来一水AV@lysav|亚洲AV无码片VR一区二区三区 |国产亚洲精久久久久久无码|视色4se成人午夜精品久久

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
  
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  人才招聘  關(guān)于我們  聯(lián)系我們
国模无码视频一区二区三区|欧美日韩午夜群交多人轮换 |GOGOGO日本免费观看视频
首頁 > 產(chǎn)品中心 > 一抗 > 產(chǎn)品信息
Rabbit Anti-VANGL2  antibody (bs-23065R)  
訂購熱線:400-901-9800
訂購郵箱:sales@73327.net
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@73327.net
說明書: 50ul  100ul  200ul
50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包裝/詢價

產(chǎn)品編號 bs-23065R
英文名稱 Rabbit Anti-VANGL2  antibody
中文名稱 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.  
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 Human (predicted: Mouse,Rat,Sheep,Cow)
產(chǎn)品應用 WB=1:500-2000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 60kDa
細胞定位 細胞膜 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human VANGL2: 11-100/521 <Cytoplasmic>
亞    型 IgG
純化方法 affinity purified by Protein A
緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產(chǎn)品介紹 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.

SWISS:
Q9ULK5

Gene ID:
57216

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



產(chǎn)品圖片
Sample: NIH/3T3(Human) Cell Lysate at 30 ug Primary: Anti-VANGL2 (bs-23065R) at 1/300 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 60 kD Observed band size: 60 kD
版權(quán)所有 2004-2026 www.73327.net 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
a片在线观看免费| 国产特黄级AAAAA片免| 性欧美大战久久久久久久久| 欧美精品视频| 国产精品久久久久久久久久久久冷| 农村熟女XXXXHD做受| 亚洲精品欧美日韩专区免费的视频| 18VIDEOSEX性欧美69| 日本一区二区精品在线| 成年免费a级毛片免费看无码| 嫩草伊人久久精品少妇AV| 色哟哟国产在线播放| 桃花色综合| 超碰人人澡人摸人人添| 欧美牲交40_50a欧美牲交aⅴ| 在线视频国产网址你懂的| 国产精品久久久三级精品久久久三级| 欧美日韩国产精品2023| 女厕偷窥一区二区三区| 少妇BBW搡BBBB搡BBBB| 久久精品国产亚洲av蜜臀久久| 欧美激情第1页| 黑人狂躁日本妞无码| 97久久久精品综合88久久| 夜夜操夜夜摸夜夜爽| 狠狠综合久久久久免费无卡av一| av片在线观看免费| 亚洲国产一区二区三区综合片| 久久综合伊人77777麻豆| 成人区色情综合小说| 免费无遮挡禁18污污网站| 天天看片天天AV免费观看| 日本午夜精品福利视频| 国语熟妇乱人乱A片久久| 久久免费看少妇高潮V片特黄| 香蕉人妻AV久久久久天天| 国产精品亚洲一区二区z| 久久人人97超碰超国产| 亚洲色欲久久久综合网东京热| CAOPOREN免费精品视频| 花房姑娘免费观看全集|