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
动漫精品视频一区二区三区,久久午夜夜伦鲁鲁片不卡
Rabbit Anti-MSX1/BF555 Conjugated antibody (bs-8512R-BF555)
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-BF555
英文名稱 Rabbit Anti-MSX1/BF555 Conjugated antibody
中文名稱 BF555標(biāo)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(xì)胞生物  免疫學(xué)  神經(jīng)生物學(xué)  信號轉(zhuǎn)導(dǎo)  干細(xì)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
在线精品自偷自拍无码 | 精品久久久久久无码不卡 | 欧美日韩精品视频一区二区三区在线观看 | 最近中文字幕完整视频大全 | 强奸伦久久久久久久久久久特级av | 国产精品后入内射日本在线观看 | 99久久综合国产精品免费 | 少妇裸体婬交视频免费看高清 | 日韩大片在线永久免费观看网站 | 内射中出日韩无国产剧情 | 美女裸身露双奶头无遮挡免费视频 | 成 人 黄 色 网 站曰本女人牲交 | 中文字幕视频在线观看 | 国语A在线看免费观看视频 我和闺蜜在公车被cao污文 | 一二三区精品国产91久久久 | 人妻无码专区一专区二专区三 | 亚洲日韩精品欧美一区二区一 | 绯色av入口一区二区三区 | 欧美在线三级艳情网站 | 成人日韩熟女高清视频一区 | 日韩一区精品视频一区二区 | 欧美一区二区视频在线观看 | 天堂8在线天堂资源BT | 免费无码又爽又刺激高潮久久 | 国产精品成人影院在线观看 | 国产精品久久久久久久人热 | 日本那些又骚又爽的视频 | 亚洲精品高清一二区久久 | 性欧美18处19处破在线观看 | 97人人超碰国产精品最新 | 久久国产欧美日韩精品免费 | 精品国语对白清晰在线 | 国禁国产you女视频网站 | 另类重口bdsm日本tv | 国产精品爱啪在线线免费观看 | 熟妇的味道HD中文字幕 | 国产在线观看无码免费视频 | 又大又紧又粗C死你视频 | 一本无码aⅴ久久久国产 | 国产极品精频在线观看 | 在线视频一区二区三区在线播放 |