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  • 最近搜索:細胞培養 微生物學(xué) 分子生物 生物化學(xué)
    首頁(yè)>>免疫學(xué)>>一抗>>周期蛋白依賴(lài)激酶抑制因子1C抗體
    周期蛋白依賴(lài)激酶抑制因子1C抗體
    • 產(chǎn)品貨號:
      BN41547R
    • 中文名稱(chēng):
      周期蛋白依賴(lài)激酶抑制因子1C抗體
    • 英文名稱(chēng):
      Rabbit anti-p57 Kip2/Cdkn1c Polyclonal antibody
    • 品牌:
      Biorigin
    • 貨號

      產(chǎn)品規格

      售價(jià)

      備注

    • BN41547R-50ul

      50ul

      ¥1486.00

      交叉反應:Rat,Mouse,Human(predicted:Sheep,Cow) 推薦應用:WB,IHC-P,IHC-F,ICC,IF,Flow-Cyt,ELISA

    • BN41547R-100ul

      100ul

      ¥2360.00

      交叉反應:Rat,Mouse,Human(predicted:Sheep,Cow) 推薦應用:WB,IHC-P,IHC-F,ICC,IF,Flow-Cyt,ELISA

    • BN41547R-200ul

      200ul

      ¥3490.00

      交叉反應:Rat,Mouse,Human(predicted:Sheep,Cow) 推薦應用:WB,IHC-P,IHC-F,ICC,IF,Flow-Cyt,ELISA

    產(chǎn)品描述

    英文名稱(chēng)p57 Kip2/Cdkn1c
    中文名稱(chēng)周期蛋白依賴(lài)激酶抑制因子1C抗體
    別    名Beckwith Wiedemann syndrome; BWCR; BWS; CDKI; CDKN 1C; CDKN1C; Cyclin dependent kinase inhibitor 1C; Cyclin dependent kinase inhibitor p57; KIP 2; KIP2; p57; p57 Kip2; p57 Kip 2; p57Kip2; WBS; IMAGE; CDN1C_HUMAN.  
    研究領(lǐng)域腫瘤  細胞生物  細胞周期蛋白  
    抗體來(lái)源Rabbit
    克隆類(lèi)型Polyclonal
    交叉反應Human, Mouse, Rat,  (predicted: Cow, Sheep, )
    產(chǎn)品應用ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 Flow-Cyt=0.2ug/test 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35kDa
    細胞定位細胞核 
    性    狀Liquid
    濃    度1mg/ml
    免 疫 原KLH conjugated synthetic peptide derived from rat Cdkn1c:291-343/343 
    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This gene is imprinted, with preferential expression of the maternal allele. The encoded protein is a tight-binding, strong inhibitor of several G1 cyclin/Cdk complexes and a negative regulator of cell proliferation. Mutations in this gene are implicated in sporadic cancers and Beckwith-Wiedemann syndorome, suggesting that this gene is a tumor suppressor candidate. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Oct 2010].

    Function:
    Potent tight-binding inhibitor of several G1 cyclin/CDK complexes (cyclin E-CDK2, cyclin D2-CDK4, and cyclin A-CDK2) and, to lesser extent, of the mitotic cyclin B-CDC2. Negative regulator of cell proliferation. May play a role in maintenance of the non-proliferative state throughout life.

    Subunit:
    Interacts with PCNA.

    Subcellular Location:
    Nucleus.

    Tissue Specificity:
    Expressed in the heart, brain, lung, skeletal muscle, kidney, pancreas and testis. Expressed in the eye. High levels are seen in the placenta while low levels are seen in the liver.

    DISEASE:
    Defects in CDKN1C are a cause of Beckwith-Wiedemann syndrome (BWS) [MIM:130650]. BWS is a genetically heterogeneous disorder characterized by anterior abdominal wall defects including exomphalos (omphalocele), pre- and postnatal overgrowth, and macroglossia. Additional less frequent complications include specific developmental defects and a predisposition to embryonal tumors.
    Defects in CDKN1C are the cause of intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies (IMAGE) [MIM:614732]. A rare condition characterized by intrauterine growth restriction, metaphyseal dysplasia, congenital adrenal hypoplasia, and genital anomalies. Patients with this condition may present shortly after birth with severe adrenal insufficiency, which can be life-threatening if not recognized early and commenced on steroid replacement therapy. Other reported features in this condition include, hypercalciuria and/or hypercalcemia, craniosynostosis, cleft palate, and scoliosis.
    Note=Defects in CDKN1C are involved in tumor formation.

    Similarity:
    Belongs to the CDI family.

    SWISS:
    E9PTV7

    Gene ID:
    246060

    Database links:

    Entrez Gene: 1028 Human

    Entrez Gene: 12577 Mouse

    Entrez Gene: 246060 Rat

    Omim: 600856 Human

    SwissProt: P49918 Human

    SwissProt: P49919 Mouse

    SwissProt: E9PTV7 Rat

    SwissProt: Q69DC0 Rat

    Unigene: 106070 Human

    Unigene: 168789 Mouse

    Unigene: 162507 Rat



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

    p57 Kip-2調控周期蛋白依賴(lài)蛋白激酶、G1 期, 是細胞周期蛋白依賴(lài)性激酶(CDK)的抑制蛋白。它通過(guò)調控細胞周期進(jìn)程,參與腫瘤細胞的增殖、分化與凋亡。在多種腫瘤中均發(fā)現p57,kip2表達異常,在某些腫瘤中是一種獨立的預后因素,與腫瘤的發(fā)生、發(fā)展及預后有著(zhù)密切關(guān)系。


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