產(chǎn)品編號(hào) | bs-6327R-BF488 |
英文名稱 | Rabbit Anti-Filaggrin/BF488 Conjugated antibody |
中文名稱 | BF488標(biāo)記的絲聚蛋白/中間絲相關(guān)蛋白抗體 |
別 名 | FLG; Epidermal filaggrin; Filaggrin precursor; Fillagrin; Profilaggrin; FILA_HUMAN. |
規(guī)格價(jià)格 | 100ul/2980元 購買 大包裝/詢價(jià) |
說 明 書 | 100ul |
研究領(lǐng)域 | 細(xì)胞生物 信號(hào)轉(zhuǎn)導(dǎo) 細(xì)胞周期蛋白 細(xì)胞類型標(biāo)志物 細(xì)胞骨架 |
抗體來源 | Rabbit |
克隆類型 | Polyclonal |
交叉反應(yīng) | Human, Rat, (predicted: Mouse, Dog, Pig, Cow, Horse, Rabbit, ) |
產(chǎn)品應(yīng)用 | IF=1:50-200
not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
分 子 量 | 447kDa |
性 狀 | Lyophilized or Liquid |
濃 度 | 1mg/ml |
免 疫 原 | KLH conjugated synthetic peptide derived from human Filaggrin |
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 | Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C. |
產(chǎn)品介紹 |
background: The protein encoded by this gene is an intermediate filament-associated protein that aggregates keratin intermediate filaments in mammalian epidermis. It is initially synthesized as a polyprotein precursor, profilaggrin (consisting of multiple filaggrin units of 324 aa each), which is localized in keratohyalin granules, and is subsequently proteolytically processed into individual functional filaggrin molecules. Mutations in this gene are associated with ichthyosis vulgaris.[provided by RefSeq, Dec 2009]. Function: Aggregates keratin intermediate filaments and promotes disulfide-bond formation among the intermediate filaments during terminal differentiation of mammalian epidermis. Tissue Specificity: Keratohyalin granules. Post-translational modifications: Filaggrin is initially synthesized as a large, insoluble, highly phosphorylated precursor containing many tandem copies of 324 AA, which are not separated by large linker sequences. During terminal differentiation it is dephosphorylated and proteolytically cleaved. The N-terminal of the mature protein is heterogeneous, and is blocked by the formation of pyroglutamate. Undergoes deimination of some arginine residues (citrullination). DISEASE: Defects in FLG are the cause of ichthyosis vulgaris (VI) [MIM:146700]; also known as ichthyosis simplex. Ichthyosis vulgaris is the most common form of ichthyosis inherited as an autosomal dominant trait. It is characterized by palmar hyperlinearity, keratosis pilaris and a fine scale that is most prominent over the lower abdomen, arms, and legs. Ichthyosis vulgaris is characterized histologically by absent or reduced keratohyalin granules in the epidermis and mild hyperkeratosis. The disease can be associated with frequent asthma, eczema or hay fever. Defects in FLG are a cause of susceptibility to dermatitis atopic type 2 (ATOD2) [MIM:605803]. Atopic dermatitis is a complex, inflammatory disease with multiple alleles at several loci thought to be involved in the pathogenesis. It commonly begins in infancy or early childhood and is characterized by a chronic relapsing form of skin inflammation, a disturbance of epidermal barrier function that culminates in dry skin, and IgE-mediated sensitization to food and environmental allergens. It is manifested by lichenification, excoriation, and crusting, mainly on the flexural surfaces of the elbow and knee. Similarity: Belongs to the S100-fused protein family. Contains 2 EF-hand domains. Contains 23 filaggrin repeats. Database links: Entrez Gene: 2312 Human Entrez Gene: 14246 Mouse Omim: 135940 Human SwissProt: P20930 Human SwissProt: P11088 Mouse Unigene: 654510 Human Unigene: 162684 Mouse Unigene: 439710 Mouse Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |
| 刚才黄色内射视频 | 欧美性爱xxxx | 91精品国产99久久久久久女少 | 免费看国产女人动态图片 | 国产日韩久久久久69影院 | 免费无码婬片AA片按摩 | 国产肥婆乱婬视频一区 | 国产精品99朵亚视频免费 | 色偷偷超碰丁香六月 | 成人午夜啪免费视频在线观看软件 | 午夜剧场三级爱爱黑人 | 美女搡BBB又爽又猛又黄www | 免费黄色视频在线观看一区二区 | 亚洲国产精品无码久久一线夕不卡 | 国产 18 爽 不卡 | 日韩精品无码中文视频 | 四虎最新成人永久网站 | 少女免费观看片哔哩哔哩在线观看视频 | 无码专区3D动漫精品免费软件 | 色哟哟在线视频免费看到爽 | 91无码人妻精品一区二区三区四 | 老司机午夜福利视频 | 免费无遮挡 视频网站 | 少妇搡BBBB搡BBB搡毛片 | 台湾少妇搡BBBB搡BBBB | 成人动漫一区二区 | 大黑人狂躁美女大BBBB小说 | 国产成人免费在线观看 | 成人女人看A片免费视频古代 | 欧美A∨男人天堂A√ | 极品熟女人妻20p白浆出来了 | 亚洲欧洲精品mv免费看 | 手机在线不卡无码操三八 | 99久久无码一区人妻贼王 | 成人精品一区二区三区无码视频 | 精品国产AⅤ无码久久久暖暖 | 少妇无套内谢太紧了A片软件 | 媚黑极品魔都绿帽人妻找黑人 | 中文字幕av在线观看 | 天天干天天射天天操天天日 |