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(guān)注公眾號(hào)           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
欧美一区二区在线观看,国产suv精品一区二区,中文字幕精品久久久久人妻红杏1 国产成人三级一区二区在线观看一
Rabbit Anti-RNF59/MID1/Cy5.5 Conjugated antibody (bs-9380R-Cy5.5)
訂購(gòu)熱線:400-901-9800
訂購(gòu)郵箱:sales@bioss.com.cn
訂購(gòu)QQ:  400-901-9800
技術(shù)支持:techsupport@bioss.com.cn
說(shuō) 明 書(shū): 100ul  
100ul/2980.00元
大包裝/詢價(jià)
產(chǎn)品編號(hào) bs-9380R-Cy5.5
英文名稱 Rabbit Anti-RNF59/MID1/Cy5.5 Conjugated antibody
中文名稱 Cy5.5標(biāo)記的環(huán)指蛋白59抗體
別    名 BBBG 1; BBBG1; Finger on X and Y mouse homolog of antibody; FXY; GBBB 1; GBBB1; MID 1; MID-1; Mid1; Midin; Midline 1 (Opitz/BBB syndrome); Midline 1; Midline 1 ring finger; Midline 1 RING finger protein; Midline-1; Midline1; OGS 1; OGS1; OS antibody; OSX; Putative transcription factor XPRF; RING finger protein 59; RNF 59; RNF59; TRI18; TRI18_HUMAN; TRIM 18; TRIM18; Tripartite motif containing protein 18; Tripartite motif protein TRIM18; Tripartite motif-containing protein 18; XPRF; Zinc finger X and Y antibody; ZNFXY.  
規(guī)格價(jià)格 100ul/2980元 購(gòu)買        大包裝/詢價(jià)
說(shuō) 明 書(shū) 100ul  
研究領(lǐng)域 細(xì)胞生物  免疫學(xué)  鋅指蛋白  
抗體來(lái)源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) (predicted: Human, Mouse, Rat, Chicken, Dog, Pig, Horse, Sheep, )
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 75kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human MID1/Midline-1/RNF59
亞    型 IgG
純化方法 affinity purified by Protein A
儲(chǔ) 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:
Midline-1 (Tripartite motif-containing protein 18, Putative transcription factor XPRF, RING finger protein 59) is a 667 amino acid protein encoded by the human gene MID1. Midline-1 belongs to the TRIM/RBCC family and contains two B box-type zinc fingers, one B30.2/SPRY domain, one COS domain, one fibronectin type-III domain and one RING-type zinc finger. Midline-1 is believed to have E3 ubiquitin ligase activity which targets the catalytic subunit of protein phosphatase 2 for degradation. It is a cytoplasmic protein found as a homodimer or heterodimer with Midline-2. It also interacts with IGBP1 (Lymphocyte signaling protein A4). Defects in MID1 are the cause of Opitz syndrome type I (OS-I). OS-I is an X-linked recessive disorder characterized by hypertelorism, genital-urinary defects such as hypospadias in males and splayed labia in females, lip-palate-laryngotracheal clefts, imperforate anus, developmental delay and congenital heart defects. OS-I mutations produce proteins with a decreased affinity for microtubules.

Function:
Has E3 ubiquitin ligase activity towards IGBP1, promoting its monoubiquitination, which results in deprotection of the catalytic subunit of protein phosphatase PP2A, and its subsequent degradation by polyubiquitination.

Subunit:
Homodimer or heterodimer with MID2. Interacts with IGBP1.

Subcellular Location:
Cytoplasm.

Tissue Specificity:
In the fetus, highest expression found in kidney, followed by brain and lung. Expressed at low levels in fetal liver. In the adult, most abundant in heart, placenta and brain.

Post-translational modifications:
Phosphorylated on serine and threonine residues.

DISEASE:
Defects in MID1 are the cause of Opitz GBBB syndrome 1 (OGS1) [MIM:300000]. A congenital midline malformation syndrome characterized by hypertelorism, genital-urinary defects such as hypospadias in males and splayed labia in females, lip-palate-laryngotracheal clefts, imperforate anus, developmental delay and congenital heart defects. Note=MID1 mutations produce proteins with a decreased affinity for microtubules.

Similarity:
Belongs to the TRIM/RBCC family.
Contains 2 B box-type zinc fingers.
Contains 1 B30.2/SPRY domain.
Contains 1 COS domain.
Contains 1 fibronectin type-III domain. [SIMILARITY] Contains 1 RING-type zinc finger.

Database links:

Entrez Gene: 4281 Human

Entrez Gene: 17318 Mouse

Entrez Gene: 54252 Rat

Omim: 300552 Human

SwissProt: O15344 Human

SwissProt: O70583 Mouse

SwissProt: P82458 Rat

Unigene: 27695 Human

Unigene: 689953 Human

Unigene: 34441 Mouse

Unigene: 444905 Mouse

Unigene: 460870 Mouse

Unigene: 15169 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 m.rvdoil.com 北京博奧森生物技術(shù)有限公司
通過(guò)國(guó)際質(zhì)量管理體系ISO 9001:2015 GB/T 19001-2016    證書(shū)編號(hào): 00124Q34771R2M/1100
通過(guò)國(guó)際醫(yī)療器械-質(zhì)量管理體系ISO 13485:2016 GB/T 42061-2022    證書(shū)編號(hào): CQC24QY10047R0M/1100
京ICP備05066980號(hào)-1         京公網(wǎng)安備110107000727號(hào)
国产AV最新精品 | 高跟丝袜一区二区自慰无码 | 在线无码精品秘 入口 | 无码精品视频在线观看 | 人妻黑人一区二区三区 | 全免费A级毛片免费看黄瓜视频 | 7777kkk亚洲综合欧美网站 | 美女mm131麻豆視頻 | 中文字幕一区二区三区四区五区 | 午夜影院在线观看视频 | 91久久无码一区人妻A片蜜桃 | 国产精品21一区二区 | 国产高清无码100% | 久久久精品无码一二三区 | 成人羞羞 国产免费 | 寡妇免费A片一级无极看 | 全免费A级毛片免费看黄瓜视频 | 久久99精品亚洲国产 | 看黄色一级免费的黄色视频 | 国产精品人成A片一区二区 国产亚洲东北熟女高潮叫床 | 无码少妇一二三四区最新版 | 四虎影视在线播免费观看 | 精品国产乱码久久久久久蜜柚 | 黄色无码免费在线观看 | 亚洲国产精品人人做人人爽 | 久久丰满人妻一区二区 | 亚洲第一区二区在线 | 黄色视频免费在线观看 | 波多野吉衣在线观看黄色 | 少妇荡乳欲伦交换A片欧美 中文字幕在线免费观看视频 | 亚洲国产成人精品无码一区二区 | 中国体内射精在线播放 | 精品国产91乱码一区二区三区 | 国产女教师一级爽A片 | 精品囯产人妻久久久久 | 特大肥婆BBBWBBBw| 近親相姦五十路の在线 | 国产剧情亚洲无码视频 | 搡老女人老妇女aaa一区麻豆 | 国偷精品无码久久久久蜜桃软件 | 啪啪免费无码人妻丰满熟妇 |