亚洲制服欧美另类-午夜激情av电影-日本高清中文字幕一区二区三区-中国欧美日韩一区二区三区-欧洲亚洲日本韩国-成人欧美激情一区二区-亚洲偷偷自拍高清

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
欧美日韩亚洲一区二区三区在线观看,免费看人与动人物XXXX,国产亚洲AV片在线观看16女人
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-MSX1/RBITC Conjugated antibody (bs-8512R-RBITC)
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-8512R-RBITC
英文名稱 Rabbit Anti-MSX1/RBITC Conjugated antibody
中文名稱 羅丹明(RBITC)標記的MSH同源蛋白1樣蛋白抗體
別    名 Msh homeobox 1 like protein; Homeobox 7; Homeobox protein Hox-7; Homeobox protein MSX 1; Homeobox protein MSX-1; Homeobox protein MSX1; Homeobox, msh like 1; Homeobox, msh-like 1; HOX 7; Hox 7.1; Hox-7; HOX7; Hox7.1; HYD 1; HYD1; msh (Drosophila) homeo box homolog 1 (formerly homeo box 7); Msh; msh homeo box 1; msh homeo box homolog 1; Msh homeobox 1; Msh homeobox 1-like protein; msh homeobox homolog 1 (Drosophila); msh homeobox homolog 1; MSH, Drosophila, Homolog of, 1; MSX 1; MSX1; MSX1_HUMAN; Muscle segment homeobox; Muscle segment homeobox, Drosophila, Homolog of, 1; OFC5; STHAG1.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領(lǐng)域 細胞生物  免疫學  神經(jīng)生物學  信號轉(zhuǎn)導  干細胞  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) Human, Mouse,  (predicted: Rat, Dog, Cow, )
產(chǎn)品應(yīng)用 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 31kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human MSX1
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:
Acts as a transcriptional repressor. May play a role in limb-pattern formation. Acts in cranofacial development and specifically in odontogenesis. Expression in the developing nail bed mesenchyme is important for nail plate thickness and integrity.

Function:
Acts as a transcriptional repressor. May play a role in limb-pattern formation. Acts in cranofacial development and specifically in odontogenesis. Expression in the developing nail bed mesenchyme is important for nail plate thickness and integrity.

Subcellular Location:
Nucleus

Tissue Specificity:
Expressed in the developing nail bed mesenchyme.

Post-translational modifications:
Sumoylated by PIAS1, desumoylated by SENP1 (By similarity).

DISEASE:
Defects in MSX1 are the cause of tooth agenesis selective type 1 (STHAG1) [MIM:106600]. A form of selective tooth agenesis, a common anomaly characterized by the congenital absence of one or more teeth. Selective tooth agenesis without associated systemic disorders has sometimes been divided into 2 types: oligodontia, defined as agenesis of 6 or more permanent teeth, and hypodontia, defined as agenesis of less than 6 teeth. The number in both cases does not include absence of third molars (wisdom teeth). Tooth agenesis selective type 1 can be associated with orofacial cleft in some patients.
Note=MSX1 is deleted in some patients with Wolf-Hirschhorn syndrome (WHS). WHS results from sub-telomeric deletions in the short arm of chromosome 4.
Defects in MSX1 are the cause of Witkop syndrome (WITS) [MIM:189500]. WITS is a form of ectodermal dyslasia also called tooth-and-nail syndrome or dysplasia of nails with hypodontia. Ectodermal dysplasias (EDs) constitute a heterogeneous group of developmental disorders affecting tissues of ectodermal origin. EDs are characterized by abnormal development of two or more ectodermal structures such as hair, teeth, nails and sweat glands, with or without any additional clinical sign. Each combination of clinical features represents a different type of ectodermal dysplasia. Witkop syndrome is characterized by abnormalities largely limited largely to teeth (some of which are missing) and nails (which are poorly formed early in life, especially toenails). This condition is distinguished from anhidrotic ectodermal dysplasia by autosomal dominant inheritance and little involvement of hair and sweat glands. The teeth are not as severely affected.
Defects in MSX1 are the cause of non-syndromic orofacial cleft type 5 (OFC5) [MIM:608874]; also called non-syndromic cleft lip with or without cleft palate 5. Non-syndromic orofacial cleft is a common birth defect consisting of cleft lips with or without cleft palate. Cleft lips are associated with cleft palate in two-third of cases. A cleft lip can occur on one or both sides and range in severity from a simple notch in the upper lip to a complete opening in the lip extending into the floor of the nostril and involving the upper gum.

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

Database links:

Entrez Gene: 4487 Human

Entrez Gene: 17701 Mouse

Entrez Gene: 81710 Rat

Entrez Gene: 692067 Rhesus monkey

Omim: 142983 Human

SwissProt: Q2VL88 Chimpanzee

SwissProt: O02786 Cow

SwissProt: P28360 Human

SwissProt: P13297 Mouse

SwissProt: Q2VL87 Rhesus monkey

Unigene: 424414 Human

Unigene: 256509 Mouse

Unigene: 18117 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 a6308.cn 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
黑人玩弄极品人妻系列 | 久久se精品一区二区国产 | 国产精品爱啪在线线免费观看 | 99狠狠噜夜夜澡人人爽人人爽 | 日批日韩在线观看 | A级毛片久久久久久精品 | 久久99精品久久久久久清纯直播 | 国产一级毛片国产 | 国产无套内射普通话对白 | 欧美日韩精品视频一区二区三区在线观看 | 一品二品三品免费看 | WWW.啪啪小白浆内射无码 | 国产一级a毛一级a看免费视频 | 十八岁以下禁止观看的1000个网站 | 欧美日韩精品一区二区三区不卡 | 狂躁美女大BBBBBB视频1 | 91露出自慰白浆一区二区 | 国产精品一区二区三区免费 | 国产精品后入内射日本在线观看 | 久久久又黄又爽免费观看下载 | 色欲精品国产一区二区三区AV | 日韩精品福利视频一区二区三区 | 国产免费看JIZZ视频 | 插我舔内射18免费视频 | 久久99热狠狠色精品一区 | 99re6这里只有精品视频在线观看 | fuli.su黑料正能量入口 | 日韩AV免费在线观看 | 欧美日韩精品国产一区在线 | 思思久久好好热精品国产 | 日本丰满熟妇被捏出奶水 | A级成人毛片免费视频 | 免费被黄动漫网站在线无网观看 | 久久中文字幕亚洲一区二区 | 动漫AV网站免费观看 | 成年网站免费人性视频a站 老司机在线精品视频网站 亚洲色熟女图激情另类图区 | 无码乱码精品少妇一级内射 | 2021亚洲中文字幕久久精品 | 超碰国产精品人人做人人爱 | 欧美性一交一乱一伦A片 | 熟妇人妻中文字幕无码老熟妇 |