亚洲中文字幕特级毛片-亚洲制服丝袜中文字幕-亚洲制服丝袜在线观看-亚洲制服欧美自拍另类-免费一级黄色-免费一级国产生活片

掃碼關注公眾號           掃碼咨詢技術支持           掃碼咨詢技術服務
  
客服熱線:400-901-9800  客服QQ:4009019800  技術答疑  技術支持  質量反饋  關于我們  聯系我們
粉嫩小仙女扒开双腿自慰 ,精品无码成人久久久久久,国产午夜不卡在线观看视频666
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-CK16/BF488 Conjugated antibody (bs-1270R-BF488)
訂購熱線:400-901-9800
訂購郵箱:sales@www.chomd.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@www.chomd.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-1270R-BF488
英文名稱 Rabbit Anti-CK16/BF488 Conjugated antibody
中文名稱 BF488標記的細胞角蛋白16抗體
別    名 Cytokeratin 16; CK 16; Focal non epidermolytic palmoplantar keratoderma; K 16; K16; K1CP; CK-16; CK16; Cytokeratin-16; FNEPPK; K1C16_HUMAN; Keratin; Keratin-16; type I cytoskeletal 16; Keratin 16; Keratin type I cytoskeletal 16; Keratin16; KRT 16; KRT16; KRT16A; NEPPK.  
規格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 腫瘤  免疫學  信號轉導  細胞骨架  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Mouse, Rat,  (predicted: Human, Dog, Cow, Horse, )
產品應用 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 51kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human CK16
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 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.
產品介紹 background:
The protein encoded by this gene is a member of the keratin gene family. The keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into cytokeratins and hair keratins. Most of the type I cytokeratins consist of acidic proteins which are arranged in pairs of heterotypic keratin chains and are clustered in a region of chromosome 17q12-q21. This keratin has been coexpressed with keratin 14 in a number of epithelial tissues, including esophagus, tongue, and hair follicles. Mutations in this gene are associated with type 1 pachyonychia congenita, non-epidermolytic palmoplantar keratoderma and unilateral palmoplantar verrucous nevus. [provided by RefSeq, Jul 2008].

Subunit:
Heterodimer of a type I and a type II keratin. KRT16 associates with KRT6 isomers. Interacts with TCHP. Interacts with TRADD (By similarity).

Tissue Specificity:
Expressed in the hair follicle, nail bed and in mucosal stratified squamous epithelia and, suprabasally, in oral epithelium and palmoplantar epidermis. Also found in luminal cells of sweat and mammary gland ducts.

DISEASE:
Pachyonychia congenita 1 (PC1) [MIM:167200]: An autosomal dominant ectodermal dysplasia characterized by hypertrophic nail dystrophy resulting in onchyogryposis (thickening and increase in curvature of the nail), palmoplantar keratoderma, follicular hyperkeratosis, and oral leukokeratosis. Hyperhidrosis of the hands and feet is usually present. Note=The disease is caused by mutations affecting the gene represented in this entry.
Keratoderma, palmoplantar, non-epidermolytic, focal (FNEPPK) [MIM:613000]: A dermatological disorder characterized by non-epidermolytic palmoplantar keratoderma limited to the pressure points on the balls of the feet, with later mild involvement on the palms. Oral, genital and follicular keratotic lesions are often present. Note=The disease is caused by mutations affecting the gene represented in this entry.
Unilateral palmoplantar verrucous nevus (UPVN) [MIM:144200]: UPVN is characterized by a localized epidermolytic hyperkeratosis in parts of the right palm and the right sole, following the lines of Blaschko. Note=The disease is caused by mutations affecting the gene represented in this entry.
Note=KRT16 and KRT17 are coexpressed only in pathological situations such as metaplasias and carcinomas of the uterine cervix and in psoriasis vulgaris.

Similarity:
Belongs to the intermediate filament family.

Database links:

Entrez Gene: 3868 Human

Omim: 148067 Human

SwissProt: P08779 Human

Unigene: 655160 Human



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
版權所有 2004-2026 www.www.chomd.com.cn 北京博奧森生物技術有限公司
通過國際質量管理體系ISO 9001:2015 GB/T 19001-2016    證書編號: 00124Q34771R2M/1100
通過國際醫療器械-質量管理體系ISO 13485:2016 GB/T 42061-2022    證書編號: CQC24QY10047R0M/1100
京ICP備05066980號-1         京公網安備110107000727號
主站蜘蛛池模板: 北条麻妃国产九九九精品小说| 亚洲精品无码少妇剧情| 久久精品免视看国产成人不卡_无码| 久久久久久久久女黄9999找换换换 | 亚洲一区二区三区丝袜中文 | 色噜噜在线视频葡京| 亚洲精品无AMM毛片鸭王2| 人妻中文字幕网曝| 国产亚洲精品国产社区| 国产内射网站免费视频观看| 在线看片毛片无码永久免费| 女厕嘘嘘嘘免费视频网站在线观看| 国产三级久久精品三级付费| 亚洲日本一本palipali2轻量| 久久99精品久久久久久国产_ | 国产suv精品一区二区3d动漫| 亚洲精品天天影视综合网 - 亚洲人成无码网站久久 | 精品久久久久久久亚洲综合网站 桃儿 | 国产毛片色av在线| 亚洲精品无码不卡在线播HEsm| 精品人妻久久久久久88精| 中文字幕日韩高清人妻无码| 日韩成a人无码精品区二区免费A片| 日韩精品一区二区三区在线观看大师 | 久久大香伊蕉在人线国产H_女人高潮抽 | 免费看黄区一区二| 100部毛片免费全部播放完整视频| 手机看片福利久久大香蕉大香蕉| 国产AV精品一区二区凹凸婷婷| 无码人妻少妇伦在线电影 人妻免费视频| 无码专区久久综合久中文字幕_亚洲A| 韩国亚洲国产日产a?v| 亚洲欧洲国产一区二区三区午夜精品 | 精品国产黑色丝袜高跟鞋h| 亚洲视频高清无码横宫七海| 国产女主播在线观看手机免费| 无码人妻精品一区二区三区久久久后入第一视角 - v8 | 久热精品视频第一页免费观看 | 亚洲午夜成激人情在线影院免费观看| 精品国产一二三产品价格新新影院| 亚洲中文字幕精品无码影视网|