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
黄色视频网站在线播放,四川妇女BBBB爽BBBB爽,深圳妇女搡BBBB搡BBBB
Rabbit Anti-VANGL2/PE-Cy5 Conjugated antibody (bs-23066R-PE-Cy5)
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-PE-Cy5
英文名稱 Rabbit Anti-VANGL2/PE-Cy5 Conjugated antibody
中文名稱 PE-Cy5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, 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 www.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
四虎精品成人免费网站 | 国产熟妇婬乱A片免费看 | 免费少妇A级毛片野外大战 蜜桃人妻一区二区三区欧美 | 国产精品久久久久久久久爆乳污 | 成人无码视频在线看 | 亚洲 日韩 欧美 91 | 初中麻豆啪啪啪黑丝免费 | 午夜成人精品一二三区 | 国產精品久久久久久久 | 特大肥肥婆爽高潮视频 | 午夜成人理论片A片AAA图片 | 成人做爰黄 片免费观看 | 亚洲一区二区三区黄瓜勒 | 国产一a毛一a毛A免费看图 | 国产精品一区二区三区小说 | 麻豆精品国产人妻无码 | 搡bbbb 搡bbb冒白浆 | 少妇精品一品二品三品在线观看 | 国产丝袜在线熟女高潮 | 红桃视频一区二区高清码 | 日韩公交车系列无码AV | 北条麻纪码免费版官方 | 精品黑人一区二区三区国语馆 | 国产妇少水多毛多高潮A片视频 | 农村拗女一区二区三区在线播放 | 欧美丝袜AAAAA片 | 午夜无码国产午夜 | 亚洲素人无码不卡中文字幕 | 污视频免费网站在线观看 | 中文字幕在线视频网 | 北京熟妇槡BBBB槡BBBB | 国产激情二级婬片免费桃 | 久久精品99国产国产精 | 西西4444www无码精品 | 丰满人妻的婬乱生活2 | 国内精品国产成人国产三级 | 中文字幕熟妇久久久人妻 | 国产三级三级三级看三级 | 天堂AV在线免费观看 | 91九色丨国产丨人妻在线 | www射我里面在线观看 |