亚洲中文字幕特级毛片-亚洲制服丝袜中文字幕-亚洲制服丝袜在线观看-亚洲制服欧美自拍另类-免费一级黄色-免费一级国产生活片

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  聯系我們
欧美成aⅴ人高清免费观看,国产精品夜间视频香蕉,亚洲av无码成人黄网站在线观看
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-Msx2/APC Conjugated antibody (bs-10158R-APC)
訂購熱線:400-901-9800
訂購郵箱:sales@www.chomd.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@www.chomd.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-10158R-APC
英文名稱 Rabbit Anti-Msx2/APC Conjugated antibody
中文名稱 APC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  神經生物學  轉錄調節因子  
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 www.www.chomd.com.cn 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         京公網安備110107000727號
主站蜘蛛池模板: av资源免费观看试看资源| 国产超碰人人做人人爱vⅤ| 狠狠色婷婷久久一区二区四季AV | 激情综合婷婷丁香五月可下载| 人人人人一摸| 乱码精品一区二区三区生孩子| 日韩精品无码一区二区三区四区我区| 少妇精品亚洲一区二区成人天海翼| 亚洲成a人v欧美综合天堂 - 亚洲精品 | 久久久久综合国产一区二区| 免费人妻精品一区二区三区小宝探花 | 国产永久免费高清在线精品18 | 老鬼色无码精品一二三区| 大黑人性群交XXX双渗透| bl道具play珠串震珠强迫男男文| 亚洲精品国偷自产在线99正片,中文成人 | 综合免费精品AⅤ| 2022中文字幕在线观看视频a三区| 中文字字幕在线乱码视频,亚洲视频| 18禁止看的免费污网站 快播 | 天堂国产一区二区三区www| 日韩蜜芽精品视频在线观看网站| 国产免费久久精品99久久,亚洲中文久久久久| 国色天香在线视频下载| 亚洲午夜福利av一区二区无码在线观看 | 国产亚洲精品无码成人一| 亚洲乱色伦图片小说精品一区二区三区久久99精品 | 丰满少妇高潮惨叫久久久久婷婷| 草莓视频在线观看版官方免费| 18禁网站免费无遮挡无码中文_日韩欧美中文| 亚洲 小说区 图片区| 久久噜噜噜久久92精品国产自产| 中文字幕资源在线日| 久久国产成人精品护士| 低头看我是怎么c哭你的高H| 色婷婷Aⅴ综合蜜核视频| 18护士一区二区三区免费| 久久人人爽人人爽人人AV麻| 亚洲综合精品伊人久久网站_国产成人蜜臀伊人 | 日日婷婷夜日日天干1469| 91精品国产自产91精品资源,色综合久 |