强伦轩一级A片在线观看,中文字幕乱码人妻二区三区,鲁鲁狠狠狠7777一区二区,西西4444www无码精品
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
一区二区三区久久,国产免费黄色视频
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-VANGL2/Cy3 Conjugated antibody (bs-23066R-Cy3)
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-23066R-Cy3
英文名稱 Rabbit Anti-VANGL2/Cy3 Conjugated antibody
中文名稱 Cy3標記的神經(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  神經(jīng)生物學  干細胞  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) Human, Mouse,  (predicted: Rat, Pig, Cow, Horse, 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 m.nmgps.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
西西大胆一级裸体A片 | 白丝女仆被 免费网站 | 小向美奈子乳巨码无在线 | 久久久久久久国产精品 | 亚洲精品久久久久久久久久久 | 自慰喷水www久久天堂 | 国产精品久久久午夜夜伦鲁鲁 | 亚洲无码成人在线观看 | 亚洲AV无码乱码在线观看性色 | 白丝女疯狂 喷水自慰爽 | 丰满老女人乱妇DVD在线播放 | 国精产品一区二区三区在线观看 | 蜜桃av网站在线浏览 | 国产露脸农村妇女对白 | AV无码秘蜜桃成人片玉蝶直播 | 成人 在线观看免费爱爱 | 四川少妇BBBw搡BBBB搡BBBB | 特级西西西4444大胆无码 | 亚洲免费AV在线 | 日本私人一二三四区色欲 | 亚洲成人中文字幕 | 亚洲精选久久久久久久 | 成人做爰黄AA片啪啪声 | 91精品国产综合久久蜜臀使用方法 | 91popny丨九色丨蜜臀 | 四川少妇一级AAAAA片 | 91极品黑色丝袜自慰喷水久久 | ,四川少妇搡BBBB搡BBBB | 无码做爰内谢免费视频 | 久久久久免费毛A片免费一瓶梅 | 性无码av免费在线观看 | 日本三级片免费观看网站 | 人妻熟妇乱子伦精品无码专区毛片 | 亚洲成人网站在线观看 | 少妇疯狂做爰XXXⅩ高潮网站 | www久久久红桃视频国产 | 在线播放国产不卡免费 | 欧美青涩亚洲日韩蜜桃 | 91在线无码精品秘 入口不卡 | 人人澡人人妻人人爽 | 媚黑无码视频一区二区 |