mm1313亚洲精品,欧美俄罗斯40老熟妇,欧美日韩在线观看视频在线,亚洲欧美国产激情综合在线

掃碼關(guān)注公眾號(hào)           掃碼咨詢技術(shù)支持           掃碼咨詢技術(shù)服務(wù)
  
客服熱線:400-901-9800  客服QQ:4009019800  技術(shù)答疑  技術(shù)支持  質(zhì)量反饋  關(guān)于我們  聯(lián)系我們
亚洲高清一区二区三区四区,日本高清一区二区三区精品,日韩电影免费在线观看网址
Rabbit Anti-WNT5A/BF350 Conjugated antibody (bs-1948R-BF350)
訂購(gòu)熱線:400-901-9800
訂購(gòu)郵箱:sales@m.p2b3.cn
訂購(gòu)QQ:  400-901-9800
技術(shù)支持:techsupport@m.p2b3.cn
說(shuō) 明 書(shū): 100ul  
100ul/2980.00元
大包裝/詢價(jià)
產(chǎn)品編號(hào) bs-1948R-BF350
英文名稱 Rabbit Anti-WNT5A/BF350 Conjugated antibody
中文名稱 BF350標(biāo)記的信號(hào)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(guī)格價(jià)格 100ul/2980元 購(gòu)買(mǎi)        大包裝/詢價(jià)
說(shuō) 明 書(shū) 100ul  
研究領(lǐng)域 腫瘤  細(xì)胞生物  信號(hào)轉(zhuǎn)導(dǎo)  
抗體來(lái)源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) Human, Mouse,  (predicted: Rat, Pig, Cow, 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 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(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 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(fā)生、轉(zhuǎn)移有關(guān)。
版權(quán)所有 2004-2026 www.m.p2b3.cn 北京博奧森生物技術(shù)有限公司
通過(guò)國(guó)際質(zhì)量管理體系ISO 9001:2015 GB/T 19001-2016    證書(shū)編號(hào): 00124Q34771R2M/1100
通過(guò)國(guó)際醫(yī)療器械-質(zhì)量管理體系ISO 13485:2016 GB/T 42061-2022    證書(shū)編號(hào): CQC24QY10047R0M/1100
京ICP備05066980號(hào)-1         京公網(wǎng)安備110107000727號(hào)
正在播放舔穴视频| 啊啊不要你那痛死爽死了直播一区| 久久国产亚洲高清| 啊啊啊男女激情插插视频| 2021最新热播国产一区二区| 视频在线观看一区@99| 国产精品视频一区二区三区八戒| 中文欧美亚洲欧日韩| av在线国产哟哟| 午夜精品福利一区二区三区蜜桃p| 搞段B片黄色全免费看看| 非洲男生操男生屁眼视频| 日韩精品诱惑一区?区三区| 粉嫩小穴被大鸡巴操视频在线观看| a一级毛片免费高清在线| 怎么样操女人的逼亚洲Av黄片段| 操批在线观看视频| 国产一区二区在线观看精品| 制服丝袜国产在线第一页| 日韩有码一区二区三区在线观看| 国产情侣色综合久久有码| 国产一区曰韩二区欧美三区| 午夜福利国产三级片| 国产青青操骚货在线观看| 无码爆一二三区免费视频| 被公侵犯人妻少妇一区二区三区| 中文字幕在线精品的视频| 60秒动态视频在线观看| 亚洲人成在线不卡网| 一区二区国产精品免费视频| 亚洲精品自拍偷拍| 亚洲av午夜福利精品一区| 大黑屌爆操日本女人| 尤物AV无码国产在线看| 爆乳喷奶水无码正在播放| 青青视频在线人视频在线| 黄色亚洲一级大片| 操老骚逼三级黄视频| 美女被插入小穴涩涩视频| 色一情一交一乱一区二区| 久久国产精品二卡|