亚洲中文字幕特级毛片-亚洲制服丝袜中文字幕-亚洲制服丝袜在线观看-亚洲制服欧美自拍另类-免费一级黄色-免费一级国产生活片

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  聯系我們
国产精品反差婊在线观看,a亚洲va欧美va国产综合,欧美性猛交xxxx乱大交极品
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-DDOST/BF350 Conjugated antibody (bs-14213R-BF350)
訂購熱線:400-901-9800
訂購郵箱:sales@www.chomd.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@www.chomd.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-14213R-BF350
英文名稱1 Rabbit Anti-DDOST/BF350 Conjugated antibody
中文名稱 BF350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.www.chomd.com.cn 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
主站蜘蛛池模板: 岛国无码在线播放一区二区无码| 久久精品一区二区三区AⅤ | 精品国产导航网址一区 | 在线播放国产999视频| 亚洲GV天堂无码男同在线观看,我才12| 老熟女chese老熟女| 久久肉色丝袜脚交| 成人羞羞视频网站app免费下载| 在线观看视频vivo新出的nex| 色婷婷狠狠五月综合舔 | 久久久久亚洲精品男人的天堂 高清少妇 | 国产91在线精品操| 亚洲精品国偷自产在线99正片,中文成人 | 岛国无码在线视频播放网页| 亚洲一区二区三区乱码漫画免费| 男女猛烈无遮挡午夜视频在线观看网址| 国产精品一区在线观看你懂的| 国产日韩精品一区二区三区在线_ 国产日韩精品一区二区三区在线观看婷欧美日韩 | 国产最新情侣在线小视频免费观看| 中文字幕乱码人妻无码久久久1.每日更新 | 99久久99久久免费精品小说儿子调教妈妈| 国产精品久久久久久妇女6080 | 精品视频一区二区三区四区政府| 在线观看亚洲精品国产成人| 久久亚洲精精品中文字幕淹川惠理| 99久久精品影院老鸭窝,国产国产成人精品久久 | 欧美另类熟妇与子伦HD| 98精品国产综合久久久久l| 中文字幕久久无码内射网站| 日韩人妻无码一级毛片水多多2008金瓶梅| 国产色综合天天综合网同性| 亚洲国产一二三精品无码不卡 站长工具| 精品免费久久久久久久无码| 亚洲熟妇Heyzo在线播放| 国产综合成人久久大片91|亚洲国产 | 亚洲熟妇无码久久精品769| 国产毛片色av在线| 日韩熟妇在线网址| 在线观看一二三四区免费| 精品国产一区二区三区弓凉| 亚洲精品成人久久久久免费网站|