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
掃碼關注公眾號           掃碼咨詢技術支持           掃碼咨詢技術服務
  
客服熱線:400-901-9800  客服QQ:4009019800  技術答疑  技術支持  質量反饋  關于我們  聯(lián)系我們
亚洲无码视频在线,17C一起草在线观看入口,四川少妇搡BBB搡BBB爽爽爽小说
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-Msx2/BF555 Conjugated antibody (bs-10158R-BF555)
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@bioss.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-10158R-BF555
英文名稱 Rabbit Anti-Msx2/BF555 Conjugated antibody
中文名稱 BF555標記的同源盒基因Msx2抗體
別    名 Msx2/Hox8; CRS 2; CRS2; FPP; Homeo box msh like 2; Homeobox protein Hox-8; Homeobox protein MSX 2; Homeobox protein MSX-2; Homeobox protein MSX2; Hox 8; Hox8; MSH; Msh homeo box 2; Msh homeo box homolog; Msh homeo box homolog 2; Msh homeobox 2; Msh homeobox homolog 2; Msx 2; Msx2; MSX2_HUMAN; Parietal foramina 1; PFM 1; PFM; PFM1.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 腫瘤  心血管  染色質和核信號  神經(jīng)生物學  轉錄調節(jié)因子  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Chicken, Dog, Cow, Horse, Rabbit, )
產品應用 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 29kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human Msx2/Hox8
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.
產品介紹 background:
This gene encodes a member of the muscle segment homeobox gene family. The encoded protein is a transcriptional repressor whose normal activity may establish a balance between survival and apoptosis of neural crest-derived cells required for proper craniofacial morphogenesis. The encoded protein may also have a role in promoting cell growth under certain conditions and may be an important target for the RAS signaling pathways. Mutations in this gene are associated with parietal foramina 1 and craniosynostosis type 2. [provided by RefSeq, Jul 2008].

Function:
Acts as a transcriptional regulator in bone development. Represses the ALPL promoter activity and antogonizes the stimulatory effect of DLX5 on ALPL expression during osteoblast differentiation. Probable morphogenetic role. May play a role in limb-pattern formation. In osteoblasts, suppresses transcription driven by the osteocalcin FGF response element (OCFRE). Binds to the homeodomain-response element of the ALPL promoter.

Subunit:
Interacts with MINT. Interacts with XRCC6 (Ku70) and XRCC5 (Ku80).

Subcellular Location:
Nucleus.

DISEASE:
Defects in MSX2 are the cause of parietal foramina 1 (PFM1) [MIM:168500]; also known as foramina parietalia permagna (FPP). PFM1 is an autosomal dominant disease characterized by oval defects of the parietal bones caused by deficient ossification around the parietal notch, which is normally obliterated during the fifth fetal month.
Defects in MSX2 are the cause of parietal foramina with cleidocranial dysplasia (PFMCCD) [MIM:168550]; also known as cleidocranial dysplasia with parietal foramina. PFMCCD combines skull defects in the form of enlarged parietal foramina and deficient ossification of the clavicles.
Defects in MSX2 are the cause of craniosynostosis type 2 (CRS2) [MIM:604757]; also known as craniosynostosis Boston-type (CSB). CRS2 is an autosomal dominant disorder characterized by the premature fusion of calvarial sutures. The craniosynostosis phenotype is either fronto-orbital recession, or frontal bossing, or turribrachycephaly, or cloverleaf skull. Associated features include severe headache, high incidence of visual problems (myopia or hyperopia), and short first metatarsals. Intelligence is normal.

Similarity:
Belongs to the Msh homeobox family.
Contains 1 homeobox DNA-binding domain.

Database links:

Entrez Gene: 4488 Human

Omim: 123101 Human

SwissProt: P35548 Human

Unigene: 89404 Human



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
版權所有 2004-2026 rvdoil.com 北京博奧森生物技術有限公司
通過國際質量管理體系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
女人18毛片A片一区二区三区 | 蜜桃狠狠狠狠狠狠狠 | 91色噜噜狠狠色婷婷 | 亚洲成人无码视频 | 中文字幕在线中文幕免费在线看免费版 | 人妻系列影片无码专区 | 911精品人妻一区二区三区A片 | 人人妻人人爱人人做人人爽性色AV | 狂躁少妇XXXX高潮无码 | 黑人猛烈一级AAA片 9l 爱剪辑视频播放 | 国产精品人妻无码专区 | 精品人妻一区二区三区线国色天香 | 国产精品久久久久久吹潮 | 国产精品久久久久毛片大屁完整版 | 91大神人妻论坛性趣 | 爆乳熟妇一区二区三区爆乳色诱 | 四色成人A片视频在线看 | 真实的国产乱XX熟妇免费 | 污视频免费网站在线观看 | AV成人网站亚洲一二区 | 中文字幕乱码亚洲中文在线 | 品善网AV无码在线播放 | 国产亚洲精品久久久久动 | 成人网站在线免费播放 | 国内揄拍国内精品人妻 | 亚洲美女一区二区三区 | 高潮白浆大鸡巴AV | 国产又粗又猛又爽又黄的视频先 | 少妇毛片一区二区三区粉嫩aV | 91成人无码看片在线观看 | 免费一级婬A片AAA毛片古女 | 久久精品无码一区三区 | 人妻无码аⅴ天堂中文在线 | 91人妻人人爽人人添夜夜爽直软件播 | 无码人妻精品一区二区蜜桃色欲 | AV无码一区二区三区 | 99久久免费看黄A片APP | 国产伦子伦视频在线观看 | 人妻 的搜索结果 - 91n | 国产极品黑丝美女裸体被操免费网站 | 国产成人精品久久二区二区 |