91精品少妇一区二区三区蜜桃臀,少妇搡BBBB搡BBB搡失恋,BBB片一毛片A片AA少妇,国产成人无码久久久久毛片朴信惠
掃碼關(guān)注公眾號           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
精品一区二区三区四区,老熟妇一区二区三区啪啪
Rabbit Anti-VANGL2/FITC Conjugated antibody (bs-23065R-FITC)
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@bioss.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-23065R-FITC
英文名稱 Rabbit Anti-VANGL2/FITC Conjugated antibody
中文名稱 FITC標(biāo)記的神經(jīng)管畸形相關(guān)蛋白VANGL2抗體
別    名 Homolog of Drosophila strabismus; KIAA1215; Loop tail associated protein; loop tail protein 1 homolog; Loop-tail protein 1 homolog; LPP 1; LPP1; LTAP; STB 1; STB1; STBM 1; STBM; STBM1; Strabismus 1; van Gogh like protein 2; Van Gogh-like protein 2; Vang (van gogh, Drosophila) like 2; Vang like 2 (van gogh, Drosophila); vang like 2; vang like protein 2; Vang-like protein 2; VANG2_HUMAN; VANGL 2; Vangl2.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領(lǐng)域 心血管  發(fā)育生物學(xué)  神經(jīng)生物學(xué)  干細(xì)胞  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) Human,  (predicted: Mouse, Rat, Cow, Sheep, )
產(chǎn)品應(yīng)用 ICC=1:50-200 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 60kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human VANGL2
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(chǎn)品介紹 background:
The Vang family of proteins are integral membrane proteins that are homologs of the Drosophila tissue polarity gene strabismus. The gene encoding for Van Gogh-like protein 1 (Vangl1), also designated Strabismus 2 (STB2), localizes to chromosome 1p11-p13.1. Van Gogh-like protein 2 (Vangl2), also designated Strabismus1 (STB1), localizes on chromosome 1q22-q23. Vangl1 is expressed in testis and ovary, but also in gastric and pancreatic cancer. Vangl proteins play a key developmental role in establishing planar cell polarity (PCP) and in regulating convergent extension (CE) movements during embryogenesis. Vangl1 and Vangl2 are both down-regulated in several cancer cell lines and primary tumors.
Involved in the control of early morphogenesis and patterning of both axial midline structures and the development of neural plate. Plays a role in the regulation of planar cell polarity, particularly in the orientation of stereociliary bundles in the cochlea. Required for polarization and movement of myocardializing cells in the outflow tract and seems to act via RHOA signaling to regulate this process.

Function:
Involved in the control of early morphogenesis and patterning of both axial midline structures and the development of neural plate. Plays a role in the regulation of planar cell polarity, particularly in the orientation of stereociliary bundles in the cochlea. Required for polarization and movement of myocardializing cells in the outflow tract and seems to act via RHOA signaling to regulate this process (By similarity).

Subunit:
Interacts through its C-terminal region with the N-terminal half of DVL1, DVL2 and DVL3. The PDZ domain of DVL1, DVL2 and DVL3 is required for the interaction. Also interacts with the PDZ domains of MAGI3, SCRIB/SCRB1 and FZD3 (By similarity).

Subcellular Location:
Membrane; Multi-pass membrane protein (Potential).

DISEASE:
Defects in VANGL2 are a cause of neural tube defects (NTD) [MIM:182940]. NTD are congenital malformations of the central nervous system and adjacent structures related to defective neural tube closure during the first trimester of pregnancy. Failure of neural tube closure can occur at any level of the embryonic axis. Common NTD forms include anencephaly, myelomeningocele and spina bifida, which result from the failure of fusion in the cranial and spinal region of the neural tube. NTDs have a multifactorial etiology encompassing both genetic and environmental components.

Similarity:
Belongs to the Vang family.

Database links:

Entrez Gene: 57216 Human

Entrez Gene: 93840 Mouse

Entrez Gene: 289229 Rat

Omim: 600533 Human

SwissProt: Q9ULK5 Human

SwissProt: Q91ZD4 Mouse

SwissProt: P84889 Rat

Unigene: 99477 Human

Unigene: 36148 Mouse

Unigene: 392110 Mouse

Unigene: 198958 Rat



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
版權(quán)所有 2004-2026 www.rvdoil.com 北京博奧森生物技術(shù)有限公司
通過國際質(zhì)量管理體系ISO 9001:2015 GB/T 19001-2016    證書編號: 00124Q34771R2M/1100
通過國際醫(yī)療器械-質(zhì)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(wǎng)安備110107000727號
特级AAAAAAA级毛片图片 | 久99热人妻偷产无码区牛牛直播 | 9l人人澡人人凄人人精品 | 成年人黄色视频在线观看 | 亚洲无码一区在线 | 午夜小视频在线观看 | 色欲狠狠躁天天躁无码中文字幕 | 国产高清乱码爆乳女 | 国产麻豆乱码精品一区二区三区 | 91三产区少妇在线观看 | 蜜桃秘 无码一区二区三区 91久久人澡人人添人人爽 | 红桃视频网站一区二区精品 | 亚洲国产精品中文视频 | 国产校花久色在线观看 | 欧洲美女淫妓A级高清视频播放 | 成人羞羞 国产免费动态 | 精品人妻无码一级A片 | 打开双腿扒开自慰喷水网站 | 无码精品一区二区免费蜜桃 | 少妇人妻偷人精品视频蜜桃 | 国产成人精品女人久久久 | 国产精品人妻熟女毛片aⅴ 99精品乱码国产在线观看 | 久久亚洲精品无码Va白人极品 | 91精品人妻一区二区三区蜜桃 | BBw揉BBBB搡BBBB动漫 | 99精品在线免费观看 | 欧美一级特黄AA大片 | 亚洲AV秘 无码一区二区三竹菊 | 台湾佬中文综合娱乐网 | 北条麻纪码免费版官方 | 国产乱人乱偷精品a人人澡 特黄三级又爽又粗又大洗澡 | 在线观看中文字幕 | 影音先锋女人aV鲁色资源网站 | 免费无码婬片A片AAA毛扒开 | 安徽BBBBB视频BBB | 午夜成人电影在线观看 | 亚洲AV吞精久久久久 | 91精品少妇一区二区三区蜜桃臀 | 2018中文字幕在线观看 | 免费黄色在线视频 | 中文字幕高清无码视频 |