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    蛋白酶體26S亞基ATP酶3相互作用蛋白抗體
    • 產品貨號:
      BN40562R
    • 中文名稱:
      蛋白酶體26S亞基ATP酶3相互作用蛋白抗體
    • 英文名稱:
      Rabbit anti-PSMC3IP Polyclonal antibody
    • 品牌:
      Biorigin
    • 貨號

      產品規格

      售價

      備注

    • BN40562R-100ul

      100ul

      ¥2360.00

      交叉反應:Mouse(predicted:Human,Rat,Dog,Horse,Rabbit) 推薦應用:IHC-P,IHC-F,ICC,IF,ELISA

    • BN40562R-200ul

      200ul

      ¥3490.00

      交叉反應:Mouse(predicted:Human,Rat,Dog,Horse,Rabbit) 推薦應用:IHC-P,IHC-F,ICC,IF,ELISA

    產品描述

    英文名稱PSMC3IP
    中文名稱蛋白酶體26S亞基ATP酶3相互作用蛋白抗體
    別    名26S protease regulatory subunit 6A; 26S proteasome AAA-ATPase subunit RPT5; Human immunodeficiency virus tat transactivator binding protein 1; MGC8487; Proteasome (prosome macropain) 26S subunit ATPase 3; Proteasome 26S ATPase subunit 3; Proteasome 26S subunit ATPase 3; Proteasome subunit P50; PRS6A_HUMAN; PSMC 3; PSMC3; Tat binding protein 1; TAT-binding protein 1; TBP-1; TBP1.  
    研究領域細胞生物  轉錄調節因子  泛素  
    抗體來源Rabbit
    克隆類型Polyclonal
    交叉反應Mouse,  (predicted: Human, Rat, Dog, Horse, Rabbit, )
    產品應用ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 (石蠟切片需做抗原修復)
    not yet tested in other applications.
    optimal dilutions/concentrations should be determined by the end user.
    分 子 量24kDa
    細胞定位細胞核 
    性    狀Liquid
    濃    度1mg/ml
    免 疫 原KLH conjugated synthetic peptide derived from human PSMC3IP:1-100/217 
    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
    產品介紹This gene encodes a protein that functions in meiotic recombination. It is a subunit of the PSMC3IP/MND1 complex, which interacts with PSMC3/TBP1 to stimulate DMC1- and RAD51-mediated strand exchange during meiosis. The protein encoded by this gene can also co-activate ligand-driven transcription mediated by estrogen, androgen, glucocorticoid, progesterone, and thyroid nuclear receptors. Mutations in this gene cause XX female gonadal dysgenesis. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Dec 2011]

    Function:
    Plays an important role in meiotic recombination. Stimulates DMC1-mediated strand exchange required for pairing homologous chromosomes during meiosis. The complex PSMC3IP/MND1 binds DNA, stimulates the recombinase activity of DMC1 as well as DMC1 D-loop formation from double-strand DNA. This complex stabilizes presynaptic RAD51 and DMC1 filaments formed on single strand DNA to capture double-strand DNA. This complex stimulates both synaptic and presynaptic critical steps in RAD51 and DMC1-promoted homologous pairing. May inhibit HIV-1 viral protein TAT activity and modulate the activity of proteasomes through association with PSMC3. Acts as a tissue specific coactivator of hormone-dependent transcription mediated by nuclear receptors.

    Subcellular Location:
    Nucleus.

    Tissue Specificity:
    Highly expressed in testis and colon.

    Post-translational modifications:
    PTM: Phosphorylated by PKA, PKC and MAPK.

    DISEASE:
    Ovarian dysgenesis 3 (ODG3) [MIM:614324]: A disorder characterized by lack of spontaneous pubertal development, primary amenorrhea, uterine hypoplasia, and hypergonadotropic hypogonadism as a result of streak gonads. Note=The disease is caused by mutations affecting the gene represented in this entry.

    Similarity:
    Belongs to the HOP2 family.

    SWISS:
    Q9P2W1

    Gene ID:
    29893

    Database links:
    ntrez Gene: 29893 Human

    Entrez Gene: 19183 Mouse

    Entrez Gene: 140938 Rat

    Omim: 608665 Human

    SwissProt: Q9P2W1 Human

    SwissProt: O35047 Mouse

    SwissProt: Q91ZY6 Rat

    Unigene: 383019 Human

    Unigene: 18344 Mouse

    Unigene: 144650 Rat



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


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