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
久久精品国产亚洲av网站,另类国产ts人妖合集,国产在线不卡一区二区三区
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-Alpha Dystroglycan/Biotin Conjugated antibody (bs-5152R-Bio)
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-5152R-Bio
英文名稱1 Rabbit Anti-Alpha Dystroglycan/Biotin Conjugated antibody
中文名稱 生物素標記的肌萎縮相關蛋白DAG1抗體
別    名 AGRNR; Alpha-DG; Beta-DG; Beta-dystroglycan; beta Dystroglycan; DAG; Dag1; DAG1_HUMAN; Dystroglycan 1 (dystrophin-associated glycoprotein 1); Dystroglycan; Dystrophin-associated glycoprotein 1; 156DAG; A3a; Dystrophin-associated glycoprotein 1.  
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  神經生物學  信號轉導  轉錄調節因子  細胞骨架  細胞外基質  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Mouse, Rat,  (predicted: Human, Chicken, Dog, Pig, Horse, Rabbit, )
產品應用 WB=1:50-200 ELISA=1:100-1000 IHC-P=1:50-200 IHC-F=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 98kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human DAG1 (501-550aa)
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:
Dystroglycan is a laminin binding component of the dystrophin-glycoprotein complex which provides a linkage between the subsarcolemmal cytoskeleton and the extracellular matrix. Dystroglycan 1 is a candidate gene for the site of the mutation in autosomal recessive muscular dystrophies. The dramatic reduction of dystroglycan 1 in Duchenne muscular dystrophy leads to a loss of linkage between the sarcolemma and extracellular matrix, rendering muscle fibers more susceptible to necrosis. Dystroglycan also functions as dual receptor for agrin and laminin-2 in the Schwann cell membrane. The muscle and nonmuscle isoforms of dystroglycan differ by carbohydrate moieties but not protein sequence. Alternative splicing results in multiple transcript variants all encoding the same protein.[provided by RefSeq, Apr 2010]

Function:
The dystroglycan complex is involved in a number of processes including laminin and basement membrane assembly, sarcolemmal stability, cell survival, peripheral nerve myelination, nodal structure, cell migration, and epithelial polarization.
Alpha-dystroglycan is an extracellular peripheral glycoprotein that acts as a receptor for both extracellular matrix proteins containing laminin-G domains, and for certain adenoviruses. Receptor for laminin-2 (LAMA2) and agrin in peripheral nerve Schwann cells. Also acts as a receptor for M.leprae in peripheral nerve Schwann cells but only in the presence of the G-domain of LAMA2, and for lymphocytic choriomeningitis virus, Old World Lassa fever virus, and clade C New World arenaviruses.
Beta-dystroglycan is a transmembrane protein that plays important roles in connecting the extracellular matrix to the cytoskeleton. Acts as a cell adhesion receptor in both muscle and non-muscle tissues. Receptor for both DMD and UTRN and, through these interactions, scaffolds axin to the cytoskeleton. Also functions in cell adhesion-mediated signaling and implicated in cell polarity.

Subunit:
Monomer. Heterodimer of alpha- and beta-dystroglycan subunits which are the central components of the dystrophin-glycoprotein complex.

Subcellular Location:
Secreted > extracellular space and Cell membrane. Cytoplasm > cytoskeleton. Nucleus > nucleoplasm. The monomeric form translocates to the nucleus via the action of importins and depends on RAN. Nuclear transport is inhibited by Tyr-892 phosphorylation. In skeletal muscle, this phosphorylated form locates to a vesicular internal membrane compartment. In peripheral nerves, localizes to the Schwann cell membrane. Colocalizes with ERM proteins in Schwann-cell microvilli.

Tissue Specificity:
Expressed in a variety of fetal and adult tissues. In epidermal tissue, located to the basement membrane. Also expressed in keratinocytes and fibroblasts.

Post-translational modifications:
O- and N-glycosylated. Alpha-dystroglycan is heavily O-glycosylated comprising of up to two thirds of its mass and the carbohydrate composition differs depending on tissue type. Mucin-type O-glycosylation is important for ligand binding activity. O-mannosylation of alpha-DAG1 is found in high abundance in both brain and muscle where the most abundant glycan is Sia-alpha-2-3-Gal-beta-1-4-Glc-NAc-beta-1-2-Man. In muscle, glycosylation on Thr-379 by a phosphorylated O-mannosyl glycan with the structure 2-(N-acetylamido)-2-deoxygalactosyl-beta-1,3-2-(N-acetylamido)-2-deoxyglucosyl-beta-1,4-6-phosphomannose is mediated by like-acetylglucosaminyltransferase (LARGE) protein and is required for laminin binding. O-mannosylation is also required for binding lymphocytic choriomeningitis virus, Old World Lassa fever virus, and clade C New World arenaviruses. The O-glycosyl hexose on Thr-367, Thr-369, Thr-372, Thr-381 and Thr-388 is probably mannose. O-glycosylated in the N-terminal region with a core 1 or possibly core 8 glycan. The beta subunit is N-glycosylated. Autolytic cleavage produces the alpha and beta subunits. In cutaneous cells, as well as in certain pathological conditions, shedding of beta-dystroglcan can occur releasing a peptide of about 30 kDa.
SRC-mediated phosphorylation of the PPXY motif of the beta subunit recruits SH2 domain-containing proteins, but inhibits binding to WWW domain-containing proteins, DMD and UTRN. This phosphorylation also inhibits nuclear entry.

Similarity:
Contains 1 peptidase S72 domain.

Database links:

Entrez Gene: 1605 Human

Entrez Gene: 13138 Mouse

Entrez Gene: 100009278 Rabbit

Entrez Gene: 114489 Rat

Omim: 128239 Human

SwissProt: Q14118 Human

SwissProt: Q62165 Mouse

Unigene: 76111 Human

Unigene: 7524 Mouse

Unigene: 36260 Rat



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: 超碰欧美日韩99| 一级做a爰全过程免费视频,日韩一区二区三区四区区区 | 国产一区二区精品久久岳,精品精品国产自在 | 国产99在线亚洲亚太| 中文字幕亚洲无线码a免费| 无码国内精品久久人妻,无码AV日韩 | 国内精品久久久久伊人av,俺来也俺去啦久久综合网 | 波多野结衣在线资源ctxl| 亚洲国产成人久久综合碰碰动漫3d,午夜... | 岛国无码在线视频nylon| 亚洲人成7777| 国产在线观看激情对白| 亚洲欧洲国产一区二区三区午夜精品 | 91麻豆精品国产91久久久久久久久| 亚洲大尺度无码专区尤物,国产情节片 | 人人爽人人爽人人片AV - 国产精 人人爽亚洲AV人人爽AV人人片 | 精品久久久久中文字幕人妻蜜臀97资源 | 成人国产一区二区三区精品不卡麻豆| 亚洲精品一卡2卡3卡四卡乱码在线 | 一二三四社区在线视频社区麻豆| 久久亚洲日韩看片无码精品| 中文字幕一区二区三区麻豆木下凛| 日韩精品一区二区三区不卡人妻视频中文字幕 | 狠狠色丁香婷婷久久综合3333视频 | 人人超碰欧美精品凸凹| 91慰在线一区二区| 久久综合给合精欧精品欧| 中文字幕人成无码人妻欧美日韩二区 | 一区二区三区视频在线播放视频国语高清观看| 手机看片福利久久大香蕉大香蕉 | 麻豆传媒新花絮预告| 中文字幕日韩一区二区三区不卡JUQ-695 | 2021精品自拍大片1998精品自拍大片 | 中文字幕日韩一区二区不卡,久青草国 | 一本色道久久综合狠狠躁篇怎么玩 | 日韩蜜芽精品视频在线观看网站| 2021国产麻豆剧果冻传媒网| 久久精品久久精品久久精品j| 亚洲欧美XXⅩXX喷水| 不卡中文字幕在线观看的av软件| 免费人妻精品一区二区三区小宝探花|