and Smad7). Smad2 consists of two highly conserved domains, the N terminal Mad homology (MH1) and the C-terminal Mad homology 2 (MH2) domains. The MH1 domain binds DNA and regulates nuclear import and transcription while the MH2 domain conserved among all the Smad's regulates Smad2 oligomerization and binding to cytoplasmic adaptors and transcription factors. Activated Smad2 associates with Smad4 and translocates as a complex into the nucleus, allowing its binding to DNA and transcription factors. This translocation of Smad2 (as well as Smad3) into the nucleus is a central event in TGF beta signaling. Phosphorylation of threonine 8 in the calmodulin binding region of the MH1 domain by extracellular signal regulated kinase 1(ERK 1) enhances Smad2 transcriptional activity, which is negatively regulated by calmodulin. The regulation of Smad2 phosphorylation on threonine 8 by ERK 1 and calmodulin is critical for Smad2 mediated signaling.

    Function:
    Receptor-regulated SMAD (R-SMAD) that is an intracellular signal transducer and transcriptional modulator activated by TGF-beta (transforming growth factor) and activin type 1 receptor kinases. Binds the TRE element in the promoter region of many genes that are regulated by TGF-beta and, on formation of the SMAD2/SMAD4 complex, activates transcription. May act as a tumor suppressor in colorectal carcinoma. Positively regulates PDPK1 kinase activity by stimulating its dissociation from the 14-3-3 protein YWHAQ which acts as a negative regulator.

    Subunit:
    Momomer; the absence of TGF-beta. Heterodimer; in the presence of TGF-beta. Forms a heterodimer with co-SMAD, SMAD4, in the nucleus to form the transactivation complex SMAD2/SMAD4. Interacts with AIP1, HGS, PML and WWP1. Interacts with NEDD4L in response to TGF-beta. Found in a complex with SMAD3 and TRIM33 upon addition of TGF-beta. Interacts with ACVR1B, SMAD3 and TRIM33. Interacts (via the MH2 domain) with ZFYVE9; may form trimers with the SMAD4 co-SMAD. Interacts with FOXH1, homeobox protein TGIF, PEBP2-alpha subunit, CREB-binding protein (CBP), EP300 and SKI. Interacts with SNON; when phosphorylated at Ser-465/467. Interacts with SKOR1 and SKOR2. Interacts with PRDM16. Interacts (via MH2 domain) with LEMD3. Interacts with RBPMS. Interacts with WWP1. Interacts (dephosphorylated form, via the MH1 and MH2 domains) with RANBP3 (via its C-terminal R domain); the interaction results in the export of dephosphorylated SMAD3 out of the nucleus and termination ot the TGF-beta signaling. Interacts with PDPK1 (via PH domain).

    Subcellular Location:
    Cytoplasm. Nucleus. Note=Cytoplasmic and nuclear in the absence of TGF-beta. On TGF-beta stimulation, migrates to the nucleus when complexed with SMAD4. On dephosphorylation by phosphatase PPM1A, released from the SMAD2/SMAD4 complex, and exported out of the nucleus by interaction with RANBP1.

    Tissue Specificity:
    Expressed at high levels in skeletal muscle, heart and placenta.

    Post-translational modifications:
    Phosphorylated on one or several of Thr-220, Ser-245, Ser-250, and Ser-255. In response to TGF-beta, phosphorylated on Ser-465/467 by TGF-beta and activin type 1 receptor kinases. Able to interact with SMURF2 when phosphorylated on Ser-465/467, recruiting other proteins, such as SNON, for degradation. In response to decorin, the naturally occurring inhibitor of TGF-beta signaling, phosphorylated on Ser-240 by CaMK2. Phosphorylated by MAPK3 upon EGF stimulation; which increases transcriptional activity and stability, and is blocked by calmodulin. Phosphorylated by PDPK1.
    In response to TGF-beta, ubiquitinated by NEDD4L; which promotes its degradation.
    Acetylated on Lys-19 by coactivators in response to TGF-beta signaling, which increases transcriptional activity. Isoform short: Acetylation increases DNA binding activity in vitro and enhances its association with target promoters in vivo. Acetylation in the nucleus by EP300 is enhanced by TGF-beta.

    Similarity:
    Belongs to the dwarfin/SMAD family.
    Contains 1 MH1 (MAD homology 1) domain.
    Contains 1 MH2 (MAD homology 2) domain.

    SWISS:
    Q15796

    Gene ID:
    4087

    Database links:

    Entrez Gene: 4087 Human

    Entrez Gene: 17126 Mouse

    Entrez Gene: 29357 Rat

    Omim: 601366 Human

    SwissProt: Q15796 Human

    SwissProt: Q62432 Mouse

    SwissProt: O70436 Rat

    Unigene: 12253 Human

    Unigene: 705764 Human

    Unigene: 391091 Mouse

    Unigene: 2755 Rat



    Important Note:
    This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic application


    亚洲乱码卡一卡二卡三| 亚洲欧洲国产综合| 亚洲韩国—中文字幕| 亚洲国产高清国产拍精品| 亚洲 欧洲 日韩 综合在线| 亚洲电影国产一区| 亚洲一区二区三区影院 | 亚洲精品中文字幕麻豆| 久久亚洲精品成人无码网站| 亚洲人色婷婷成人网站在线观看| 最新亚洲成av人免费看| 久久久久噜噜噜亚洲熟女综合| 国产av无码专区亚洲国产精品| 国产精品手机在线亚洲| 亚洲福利在线播放| 久久亚洲国产成人精品无码区| 国产精品亚洲mnbav网站| 亚洲中文字幕无码一区 | 一本色道久久88亚洲精品综合| 亚洲人成电影网站久久| 亚洲天然素人无码专区| 国产精品无码亚洲精品2021| 校园亚洲春色另类小说合集| 国产AV日韩A∨亚洲AV电影 | 亚洲福利一区二区| 精品久久亚洲中文无码| 亚洲中文字幕久久无码| 亚洲AV成人无码久久WWW| www.亚洲色图| 一本久久a久久精品亚洲| 亚洲成AV人片在线观看无| 久久久久亚洲Av无码专| 亚洲国产精品成人精品小说| 欧洲 亚洲 国产图片综合| 久久亚洲精品高潮综合色a片| 另类图片亚洲校园小说区| 久久精品国产精品亚洲| 久久青青草原亚洲AV无码麻豆 | 亚洲电影日韩精品 | 亚洲中文字幕第一页在线| 久久国产亚洲电影天堂|