吃奶呻吟打开双腿做受动态图 -亚洲色偷偷色噜噜狠狠99网-日韩精品极品视频在线观看免费-来一水AV@lysav

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  人才招聘  關于我們  聯(lián)系我們
成人AAA片一区国产精品,国产乱码一区二区三区
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-DDOST/PE-Cy5 Conjugated antibody (bs-14213R-PE-Cy5)
訂購熱線:400-901-9800
訂購郵箱:sales@xucheq.com
訂購QQ:  400-901-9800
技術支持:techsupport@xucheq.com
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-14213R-PE-Cy5
英文名稱1 Rabbit Anti-DDOST/PE-Cy5 Conjugated antibody
中文名稱 PE-Cy5標記的晚期糖基化終產物受體1抗體
別    名 Advanced glycation endproduct receptor 1; AGE R1; AGER1; CDG1R; DDOST 48 kDa subunit; Dolichyl diphosphooligosaccharide protein glycosyltransferase subunit (non catalytic); Dolichyl-diphosphooligosaccharide--protein glycosyltransferase 48 kDa subunit; Dolichyl-diphosphooligosaccharide-protein glycosyltransferase; EC 2.4.1.119; KIAA0115; MGC2191; OK/SW-cl.45; OKSWcl45; Oligosaccharyl transferase 48 kDa subunit; Oligosaccharyltransferase 48 kDa subunit; Oligosaccharyltransferase subunit 48; OST; OST48; OST48_HUMAN; RP23-25C1.4; WBP1; wu:fa11d01; zgc:66068; zgc:77478.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 免疫學  糖尿病  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Chicken, Dog, Cow, Horse, Zebrafish, Sheep, )
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 43kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human DDOST/AGER1
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 component of the oligosaccharyltransferase complex which catalyzes the transfer of high-mannose oligosaccharides to asparagine residues on nascent polypeptides in the lumen of the rough endoplasmic reticulum. The protein complex co-purifies with ribosomes. The product of this gene is also implicated in the processing of advanced glycation endproducts (AGEs), which form from non-enzymatic reactions between sugars and proteins or lipids and are associated with aging and hyperglycemia. [provided by RefSeq, Jul 2008]

Function:
DDOST (Dolichyl-diphosphooligosaccharide-protein glycosyltransferase) is a component of the oligosaccharyltransferase complex. This complex catalyzes the transfer of high-mannose oligosaccharides to asparagine residues on nascent polypeptides in the lumen of the rough endoplasmic reticulum and co-purifies with ribosomes. DDOST is also implicated in the processing of advanced glycation endproducts (AGEs), which form from non-enzymatic reactions between sugars and proteins or lipids and are associated with aging and hyperglycemia.

Subunit:
Component of the oligosaccharyltransferase (OST) complex. OST seems to exist in different forms which contain at least RPN1, RPN2, OST48, DAD1, OSTC, KRTCAP2 and either STT3A or STT3B. OST can form stable complexes with the Sec61 complex or with both the Sec61 and TRAP complexes even after release from the ribosome.

Subcellular Location:
Endoplasmic reticulum membrane; Single-pass type I membrane protein. Database links.

DISEASE:
Congenital disorder of glycosylation 1R (CDG1R) [MIM:614507]: A multisystem disorder caused by a defect in glycoprotein biosynthesis and characterized by under-glycosylated serum glycoproteins. Congenital disorders of glycosylation result in a wide variety of clinical features, such as defects in the nervous system development, psychomotor retardation, dysmorphic features, hypotonia, coagulation disorders, and immunodeficiency. The broad spectrum of features reflects the critical role of N-glycoproteins during embryonic development, differentiation, and maintenance of cell functions. Note=The disease is caused by mutations affecting the gene represented in this entry.

Similarity:
Belongs to the DDOST 48 kDa subunit family.

Database links:

Entrez Gene: 1650 Human

Entrez Gene: 425542 Chicken

Entrez Gene: 510682 Cow

Entrez Gene: 404012 Dog

Entrez Gene: 13200 Mouse

Entrez Gene: 313648 Rat

Entrez Gene: 444283 Xenopus laevis

Entrez Gene: 100145597 Xenopus tropicalis

Entrez Gene: 406408 Zebrafish

Omim: 602202 Human

SwissProt: P48440 Chicken

SwissProt: A6QPY0 Cow

SwissProt: Q05052 Dog

SwissProt: P39656 Human

SwissProt: O54734 Mouse

SwissProt: Q641Y0 Rat

SwissProt: Q6GNR9 Xenopus laevis

SwissProt: B1H3C9 Xenopus tropicalis

SwissProt: Q6NYS8 Zebrafish

Unigene: 523145 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.xucheq.com 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(yī)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
亚洲精品无码国产| 欧美电影在线观看| 无码人妻精品中文字幕 | 国模冰莲自慰肥美胞极品人体图| 亚洲人成无码网站久久99热国产| 婷婷人人爽人人爽人人片| AV动漫| 久久久久亚洲AV无码专区首JN| 偷偷色噜狠狠狠狠的777米奇| 日日躁夜夜躁狠狠躁| 国产chinasex对白videos麻豆| 精品久久久久久无码中文野结衣| 玩弄人妻少妇500系列视频| 久久久久久久99精品免费观看| 国产亚洲精品久久久久久| 大肉大捧一进一出的视频| 后入内射无码人妻一区| 亚洲精品午夜国产VA久久成人| 亚洲AV色香蕉一区二区三区| 国内精品一区二区三区 | 中文字幕人妻女友一区蜜芽视频 | 国产美女自慰在线观看| 性欧美大战久久久久久久久| 男男做爰猛烈叫床视频GV| 秋霞无码AV久久久精品小说| 少妇人妻精品一区二区三区| 实拍各种胸走光见奶头 | 亚洲精品乱码久久久久蜜桃| 狂飙大嫂是谁扮演的| 人妻少妇精品中文字幕av蜜桃| 亚洲精品久久久久AV无码| 午夜精品久久久久久毛片| 国产+成+人+亚洲欧洲自| 男男做爰猛烈叫床视频GV| 色综合久久无码五十路人妻| 天堂А√在线中文在线新版| 88久久精品无码一区二区毛片| 亚洲中文字幕无码AV| 免费无码毛片一区二区APP| 护士的小嫩嫩好紧好爽| 高潮H跪趴扩张调教男男视频|