最近搜索:細(xì)胞培養(yǎng) 微生物學(xué) 分子生物 生物化學(xué)
    首頁(yè)>>免疫學(xué)>>一抗>>細(xì)胞角蛋白2e重組兔單克隆抗體
    細(xì)胞角蛋白2e重組兔單克隆抗體
    • 產(chǎn)品貨號(hào):
      BN42077R
    • 中文名稱(chēng):
      細(xì)胞角蛋白2e重組兔單克隆抗體
    • 英文名稱(chēng):
      Rabbit anti-Cytokeratin 2e Monoclonal antibody
    • 品牌:
      Biorigin
    • 貨號(hào)

      產(chǎn)品規(guī)格

      售價(jià)

      備注

    • BN42077R-50ul

      50ul

      ¥2020.00

      交叉反應(yīng):Human 推薦應(yīng)用:WB,IHC-P,IHC-F,ICC,IF,ELISA

    • BN42077R-100ul

      100ul

      ¥3240.00

      交叉反應(yīng):Human 推薦應(yīng)用:WB,IHC-P,IHC-F,ICC,IF,ELISA

    產(chǎn)品描述

    英文名稱(chēng)Cytokeratin 2e
    中文名稱(chēng)細(xì)胞角蛋白2e重組兔單克隆抗體
    別    名K 2e; Cytokeratin-2e; Epithelial keratin-2e; K2e; Keratin type II cytoskeletal 2 epidermal; Keratin-2 epidermis; KRT2; K22E_HUMAN; KRT2A; KRT2E; Type-II keratin Kb2.  
    研究領(lǐng)域信號(hào)轉(zhuǎn)導(dǎo)  
    抗體來(lái)源Rabbit
    克隆類(lèi)型Monoclonal
    克 隆 號(hào)2F7
    交叉反應(yīng)Human, 
    產(chǎn)品應(yīng)用WB=1:500-1000 ELISA=1:5000-10000 IHC-P=1:50-200 IHC-F=1:50-200 ICC=1:50-200 IF=1:50-200 (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70kDa
    細(xì)胞定位細(xì)胞漿 
    性    狀Liquid
    濃    度1mg/ml
    免 疫 原Recombinant human Cytokeratin 2e protein, around 350-500aa: 
    亞    型IgG
    純化方法affinity purified by Protein A
    儲(chǔ) 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The protein encoded by this gene is a member of the keratin gene family. The type II cytokeratins consist of basic or neutral proteins which are arranged in pairs of heterotypic keratin chains coexpressed during differentiation of simple and stratified epithelial tissues. This type II cytokeratin is expressed largely in the upper spinous layer of epidermal keratinocytes and mutations in this gene have been associated with bullous congenital ichthyosiform erythroderma. The type II cytokeratins are clustered in a region of chromosome 12q12-q13. [provided by RefSeq, Jul 2008]

    Function:
    Keratins are the major gene product of keratinocytes and form the intermediate filament cytoskeletal network in these cells. In cells of the upper spinous layer, KRT2E and KRT9 are expressed. Although the expression of KRT9 is limited to palmoplantar epidermis, KRT2E is expressed not only in this tissue but also in other regions, notably the epidermis covering the knee, thigh, and groin. It is not known whether these keratins simply replace their respective type I or type II counterpart in the preexisting KRT1/KRT10 network or dimerize with another, as yet undiscovered keratin partner.

    Subunit:
    Heterotetramer of two type I and two type II keratins. Associates with KRT10.

    Subcellular Location:
    Cytoplasmic.

    Tissue Specificity:
    Expressed in the upper spinous and granular suprabasal layers of normal adult epidermal tissues from most body sites including thigh, breast nipple, foot sole, penile shaft and axilla. Not present in foreskin, squamous metaplasias and carcinomas. Expression in hypertrophic and keloid scars begins in the deepest suprabasal layer. Weakly expressed in normal gingival and tongue, however expression is induced in benign keratoses of lingual mucosa and in mild-to-moderate oral dysplasia with orthokeratinization.

    DISEASE:
    Ichthyosis bullosa of Siemens (IBS) [MIM:146800]: A rare autosomal dominant skin disorder displaying a type of epidermolytic hyperkeratosis characterized by generalized erythema and extensive blistering from birth. Large, dark gray hyperkeratoses are observed in later weeks. The skin of IBS patients is unusually fragile and has a tendency to shed the outer layers of the epidermis, producing localized denuded areas (molting effect). IBS usually improves with age so that in most middle-aged patients the hyperkeratosis and keratotic lichenification is limited to the flexural folds of the major joints. Note=The disease is caused by mutations affecting the gene represented in this entry.

    Similarity:
    Belongs to the intermediate filament family.

    SWISS:
    P35908

    Gene ID:
    3849

    Database links:

    Entrez Gene: 3849 Human

    Omim: 600194 Human

    SwissProt: P35908 Human

    Unigene: 707 Human



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


    亚洲AV无码成人专区| 国产性爱在线观看亚洲黄色一级片| 在线观看亚洲电影| 亚洲乱码无人区卡1卡2卡3| 亚洲伊人久久大香线蕉影院| 亚洲视频一区网站| 亚洲系列中文字幕| 亚洲色图黄色小说| 亚洲伊人久久精品| 国产成人精品日本亚洲专| 亚洲jjzzjjzz在线播放| 亚洲一区二区三区高清视频| 亚洲w码欧洲s码免费| 亚洲av无码久久忘忧草| 亚洲kkk4444在线观看| 亚洲欧美自偷自拍另类视 | 亚洲精品无码aⅴ中文字幕蜜桃| 亚洲精品第一综合99久久| 亚洲熟妇丰满xxxxx| 亚洲国产成人精品无码区二本| 久久亚洲AV成人无码国产电影 | 亚洲AV无码不卡在线播放| 亚洲精品天天影视综合网| 97se亚洲综合在线| 亚洲国产日韩在线| 日韩亚洲人成在线| 亚洲国产成人AV在线播放| 国产成人不卡亚洲精品91| 国产a v无码专区亚洲av| 亚洲五月综合缴情在线观看| 亚洲成AV人片在| 亚洲第一中文字幕| 亚洲成综合人影院在院播放| 亚洲天堂免费在线| 欧美日韩亚洲精品| 久久久久亚洲精品天堂久久久久久| 九月丁香婷婷亚洲综合色| 日产亚洲一区二区三区| 亚洲最大的黄色网| 国产精品亚洲专区无码WEB| 久久精品国产精品亚洲下载|