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
午夜理论影院第九电影院,午夜a一级毛片一.成,国产免费久久精品丫丫
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-Msx2/BF647 Conjugated antibody (bs-10158R-BF647)
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-BF647
英文名稱 Rabbit Anti-Msx2/BF647 Conjugated antibody
中文名稱 BF647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: 久久国产亚洲高清观看5388,国产日韩欧美二区_ | 中文字幕无码综合插插| 色婷婷Aⅴ综合蜜核视频| 中日韩精品视频在线观看黑人| 国产成人精品综合久久久久 久久综 | 在线播放无码不卡免费疯马秀av| 亚洲精品无AMM毛片鸭王2| 在线观看亚洲精品国产欧美| 婷婷丁香五月激情综合图片视频| 亚洲第一精品福利网址导航章节| 亚洲美女大胸诱惑视频在线观看 | 久久久无码少妇超碰| 久久久久国产一级毛片高清版版新婚91 | 精品人妻无码专区| 精品久久久久久久久久中文字幕,天天爽夜夜爽人 | 丰满少妇大力进入动态视频| 国产精品久久久区三区天天噜| 久久91精品国产91久久蘑菇| 99精品一区二区三区在这里 | 欧美性猛片XXXXX免费中国| 久久综合九色综合久99-日韩精品无码| 欧洲成人午夜精品无码区久久_精品国产免| 国产综合成人久久大片91亚洲国产成| 国产亚洲一区二区在线观看一区二区在线观看 | 亚洲欧洲精品久久99| 亚洲成a人v欧美综合天堂麻豆 | 综合色热一本加勒比| 亚洲秘?AV无码一区二区qq群 | 熟妇中国伦片| 超碰欧美日韩99| 永久免费不收费免费的app | 久久91亚洲精品中文字幕奶水久久| 中文字幕无码少妇HD| 久久精品免费一区二区三区y| 中文字幕第30页一区二区| 亚洲精品无码AV中文永久在线| 韩国亚洲国产日产a?v| 亚洲成a人片在线观看国产,青青视频 | 91无码人妻精品一区二区三区四| 在线播放无码不卡桥本有菜| 久久精品黄AA片一区二区三区无码|