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(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
动漫精品中文无码卡通动漫,欧美激情一区二区三区蜜桃视频,日本BBW丰满牲交片
Rabbit Anti-PEPD/Cy5.5 Conjugated antibody (bs-12616R-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: 100ul  
100ul/2980.00元
大包裝/詢價(jià)
產(chǎn)品編號(hào) bs-12616R-Cy5.5
英文名稱 Rabbit Anti-PEPD/Cy5.5 Conjugated antibody
中文名稱 Cy5.5標(biāo)記的脯氨酸二肽酶抗體
別    名 Aminoacyl L proline hydrolase; Imidodipeptidase; MGC10905; MGC95081; Pep 4; Pep4; pepD; PEPD_HUMAN; Peptidase 4; Peptidase D; Prolidase; Proline dipeptidase; X pro dipeptidase; X-Pro dipeptidase; Xaa-Pro dipeptidase.  
規(guī)格價(jià)格 100ul/2980元 購(gòu)買        大包裝/詢價(jià)
說(shuō) 明 書 100ul  
研究領(lǐng)域 細(xì)胞生物  信號(hào)轉(zhuǎn)導(dǎo)  細(xì)胞骨架  泛素  
抗體來(lái)源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) Human,  (predicted: Mouse, Rat, Chicken, Dog, Pig, Horse, Zebrafish, )
產(chǎn)品應(yīng)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 55kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human PEPD
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:
This gene encodes a member of the peptidase family. The protein forms a homodimer that hydrolyzes dipeptides or tripeptides with C-terminal proline or hydroxyproline residues. The enzyme serves an important role in the recycling of proline, and may be rate limiting for the production of collagen. Mutations in this gene result in prolidase deficiency, which is characterized by the excretion of large amount of di- and tri-peptides containing proline. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Oct 2009]

Function:
Splits dipeptides with a prolyl or hydroxyprolyl residue in the C-terminal position. Plays an important role in collagen metabolism because the high level of iminoacids in collagen.

Subunit:
Interacts with TRAF6, IRAK1, IRAK4 and MAP3K7. Interacts with BCL10; this interaction is impaired by SOCS3 (By similarity).

Post-translational modifications:
Phosphorylated by IRAK1 and IRAK4 enhancing its E3 ligase activity.

DISEASE:
Defects in PEPD are a cause of prolidase deficiency (PD) [MIM:170100]. Prolidase deficiency is an autosomal recessive disorder associated with iminodipeptiduria. The clinical phenotype includes skin ulcers, mental retardation, recurrent infections, and a characteristic facies. These features, however are incompletely penetrant and highly variable in both age of onset and severity. There is a tight linkage between the polymorphisms of prolidase and the myotonic dystrophy trait.

Similarity:
Belongs to the peptidase M24B family.
Eukaryotic-type prolidase subfamily.

Database links:

Entrez Gene: 5184 Human

Entrez Gene: 18624 Mouse

Entrez Gene: 292808 Rat

Omim: 613230 Human

SwissProt: P12955 Human

SwissProt: Q11136 Mouse

SwissProt: Q5I0D7 Rat

Unigene: 36473 Human

Unigene: 69751 Mouse

Unigene: 101639 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 www.a6308.cn 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    證書編號(hào): CQC24QY10047R0M/1100
京ICP備05066980號(hào)-1         京公網(wǎng)安備110107000727號(hào)
国产日韩精品中文字无码国产精品 | 国产精品看高国产精品不卡 | 无码乱人伦一区二区亚洲一 | 99精品亚洲国产精品久久不卡 | 国产乱来乱子视频 | 日韩在线视频网站 | 婷婷色婷婷开心五月四房播播久久 | 妇女BBBB插插插视频 | 国产女主播喷水视频在线观看 | 韩国美女精品久久久久久久 | 精品无码国产污污污免费网站 | 国产一区二区三区AV天堂 | 国产成人精品一区二区三区免费 | 欧美精品做人一级爱免费 | 国产精品酒店性爱视频 | 一级成人欧美一区在线观看 | 狠狠综合久久AV一区二区三区 | 亚洲综合激情另类小说区 | 激情爆乳一区二区三区 | 欧美97色伦欧美一区二区日韩 | 欧美一性一交一免费看 | 欧美激情一区二区三区视频 | 久久久久久成人毛片免费看 | 视频一本大道香蕉久在线播放 | 国产乱婬AV一区二区三区 | 日韩中文字幕无码R级电影 色婷婷AV一区二区三区在线观看 | 惩罚抽插校花嗯啊白浆 | 国产精品毛片一级久久 | gvg454真实性教育在线播放 | 最近免费中文字幕大全高清大全10 | 51视频精品全部免费的意义在哪里 | 亚洲美女又黄又爽在线观看 | 国产美女69视频免费观看 | 人妻少妇看A偷人无码精品 荡公乱妇蒂芙尼中文字幕 爆乳JK美女脱内衣裸体网站 | 国产不卡高清在线观看视频 | 午夜色大片在线观看 | 欧美XXXXX高潮喷水麻豆 | 国产激情艳情在线看视频 | 亚洲AV√最新天堂版资源地址在线官网 | 无码人妻精品一区二区三区千菊 | 国内精品伊人久久久久 |