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
在线二区人妖系列,初尝黑人巨砲波多野结衣,成人免费无遮挡无码黄漫视频
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-WNT5A/PE Conjugated antibody (bs-1948R-PE)
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-1948R-PE
英文名稱 Rabbit Anti-WNT5A/PE Conjugated antibody
中文名稱 PE標記的信號通路Wnt5a抗體
別    名 wingless-related MMTV integration site 5A; hWNT 5A; hWNT5A; Protein Wnt 5a; Protein Wnt5a; Wingless type MMTV integration site family member 5A; Wnt-5a; WNT 5A protein precursor; WNT5A protein precursor; WNT5A_HUMAN.  
規格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 腫瘤  細胞生物  信號轉導  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Human, Mouse,  (predicted: Rat, Pig, Cow, Rabbit, )
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 35kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human WNT5A
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 WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene encodes a member of the WNT family that signals through both the canonical and non-canonical WNT pathways. This protein is a ligand for the seven transmembrane receptor frizzled-5 and the tyrosine kinase orphan receptor 2. This protein plays an essential role in regulating developmental pathways during embryogenesis. This protein may also play a role in oncogenesis. Mutations in this gene are the cause of autosomal dominant Robinow syndrome. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2012].

Function:
Ligand for members of the frizzled family of seven transmembrane receptors. Can activate or inhibit canonical Wnt signaling, depending on receptor context. In the presence of FZD4, activates beta-catenin signaling. In the presence of ROR2, inhibits the canonical Wnt pathway by promoting beta-catenin degradation through a GSK3-independent pathway which involves down-regulation of beta-catenin-induced reporter gene expression. Suppression of the canonical pathway allows chondrogenesis to occur and inhibits tumor formation. Stimulates cell migration. Decreases proliferation, migration, invasiveness and clonogenicity of carcinoma cells and may act as a tumor suppressor. Mediates motility of melanoma cells. Required during embryogenesis for extension of the primary anterior-posterior axis and for outgrowth of limbs and the genital tubercle. Inhibits type II collagen expression in chondrocytes.

Subunit:
Interacts with PORCN. Interacts with WLS.

Subcellular Location:
Secreted, extracellular space, extracellular matrix.

Tissue Specificity:
Expression is increased in differentiated thyroid carcinomas compared to normal thyroid tissue and anaplastic thyroid tumors where expression is low or undetectable. Expression is found in thyrocytes but not in stromal cells (at protein level).

Post-translational modifications:
Palmitoylation is necessary for stimulation of cell migration, inhibition of the beta-catenin pathway and receptor binding.
Glycosylation is necessary for secretion but not for activity.

DISEASE:
Defects in WNT5A are the cause of Robinow syndrome autosomal dominant (DRS) [MIM:180700]. A disease characterized by short-limb dwarfism, costovertebral segmentation defects and abnormalities of the head, face and external genitalia. The clinical signs are generally milder in dominant cases.

Similarity:
Belongs to the Wnt family.

Database links:

Entrez Gene: 7474 Human

Entrez Gene: 530005 Cow

Entrez Gene: 22418 Mouse

Entrez Gene: 64566 Rat

Omim: 164975 Human

SwissProt: P41221 Human

SwissProt: P22725 Mouse

SwissProt: Q5PY99 Rat

SwissProt: Q9QXQ7 Rat

Unigene: 643085 Human

Unigene: 287544 Mouse

Unigene: 48749 Rat



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

WNT5A蛋白屬于Wnt原癌基因家族中的一種。Wnt5a與腫瘤、發生、轉移有關。
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: 久久99热只有频精品6的演员| 国产三级在线观看播放视频色精屋 | 亚洲岛国无码爱情动作片在线观看 | 精品久久久久久久亚洲ll| 国产在线AAA片一区二区99国产| 亚洲美女又黄又爽在线观看动漫穿越 | 波多野结衣中文字幕久久丝袜 | 亚洲 中文字幕 人妻制服| 人妻少妇激情久久精品免下载| 伊人色综合久久| 亚洲第一页在线播放可搜索| 久久人人爽人人爽人人片av高清新婚之夜 | 无码精品人妻一区二区三区ap小说 | 国产69精品久久久久9999|精品久久久| 肉感无码色色色不卡视频| 久9re热视频这里只有精品免费_第1集| 性刺激久久久久久久久九色下载 | 又粗又猛又色又骚Av| 色综合久久综合中文综合网,国产AⅤ| 中文字幕乱码人妻一区二区三区,99精品久久久久久 | 丰满少妇人妻久久久久久_| 亚洲熟妇久久精品漫画人桃蜜 | 国精品无码一区二区三区D七天| 桃花岛AV偷窥盗摄| 精品综合久久久久久98_另类国产| 免费无码又爽视频在线观看王钟瑶| 亚洲第一网站男人都懂2023| 国产在线观看高清精品8X| 在线丝袜av更新网站| 久久久国产99久久国产久麻| 中文字幕亚洲乱码熟女一区二区图片 | 亚洲国产专区一区二区麻豆99视频| 一区 二区 三区 中文字幕 无码| AAAAA级毛片好多水| 日韩人妻无码一级毛片水多多2008金瓶梅| 亚洲国产熟女精品网站 | 色婷婷狠狠五月综合天色拍sewuji | 亚洲AV成人无码网站18禁在线男男| 精品成人免费自拍视频网站| 99精品免费观看爱V| 久久午夜无码鲁丝秋霞黄片|